Difference between revisions of "Osteosarcoma"

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!colspan="2" align="center" style="color:white; font-size:125%; background-color:#08519c"|'''Section editor'''
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[[#top|Back to Top]]
|style="background-color:#F0F0F0"|[[File:Elizabethdavis2.jpg|frameless|upright=0.3|center]]
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|<big>[[User:Elizabethdavis|Elizabeth J. Davis, MD]]<br>Vanderbilt University<br>Nashville, TN</big><br>[[File:Social-twitter-icon.png|frameless|upright=0.1]] [https://twitter.com/ejdavis25 ejdavis25]
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{{#lst:Editorial board transclusions|sarcoma}}
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''Are you looking for a regimen but can't find it here? It is possible that we've moved it to the [[Osteosarcoma_-_historical|historical regimens page]]. For placebo or observational studies in this condition, please visit [[Osteosarcoma - null regimens|this page]]. If you still can't find it, please let us know so we can add it!''
 
''Are you looking for a regimen but can't find it here? It is possible that we've moved it to the [[Osteosarcoma_-_historical|historical regimens page]]. For placebo or observational studies in this condition, please visit [[Osteosarcoma - null regimens|this page]]. If you still can't find it, please let us know so we can add it!''
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*'''[[Osteosarcoma, pediatric|Pediatric osteosarcoma]] regimens can be found here.'''</big>
 
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=Guidelines=
 
=Guidelines=
==[http://www.esmo.org/ ESMO]==
+
'''Given the rapid change in evidence in many areas of hematology/oncology, readers are encouraged to consider any guideline published 5+ years ago to be for historical purposes, only.'''
*'''2014:''' [http://annonc.oxfordjournals.org/content/25/suppl_3/iii113.full.pdf+html Bone sarcomas: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up.] [https://pubmed.ncbi.nlm.nih.gov/25210081 PubMed]
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==[https://www.esmo.org/ ESMO]==
==ESMO/PaedCan/EURACAN==
+
*'''2009:''' Bielack et al. [https://doi.org/10.1093/annonc/mdp154 Osteosarcoma: ESMO clinical recommendations for diagnosis, treatment and follow-up] [https://pubmed.ncbi.nlm.nih.gov/19454435/ PubMed]
*'''2018:''' Casali et al. [https://www.esmo.org/Guidelines/Sarcoma-and-GIST/Bone-Sarcomas Bone sarcomas: ESMO–PaedCan–EURACAN Clinical Practice Guidelines for diagnosis, treatment and follow-up]
+
**'''2008:''' Bielack et al. [https://doi.org/10.1093/annonc/mdn102 Osteosarcoma: ESMO clinical recommendations for diagnosis, treatment and follow-up] [https://pubmed.ncbi.nlm.nih.gov/18456784/ PubMed]
==[https://www.nccn.org/ NCCN]==
+
**'''2003:''' Saeter. [https://doi.org/10.1093/annonc/mdg336 ESMO Minimum Clinical Recommendations for diagnosis, treatment and follow-up of osteosarcoma] [https://pubmed.ncbi.nlm.nih.gov/12881369/ PubMed]
*[https://www.nccn.org/professionals/physician_gls/pdf/bone.pdf NCCN Guidelines - Bone Cancer]
 
 
 
 
 
=Karan=
 
 
 
=COG AOST0331 MAP Group=
 
==Induction==
 
Received by all patients and consists of 2 cycles of MAP.
 
===Chemotherapy===
 
*[[Cisplatin (Platinol)]] 60 mg/m<sup>2</sup> IV infusion over 4 hours, started on day 1 of weeks 1 and 6
 
*[[Doxorubicin (Adriamycin)]] 37.5 mg/m<sup>2</sup>/day (total dose is 75 mg/m<sup>2</sup> given as a 48 hour infusion) on days 1 to 2 of Weeks 1 and 6
 
*[[Methotrexate (MTX)]] 12 g/m<sup>2</sup> (MAX DOSE = 20 grams) IV over 4 hours once on day 1 of weeks 4, 5, 9, and 10.
 
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> PO or IV every 6 hours beginning 24 hours after the beginning of the [[Methotrexate (MTX)]] infusion and continuing until the serum [[Methotrexate (MTX)]] level is less than 0.1 μM.
 
 
 
'''10 Week Course'''
 
 
 
===References===
 
#'''COG AOST0331:''' Marina NM, Smeland S, Bielack SS, Bernstein M, Jovic G, Krailo MD, Hook JM, Arndt C, Berg H, Brennan B, Brichard B, Brown KLB, Butterfass-Bahloul T, Calaminus G, Daldrup-Link HE, Eriksson M, Gebhardt MC, Gelderblom H, Gerss J, Goldsby R,  Goorin A, Gorlick R, Grier H, Hale JP, Hall KS, Hardes J, Hawkins DS, Helmke K, Hogendoorn PCW, Isakoff MS, JAneway KA, Jurgens H, Kager L, Kuhne T, Lau CC, Leavey PJ, Lessnick SL, Mascarenhas L, Meyers PA, Mottl H, Nathrath M, Papai Z, Randall RL, Reichardt P, Renard M, Safwat AA, Schwartz CL, Stevens MCG, Strauss SJ, Teot L, Werner M, Sydes MR, Whelan JS. Comparison of MAPIE versus MAP in patients with a poor response to preoperative chemotherapy for newly diagnosed high-grade osteosarcoma (EURAMOS-1): an open-label, international randomized controlled trial. J Clin Oncol. 2020 Feb 20;38(6):602-612. Epub 2019 Dec 11. [https://doi.org/10.1016/s1470-2045(16)30214-5 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052459/ link to PMC article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/27569442/ PubMed] NCT00134030
 
 
 
==MAP Cycles 3-4==
 
Good Responders and Poor Responders
 
 
 
===Chemotherapy===
 
*[[Cisplatin (Platinol)]] 60 mg/m<sup>2</sup> IV infusion over 4 hours, started on day 1 of weeks 12 and 17
 
*[[Doxorubicin (Adriamycin)]] 37.5 mg/m<sup>2</sup>/day (total dose is 75 mg/m<sup>2</sup> given as a 48 hour infusion) on days 1 to 2 of Weeks 12 and 17.
 
*[[Methotrexate (MTX)]] 12 g/m<sup>2</sup> (MAX DOSE = 20 grams) IV over 4 hours once on day 1 of weeks 15, 16, 20, and 21.
 
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> PO or IV every 6 hours beginning 24 hours after the beginning of the [[Methotrexate (MTX)]] infusion and continuing until the serum [[Methotrexate (MTX)]] level is less than 0.1 μM.
 
 
 
'''10 Week Course'''
 
 
 
===References===
 
#'''COG AOST0331:''' Marina NM, Smeland S, Bielack SS, Bernstein M, Jovic G, Krailo MD, Hook JM, Arndt C, Berg H, Brennan B, Brichard B, Brown KLB, Butterfass-Bahloul T, Calaminus G, Daldrup-Link HE, Eriksson M, Gebhardt MC, Gelderblom H, Gerss J, Goldsby R,  Goorin A, Gorlick R, Grier H, Hale JP, Hall KS, Hardes J, Hawkins DS, Helmke K, Hogendoorn PCW, Isakoff MS, JAneway KA, Jurgens H, Kager L, Kuhne T, Lau CC, Leavey PJ, Lessnick SL, Mascarenhas L, Meyers PA, Mottl H, Nathrath M, Papai Z, Randall RL, Reichardt P, Renard M, Safwat AA, Schwartz CL, Stevens MCG, Strauss SJ, Teot L, Werner M, Sydes MR, Whelan JS. Comparison of MAPIE versus MAP in patients with a poor response to preoperative chemotherapy for newly diagnosed high-grade osteosarcoma (EURAMOS-1): an open-label, international randomized controlled trial. J Clin Oncol. 2020 Feb 20;38(6):602-612. Epub 2019 Dec 11. [https://doi.org/10.1016/s1470-2045(16)30214-5 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052459/ link to PMC article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/27569442/ PubMed] NCT00134030
 
 
 
==MAP Cycles 5-6==
 
Good Responders and Poor Responders
 
 
 
===Chemotherapy===
 
*[[Doxorubicin (Adriamycin)]] 37.5 mg/m<sup>2</sup>/day (total dose is 75 mg/m<sup>2</sup> given as a 48 hour infusion) on days 1 to 2 of Weeks 22 and 26.
 
*[[Methotrexate (MTX)]] 12 g/m<sup>2</sup> (MAX DOSE = 20 grams) IV over 4 hours once on day 1 of weeks 24, 25, 28, and 29.
 
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> PO or IV every 6 hours beginning 24 hours after the beginning of the [[Methotrexate (MTX)]] infusion and continuing until the serum [[Methotrexate (MTX)]] level is less than 0.1 μM.
 
 
 
'''10 Week Course'''
 
 
 
===References===
 
#'''COG AOST0331:''' Marina NM, Smeland S, Bielack SS, Bernstein M, Jovic G, Krailo MD, Hook JM, Arndt C, Berg H, Brennan B, Brichard B, Brown KLB, Butterfass-Bahloul T, Calaminus G, Daldrup-Link HE, Eriksson M, Gebhardt MC, Gelderblom H, Gerss J, Goldsby R,  Goorin A, Gorlick R, Grier H, Hale JP, Hall KS, Hardes J, Hawkins DS, Helmke K, Hogendoorn PCW, Isakoff MS, JAneway KA, Jurgens H, Kager L, Kuhne T, Lau CC, Leavey PJ, Lessnick SL, Mascarenhas L, Meyers PA, Mottl H, Nathrath M, Papai Z, Randall RL, Reichardt P, Renard M, Safwat AA, Schwartz CL, Stevens MCG, Strauss SJ, Teot L, Werner M, Sydes MR, Whelan JS. Comparison of MAPIE versus MAP in patients with a poor response to preoperative chemotherapy for newly diagnosed high-grade osteosarcoma (EURAMOS-1): an open-label, international randomized controlled trial. J Clin Oncol. 2020 Feb 20;38(6):602-612. Epub 2019 Dec 11. [https://doi.org/10.1016/s1470-2045(16)30214-5 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052459/ link to PMC article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/27569442/ PubMed] NCT00134030
 
 
 
=COG AOST0331 MAPifn Group=
 
==Induction==
 
Received by all patients and consists of 2 cycles of MAP.
 
===Chemotherapy===
 
*[[Cisplatin (Platinol)]] 60 mg/m<sup>2</sup> IV infusion over 4 hours, started on day 1 of weeks 1 and 6
 
*[[Doxorubicin (Adriamycin)]] 37.5 mg/m<sup>2</sup>/day (total dose is 75 mg/m<sup>2</sup> given as a 48 hour infusion) on days 1 to 2 of Weeks 1 and 6
 
*[[Methotrexate (MTX)]] 12 g/m<sup>2</sup> (MAX DOSE = 20 grams) IV over 4 hours once on day 1 of weeks 4, 5, 9, and 10.
 
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> PO or IV every 6 hours beginning 24 hours after the beginning of the [[Methotrexate (MTX)]] infusion and continuing until the serum [[Methotrexate (MTX)]] level is less than 0.1 μM.
 
 
 
'''10 Week Course'''
 
 
 
===References===
 
#'''COG AOST0331:''' Marina NM, Smeland S, Bielack SS, Bernstein M, Jovic G, Krailo MD, Hook JM, Arndt C, Berg H, Brennan B, Brichard B, Brown KLB, Butterfass-Bahloul T, Calaminus G, Daldrup-Link HE, Eriksson M, Gebhardt MC, Gelderblom H, Gerss J, Goldsby R,  Goorin A, Gorlick R, Grier H, Hale JP, Hall KS, Hardes J, Hawkins DS, Helmke K, Hogendoorn PCW, Isakoff MS, JAneway KA, Jurgens H, Kager L, Kuhne T, Lau CC, Leavey PJ, Lessnick SL, Mascarenhas L, Meyers PA, Mottl H, Nathrath M, Papai Z, Randall RL, Reichardt P, Renard M, Safwat AA, Schwartz CL, Stevens MCG, Strauss SJ, Teot L, Werner M, Sydes MR, Whelan JS. Comparison of MAPIE versus MAP in patients with a poor response to preoperative chemotherapy for newly diagnosed high-grade osteosarcoma (EURAMOS-1): an open-label, international randomized controlled trial. J Clin Oncol. 2020 Feb 20;38(6):602-612. Epub 2019 Dec 11. [https://doi.org/10.1016/s1470-2045(16)30214-5 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052459/ link to PMC article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/27569442/ PubMed] NCT00134030
 
 
 
==MAPifn Cycles 3-4==
 
Good Responders
 
 
 
===Chemotherapy===
 
*[[Cisplatin (Platinol)]] 60 mg/m<sup>2</sup> IV infusion over 4 hours, started on day 1 of weeks 12 and 17
 
*[[Doxorubicin (Adriamycin)]] 37.5 mg/m<sup>2</sup>/day (total dose is 75 mg/m<sup>2</sup> given as a 48 hour infusion) on days 1 to 2 of Weeks 12 and 17.
 
*[[Methotrexate (MTX)]] 12 g/m<sup>2</sup> (MAX DOSE = 20 grams) IV over 4 hours once on day 1 of weeks 15, 16, 20, and 21.
 
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> PO or IV every 6 hours beginning 24 hours after the beginning of the [[Methotrexate (MTX)]] infusion and continuing until the serum [[Methotrexate (MTX)]] level is less than 0.1 μM.
 
 
 
'''10 Week Course'''
 
 
 
===References===
 
#'''COG AOST0331:''' Marina NM, Smeland S, Bielack SS, Bernstein M, Jovic G, Krailo MD, Hook JM, Arndt C, Berg H, Brennan B, Brichard B, Brown KLB, Butterfass-Bahloul T, Calaminus G, Daldrup-Link HE, Eriksson M, Gebhardt MC, Gelderblom H, Gerss J, Goldsby R,  Goorin A, Gorlick R, Grier H, Hale JP, Hall KS, Hardes J, Hawkins DS, Helmke K, Hogendoorn PCW, Isakoff MS, JAneway KA, Jurgens H, Kager L, Kuhne T, Lau CC, Leavey PJ, Lessnick SL, Mascarenhas L, Meyers PA, Mottl H, Nathrath M, Papai Z, Randall RL, Reichardt P, Renard M, Safwat AA, Schwartz CL, Stevens MCG, Strauss SJ, Teot L, Werner M, Sydes MR, Whelan JS. Comparison of MAPIE versus MAP in patients with a poor response to preoperative chemotherapy for newly diagnosed high-grade osteosarcoma (EURAMOS-1): an open-label, international randomized controlled trial. J Clin Oncol. 2020 Feb 20;38(6):602-612. Epub 2019 Dec 11. [https://doi.org/10.1016/s1470-2045(16)30214-5 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052459/ link to PMC article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/27569442/ PubMed] NCT00134030
 
 
 
==MAPifn Cycles 5-6==
 
Good Responders
 
 
 
===Chemotherapy===
 
*[[Doxorubicin (Adriamycin)]] 37.5 mg/m<sup>2</sup>/day (total dose is 75 mg/m<sup>2</sup> given as a 48 hour infusion) on days 1 to 2 of Weeks 22 and 26.
 
*[[Methotrexate (MTX)]] 12 g/m<sup>2</sup> (MAX DOSE = 20 grams) IV over 4 hours once on day 1 of weeks 24, 25, 28, and 29.
 
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> PO or IV every 6 hours beginning 24 hours after the beginning of the [[Methotrexate (MTX)]] infusion and continuing until the serum [[Methotrexate (MTX)]] level is less than 0.1 μM.
 
 
 
'''10 Week Course'''
 
 
 
===References===
 
#'''COG AOST0331:''' Marina NM, Smeland S, Bielack SS, Bernstein M, Jovic G, Krailo MD, Hook JM, Arndt C, Berg H, Brennan B, Brichard B, Brown KLB, Butterfass-Bahloul T, Calaminus G, Daldrup-Link HE, Eriksson M, Gebhardt MC, Gelderblom H, Gerss J, Goldsby R,  Goorin A, Gorlick R, Grier H, Hale JP, Hall KS, Hardes J, Hawkins DS, Helmke K, Hogendoorn PCW, Isakoff MS, JAneway KA, Jurgens H, Kager L, Kuhne T, Lau CC, Leavey PJ, Lessnick SL, Mascarenhas L, Meyers PA, Mottl H, Nathrath M, Papai Z, Randall RL, Reichardt P, Renard M, Safwat AA, Schwartz CL, Stevens MCG, Strauss SJ, Teot L, Werner M, Sydes MR, Whelan JS. Comparison of MAPIE versus MAP in patients with a poor response to preoperative chemotherapy for newly diagnosed high-grade osteosarcoma (EURAMOS-1): an open-label, international randomized controlled trial. J Clin Oncol. 2020 Feb 20;38(6):602-612. Epub 2019 Dec 11. [https://doi.org/10.1016/s1470-2045(16)30214-5 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052459/ link to PMC article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/27569442/ PubMed] NCT00134030
 
 
 
==MAPifn Weeks 30-104==
 
Good Responders
 
===Chemotherapy===
 
*[[Peginterferon alfa-2b (PegIntron)]] 0.5 μg/kg/day (MAX DOSE = 50 μg) subcutaneously on day 1 of Weeks 30, 31, 32, and 33.
 
**If well tolerated during first 4 weeks of therapy, escalate dose.
 
*[[Peginterferon alfa-2b (PegIntron)]] 1 μg/kg/day (MAX DOSE = 100 μg) subcutaneously on day 1 of Weeks 34 through 104.
 
 
 
'''75 Week Course'''
 
 
 
===References===
 
#'''COG AOST0331:''' Marina NM, Smeland S, Bielack SS, Bernstein M, Jovic G, Krailo MD, Hook JM, Arndt C, Berg H, Brennan B, Brichard B, Brown KLB, Butterfass-Bahloul T, Calaminus G, Daldrup-Link HE, Eriksson M, Gebhardt MC, Gelderblom H, Gerss J, Goldsby R,  Goorin A, Gorlick R, Grier H, Hale JP, Hall KS, Hardes J, Hawkins DS, Helmke K, Hogendoorn PCW, Isakoff MS, JAneway KA, Jurgens H, Kager L, Kuhne T, Lau CC, Leavey PJ, Lessnick SL, Mascarenhas L, Meyers PA, Mottl H, Nathrath M, Papai Z, Randall RL, Reichardt P, Renard M, Safwat AA, Schwartz CL, Stevens MCG, Strauss SJ, Teot L, Werner M, Sydes MR, Whelan JS. Comparison of MAPIE versus MAP in patients with a poor response to preoperative chemotherapy for newly diagnosed high-grade osteosarcoma (EURAMOS-1): an open-label, international randomized controlled trial. J Clin Oncol. 2020 Feb 20;38(6):602-612. Epub 2019 Dec 11. [https://doi.org/10.1016/s1470-2045(16)30214-5 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052459/ link to PMC article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/27569442/ PubMed] NCT00134030
 
 
 
=COG AOST0331 MAPIE Group=
 
==Induction==
 
Received by all patients and consists of 2 cycles of MAP.
 
===Chemotherapy===
 
*[[Cisplatin (Platinol)]] 60 mg/m<sup>2</sup> IV infusion over 4 hours, started on day 1 of weeks 1 and 6
 
*[[Doxorubicin (Adriamycin)]] 37.5 mg/m<sup>2</sup>/day (total dose is 75 mg/m<sup>2</sup> given as a 48 hour infusion) on days 1 to 2 of Weeks 1 and 6
 
*[[Methotrexate (MTX)]] 12 g/m<sup>2</sup> (MAX DOSE = 20 grams) IV over 4 hours once on day 1 of weeks 4, 5, 9, and 10.
 
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> PO or IV every 6 hours beginning 24 hours after the beginning of the [[Methotrexate (MTX)]] infusion and continuing until the serum [[Methotrexate (MTX)]] level is less than 0.1 μM.
 
 
 
'''10 Week Course'''
 
 
 
===References===
 
#'''COG AOST0331:''' Marina NM, Smeland S, Bielack SS, Bernstein M, Jovic G, Krailo MD, Hook JM, Arndt C, Berg H, Brennan B, Brichard B, Brown KLB, Butterfass-Bahloul T, Calaminus G, Daldrup-Link HE, Eriksson M, Gebhardt MC, Gelderblom H, Gerss J, Goldsby R,  Goorin A, Gorlick R, Grier H, Hale JP, Hall KS, Hardes J, Hawkins DS, Helmke K, Hogendoorn PCW, Isakoff MS, JAneway KA, Jurgens H, Kager L, Kuhne T, Lau CC, Leavey PJ, Lessnick SL, Mascarenhas L, Meyers PA, Mottl H, Nathrath M, Papai Z, Randall RL, Reichardt P, Renard M, Safwat AA, Schwartz CL, Stevens MCG, Strauss SJ, Teot L, Werner M, Sydes MR, Whelan JS. Comparison of MAPIE versus MAP in patients with a poor response to preoperative chemotherapy for newly diagnosed high-grade osteosarcoma (EURAMOS-1): an open-label, international randomized controlled trial. J Clin Oncol. 2020 Feb 20;38(6):602-612. Epub 2019 Dec 11. [https://doi.org/10.1016/s1470-2045(16)30214-5 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052459/ link to PMC article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/27569442/ PubMed] NCT00134030
 
 
 
==MAPIE Cycles 3 and 7==
 
Poor Responders
 
 
 
===Chemotherapy===
 
*[[Cisplatin (Platinol)]] 60 mg/m<sup>2</sup> IV infusion over 4 hours, started on day 1 of weeks 12 and 28
 
*[[Doxorubicin (Adriamycin)]] 37.5 mg/m<sup>2</sup>/day (total dose is 75 mg/m<sup>2</sup> given as a 48 hour infusion) on days 1 to 2 of Weeks 12 and 28.
 
*[[Methotrexate (MTX)]] 12 g/m<sup>2</sup> (MAX DOSE = 20 grams) IV over 4 hours once on day 1 of weeks 15 and 31.
 
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> PO or IV every 6 hours beginning 24 hours after the beginning of the [[Methotrexate (MTX)]] infusion and continuing until the serum [[Methotrexate (MTX)]] level is less than 0.1 μM.
 
 
 
'''5-Week Courses'''
 
 
 
===References===
 
#'''COG AOST0331:''' Marina NM, Smeland S, Bielack SS, Bernstein M, Jovic G, Krailo MD, Hook JM, Arndt C, Berg H, Brennan B, Brichard B, Brown KLB, Butterfass-Bahloul T, Calaminus G, Daldrup-Link HE, Eriksson M, Gebhardt MC, Gelderblom H, Gerss J, Goldsby R,  Goorin A, Gorlick R, Grier H, Hale JP, Hall KS, Hardes J, Hawkins DS, Helmke K, Hogendoorn PCW, Isakoff MS, JAneway KA, Jurgens H, Kager L, Kuhne T, Lau CC, Leavey PJ, Lessnick SL, Mascarenhas L, Meyers PA, Mottl H, Nathrath M, Papai Z, Randall RL, Reichardt P, Renard M, Safwat AA, Schwartz CL, Stevens MCG, Strauss SJ, Teot L, Werner M, Sydes MR, Whelan JS. Comparison of MAPIE versus MAP in patients with a poor response to preoperative chemotherapy for newly diagnosed high-grade osteosarcoma (EURAMOS-1): an open-label, international randomized controlled trial. J Clin Oncol. 2020 Feb 20;38(6):602-612. Epub 2019 Dec 11. [https://doi.org/10.1016/s1470-2045(16)30214-5 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052459/ link to PMC article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/27569442/ PubMed] NCT00134030
 
 
 
==MAP Cycles 4, 6, and 8==
 
Poor Responders
 
 
 
===Chemotherapy===
 
*[[Ifosfamide (Ifex)]] 2.8 g/m<sup>2</sup>/dose IV over 4 hours once per day on days 1 through 5 of weeks 16, 24, and 32.
 
*[[Etoposide (Vepesid)]] 100 mg/m<sup>2</sup>/dose IV over 60 minutes once per day on days 1 through 5 of weeks 16, 24, and 32.
 
*[[Mesna (Mesnex)]] 2.8 g/m<sup>2</sup>/24 hours IV continuous infusion over 24 hours on days 1 through 5 of weeks 16, 24, and 32.
 
*[[Methotrexate (MTX)]] 12 g/m<sup>2</sup> (MAX DOSE = 20 grams) IV over 4 hours once on day 1 of weeks 19, 27, and 35.
 
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> PO or IV every 6 hours beginning 24 hours after the beginning of the [[Methotrexate (MTX)]] infusion and continuing until the serum [[Methotrexate (MTX)]] level is less than 0.1 μM.
 
 
 
'''5-Week Courses'''
 
 
 
===References===
 
#'''COG AOST0331:''' Marina NM, Smeland S, Bielack SS, Bernstein M, Jovic G, Krailo MD, Hook JM, Arndt C, Berg H, Brennan B, Brichard B, Brown KLB, Butterfass-Bahloul T, Calaminus G, Daldrup-Link HE, Eriksson M, Gebhardt MC, Gelderblom H, Gerss J, Goldsby R,  Goorin A, Gorlick R, Grier H, Hale JP, Hall KS, Hardes J, Hawkins DS, Helmke K, Hogendoorn PCW, Isakoff MS, JAneway KA, Jurgens H, Kager L, Kuhne T, Lau CC, Leavey PJ, Lessnick SL, Mascarenhas L, Meyers PA, Mottl H, Nathrath M, Papai Z, Randall RL, Reichardt P, Renard M, Safwat AA, Schwartz CL, Stevens MCG, Strauss SJ, Teot L, Werner M, Sydes MR, Whelan JS. Comparison of MAPIE versus MAP in patients with a poor response to preoperative chemotherapy for newly diagnosed high-grade osteosarcoma (EURAMOS-1): an open-label, international randomized controlled trial. J Clin Oncol. 2020 Feb 20;38(6):602-612. Epub 2019 Dec 11. [https://doi.org/10.1016/s1470-2045(16)30214-5 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052459/ link to PMC article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/27569442/ PubMed] NCT00134030
 
 
 
==MAP Cycle 5==
 
Poor Responders
 
  
===Chemotherapy===
+
==NCCN==
*[[Doxorubicin (Adriamycin)]] 37.5 mg/m<sup>2</sup>/day (total dose is 75 mg/m<sup>2</sup> given as a 48 hour infusion) on days 1 to 2 of Week 20.
+
*''NCCN does not currently have guidelines at this granular level; please see [https://www.nccn.org/guidelines/guidelines-detail?category=1&id=1418 NCCN Guidelines - Bone Cancer].''
*[[Ifosfamide (Ifex)]] 3 g/m<sup>2</sup>/dose IV over 4 hours once per day on days 1, 2, and 3 of weeks 20.
 
*[[Mesna (Mesnex)]] 3 g/m<sup>2</sup>/24 hours IV continuous infusion over 24 hours on days 1, 2, and 3 of weeks 20.
 
*[[Methotrexate (MTX)]] 12 g/m<sup>2</sup> (MAX DOSE = 20 grams) IV over 4 hours once on day 1 of weeks 23.
 
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> PO or IV every 6 hours beginning 24 hours after the beginning of the [[Methotrexate (MTX)]] infusion and continuing until the serum [[Methotrexate (MTX)]] level is less than 0.1 μM.
 
 
 
'''5-Week Courses'''
 
 
 
===References===
 
#'''COG AOST0331:''' Marina NM, Smeland S, Bielack SS, Bernstein M, Jovic G, Krailo MD, Hook JM, Arndt C, Berg H, Brennan B, Brichard B, Brown KLB, Butterfass-Bahloul T, Calaminus G, Daldrup-Link HE, Eriksson M, Gebhardt MC, Gelderblom H, Gerss J, Goldsby R,  Goorin A, Gorlick R, Grier H, Hale JP, Hall KS, Hardes J, Hawkins DS, Helmke K, Hogendoorn PCW, Isakoff MS, JAneway KA, Jurgens H, Kager L, Kuhne T, Lau CC, Leavey PJ, Lessnick SL, Mascarenhas L, Meyers PA, Mottl H, Nathrath M, Papai Z, Randall RL, Reichardt P, Renard M, Safwat AA, Schwartz CL, Stevens MCG, Strauss SJ, Teot L, Werner M, Sydes MR, Whelan JS. Comparison of MAPIE versus MAP in patients with a poor response to preoperative chemotherapy for newly diagnosed high-grade osteosarcoma (EURAMOS-1): an open-label, international randomized controlled trial. J Clin Oncol. 2020 Feb 20;38(6):602-612. Epub 2019 Dec 11. [https://doi.org/10.1016/s1470-2045(16)30214-5 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052459/ link to PMC article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/27569442/ PubMed] NCT00134030
 
 
 
==MAP Cycle 9==
 
Poor Responders
 
 
 
===Chemotherapy===
 
*[[Doxorubicin (Adriamycin)]] 37.5 mg/m<sup>2</sup>/day (total dose is 75 mg/m<sup>2</sup> given as a 48 hour infusion) on days 1 to 2 of Week 36.
 
*[[Ifosfamide (Ifex)]] 3 g/m<sup>2</sup>/dose IV over 4 hours once per day on days 1, 2, and 3 of weeks 36.
 
*[[Mesna (Mesnex)]] 3 g/m<sup>2</sup>/24 hours IV continuous infusion over 24 hours on days 1, 2, and 3 of weeks 36.
 
*[[Methotrexate (MTX)]] 12 g/m<sup>2</sup> (MAX DOSE = 20 grams) IV over 4 hours once on day 1 of weeks 39 and 40.
 
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> PO or IV every 6 hours beginning 24 hours after the beginning of the [[Methotrexate (MTX)]] infusion and continuing until the serum [[Methotrexate (MTX)]] level is less than 0.1 μM.
 
 
 
'''5-Week Courses'''
 
 
 
===References===
 
#'''COG AOST0331:''' Marina NM, Smeland S, Bielack SS, Bernstein M, Jovic G, Krailo MD, Hook JM, Arndt C, Berg H, Brennan B, Brichard B, Brown KLB, Butterfass-Bahloul T, Calaminus G, Daldrup-Link HE, Eriksson M, Gebhardt MC, Gelderblom H, Gerss J, Goldsby R,  Goorin A, Gorlick R, Grier H, Hale JP, Hall KS, Hardes J, Hawkins DS, Helmke K, Hogendoorn PCW, Isakoff MS, JAneway KA, Jurgens H, Kager L, Kuhne T, Lau CC, Leavey PJ, Lessnick SL, Mascarenhas L, Meyers PA, Mottl H, Nathrath M, Papai Z, Randall RL, Reichardt P, Renard M, Safwat AA, Schwartz CL, Stevens MCG, Strauss SJ, Teot L, Werner M, Sydes MR, Whelan JS. Comparison of MAPIE versus MAP in patients with a poor response to preoperative chemotherapy for newly diagnosed high-grade osteosarcoma (EURAMOS-1): an open-label, international randomized controlled trial. J Clin Oncol. 2020 Feb 20;38(6):602-612. Epub 2019 Dec 11. [https://doi.org/10.1016/s1470-2045(16)30214-5 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052459/ link to PMC article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/27569442/ PubMed] NCT00134030
 
  
 
=Neoadjuvant therapy=
 
=Neoadjuvant therapy=
 
 
==Cisplatin & Doxorubicin {{#subobject:ae685c|Regimen=1}}==
 
==Cisplatin & Doxorubicin {{#subobject:ae685c|Regimen=1}}==
{| class="wikitable" style="float:right; margin-left: 5px;"
 
|-
 
|[[#top|back to top]]
 
|}
 
 
AP: '''<u>A</u>'''driamycin (Doxorubicin) & '''<u>P</u>'''latinol (Cisplatin)
 
AP: '''<u>A</u>'''driamycin (Doxorubicin) & '''<u>P</u>'''latinol (Cisplatin)
 +
<div class="toccolours" style="background-color:#eeeeee">
 
===Regimen variant #1 {{#subobject:248bc1|Variant=1}}===
 
===Regimen variant #1 {{#subobject:248bc1|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
!style="width: 20%"|Years of enrollment
+
!style="width: 20%"|Dates of enrollment
 
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|Comparator
 
!style="width: 20%"|Comparator
Line 210: Line 37:
 
|[https://doi.org/10.1200/jco.1992.10.10.1579 Bramwell et al. 1992]
 
|[https://doi.org/10.1200/jco.1992.10.10.1579 Bramwell et al. 1992]
 
|1983-1986
 
|1983-1986
|style="background-color:#1a9851"|Phase III (E-switch-ic)
+
|style="background-color:#1a9851"|Phase 3 (E-switch-ic)
 
|[[#MAP|MAP]]
 
|[[#MAP|MAP]]
 
|style="background-color:#91cf60"|Seems to have superior DFS
 
|style="background-color:#91cf60"|Seems to have superior DFS
 
|-
 
|-
|[https://www.thelancet.com/journals/lancet/article/PIIS0140-6736%2897%2902307-6/fulltext Souhami et al. 1997]
+
|[https://doi.org/10.1016/S0140-6736(97)02307-6 Souhami et al. 1997]
 
|1986-1991
 
|1986-1991
|style="background-color:#1a9851"|Phase III (E-de-esc)
+
|style="background-color:#1a9851"|Phase 3 (E-de-esc)
|Multi-drug T10 protocol
+
|[[#T10_protocol_888|Multi-drug T10 protocol]]
|style="background-color:#ffffbf"|Did not meet primary endpoints of PFS/OS
+
|style="background-color:#ffffbf"|Did not meet co-primary endpoints of PFS/OS
 
|-
 
|-
 
|}
 
|}
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
 
*[[Cisplatin (Platinol)]] 100 mg/m<sup>2</sup> IV continuous infusion over 24 hours, started on day 1
 
*[[Cisplatin (Platinol)]] 100 mg/m<sup>2</sup> IV continuous infusion over 24 hours, started on day 1
 
*[[Doxorubicin (Adriamycin)]] 25 mg/m<sup>2</sup> IV bolus once per day on days 1 to 3
 
*[[Doxorubicin (Adriamycin)]] 25 mg/m<sup>2</sup> IV bolus once per day on days 1 to 3
 
+
====Supportive therapy====
====Supportive medications====
+
*Prehydration: normal saline 400 mL/m<sup>2</sup> and D5W 400 mL/m<sup>2</sup> IV over 2 hours--the reference did not clarify if these two solutions are given at the same time
*Prehydration: normal saline 400 mL/m<sup>2</sup> and D5W 400 mL/m<sup>2</sup> over 2 hours--the reference did not clarify if these two solutions are given at the same time
 
 
*The volume of fluid for cisplatin continuous infusion is 2400 mL/m<sup>2</sup> NS, with KCl 80 mEq/L and mannitol 32,000 mg/m<sup>2</sup>
 
*The volume of fluid for cisplatin continuous infusion is 2400 mL/m<sup>2</sup> NS, with KCl 80 mEq/L and mannitol 32,000 mg/m<sup>2</sup>
 
*Posthydration: D5W 600 mL/m<sup>2</sup> over 6 hours, with KCl 20 mEq/L and mannitol 8000 mg/m<sup>2</sup>; and NS 600 mL/m<sup>2</sup> over 6 hours, with KCl 20 mEq/L, magnesium sulfate 2 mmol/L, and calcium gluconate 0.6 mmol/L--the reference did not clarify if these two solutions are given at the same time. Then D5W 600 mL/m<sup>2</sup> over 12 hours, with KCl 20 mEq/L and mannitol 8000 mg/m<sup>2</sup>.
 
*Posthydration: D5W 600 mL/m<sup>2</sup> over 6 hours, with KCl 20 mEq/L and mannitol 8000 mg/m<sup>2</sup>; and NS 600 mL/m<sup>2</sup> over 6 hours, with KCl 20 mEq/L, magnesium sulfate 2 mmol/L, and calcium gluconate 0.6 mmol/L--the reference did not clarify if these two solutions are given at the same time. Then D5W 600 mL/m<sup>2</sup> over 12 hours, with KCl 20 mEq/L and mannitol 8000 mg/m<sup>2</sup>.
 
*[[Furosemide (Lasix)]] 20 to 40 mg IV if urine output is less than 400 mL/m<sup>2</sup> over 6 hours
 
*[[Furosemide (Lasix)]] 20 to 40 mg IV if urine output is less than 400 mL/m<sup>2</sup> over 6 hours
 
 
'''21-day cycle for 3 cycles'''
 
'''21-day cycle for 3 cycles'''
 +
</div>
 +
<div class="toccolours" style="background-color:#cbd5e7">
 
====Subsequent treatment====
 
====Subsequent treatment====
*Definitive [[Surgery#Surgical_resection|surgery]] on week 9, then [[#Cisplatin_.26_Doxorubicin_2|adjuvant AP]] that starts 14 to 28 days after surgery
+
*Definitive [[Surgery#Surgical_resection|surgery]] on week 9, then adjuvant [[#Cisplatin_.26_Doxorubicin_2|AP]] that starts 14 to 28 days after surgery
 
+
</div></div><br>
 +
<div class="toccolours" style="background-color:#eeeeee">
 
===Regimen variant #2 {{#subobject:33e180|Variant=1}}===
 
===Regimen variant #2 {{#subobject:33e180|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
!style="width: 20%"|Years of enrollment
+
!style="width: 20%"|Dates of enrollment
 
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|Comparator
 
!style="width: 20%"|Comparator
Line 245: Line 74:
 
|[http://jnci.oxfordjournals.org/content/99/2/112.full Lewis et al. 2007 (EORTC 80931)]
 
|[http://jnci.oxfordjournals.org/content/99/2/112.full Lewis et al. 2007 (EORTC 80931)]
 
|1993-2002
 
|1993-2002
|style="background-color:#1a9851"|Phase III (C)
+
|style="background-color:#1a9851"|Phase 3 (C)
 
|[[#Cisplatin_.26_Doxorubicin|Cisplatin & Doxorubicin]]; dose-intense
 
|[[#Cisplatin_.26_Doxorubicin|Cisplatin & Doxorubicin]]; dose-intense
 
|style="background-color:#ffffbf"|Did not meet primary endpoint of OS
 
|style="background-color:#ffffbf"|Did not meet primary endpoint of OS
 
|-
 
|-
 
|}
 
|}
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
 
*[[Cisplatin (Platinol)]] 100 mg/m<sup>2</sup> IV continuous infusion over 24 hours, started on day 1
 
*[[Cisplatin (Platinol)]] 100 mg/m<sup>2</sup> IV continuous infusion over 24 hours, started on day 1
 
*[[Doxorubicin (Adriamycin)]] 25 mg/m<sup>2</sup> IV over 4 hours once per day on days 1 to 3
 
*[[Doxorubicin (Adriamycin)]] 25 mg/m<sup>2</sup> IV over 4 hours once per day on days 1 to 3
 
+
====Supportive therapy====
====Supportive medications====
 
 
*4 hours of prehydration prior to cisplatin
 
*4 hours of prehydration prior to cisplatin
 
*24 hours of posthydration & mannitol after cisplatin
 
*24 hours of posthydration & mannitol after cisplatin
 
*Recommended that fluid for cisplatin is isotonic saline with potassium chloride and mannitol
 
*Recommended that fluid for cisplatin is isotonic saline with potassium chloride and mannitol
 
 
'''21-day cycle for 2 cycles'''
 
'''21-day cycle for 2 cycles'''
 +
</div>
 +
<div class="toccolours" style="background-color:#cbd5e7">
 
====Subsequent treatment====
 
====Subsequent treatment====
*Definitive [[Surgery#Surgical_resection|surgery]] in a 14-day window between cycles 2 & 3, then [[#Cisplatin_.26_Doxorubicin_2|adjuvant AP]]
+
*Definitive [[Surgery#Surgical_resection|surgery]] in a 14-day window between cycles 2 & 3, then adjuvant [[#Cisplatin_.26_Doxorubicin_2|AP]]
 
+
</div></div>
 
===References===
 
===References===
# Bramwell VH, Burgers M, Sneath R, Souhami R, van Oosterom AT, Voûte PA, Rouesse J, Spooner D, Craft AW, Somers R, Pringle J, Malcolm AJ, van der Eiiken J, Thomas D, Uscinska B, Machin D, van Glabbeke M; European Osteosarcoma Intergroup. A comparison of two short intensive adjuvant chemotherapy regimens in operable osteosarcoma of limbs in children and young adults: the first study of the European Osteosarcoma Intergroup. J Clin Oncol. 1992 Oct;10(10):1579-91. [https://doi.org/10.1200/jco.1992.10.10.1579 link to original article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/1403038 PubMed]
+
# Bramwell VH, Burgers M, Sneath R, Souhami R, van Oosterom AT, Voûte PA, Rouesse J, Spooner D, Craft AW, Somers R, Pringle J, Malcolm AJ, van der Eiiken J, Thomas D, Uscinska B, Machin D, van Glabbeke M; European Osteosarcoma Intergroup. A comparison of two short intensive adjuvant chemotherapy regimens in operable osteosarcoma of limbs in children and young adults: the first study of the European Osteosarcoma Intergroup. J Clin Oncol. 1992 Oct;10(10):1579-91. [https://doi.org/10.1200/jco.1992.10.10.1579 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/1403038/ PubMed]
# Souhami RL, Craft AW, Van der Eijken JW, Nooij M, Spooner D, Bramwell VH, Wierzbicki R, Malcolm AJ, Kirkpatrick A, Uscinska BM, Van Glabbeke M, Machin D; European Osteosarcoma Intergroup. Randomised trial of two regimens of chemotherapy in operable osteosarcoma: a study of the European Osteosarcoma Intergroup. Lancet. 1997 Sep 27;350(9082):911-7. [https://www.thelancet.com/journals/lancet/article/PIIS0140-6736%2897%2902307-6/fulltext link to original article] [https://pubmed.ncbi.nlm.nih.gov/9314869 PubMed]
+
# Souhami RL, Craft AW, Van der Eijken JW, Nooij M, Spooner D, Bramwell VH, Wierzbicki R, Malcolm AJ, Kirkpatrick A, Uscinska BM, Van Glabbeke M, Machin D; European Osteosarcoma Intergroup. Randomised trial of two regimens of chemotherapy in operable osteosarcoma: a study of the European Osteosarcoma Intergroup. Lancet. 1997 Sep 27;350(9082):911-7. [https://doi.org/10.1016/S0140-6736(97)02307-6 link to original article] [https://pubmed.ncbi.nlm.nih.gov/9314869/ PubMed]
# '''EORTC 80931:''' Lewis IJ, Nooij MA, Whelan J, Sydes MR, Grimer R, Hogendoorn PC, Memon MA, Weeden S, Uscinska BM, van Glabbeke M, Kirkpatrick A, Hauben EI, Craft AW, Taminiau AH; MRC BO06 and EORTC 80931 collaborators; European Osteosarcoma Intergroup. Improvement in histologic response but not survival in osteosarcoma patients treated with intensified chemotherapy: a randomized phase III trial of the European Osteosarcoma Intergroup. J Natl Cancer Inst. 2007 Jan 17;99(2):112-28. [http://jnci.oxfordjournals.org/content/99/2/112.full link to original article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/17227995 PubMed] NCT00002539
+
# '''EORTC 80931:''' Lewis IJ, Nooij MA, Whelan J, Sydes MR, Grimer R, Hogendoorn PC, Memon MA, Weeden S, Uscinska BM, van Glabbeke M, Kirkpatrick A, Hauben EI, Craft AW, Taminiau AH; MRC BO06 and EORTC 80931 collaborators; European Osteosarcoma Intergroup. Improvement in histologic response but not survival in osteosarcoma patients treated with intensified chemotherapy: a randomized phase III trial of the European Osteosarcoma Intergroup. J Natl Cancer Inst. 2007 Jan 17;99(2):112-28. [http://jnci.oxfordjournals.org/content/99/2/112.full link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/17227995/ PubMed] [https://clinicaltrials.gov/study/NCT00002539 NCT00002539]
 
 
 
==Cisplatin, Epirubicin, Ifosfamide {{#subobject:57c6cd|Regimen=1}}==
 
==Cisplatin, Epirubicin, Ifosfamide {{#subobject:57c6cd|Regimen=1}}==
{| class="wikitable" style="float:right; margin-left: 5px;"
+
<div class="toccolours" style="background-color:#eeeeee">
|-
 
|[[#top|back to top]]
 
|}
 
 
===Regimen {{#subobject:f6b024|Variant=1}}===
 
===Regimen {{#subobject:f6b024|Variant=1}}===
 
{| class="wikitable" style="width: 40%; text-align:center;"  
 
{| class="wikitable" style="width: 40%; text-align:center;"  
Line 278: Line 104:
 
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|-
|[http://content.karger.com/produktedb/produkte.asp?DOI=10.1159/000113017 Basaran et al. 2007]
+
|[https://doi.org/10.1159/000113017 Basaran et al. 2007]
|style="background-color:#91cf61"|Phase II
+
|style="background-color:#91cf61"|Phase 2
 
|-
 
|-
 
|}
 
|}
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
 
*[[Cisplatin (Platinol)]] 100 mg/m<sup>2</sup> IV over 2 hours once on day 1
 
*[[Cisplatin (Platinol)]] 100 mg/m<sup>2</sup> IV over 2 hours once on day 1
 
*[[Epirubicin (Ellence)]] 90 mg/m<sup>2</sup> IV over 15 minutes once on day 1
 
*[[Epirubicin (Ellence)]] 90 mg/m<sup>2</sup> IV over 15 minutes once on day 1
*[[Ifosfamide (Ifex)]] 2000 mg/m<sup>2</sup> IV over 4 hours once per day on days 2 to 4, '''given with [[Mesna (Mesnex)]]'''
+
*[[Ifosfamide (Ifex)]] 2000 mg/m<sup>2</sup> IV over 4 hours once per day on days 2 to 4, '''given with mesna'''
 
+
====Supportive therapy====
====Supportive medications====
+
*[[Mesna (Mesnex)]] 2000 mg/m<sup>2</sup> IV over 4 hours once per day on days 2 to 4, '''given with ifosfamide'''
*[[Mesna (Mesnex)]] 2000 mg/m<sup>2</sup> IV over 4 hours once per day on days 2 to 4, '''given with [[Ifosfamide (Ifex)]]'''
+
*Pre- and post-[[:Category:Hydration|hydration]] with mannitol diuresis for cisplatin
*Prehydration and posthydration with mannitol diuresis for [[Cisplatin (Platinol)]]
 
 
 
 
'''21-day cycle for 3 cycles'''
 
'''21-day cycle for 3 cycles'''
 +
</div>
 +
<div class="toccolours" style="background-color:#cbd5e7">
 
====Subsequent treatment====
 
====Subsequent treatment====
*[[Surgery#Surgical_resection|Surgery]], then [[#Cisplatin.2C_Epirubicin.2C_Ifosfamide_2|adjuvant cisplatin, epirubicin, ifosfamide]]
+
*[[Surgery#Surgical_resection|Surgery]], then adjuvant [[#Cisplatin.2C_Epirubicin.2C_Ifosfamide_2|cisplatin, epirubicin, ifosfamide]]
 
+
</div></div>
 
===References===
 
===References===
# Basaran M, Bavbek ES, Saglam S, Eralp L, Sakar B, Atalar AC, Bilgic B, Ozger H, Onat H. A phase II study of cisplatin, ifosfamide and epirubicin combination chemotherapy in adults with nonmetastatic and extremity osteosarcomas. Oncology. 2007;72(3-4):255-60. Epub 2008 Jan 10. [http://content.karger.com/produktedb/produkte.asp?DOI=10.1159/000113017 link to original article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/18185020 PubMed]
+
# Basaran M, Bavbek ES, Saglam S, Eralp L, Sakar B, Atalar AC, Bilgic B, Ozger H, Onat H. A phase II study of cisplatin, ifosfamide and epirubicin combination chemotherapy in adults with nonmetastatic and extremity osteosarcomas. Oncology. 2007;72(3-4):255-60. Epub 2008 Jan 10. [https://doi.org/10.1159/000113017 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/18185020/ PubMed]
 
 
 
==MA {{#subobject:770fb2|Regimen=1}}==
 
==MA {{#subobject:770fb2|Regimen=1}}==
{| class="wikitable" style="float:right; margin-left: 5px;"
 
|-
 
|[[#top|back to top]]
 
|}
 
 
MA: High-dose '''<u>M</u>'''ethotrexate, '''<u>A</u>'''driamycin (Doxorubicin)
 
MA: High-dose '''<u>M</u>'''ethotrexate, '''<u>A</u>'''driamycin (Doxorubicin)
 
+
<div class="toccolours" style="background-color:#eeeeee">
 
===Regimen {{#subobject:216b6e|Variant=1}}===
 
===Regimen {{#subobject:216b6e|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
!style="width: 20%"|Years of enrollment
+
!style="width: 20%"|Dates of enrollment
 
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|Comparator
 
!style="width: 20%"|Comparator
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|[https://www.ejcancer.com/article/S0959-8049(06)01072-0/fulltext Le Deley et al. 2007 (SFOP OS94)]
+
|[https://doi.org/10.1016/j.ejca.2006.10.023 Le Deley et al. 2007 (SFOP OS94)]
 
|1994-2001
 
|1994-2001
|style="background-color:#1a9851"|Phase III (C)
+
|style="background-color:#1a9851"|Phase 3 (C)
 
|[[#M-EI|M-EI]]
 
|[[#M-EI|M-EI]]
 
|style="background-color:#fee08b"|Might have inferior EFS
 
|style="background-color:#fee08b"|Might have inferior EFS
 
|-
 
|-
 
|}
 
|}
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
 
*[[Methotrexate (MTX)]] as follows:
 
*[[Methotrexate (MTX)]] as follows:
 
**Cycles 1, 2, 3, 6, 7, 10, 11: 12,000 mg/m<sup>2</sup> IV over 4 hours once on day 1  
 
**Cycles 1, 2, 3, 6, 7, 10, 11: 12,000 mg/m<sup>2</sup> IV over 4 hours once on day 1  
**Given in D5W 1L with sodium bicarbonate 1 mEq/kg
+
***Given in D5W 1L with sodium bicarbonate 1 mEq/kg
 
*[[Doxorubicin (Adriamycin)]] as follows:
 
*[[Doxorubicin (Adriamycin)]] as follows:
 
**Cycles 4 & 8: 70 mg/m<sup>2</sup> IV over 6 hours once on day 1
 
**Cycles 4 & 8: 70 mg/m<sup>2</sup> IV over 6 hours once on day 1
 
+
====Supportive therapy====
====Supportive medications====
+
*[[Leucovorin (Folinic acid)]] 15 mg PO every 6 hours for up to 11 doses on weeks 1, 2, 3, 6, 7, 10, 11, starting 20 hours after the completion of methotrexate infusion
*[[Folinic acid (Leucovorin)]] 15 mg PO every 6 hours for up to 11 doses on weeks 1, 2, 3, 6, 7, 10, 11, starting 20 hours after the completion of [[Methotrexate (MTX)]] infusion
 
 
*For methotrexate: hydration & urine alkalinization by PO and IV routes to maintain 1.6 L/m<sup>2</sup> urine output over the first 24 hours and 2 L/m<sup>2</sup> on days 2 & 3, with urine pH greater than 7
 
*For methotrexate: hydration & urine alkalinization by PO and IV routes to maintain 1.6 L/m<sup>2</sup> urine output over the first 24 hours and 2 L/m<sup>2</sup> on days 2 & 3, with urine pH greater than 7
 
*Daily monitoring of methotrexate levels and creatinine
 
*Daily monitoring of methotrexate levels and creatinine
 
 
'''7-day cycle for 11 cycles'''
 
'''7-day cycle for 11 cycles'''
 +
</div>
 +
<div class="toccolours" style="background-color:#cbd5e7">
 
====Subsequent treatment====
 
====Subsequent treatment====
*[[Surgery#Surgical_resection|Surgery]] occurs during week 12, with risk-adapted treatment as follows:
+
*[[Surgery#Surgical_resection|Surgery]] occurs during week 12, with risk-adapted treatment by the following response-based criteria:
**Patients with good response: [[#MA|Adjuvant MA]]
+
**SFOP OS94, patients with good response: Adjuvant [[#MA|MA]]
**Patients with poor response: [[#IE|Adjuvant IE]]
+
**SFOP OS94, patients with poor response: Adjuvant [[#IE|IE]]
 
+
</div></div>
 
===References===
 
===References===
# '''SFOP OS94:''' Le Deley MC, Guinebretière JM, Gentet JC, Pacquement H, Pichon F, Marec-Bérard P, Entz-Werlé N, Schmitt C, Brugières L, Vanel D, Dupoüy N, Tabone MD, Kalifa C; Société Française d'Oncologie Pédiatrique (SFOP). SFOP OS94: a randomised trial comparing preoperative high-dose methotrexate plus doxorubicin to high-dose methotrexate plus etoposide and ifosfamide in osteosarcoma patients. Eur J Cancer. 2007 Mar;43(4):752-61. Epub 2007 Jan 30. [https://www.ejcancer.com/article/S0959-8049(06)01072-0/abstract link to original article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/17267204 PubMed] NCT00180908
+
# '''SFOP OS94:''' Le Deley MC, Guinebretière JM, Gentet JC, Pacquement H, Pichon F, Marec-Bérard P, Entz-Werlé N, Schmitt C, Brugières L, Vanel D, Dupoüy N, Tabone MD, Kalifa C; Société Française d'Oncologie Pédiatrique (SFOP). SFOP OS94: a randomised trial comparing preoperative high-dose methotrexate plus doxorubicin to high-dose methotrexate plus etoposide and ifosfamide in osteosarcoma patients. Eur J Cancer. 2007 Mar;43(4):752-61. Epub 2007 Jan 30. [https://doi.org/10.1016/j.ejca.2006.10.023 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/17267204/ PubMed] [https://clinicaltrials.gov/study/NCT00180908 NCT00180908]
 
 
 
==MAP {{#subobject:c479f6|Regimen=1}}==
 
==MAP {{#subobject:c479f6|Regimen=1}}==
{| class="wikitable" style="float:right; margin-left: 5px;"
 
|-
 
|[[#top|back to top]]
 
|}
 
 
MAP: High-dose '''<u>M</u>'''ethotrexate, '''<u>A</u>'''driamycin (Doxorubicin), '''<u>P</u>'''latinol (Cisplatin)
 
MAP: High-dose '''<u>M</u>'''ethotrexate, '''<u>A</u>'''driamycin (Doxorubicin), '''<u>P</u>'''latinol (Cisplatin)
 +
<div class="toccolours" style="background-color:#eeeeee">
 
===Regimen variant #1 {{#subobject:726dd7|Variant=1}}===
 
===Regimen variant #1 {{#subobject:726dd7|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
!style="width: 20%"|Years of enrollment
+
!style="width: 20%"|Dates of enrollment
 
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|Comparator
 
!style="width: 20%"|Comparator
Line 357: Line 176:
 
|[https://doi.org/10.1200/jco.1992.10.10.1579 Bramwell et al. 1992]
 
|[https://doi.org/10.1200/jco.1992.10.10.1579 Bramwell et al. 1992]
 
|1983-1986
 
|1983-1986
|style="background-color:#1a9851"|Phase III (E-esc)
+
|style="background-color:#1a9851"|Phase 3 (E-esc)
 
|[[#Cisplatin_.26_Doxorubicin|Cisplatin & Doxorubicin]]
 
|[[#Cisplatin_.26_Doxorubicin|Cisplatin & Doxorubicin]]
 
|style="background-color:#fc8d59"|Seems to have inferior DFS
 
|style="background-color:#fc8d59"|Seems to have inferior DFS
Line 363: Line 182:
 
|}
 
|}
 
''Note: The body of Bramwell et al. 1992 says that methotrexate is given over 4 hours, whereas Bramwell et al. 1992 figure 1's text says that methotrexate is given over 6 hours.''
 
''Note: The body of Bramwell et al. 1992 says that methotrexate is given over 4 hours, whereas Bramwell et al. 1992 figure 1's text says that methotrexate is given over 6 hours.''
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
 
*[[Methotrexate (MTX)]] 8000 mg/m<sup>2</sup> IV over 4 to 6 hours once on day 1
 
*[[Methotrexate (MTX)]] 8000 mg/m<sup>2</sup> IV over 4 to 6 hours once on day 1
 
*[[Doxorubicin (Adriamycin)]] 25 mg/m<sup>2</sup> IV bolus once per day on days 11 to 13
 
*[[Doxorubicin (Adriamycin)]] 25 mg/m<sup>2</sup> IV bolus once per day on days 11 to 13
 
*[[Cisplatin (Platinol)]] 100 mg/m<sup>2</sup> IV continuous infusion over 24 hours, started on day 11
 
*[[Cisplatin (Platinol)]] 100 mg/m<sup>2</sup> IV continuous infusion over 24 hours, started on day 11
 
+
====Supportive therapy====
====Supportive medications====
+
*[[Leucovorin (Folinic acid)]] 12 mg/m<sup>2</sup> IV every 6 hours x 10 doses or 15 mg/m<sup>2</sup> PO every 6 hours x 10 doses, starting 24 hours after the start of methotrexate infusion
*[[Folinic acid (Leucovorin)]] 12 mg/m<sup>2</sup> IV every 6 hours x 10 doses or 15 mg/m<sup>2</sup> PO every 6 hours x 10 doses, starting 24 hours after the start of [[Methotrexate (MTX)]] infusion
 
 
**Monitor methotrexate level at "24 hours and 48 hours"--it is unclear in the reference if this is time after the start/end of methotrexate, beginning of leucovorin, or something else
 
**Monitor methotrexate level at "24 hours and 48 hours"--it is unclear in the reference if this is time after the start/end of methotrexate, beginning of leucovorin, or something else
 
**Methotrexate levels higher than 100 nmol/L at 48 hours required additional leucovorin rescue
 
**Methotrexate levels higher than 100 nmol/L at 48 hours required additional leucovorin rescue
Line 376: Line 195:
 
*Posthydration for methotrexate: Alternating liters of D5W and NS 3000 mL/m<sup>2</sup> over 24 hours, with KCl 60 mEq/L.
 
*Posthydration for methotrexate: Alternating liters of D5W and NS 3000 mL/m<sup>2</sup> over 24 hours, with KCl 60 mEq/L.
 
*Sodium bicarbonate 3 g PO Q6H, starting 12 hours before methotrexate, and sodium bicarbonate 167 mmol/L IV until serum methotrexate level is less than 8000 to 10,000 nmol/L. Note: the reference is not clear about when/if PO sodium bicarbonate is stopped, when IV sodium bicarbonate is started, or the administration rate of IV sodium bicarbonate.
 
*Sodium bicarbonate 3 g PO Q6H, starting 12 hours before methotrexate, and sodium bicarbonate 167 mmol/L IV until serum methotrexate level is less than 8000 to 10,000 nmol/L. Note: the reference is not clear about when/if PO sodium bicarbonate is stopped, when IV sodium bicarbonate is started, or the administration rate of IV sodium bicarbonate.
*Prehydration for [[Cisplatin (Platinol)]]: normal saline 400 mL/m<sup>2</sup> and D5W 400 mL/m<sup>2</sup> over 2 hours--the reference did not clarify if these two solutions are given at the same time
+
*Prehydration for cisplatin: [[normal saline]] 400 mL/m<sup>2</sup> and D5W 400 mL/m<sup>2</sup> IV over 2 hours--the reference did not clarify if these two solutions are given at the same time
 
*The volume of fluid for cisplatin continuous infusion is 2400 mL/m<sup>2</sup> NS, with KCl 80 mEq/L and mannitol 32,000 mg/m<sup>2</sup>
 
*The volume of fluid for cisplatin continuous infusion is 2400 mL/m<sup>2</sup> NS, with KCl 80 mEq/L and mannitol 32,000 mg/m<sup>2</sup>
*Posthydration for [[Cisplatin (Platinol)]]: D5W 600 mL/m<sup>2</sup> over 6 hours, with KCl 20 mEq/L and mannitol 8000 mg/m<sup>2</sup>; and NS 600 mL/m<sup>2</sup> over 6 hours, with KCl 20 mEq/L, magnesium sulfate 2 mmol/L, and calcium gluconate 0.6 mmol/L--the reference did not clarify if these two solutions are given at the same time. Then D5W 600 mL/m<sup>2</sup> over 12 hours, with KCl 20 mEq/L and mannitol 8000 mg/m<sup>2</sup>.
+
*Posthydration for cisplatin: D5W 600 mL/m<sup>2</sup> over 6 hours, with KCl 20 mEq/L and mannitol 8000 mg/m<sup>2</sup>; and NS 600 mL/m<sup>2</sup> over 6 hours, with KCl 20 mEq/L, magnesium sulfate 2 mmol/L, and calcium gluconate 0.6 mmol/L--the reference did not clarify if these two solutions are given at the same time. Then D5W 600 mL/m<sup>2</sup> over 12 hours, with KCl 20 mEq/L and mannitol 8000 mg/m<sup>2</sup>.
*[[Furosemide (Lasix)]] 20 to 40 mg IV if urine output is less than 400 mL/m<sup>2</sup> over 6 hours during [[Cisplatin (Platinol)]]
+
*[[Furosemide (Lasix)]] 20 to 40 mg IV if urine output is less than 400 mL/m<sup>2</sup> over 6 hours during cisplatin
 
 
 
'''21-day cycle for 2 cycles'''
 
'''21-day cycle for 2 cycles'''
 +
</div>
 +
<div class="toccolours" style="background-color:#cbd5e7">
 
====Subsequent treatment====
 
====Subsequent treatment====
*Definitive [[Surgery#Surgical_resection|surgery]] on week 9, then [[#MAP_2|adjuvant MAP]] that starts 14 to 28 days after surgery
+
*Definitive [[Surgery#Surgical_resection|surgery]] on week 9, then adjuvant [[#MAP_2|MAP]] that starts 14 to 28 days after surgery
 
+
</div></div><br>
 +
<div class="toccolours" style="background-color:#eeeeee">
 
===Regimen variant #2 {{#subobject:9f5a4e|Variant=1}}===
 
===Regimen variant #2 {{#subobject:9f5a4e|Variant=1}}===
 
{| class="wikitable" style="width: 40%; text-align:center;"  
 
{| class="wikitable" style="width: 40%; text-align:center;"  
Line 390: Line 211:
 
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|-
|[https://onlinelibrary.wiley.com/doi/10.1002/1097-0142(19931201)72:11%3C3227::AID-CNCR2820721116%3E3.0.CO;2-C/abstract Bacci et al. 1993 (IOR/OS-2)]
+
|[https://doi.org/10.1002/1097-0142(19931201)72:11%3C3227::AID-CNCR2820721116%3E3.0.CO;2-C Bacci et al. 1993 (IOR/OS-2)]
|style="background-color:#91cf61"|Phase II
+
|style="background-color:#91cf61"|Phase 2
 
|-
 
|-
 
|}
 
|}
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
 
*[[Methotrexate (MTX)]] 8000 mg/m<sup>2</sup> IV over 6 hours once on day 1
 
*[[Methotrexate (MTX)]] 8000 mg/m<sup>2</sup> IV over 6 hours once on day 1
 
*[[Doxorubicin (Adriamycin)]] 60 mg/m<sup>2</sup> IV over 8 hours once on day 9, '''starting 48 hours after the start of cisplatin'''
 
*[[Doxorubicin (Adriamycin)]] 60 mg/m<sup>2</sup> IV over 8 hours once on day 9, '''starting 48 hours after the start of cisplatin'''
 
*[[Cisplatin (Platinol)]] 40 mg/m<sup>2</sup>/day IA continuous infusion over 72 hours, started on day 7 (total dose per cycle: 120 mg/m<sup>2</sup>)
 
*[[Cisplatin (Platinol)]] 40 mg/m<sup>2</sup>/day IA continuous infusion over 72 hours, started on day 7 (total dose per cycle: 120 mg/m<sup>2</sup>)
 
+
====Supportive therapy====
====Supportive medications====
+
*[[Leucovorin (Folinic acid)]] 15 mg IV every 6 hours x 11 doses on days 2 to 4, starting 24 hours after the start of methotrexate infusion
*[[Folinic acid (Leucovorin)]] 15 mg IV every 6 hours x 11 doses on days 2 to 4, starting 24 hours after the start of [[Methotrexate (MTX)]] infusion
+
*Hydration during and after methotrexate infusion
*Hydration during and after [[Methotrexate (MTX)]] infusion
 
 
 
 
'''27-day cycle for 2 cycles'''
 
'''27-day cycle for 2 cycles'''
 +
</div>
 +
<div class="toccolours" style="background-color:#cbd5e7">
 
====Subsequent treatment====
 
====Subsequent treatment====
 
*Definitive [[Surgery#Surgical_resection|surgery]], then risk-adapted therapy. Amputated patients restart chemotherapy 3 to 5 days after surgery; patients who undergo limb salvage or rotation plasty restart chemotherapy 10 to 21 days after surgery.
 
*Definitive [[Surgery#Surgical_resection|surgery]], then risk-adapted therapy. Amputated patients restart chemotherapy 3 to 5 days after surgery; patients who undergo limb salvage or rotation plasty restart chemotherapy 10 to 21 days after surgery.
**At least 90% tumor necrosis in the surgically removed specimen: [[#MAP_2|Adjuvant MAP]]
+
**IOR/OS-2, at least 90% tumor necrosis in the surgically removed specimen: Adjuvant [[#MAP_2|MAP]]
**Less than 90% tumor necrosis in the surgically removed specimen: [[#MAPIE|Adjuvant MAPIE]]
+
**IOR/OS-2, less than 90% tumor necrosis in the surgically removed specimen: Adjuvant [[#MAPIE|MAPIE]]
 
+
</div></div><br>
 +
<div class="toccolours" style="background-color:#eeeeee">
 
===Regimen variant #3 {{#subobject:727eb0|Variant=1}}===
 
===Regimen variant #3 {{#subobject:727eb0|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
!style="width: 20%"|Years of enrollment
+
!style="width: 20%"|Dates of enrollment
 
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|Comparator
 
!style="width: 20%"|Comparator
Line 419: Line 242:
 
|[https://doi.org/10.1200/jco.1988.6.2.329 Winkler et al. 1988 (COSS-82)]
 
|[https://doi.org/10.1200/jco.1988.6.2.329 Winkler et al. 1988 (COSS-82)]
 
|1982-1984
 
|1982-1984
|style="background-color:#1a9851"|Phase III (E-switch-ic)
+
|style="background-color:#1a9851"|Phase 3 (E-switch-ic)
 
|[[Osteosarcoma_-_historical#M-BCD|M-BCD]]
 
|[[Osteosarcoma_-_historical#M-BCD|M-BCD]]
 
|style="background-color:#1a9850"|Superior ORR
 
|style="background-color:#1a9850"|Superior ORR
Line 425: Line 248:
 
|}
 
|}
 
''Note: The exact schedule is unclear based on limited information in the reference, as schedule of doses is primarily extrapolated from Figure 1, which does not contain clear delineations in time. The dose/schedule of cisplatin reflects the protocol amendment that was done because of nephrotoxicity.''
 
''Note: The exact schedule is unclear based on limited information in the reference, as schedule of doses is primarily extrapolated from Figure 1, which does not contain clear delineations in time. The dose/schedule of cisplatin reflects the protocol amendment that was done because of nephrotoxicity.''
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
 
*[[Methotrexate (MTX)]] 12,000 mg/m<sup>2</sup> (maximum dose of 20,000 mg) IV over 4 hours once per day on days 22 & 29
 
*[[Methotrexate (MTX)]] 12,000 mg/m<sup>2</sup> (maximum dose of 20,000 mg) IV over 4 hours once per day on days 22 & 29
Line 430: Line 254:
 
*[[Doxorubicin (Adriamycin)]] 30 mg/m<sup>2</sup> IV bolus once per day on days 1 & 2
 
*[[Doxorubicin (Adriamycin)]] 30 mg/m<sup>2</sup> IV bolus once per day on days 1 & 2
 
*[[Cisplatin (Platinol)]] 90 mg/m<sup>2</sup> IV over 4 hours once on day 3
 
*[[Cisplatin (Platinol)]] 90 mg/m<sup>2</sup> IV over 4 hours once on day 3
 
+
====Supportive therapy====
====Supportive medications====
+
*[[Leucovorin (Folinic acid)]] 15 mg/m<sup>2</sup> PO every 6 hours x 12 hours once per day on days 23 & 30, starting 24 hours after the completion of methotrexate infusion; additional leucovorin used for delayed methotrexate elimination
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> PO every 6 hours x 12 hours once per day on days 23 & 30, starting 24 hours after the completion of [[Methotrexate (MTX)]] infusion; additional leucovorin used for delayed methotrexate elimination
+
*[[Sodium bicarbonate]] urine alkalinization prior to high-dose methotrexate
*Sodium bicarbonate urine alkalinization prior to high-dose [[Methotrexate (MTX)]]
+
*[[Normal saline|NS]] 4.5 L/m<sup>2</sup> on day 1 after methotrexate; NS 3 L/m<sup>2</sup> on day 2, with adjustments made to keep urine pH greater than 7.4
*NS 4.5 L/m<sup>2</sup> on day 1 after methotrexate; NS 3 L/m<sup>2</sup> on day 2, with adjustments made to keep urine pH greater than 7.4
+
*12 hours of [[:Category:Hydration|hydration]] prior to cisplatin & 20 hours of hydration after cisplatin; total amount of fluid given over 36hours of prehydration, cisplatin, and posthydration is NS 6 L/m<sup>2</sup> with mannitol 8 g/L and potassium 20 mval/L.
*12 hours of hydration prior to [[Cisplatin (Platinol)]] & 20 hours of hydration after [[Cisplatin (Platinol)]]; total amount of fluid given over 36hours of prehydration, cisplatin, and posthydration is NS 6 L/m<sup>2</sup> with mannitol 8 g/L and potassium 20 mval/L.
 
 
*Magnesium 180 mg/m<sup>2</sup> PO "per day throughout the whole chemotherapy time"--as described in COSS-80
 
*Magnesium 180 mg/m<sup>2</sup> PO "per day throughout the whole chemotherapy time"--as described in COSS-80
 
 
'''35-day cycle for 2 cycles'''
 
'''35-day cycle for 2 cycles'''
 +
</div>
 +
<div class="toccolours" style="background-color:#cbd5e7">
 
====Subsequent treatment====
 
====Subsequent treatment====
 
*[[Surgery#Surgical_resection|Surgery]], then risk-adapted treatment:
 
*[[Surgery#Surgical_resection|Surgery]], then risk-adapted treatment:
**Good response: [[#MAP_2|Adjuvant MAP]]
+
**COSS-82, good response: Adjuvant [[#MAP_2|MAP]]
**Poor response: [[Osteosarcoma_-_historical#IP-BCD|adjuvant IP-BCD]]
+
**COSS-82, poor response: Adjuvant [[Osteosarcoma_-_historical#IP-BCD|IP-BCD]]
 
+
</div></div><br>
===Protocol variant #4 {{#subobject:267572|Variant=1}}===
+
<div class="toccolours" style="background-color:#eeeeee">
 +
===Regimen variant #4 {{#subobject:267572|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
!style="width: 20%"|Years of enrollment
+
!style="width: 20%"|Dates of enrollment
 
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|Comparator
 
!style="width: 20%"|Comparator
Line 454: Line 279:
 
|[https://doi.org/10.1200/jco.1984.2.6.617 Winkler et al. 1984 (COSS-80)]
 
|[https://doi.org/10.1200/jco.1984.2.6.617 Winkler et al. 1984 (COSS-80)]
 
|1979-1982
 
|1979-1982
|style="background-color:#1a9851"|Phase III (E-switch-ic)
+
|style="background-color:#1a9851"|Phase 3 (E-switch-ic)
 
|[[#Osteosarcoma_-_historical#MA-BCD|MA-BCD]]
 
|[[#Osteosarcoma_-_historical#MA-BCD|MA-BCD]]
 
|style="background-color:#ffffbf"|Did not meet primary endpoint of CDF rate
 
|style="background-color:#ffffbf"|Did not meet primary endpoint of CDF rate
Line 460: Line 285:
 
|}
 
|}
 
''Note: The exact schedule is unclear based on limited/conflicting information in the reference. For example, Figure 1 appears to depict high-dose methotrexate starting 2 weeks after adriamycin, but the text says that methotrexate begins after a 3-week rest period. Additionally, the diagram in Figure 1 implies that the later therapies are given 4 times (once, then repeated x 3 cycles), but based on the cumulative doses listed, they are only given for a total of 3 cycles. The optional interferon arm is omitted given lack of benefit seen in the study.''
 
''Note: The exact schedule is unclear based on limited/conflicting information in the reference. For example, Figure 1 appears to depict high-dose methotrexate starting 2 weeks after adriamycin, but the text says that methotrexate begins after a 3-week rest period. Additionally, the diagram in Figure 1 implies that the later therapies are given 4 times (once, then repeated x 3 cycles), but based on the cumulative doses listed, they are only given for a total of 3 cycles. The optional interferon arm is omitted given lack of benefit seen in the study.''
====Chemotherapy, part 1====
+
<div class="toccolours" style="background-color:#b3e2cd">
*[[Doxorubicin (Adriamycin)]] 45 mg/m<sup>2</sup> IV bolus once per day on days 1 & 2
+
====Chemotherapy====
 
+
*[[Methotrexate (MTX)]] as follows:
'''21-day course, followed by:'''
+
**Cycle 1: 12,000 mg/m<sup>2</sup> (maximum dose of 20,000 mg) IV over 4 hours once per day on days 29 & 36
 
+
**Cycles 2 to 4: 12,000 mg/m<sup>2</sup> (maximum dose of 20,000 mg) IV over 4 hours once per day on days 1, 8, 29, 36
====Chemotherapy, part 2====
 
''See note above about uncertainty about the exact schedule.''
 
*[[Methotrexate (MTX)]] 12,000 mg/m<sup>2</sup> (maximum dose of 20,000 mg) IV over 4 hours once per day on days 1 & 8
 
 
**MTX is dissolved at a concentration of 20,000 mg/L in a solution containing 5% glucose
 
**MTX is dissolved at a concentration of 20,000 mg/L in a solution containing 5% glucose
*[[Cisplatin (Platinol)]] 120 mg/m<sup>2</sup> IV over 5 hours once on day 15
+
*[[Doxorubicin (Adriamycin)]] as follows:
 
+
**Cycles 1, 3, 4: 45 mg/m<sup>2</sup> IV bolus once per day on days 1 & 2
====Supportive medications====
+
**Cycle 2: 45 mg/m<sup>2</sup> IV bolus once per day on days 15 & 16 (delayed during cycle 2 until after surgery)
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> PO every 6 hours x 12 hours once per day on days 2 & 9, starting 24 hours after the completion of [[Methotrexate (MTX)]] infusion; additional leucovorin used for delayed methotrexate elimination
 
*Sodium bicarbonate urine alkalinization prior to high-dose [[Methotrexate (MTX)]]
 
*NS 4.5 L/m<sup>2</sup> on day 1 after [[Methotrexate (MTX)]]; NS 3 L/m<sup>2</sup> on day 2, with adjustments made to keep urine pH greater than 7.4
 
*3 hours of hydration prior to [[Cisplatin (Platinol)]] & 3 hours of hydration after [[Cisplatin (Platinol)]]; total amount of fluid given over 11 hours of prehydration, cisplatin, and posthydration is NS 2.5 L/m<sup>2</sup> with mannitol 8 g/L and potassium 20 mval/L.
 
*Magnesium 180 mg/m<sup>2</sup> PO "per day throughout the whole chemotherapy time" with [[Cisplatin (Platinol)]]
 
 
 
'''35-day course, followed by:'''
 
 
 
====Chemotherapy, part 3====
 
''See note above about uncertainty about the exact schedule.''
 
*[[Methotrexate (MTX)]] 12,000 mg/m<sup>2</sup> (maximum dose of 20,000 mg) IV over 4 hours once per day on days 1, 8, 29, 36
 
**MTX is dissolved at a concentration of 20,000 mg/L in a solution containing 5% glucose
 
*[[Doxorubicin (Adriamycin)]] 45 mg/m<sup>2</sup> IV bolus once per day on days 15 & 16 (delayed during cycle 1 until after surgery)
 
 
*[[Cisplatin (Platinol)]] 120 mg/m<sup>2</sup> IV over 5 hours once on day 43
 
*[[Cisplatin (Platinol)]] 120 mg/m<sup>2</sup> IV over 5 hours once on day 43
 
+
====Supportive therapy====
====Supportive medications====
+
*[[Leucovorin (Folinic acid)]] 15 mg/m<sup>2</sup> PO every 6 hours x 12 hours once per day on days 2, 9, 30, 37, starting 24 hours after the completion of methotrexate infusion; additional leucovorin used for delayed methotrexate elimination
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> PO every 6 hours x 12 hours once per day on days 2, 9, 30, 37, starting 24 hours after the completion of [[Methotrexate (MTX)]] infusion; additional leucovorin used for delayed methotrexate elimination
+
*[[Sodium bicarbonate]] urine alkalinization prior to high-dose methotrexate
*Sodium bicarbonate urine alkalinization prior to high-dose [[Methotrexate (MTX)]]
+
*[[Normal saline|NS]] 4.5 L/m<sup>2</sup> on day 1 after methotrexate; NS 3 L/m<sup>2</sup> on day 2, with adjustments made to keep urine pH greater than 7.4
*NS 4.5 L/m<sup>2</sup> on day 1 after [[Methotrexate (MTX)]]; NS 3 L/m<sup>2</sup> on day 2, with adjustments made to keep urine pH greater than 7.4
+
*3 hours of [[:Category:Hydration|hydration]] prior to cisplatin & 3 hours of [[:Category:Hydration|hydration]] after cisplatin; total amount of fluid given over 11 hours of prehydration, cisplatin, and posthydration is NS 2.5 L/m<sup>2</sup> with mannitol 8 g/L and potassium 20 mval/L.
*3 hours of hydration prior to [[Cisplatin (Platinol)]] & 3 hours of hydration after [[Cisplatin (Platinol)]]; total amount of fluid given over 11 hours of prehydration, cisplatin, and posthydration is NS 2.5 L/m<sup>2</sup> with mannitol 8 g/L and potassium 20 mval/L.
+
*Magnesium 180 mg/m<sup>2</sup> PO "per day throughout the whole chemotherapy time" with cisplatin
*Magnesium 180 mg/m<sup>2</sup> PO "per day throughout the whole chemotherapy time" with [[Cisplatin (Platinol)]]
+
'''8-week cycle for 4 cycles, with surgery done during cycle 2 before doxorubicin'''; surgery is done 9 to 18 weeks after the start of chemotherapy
 
+
</div></div>
'''8-week cycle for 3 cycles, with surgery done during cycle 1 before doxorubicin'''; surgery is done 9 to 18 weeks after the start of chemotherapy
 
  
 
===References===
 
===References===
# '''COSS-80:''' Winkler K, Beron G, Kotz R, Salzer-Kuntschik M, Beck J, Beck W, Brandeis W, Ebell W, Erttmann R, Göbel U, Havers W, Henze G, Hinderfeld L, Höcker P, Jobke A, Jürgens H, Kabisch H, Preusser P, Prindull G, Ramach W, Ritter J, Sekera J, Treuner J, Wist G, Landbeck G. Neoadjuvant chemotherapy for osteogenic sarcoma: results of a Cooperative German/Austrian study. J Clin Oncol. 1984 Jun;2(6):617-24. [https://doi.org/10.1200/jco.1984.2.6.617 link to original article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/6202851 PubMed]
+
# '''COSS-80:''' Winkler K, Beron G, Kotz R, Salzer-Kuntschik M, Beck J, Beck W, Brandeis W, Ebell W, Erttmann R, Göbel U, Havers W, Henze G, Hinderfeld L, Höcker P, Jobke A, Jürgens H, Kabisch H, Preusser P, Prindull G, Ramach W, Ritter J, Sekera J, Treuner J, Wist G, Landbeck G. Neoadjuvant chemotherapy for osteogenic sarcoma: results of a Cooperative German/Austrian study. J Clin Oncol. 1984 Jun;2(6):617-24. [https://doi.org/10.1200/jco.1984.2.6.617 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/6202851/ PubMed]
# '''COSS-82:''' Winkler K, Beron G, Delling G, Heise U, Kabisch H, Purfürst C, Berger J, Ritter J, Jürgens H, Gerein V, Graf N, Russe W, Gruemayer ER, Ertelt W, Kotz R, Preuzzer P, Prindull G, Brandeis W, Landbeck G. Neoadjuvant chemotherapy of osteosarcoma: results of a randomized cooperative trial (COSS-82) with salvage chemotherapy based on histological tumor response. J Clin Oncol. 1988 Feb;6(2):329-37. [https://doi.org/10.1200/jco.1988.6.2.329 link to original article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/2448428 PubMed]
+
# '''COSS-82:''' Winkler K, Beron G, Delling G, Heise U, Kabisch H, Purfürst C, Berger J, Ritter J, Jürgens H, Gerein V, Graf N, Russe W, Gruemayer ER, Ertelt W, Kotz R, Preuzzer P, Prindull G, Brandeis W, Landbeck G. Neoadjuvant chemotherapy of osteosarcoma: results of a randomized cooperative trial (COSS-82) with salvage chemotherapy based on histological tumor response. J Clin Oncol. 1988 Feb;6(2):329-37. [https://doi.org/10.1200/jco.1988.6.2.329 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/2448428/ PubMed]
# Bramwell VH, Burgers M, Sneath R, Souhami R, van Oosterom AT, Voûte PA, Rouesse J, Spooner D, Craft AW, Somers R, Pringle J, Malcolm AJ, van der Eiiken J, Thomas D, Uscinska B, Machin D, van Glabbeke M; European Osteosarcoma Intergroup. A comparison of two short intensive adjuvant chemotherapy regimens in operable osteosarcoma of limbs in children and young adults: the first study of the European Osteosarcoma Intergroup. J Clin Oncol. 1992 Oct;10(10):1579-91. [https://doi.org/10.1200/jco.1992.10.10.1579 link to original article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/1403038 PubMed] content property of [http://hemonc.org HemOnc.org]
+
# Bramwell VH, Burgers M, Sneath R, Souhami R, van Oosterom AT, Voûte PA, Rouesse J, Spooner D, Craft AW, Somers R, Pringle J, Malcolm AJ, van der Eiiken J, Thomas D, Uscinska B, Machin D, van Glabbeke M; European Osteosarcoma Intergroup. A comparison of two short intensive adjuvant chemotherapy regimens in operable osteosarcoma of limbs in children and young adults: the first study of the European Osteosarcoma Intergroup. J Clin Oncol. 1992 Oct;10(10):1579-91. [https://doi.org/10.1200/jco.1992.10.10.1579 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/1403038/ PubMed] content property of [https://hemonc.org HemOnc.org]
# '''IOR/OS-2:''' Bacci G, Picci P, Ferrari S, Ruggieri P, Casadei R, Tienghi A, Brach del Prever A, Gherlinzoni F, Mercuri M, Monti C. Primary chemotherapy and delayed surgery for nonmetastatic osteosarcoma of the extremities: results in 164 patients preoperatively treated with high doses of methotrexate followed by cisplatin and doxorubicin. Cancer. 1993 Dec 1;72(11):3227-38. [https://onlinelibrary.wiley.com/doi/10.1002/1097-0142(19931201)72:11%3C3227::AID-CNCR2820721116%3E3.0.CO;2-C/abstract link to original article] [https://pubmed.ncbi.nlm.nih.gov/8242546 PubMed]
+
# '''IOR/OS-2:''' Bacci G, Picci P, Ferrari S, Ruggieri P, Casadei R, Tienghi A, Brach del Prever A, Gherlinzoni F, Mercuri M, Monti C. Primary chemotherapy and delayed surgery for nonmetastatic osteosarcoma of the extremities: results in 164 patients preoperatively treated with high doses of methotrexate followed by cisplatin and doxorubicin. Cancer. 1993 Dec 1;72(11):3227-38. [https://doi.org/10.1002/1097-0142(19931201)72:11%3C3227::AID-CNCR2820721116%3E3.0.CO;2-C link to original article] [https://pubmed.ncbi.nlm.nih.gov/8242546/ PubMed]
## '''Update:''' Bacci G, Ferrari S, Bertoni F, Ruggieri P, Picci P, Longhi A, Casadei R, Fabbri N, Forni C, Versari M, Campanacci M. Long-term outcome for patients with nonmetastatic osteosarcoma of the extremity treated at the Istituto Ortopedico Rizzoli according to the Istituto Ortopedico Rizzoli/Osteosarcoma-2 protocol: an updated report. J Clin Oncol. 2000 Dec 15;18(24):4016-27. [https://doi.org/10.1200/jco.2000.18.24.4016 link to original article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/11118462 PubMed]
+
## '''Update:''' Bacci G, Ferrari S, Bertoni F, Ruggieri P, Picci P, Longhi A, Casadei R, Fabbri N, Forni C, Versari M, Campanacci M. Long-term outcome for patients with nonmetastatic osteosarcoma of the extremity treated at the Istituto Ortopedico Rizzoli according to the Istituto Ortopedico Rizzoli/Osteosarcoma-2 protocol: an updated report. J Clin Oncol. 2000 Dec 15;18(24):4016-27. [https://doi.org/10.1200/jco.2000.18.24.4016 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/11118462/ PubMed]
 
 
 
==MAPI {{#subobject:8fa44|Regimen=1}}==
 
==MAPI {{#subobject:8fa44|Regimen=1}}==
{| class="wikitable" style="float:right; margin-left: 5px;"
 
|-
 
|[[#top|back to top]]
 
|}
 
 
MAPI: High-dose '''<u>M</u>'''ethotrexate, '''<u>A</u>'''driamycin (Doxorubicin), '''<u>P</u>'''latinol (Cisplatin), '''<u>I</u>'''fosfamide
 
MAPI: High-dose '''<u>M</u>'''ethotrexate, '''<u>A</u>'''driamycin (Doxorubicin), '''<u>P</u>'''latinol (Cisplatin), '''<u>I</u>'''fosfamide
 +
<div class="toccolours" style="background-color:#eeeeee">
 
===Regimen {{#subobject:ad261e|Variant=1}}===
 
===Regimen {{#subobject:ad261e|Variant=1}}===
 
{| class="wikitable" style="width: 40%; text-align:center;"  
 
{| class="wikitable" style="width: 40%; text-align:center;"  
Line 515: Line 319:
 
|-
 
|-
 
|[https://doi.org/10.1093/annonc/mdg286 Bacci et al. 2003]
 
|[https://doi.org/10.1093/annonc/mdg286 Bacci et al. 2003]
|style="background-color:#91cf61"|Phase II
+
|style="background-color:#91cf61"|Phase 2
 
|-
 
|-
 
|}
 
|}
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
 
*[[Methotrexate (MTX)]] 12,000 mg/m<sup>2</sup> IV over 4 hours once on day 1
 
*[[Methotrexate (MTX)]] 12,000 mg/m<sup>2</sup> IV over 4 hours once on day 1
**If 4-hour methotrexate level is less than 10,000 nmol/L, the next cycle's dose is increased by 2000 mg/m<sup>2</sup>
 
 
*[[Cisplatin (Platinol)]] 60 mg/m<sup>2</sup>/day IV continuous infusion over 48 hours, started on day 8 (total dose per cycle: 120 mg/m<sup>2</sup>)
 
*[[Cisplatin (Platinol)]] 60 mg/m<sup>2</sup>/day IV continuous infusion over 48 hours, started on day 8 (total dose per cycle: 120 mg/m<sup>2</sup>)
 
*[[Doxorubicin (Adriamycin)]] 75 mg/m<sup>2</sup> IV continuous infusion over 24 hours, started on day 10
 
*[[Doxorubicin (Adriamycin)]] 75 mg/m<sup>2</sup> IV continuous infusion over 24 hours, started on day 10
*[[Ifosfamide (Ifex)]] 3000 mg/m<sup>2</sup>/day IV continuous infusion over 120 hours, started on day 29, '''given with [[Mesna (Mesnex)]]''' (total dose per cycle: 15,000 mg/m<sup>2</sup>)
+
*[[Ifosfamide (Ifex)]] 3000 mg/m<sup>2</sup>/day IV continuous infusion over 120 hours, started on day 29, '''given with mesna''' (total dose per cycle: 15,000 mg/m<sup>2</sup>)
 
+
====Supportive therapy====
====Supportive medications====
+
*[[Leucovorin (Folinic acid)]] 15 mg (route not specified) every 6 hours x 11 doses (note: the reference says "11 cycles," but it is assumed this is the intended meaning), starting day 2, 24 hours after the start of methotrexate
*[[Folinic acid (Leucovorin)]] 15 mg (route not specified) every 6 hours x 11 doses (note: the reference says "11 cycles," but it is assumed this is the intended meaning), starting day 2, 24 hours after the start of [[Methotrexate (MTX)]]
+
*Hydration during and after methotrexate as described by: Rosen G, Nirenberg A. Chemotherapy for osteogenic sarcoma: an investigative method, not a recipe. Cancer Treat Rep. 1982 Sep;66(9):1687-97. [https://pubmed.ncbi.nlm.nih.gov/6981454/ PubMed]
*Hydration during and after methotrexate as described by: Rosen G, Nirenberg A. Chemotherapy for osteogenic sarcoma: an investigative method, not a recipe. Cancer Treat Rep. 1982 Sep;66(9):1687-97. [https://pubmed.ncbi.nlm.nih.gov/6981454 PubMed]
+
*[[Mesna (Mesnex)]] 3000 mg/m<sup>2</sup>/day IV continuous infusion over 120 hours, started on day 29, '''given with ifosfamide''' (total dose: 15,000 mg/m<sup>2</sup>)
*[[Mesna (Mesnex)]] 3000 mg/m<sup>2</sup>/day IV continuous infusion over 120 hours, started on day 29, '''given with [[Ifosfamide (Ifex)]]''' (total dose: 15,000 mg/m<sup>2</sup>)
 
 
 
 
'''42-day cycle for 2 cycles'''
 
'''42-day cycle for 2 cycles'''
 +
</div>
 +
<div class="toccolours" style="background-color:#cbd5e7">
 
====Subsequent treatment====
 
====Subsequent treatment====
*[[Surgery#Surgical_resection|Surgery]], then [[#MAPI_2|adjuvant MAPI]]
+
*[[Surgery#Surgical_resection|Surgery]], then adjuvant [[#MAPI_2|MAPI]]
 
+
</div>
 +
<div class="toccolours" style="background-color:#fff2ae">
 +
====Dose and schedule modifications====
 +
*If 4-hour methotrexate level is less than 10,000 nmol/L, the next cycle's methotrexate dose is increased by 2000 mg/m<sup>2</sup>
 +
</div></div>
 
===References===
 
===References===
# Bacci G, Briccoli A, Rocca M, Ferrari S, Donati D, Longhi A, Bertoni F, Bacchini P, Giacomini S, Forni C, Manfrini M, Galletti S. Neoadjuvant chemotherapy for osteosarcoma of the extremities with metastases at presentation: recent experience at the Rizzoli Institute in 57 patients treated with cisplatin, doxorubicin, and a high dose of methotrexate and ifosfamide. Ann Oncol. 2003 Jul;14(7):1126-34. [https://doi.org/10.1093/annonc/mdg286 link to original article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/12853357 PubMed]
+
# Bacci G, Briccoli A, Rocca M, Ferrari S, Donati D, Longhi A, Bertoni F, Bacchini P, Giacomini S, Forni C, Manfrini M, Galletti S. Neoadjuvant chemotherapy for osteosarcoma of the extremities with metastases at presentation: recent experience at the Rizzoli Institute in 57 patients treated with cisplatin, doxorubicin, and a high dose of methotrexate and ifosfamide. Ann Oncol. 2003 Jul;14(7):1126-34. [https://doi.org/10.1093/annonc/mdg286 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/12853357/ PubMed]
 
 
 
==M-EI {{#subobject:ac6075|Regimen=1}}==
 
==M-EI {{#subobject:ac6075|Regimen=1}}==
{| class="wikitable" style="float:right; margin-left: 5px;"
 
|-
 
|[[#top|back to top]]
 
|}
 
 
M-EI: '''<u>M</u>'''ethotrexate, '''<u>E</u>'''toposide, '''<u>I</u>'''fosfamide
 
M-EI: '''<u>M</u>'''ethotrexate, '''<u>E</u>'''toposide, '''<u>I</u>'''fosfamide
 +
<div class="toccolours" style="background-color:#eeeeee">
 
===Regimen {{#subobject:9ed88a|Variant=1}}===
 
===Regimen {{#subobject:9ed88a|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
!style="width: 20%"|Years of enrollment
+
!style="width: 20%"|Dates of enrollment
 
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|Comparator
 
!style="width: 20%"|Comparator
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|[https://www.ejcancer.com/article/S0959-8049(06)01072-0/fulltext Le Deley et al. 2007 (SFOP OS94)]
+
|[https://doi.org/10.1016/j.ejca.2006.10.023 Le Deley et al. 2007 (SFOP OS94)]
 
|1994-2001
 
|1994-2001
|style="background-color:#1a9851"|Phase III (E-switch-ic)
+
|style="background-color:#1a9851"|Phase 3 (E-switch-ic)
 
|[[#MA|MA]]
 
|[[#MA|MA]]
 
|style="background-color:#d9ef8b"|Might have superior EFS
 
|style="background-color:#d9ef8b"|Might have superior EFS
 
|-
 
|-
|[https://www.thelancet.com/journals/lanonc/article/PIIS1470-2045(16)30096-1/fulltext Piperno-Neumann et al. 2016 (OS2006)]
+
|[https://doi.org/10.1016/S1470-2045(16)30096-1 Piperno-Neumann et al. 2016 (OS2006)]
 
|2007-2014
 
|2007-2014
|style="background-color:#1a9851"|Phase III (C)
+
|style="background-color:#1a9851"|Phase 3 (C)
|M-EI & Zoledronic acid
+
|[[#M-EI_.26_Zoledronic_acid_999|M-EI & Zoledronic acid]]
|style="background-color:#d9ef8b"|Might have superior EFS
+
|style="background-color:#d9ef8b"|Might have superior EFS<br>EFS36: 63.4% vs 57.1%<br>(HR 0.74, 95% CI 0.51-1.05)
 
|-
 
|-
 
|}
 
|}
 
''Note: this regimen information is from SFOP OS94.''
 
''Note: this regimen information is from SFOP OS94.''
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
 
*[[Methotrexate (MTX)]] as follows:
 
*[[Methotrexate (MTX)]] as follows:
 
**Cycles 1, 2, 3, 7, 8, 12, 13: 12,000 mg/m<sup>2</sup> IV over 4 hours once on day 1  
 
**Cycles 1, 2, 3, 7, 8, 12, 13: 12,000 mg/m<sup>2</sup> IV over 4 hours once on day 1  
**Given in D5W 1L with sodium bicarbonate 1 mEq/kg
+
***Given in D5W 1L with sodium bicarbonate 1 mEq/kg
 
*[[Etoposide (Vepesid)]] as follows:
 
*[[Etoposide (Vepesid)]] as follows:
 
**Cycles 4 & 9: 75 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1 to 4
 
**Cycles 4 & 9: 75 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1 to 4
**Given in NS 250 to 500 mL
+
***Given in NS 250 to 500 mL
 
*[[Ifosfamide (Ifex)]] as follows:
 
*[[Ifosfamide (Ifex)]] as follows:
**Cycles 4 & 9: 3000 mg/m<sup>2</sup> IV over 3 hours once per day on days 1 to 4, '''given with [[Mesna (Mesnex)]]'''
+
**Cycles 4 & 9: 3000 mg/m<sup>2</sup> IV over 3 hours once per day on days 1 to 4, '''given with mesna'''
**Given in NS 250 to 500 mL
+
***Given in NS 250 to 500 mL
 
+
====Supportive therapy====
====Supportive medications====
+
*[[Leucovorin (Folinic acid)]] 15 mg PO every 6 hours for up to 11 doses on weeks 1, 2, 3, 7, 8, 12, 13, starting 20 hours after the completion of methotrexate infusion
*[[Folinic acid (Leucovorin)]] 15 mg PO every 6 hours for up to 11 doses on weeks 1, 2, 3, 7, 8, 12, 13, starting 20 hours after the completion of methotrexate infusion
 
 
*For methotrexate: hydration & urine alkalinization by PO and IV routes to maintain 1.6 L/m<sup>2</sup> urine output over the first 24 hours and 2 L/m<sup>2</sup> on days 2 & 3, with urine pH greater than 7
 
*For methotrexate: hydration & urine alkalinization by PO and IV routes to maintain 1.6 L/m<sup>2</sup> urine output over the first 24 hours and 2 L/m<sup>2</sup> on days 2 & 3, with urine pH greater than 7
 
*Daily monitoring of methotrexate levels and creatinine
 
*Daily monitoring of methotrexate levels and creatinine
*[[Mesna (Mesnex)]] 3600 mg/m<sup>2</sup>/day IV continuous infusion over 96 hours, started on day 22 (week 4) and 57 (week 9), '''given with [[Ifosfamide (Ifex)]]''' (total dose: 14,400 mg/m<sup>2</sup>)
+
*[[Mesna (Mesnex)]] 3600 mg/m<sup>2</sup>/day IV continuous infusion over 96 hours, started on day 22 (week 4) and 57 (week 9), '''given with ifosfamide''' (total dose: 14,400 mg/m<sup>2</sup>)
 
*Up to 2 L/day hydration with ifosfamide & mesna
 
*Up to 2 L/day hydration with ifosfamide & mesna
 
'''7-day cycle for 13 cycles'''
 
'''7-day cycle for 13 cycles'''
 +
</div>
 +
<div class="toccolours" style="background-color:#cbd5e7">
 
====Subsequent treatment====
 
====Subsequent treatment====
 
*[[Surgery#Surgical_resection|Surgery]] occurs during week 14, with further treatment based on pathologic response:
 
*[[Surgery#Surgical_resection|Surgery]] occurs during week 14, with further treatment based on pathologic response:
**Patients with good response: [[#M-EI_2|Adjuvant M-EI]]
+
**SFOP OS94, patients with good response: Adjuvant [[#M-EI_2|M-EI]]
**Patients with poor response: [[#Cisplatin_.26_Doxorubicin_2|Adjuvant AP]]
+
**SFOP OS94, patients with poor response: Adjuvant [[#Cisplatin_.26_Doxorubicin_2|AP]]
 
+
</div></div>
 
===References===
 
===References===
# '''SFOP OS94:''' Le Deley MC, Guinebretière JM, Gentet JC, Pacquement H, Pichon F, Marec-Bérard P, Entz-Werlé N, Schmitt C, Brugières L, Vanel D, Dupoüy N, Tabone MD, Kalifa C; Société Française d'Oncologie Pédiatrique (SFOP). SFOP OS94: a randomised trial comparing preoperative high-dose methotrexate plus doxorubicin to high-dose methotrexate plus etoposide and ifosfamide in osteosarcoma patients. Eur J Cancer. 2007 Mar;43(4):752-61. Epub 2007 Jan 30. [https://www.ejcancer.com/article/S0959-8049(06)01072-0/abstract link to original article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/17267204 PubMed] NCT00180908
+
# '''SFOP OS94:''' Le Deley MC, Guinebretière JM, Gentet JC, Pacquement H, Pichon F, Marec-Bérard P, Entz-Werlé N, Schmitt C, Brugières L, Vanel D, Dupoüy N, Tabone MD, Kalifa C; Société Française d'Oncologie Pédiatrique (SFOP). SFOP OS94: a randomised trial comparing preoperative high-dose methotrexate plus doxorubicin to high-dose methotrexate plus etoposide and ifosfamide in osteosarcoma patients. Eur J Cancer. 2007 Mar;43(4):752-61. Epub 2007 Jan 30. [https://doi.org/10.1016/j.ejca.2006.10.023 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/17267204/ PubMed] [https://clinicaltrials.gov/study/NCT00180908 NCT00180908]
# '''OS2006:''' Piperno-Neumann S, Le Deley MC, Rédini F, Pacquement H, Marec-Bérard P, Petit P, Brisse H, Lervat C, Gentet JC, Entz-Werlé N, Italiano A, Corradini N, Bompas E, Penel N, Tabone MD, Gomez-Brouchet A, Guinebretière JM, Mascard E, Gouin F, Chevance A, Bonnet N, Blay JY, Brugières L; Sarcoma Group of UNICANCER; SFCE; GSF-GETO. Zoledronate in combination with chemotherapy and surgery to treat osteosarcoma (OS2006): a randomised, multicentre, open-label, phase 3 trial. Lancet Oncol. 2016 Aug;17(8):1070-1080. Epub 2016 Jun 17. [https://www.thelancet.com/journals/lanonc/article/PIIS1470-2045(16)30096-1/fulltext link to original article] [https://pubmed.ncbi.nlm.nih.gov/27324280 PubMed] NCT00470223
+
# '''OS2006:''' Piperno-Neumann S, Le Deley MC, Rédini F, Pacquement H, Marec-Bérard P, Petit P, Brisse H, Lervat C, Gentet JC, Entz-Werlé N, Italiano A, Corradini N, Bompas E, Penel N, Tabone MD, Gomez-Brouchet A, Guinebretière JM, Mascard E, Gouin F, Chevance A, Bonnet N, Blay JY, Brugières L; Sarcoma Group of UNICANCER; SFCE; GSF-GETO. Zoledronate in combination with chemotherapy and surgery to treat osteosarcoma (OS2006): a randomised, multicentre, open-label, phase 3 trial. Lancet Oncol. 2016 Aug;17(8):1070-1080. Epub 2016 Jun 17. [https://doi.org/10.1016/S1470-2045(16)30096-1 link to original article] [https://pubmed.ncbi.nlm.nih.gov/27324280/ PubMed] [https://clinicaltrials.gov/study/NCT00470223 NCT00470223]
## '''Update:''' Gaspar N, Occean BV, Pacquement H, Bompas E, Bouvier C, Brisse HJ, Castex MP, Cheurfa N, Corradini N, Delaye J, Entz-Werlé N, Gentet JC, Italiano A, Lervat C, Marec-Berard P, Mascard E, Redini F, Saumet L, Schmitt C, Tabone MD, Verite-Goulard C, Le Deley MC, Piperno-Neumann S, Brugieres L; SFCE; GSF-GETO; UNICANCER sarcoma group. Results of methotrexate-etoposide-ifosfamide based regimen (M-EI) in osteosarcoma patients included in the French OS2006/sarcome-09 study. Eur J Cancer. 2018 Jan;88:57-66. Epub 2017 Nov 28. [https://www.ejcancer.com/article/S0959-8049(17)31339-4/fulltext link to original article] [https://pubmed.ncbi.nlm.nih.gov/29190507 PubMed]
+
## '''Update:''' Gaspar N, Occean BV, Pacquement H, Bompas E, Bouvier C, Brisse HJ, Castex MP, Cheurfa N, Corradini N, Delaye J, Entz-Werlé N, Gentet JC, Italiano A, Lervat C, Marec-Berard P, Mascard E, Redini F, Saumet L, Schmitt C, Tabone MD, Verite-Goulard C, Le Deley MC, Piperno-Neumann S, Brugieres L; SFCE; GSF-GETO; UNICANCER sarcoma group. Results of methotrexate-etoposide-ifosfamide based regimen (M-EI) in osteosarcoma patients included in the French OS2006/sarcome-09 study. Eur J Cancer. 2018 Jan;88:57-66. Epub 2017 Nov 28. [https://doi.org/10.1016/j.ejca.2017.09.036 link to original article] [https://pubmed.ncbi.nlm.nih.gov/29190507/ PubMed]
 
 
 
=Adjuvant therapy=
 
=Adjuvant therapy=
 
 
==Cisplatin & Doxorubicin {{#subobject:267127|Regimen=1}}==
 
==Cisplatin & Doxorubicin {{#subobject:267127|Regimen=1}}==
{| class="wikitable" style="float:right; margin-left: 5px;"
 
|-
 
|[[#top|back to top]]
 
|}
 
 
AP: '''<u>A</u>'''driamycin (Doxorubicin) & '''<u>P</u>'''latinol (Cisplatin)
 
AP: '''<u>A</u>'''driamycin (Doxorubicin) & '''<u>P</u>'''latinol (Cisplatin)
 +
<div class="toccolours" style="background-color:#eeeeee">
 
===Regimen variant #1 {{#subobject:602292|Variant=1}}===
 
===Regimen variant #1 {{#subobject:602292|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
!style="width: 20%"|Years of enrollment
+
!style="width: 20%"|Dates of enrollment
 
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|Comparator
 
!style="width: 20%"|Comparator
Line 611: Line 412:
 
|[https://doi.org/10.1200/jco.1992.10.10.1579 Bramwell et al. 1992]
 
|[https://doi.org/10.1200/jco.1992.10.10.1579 Bramwell et al. 1992]
 
|1983-1986
 
|1983-1986
|style="background-color:#1a9851"|Phase III (E-esc)
+
|style="background-color:#1a9851"|Phase 3 (E-esc)
 
|[[#MAP|MAP]]
 
|[[#MAP|MAP]]
 
|style="background-color:#91cf60"|Seems to have superior DFS
 
|style="background-color:#91cf60"|Seems to have superior DFS
 
|-
 
|-
|[https://www.thelancet.com/journals/lancet/article/PIIS0140-6736%2897%2902307-6/fulltext Souhami et al. 1997]
+
|[https://doi.org/10.1016/S0140-6736(97)02307-6 Souhami et al. 1997]
 
|1986-1991
 
|1986-1991
|style="background-color:#1a9851"|Phase III (E-de-esc)
+
|style="background-color:#1a9851"|Phase 3 (E-de-esc)
|Multi-drug T10 protocol
+
|[[#T10_protocol_888|Multi-drug T10 protocol]]
|style="background-color:#ffffbf"|Did not meet primary endpoints of PFS/OS
+
|style="background-color:#ffffbf"|Did not meet co-primary endpoints of PFS/OS
 
|-
 
|-
 
|}
 
|}
 +
<div class="toccolours" style="background-color:#cbd5e8">
 
====Preceding treatment====
 
====Preceding treatment====
*[[#Cisplatin_.26_Doxorubicin|Neoadjuvant AP]], then [[Surgery#Surgical_resection|surgery]]
+
*Neoadjuvant [[#Cisplatin_.26_Doxorubicin|AP]], then [[Surgery#Surgical_resection|surgery]]
 +
</div>
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
 
*[[Cisplatin (Platinol)]] 100 mg/m<sup>2</sup> IV continuous infusion over 24 hours, started on day 1
 
*[[Cisplatin (Platinol)]] 100 mg/m<sup>2</sup> IV continuous infusion over 24 hours, started on day 1
 
*[[Doxorubicin (Adriamycin)]] 25 mg/m<sup>2</sup> IV bolus once per day on days 1 to 3
 
*[[Doxorubicin (Adriamycin)]] 25 mg/m<sup>2</sup> IV bolus once per day on days 1 to 3
 
+
====Supportive therapy====
====Supportive medications====
+
*Prehydration: normal saline 400 mL/m<sup>2</sup> and D5W 400 mL/m<sup>2</sup> IV over 2 hours--the reference did not clarify if these two solutions are given at the same time
*Prehydration: normal saline 400 mL/m<sup>2</sup> and D5W 400 mL/m<sup>2</sup> over 2 hours--the reference did not clarify if these two solutions are given at the same time
 
 
*The volume of fluid for cisplatin continuous infusion is 2400 mL/m<sup>2</sup> NS, with KCl 80 mEq/L and mannitol 32,000 mg/m<sup>2</sup>
 
*The volume of fluid for cisplatin continuous infusion is 2400 mL/m<sup>2</sup> NS, with KCl 80 mEq/L and mannitol 32,000 mg/m<sup>2</sup>
 
*Posthydration: D5W 600 mL/m<sup>2</sup> over 6 hours, with KCl 20 mEq/L and mannitol 8000 mg/m<sup>2</sup>; and NS 600 mL/m<sup>2</sup> over 6 hours, with KCl 20 mEq/L, magnesium sulfate 2 mmol/L, and calcium gluconate 0.6 mmol/L--the reference did not clarify if these two solutions are given at the same time. Then D5W 600 mL/m<sup>2</sup> over 12 hours, with KCl 20 mEq/L and mannitol 8000 mg/m<sup>2</sup>.
 
*Posthydration: D5W 600 mL/m<sup>2</sup> over 6 hours, with KCl 20 mEq/L and mannitol 8000 mg/m<sup>2</sup>; and NS 600 mL/m<sup>2</sup> over 6 hours, with KCl 20 mEq/L, magnesium sulfate 2 mmol/L, and calcium gluconate 0.6 mmol/L--the reference did not clarify if these two solutions are given at the same time. Then D5W 600 mL/m<sup>2</sup> over 12 hours, with KCl 20 mEq/L and mannitol 8000 mg/m<sup>2</sup>.
 
*[[Furosemide (Lasix)]] 20 to 40 mg IV if urine output is less than 400 mL/m<sup>2</sup> over 6 hours
 
*[[Furosemide (Lasix)]] 20 to 40 mg IV if urine output is less than 400 mL/m<sup>2</sup> over 6 hours
 
 
'''21-day cycle for 3 cycles'''
 
'''21-day cycle for 3 cycles'''
 
+
</div></div><br>
 +
<div class="toccolours" style="background-color:#eeeeee">
 
===Regimen variant #2 {{#subobject:32db86|Variant=1}}===
 
===Regimen variant #2 {{#subobject:32db86|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
!style="width: 20%"|Years of enrollment
+
!style="width: 20%"|Dates of enrollment
 
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|Comparator
 
!style="width: 20%"|Comparator
Line 646: Line 449:
 
|[http://jnci.oxfordjournals.org/content/99/2/112.full Lewis et al. 2007 (EORTC 80931)]
 
|[http://jnci.oxfordjournals.org/content/99/2/112.full Lewis et al. 2007 (EORTC 80931)]
 
|1993-2002
 
|1993-2002
|style="background-color:#1a9851"|Phase III (C)
+
|style="background-color:#1a9851"|Phase 3 (C)
 
|[[#Cisplatin_.26_Doxorubicin_2|Cisplatin & Doxorubicin]]; dose-intense
 
|[[#Cisplatin_.26_Doxorubicin_2|Cisplatin & Doxorubicin]]; dose-intense
|style="background-color:#d73027"|Inferior good histologic response rate
+
|style="background-color:#ffffbf"|Did not meet primary endpoint of OS
 
|-
 
|-
 
|}
 
|}
 +
<div class="toccolours" style="background-color:#cbd5e8">
 
====Preceding treatment====
 
====Preceding treatment====
*[[#Cisplatin_.26_Doxorubicin|Neoadjuvant AP]], then [[Surgery#Surgical_resection|surgery]]
+
*Neoadjuvant [[#Cisplatin_.26_Doxorubicin|AP]], then [[Surgery#Surgical_resection|surgery]]
 +
</div>
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
 
*[[Cisplatin (Platinol)]] 100 mg/m<sup>2</sup> IV continuous infusion over 24 hours, started on day 1
 
*[[Cisplatin (Platinol)]] 100 mg/m<sup>2</sup> IV continuous infusion over 24 hours, started on day 1
 
*[[Doxorubicin (Adriamycin)]] 25 mg/m<sup>2</sup> IV over 4 hours once per day on days 1 to 3
 
*[[Doxorubicin (Adriamycin)]] 25 mg/m<sup>2</sup> IV over 4 hours once per day on days 1 to 3
 
+
====Supportive therapy====
====Supportive medications====
 
 
*4 hours of prehydration prior to cisplatin
 
*4 hours of prehydration prior to cisplatin
 
*24 hours of posthydration & mannitol after cisplatin
 
*24 hours of posthydration & mannitol after cisplatin
 
*Recommended that fluid for cisplatin is isotonic saline with potassium chloride and mannitol
 
*Recommended that fluid for cisplatin is isotonic saline with potassium chloride and mannitol
 
 
'''21-day cycle for 4 cycles'''
 
'''21-day cycle for 4 cycles'''
 
+
</div></div><br>
 +
<div class="toccolours" style="background-color:#eeeeee">
 
===Regimen variant #3, dose intense {{#subobject:d1ecd3|Variant=1}}===
 
===Regimen variant #3, dose intense {{#subobject:d1ecd3|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
!style="width: 20%"|Years of enrollment
+
!style="width: 20%"|Dates of enrollment
 
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|Comparator
 
!style="width: 20%"|Comparator
Line 674: Line 479:
 
|[http://jnci.oxfordjournals.org/content/99/2/112.full Lewis et al. 2007 (EORTC 80931)]
 
|[http://jnci.oxfordjournals.org/content/99/2/112.full Lewis et al. 2007 (EORTC 80931)]
 
|1993-2002
 
|1993-2002
|style="background-color:#1a9851"|Phase III (E-esc)
+
|style="background-color:#1a9851"|Phase 3 (E-esc)
 
|[[#Cisplatin_.26_Doxorubicin|Cisplatin & Doxorubicin]]; conventional
 
|[[#Cisplatin_.26_Doxorubicin|Cisplatin & Doxorubicin]]; conventional
|style="background-color:#1a9850"|Superior good histologic response rate
+
|style="background-color:#ffffbf"|Did not meet primary endpoint of OS
 
|-
 
|-
 
|}
 
|}
 +
<div class="toccolours" style="background-color:#cbd5e8">
 
====Preceding treatment====
 
====Preceding treatment====
*[[#Cisplatin_.26_Doxorubicin|Neoadjuvant AP]], then [[Surgery#Surgical_resection|surgery]]
+
*Neoadjuvant [[#Cisplatin_.26_Doxorubicin|AP]], then [[Surgery#Surgical_resection|surgery]]
 +
</div>
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
 
*[[Cisplatin (Platinol)]] 100 mg/m<sup>2</sup> IV continuous infusion over 24 hours, started on day 1
 
*[[Cisplatin (Platinol)]] 100 mg/m<sup>2</sup> IV continuous infusion over 24 hours, started on day 1
 
*[[Doxorubicin (Adriamycin)]] 25 mg/m<sup>2</sup> IV over 4 hours once per day on days 1 to 3
 
*[[Doxorubicin (Adriamycin)]] 25 mg/m<sup>2</sup> IV over 4 hours once per day on days 1 to 3
 
+
====Supportive therapy====
====Supportive medications====
 
 
*Growth factor suppor with ONE of the following:
 
*Growth factor suppor with ONE of the following:
 
**[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day on days 4 to 13
 
**[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day on days 4 to 13
 
**[[Lenograstim (Granocyte)]] 5 mcg/kg SC once per day on days 4 to 13
 
**[[Lenograstim (Granocyte)]] 5 mcg/kg SC once per day on days 4 to 13
*4 hours of prehydration prior to [[Cisplatin (Platinol)]]
+
*4 hours of prehydration prior to cisplatin
*24 hours of posthydration & mannitol after [[Cisplatin (Platinol)]]
+
*24 hours of posthydration & mannitol after cisplatin
 
*Recommended that fluid for cisplatin is isotonic saline with potassium chloride and mannitol
 
*Recommended that fluid for cisplatin is isotonic saline with potassium chloride and mannitol
 
 
'''14-day cycle for 3 cycles'''
 
'''14-day cycle for 3 cycles'''
 
+
</div></div><br>
 +
<div class="toccolours" style="background-color:#eeeeee">
 
===Regimen variant #4 {{#subobject:44bba3|Variant=1}}===
 
===Regimen variant #4 {{#subobject:44bba3|Variant=1}}===
{| class="wikitable" style="width: 40%; text-align:center;"  
+
{| class="wikitable sortable" style="width: 60%; text-align:center;"  
!style="width: 25%"|Study
+
!style="width: 33%"|Study
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
+
!style="width: 33%"|Dates of enrollment
 +
!style="width: 33%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|-
 
|[https://doi.org/10.1200/jco.1988.6.2.329 Winkler et al. 1988 (COSS-82)]
 
|[https://doi.org/10.1200/jco.1988.6.2.329 Winkler et al. 1988 (COSS-82)]
|style="background-color:#91cf61"|Non-randomized portion of RCT
+
|1982-1984
 +
|style="background-color:#91cf61"|Non-randomized part of phase 3 RCT
 
|-
 
|-
 
|}
 
|}
 
''Note: The exact schedule is unclear based on limited information in the reference, as schedule of doses is primarily extrapolated from Figure 1, which does not contain clear delineations in time.''
 
''Note: The exact schedule is unclear based on limited information in the reference, as schedule of doses is primarily extrapolated from Figure 1, which does not contain clear delineations in time.''
 +
<div class="toccolours" style="background-color:#cbd5e8">
 
====Preceding treatment====
 
====Preceding treatment====
*[[Osteosarcoma_-_historical#M-BCD|Neoadjuvant M-BCD]], then [[Surgery#Surgical_resection|surgery]], with poor response
+
*Neoadjuvant [[Osteosarcoma_-_historical#M-BCD|M-BCD]], then [[Surgery#Surgical_resection|surgery]], with poor response
 +
</div>
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
 
*[[Cisplatin (Platinol)]] 90 mg/m<sup>2</sup> IV over 4 hours once on day 3
 
*[[Cisplatin (Platinol)]] 90 mg/m<sup>2</sup> IV over 4 hours once on day 3
 
*[[Doxorubicin (Adriamycin)]] 30 mg/m<sup>2</sup> IV bolus once per day on days 1 & 2
 
*[[Doxorubicin (Adriamycin)]] 30 mg/m<sup>2</sup> IV bolus once per day on days 1 & 2
 
+
====Supportive therapy====
====Supportive medications====
 
 
*12 hours of hydration prior to cisplatin & 20 hours of hydration after cisplatin; total amount of fluid given over 36hours of prehydration, cisplatin, and posthydration is NS 6 L/m<sup>2</sup> with mannitol 8 g/L and potassium 20 mval/L.
 
*12 hours of hydration prior to cisplatin & 20 hours of hydration after cisplatin; total amount of fluid given over 36hours of prehydration, cisplatin, and posthydration is NS 6 L/m<sup>2</sup> with mannitol 8 g/L and potassium 20 mval/L.
 
*Magnesium 180 mg/m<sup>2</sup> PO "per day throughout the whole chemotherapy time"--as described in COSS-80
 
*Magnesium 180 mg/m<sup>2</sup> PO "per day throughout the whole chemotherapy time"--as described in COSS-80
 
 
'''21-day cycle for 6 cycles'''
 
'''21-day cycle for 6 cycles'''
 
+
</div></div><br>
 +
<div class="toccolours" style="background-color:#eeeeee">
 
===Regimen variant #5 {{#subobject:7fc4e3|Variant=1}}===
 
===Regimen variant #5 {{#subobject:7fc4e3|Variant=1}}===
{| class="wikitable" style="width: 40%; text-align:center;"  
+
{| class="wikitable sortable" style="width: 60%; text-align:center;"  
!style="width: 25%"|Study
+
!style="width: 33%"|Study
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
+
!style="width: 33%"|Dates of enrollment
 +
!style="width: 33%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|-
|[https://www.ejcancer.com/article/S0959-8049(06)01072-0/abstract Le Deley et al. 2007 (SFOP OS94)]
+
|[https://doi.org/10.1016/j.ejca.2006.10.023 Le Deley et al. 2007 (SFOP OS94)]
|style="background-color:#91cf61"|Non-randomized portion of RCT
+
|1994-2001
 +
|style="background-color:#91cf61"|Non-randomized part of phase 3 RCT
 
|-
 
|-
 
|}
 
|}
 
''Details were not listed about the precise schedule. Other regimens have used both medications both on day 1, with 21-day cycles.''
 
''Details were not listed about the precise schedule. Other regimens have used both medications both on day 1, with 21-day cycles.''
 +
<div class="toccolours" style="background-color:#cbd5e8">
 
====Preceding treatment====
 
====Preceding treatment====
*[[#M-EI|Neoadjuvant M-EI]], then [[Surgery#Surgical_resection|surgery]], with poor response
+
*Neoadjuvant [[#M-EI|M-EI]], then [[Surgery#Surgical_resection|surgery]], with poor response
 +
</div>
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
*[[Cisplatin (Platinol)]] 120 mg/m<sup>2</sup>
+
*[[Cisplatin (Platinol)]] 120 mg/m<sup>2</sup> IV (schedule not specified)
*[[Doxorubicin (Adriamycin)]] 70 mg/m<sup>2</sup> IV over 6 hours
+
*[[Doxorubicin (Adriamycin)]] 70 mg/m<sup>2</sup> IV over 6 hours (schedule not specified)
 
   
 
   
 
'''5 cycles (length not specified)'''
 
'''5 cycles (length not specified)'''
 +
</div></div>
  
 
===References===
 
===References===
# '''COSS-82:''' Winkler K, Beron G, Delling G, Heise U, Kabisch H, Purfürst C, Berger J, Ritter J, Jürgens H, Gerein V, Graf N, Russe W, Gruemayer ER, Ertelt W, Kotz R, Preuzzer P, Prindull G, Brandeis W, Landbeck G. Neoadjuvant chemotherapy of osteosarcoma: results of a randomized cooperative trial (COSS-82) with salvage chemotherapy based on histological tumor response. J Clin Oncol. 1988 Feb;6(2):329-37. [https://doi.org/10.1200/jco.1988.6.2.329 link to original article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/2448428 PubMed]
+
# '''COSS-82:''' Winkler K, Beron G, Delling G, Heise U, Kabisch H, Purfürst C, Berger J, Ritter J, Jürgens H, Gerein V, Graf N, Russe W, Gruemayer ER, Ertelt W, Kotz R, Preuzzer P, Prindull G, Brandeis W, Landbeck G. Neoadjuvant chemotherapy of osteosarcoma: results of a randomized cooperative trial (COSS-82) with salvage chemotherapy based on histological tumor response. J Clin Oncol. 1988 Feb;6(2):329-37. [https://doi.org/10.1200/jco.1988.6.2.329 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/2448428/ PubMed]
# Bramwell VH, Burgers M, Sneath R, Souhami R, van Oosterom AT, Voûte PA, Rouesse J, Spooner D, Craft AW, Somers R, Pringle J, Malcolm AJ, van der Eiiken J, Thomas D, Uscinska B, Machin D, van Glabbeke M; European Osteosarcoma Intergroup. A comparison of two short intensive adjuvant chemotherapy regimens in operable osteosarcoma of limbs in children and young adults: the first study of the European Osteosarcoma Intergroup. J Clin Oncol. 1992 Oct;10(10):1579-91. [https://doi.org/10.1200/jco.1992.10.10.1579 link to original article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/1403038 PubMed]
+
# Bramwell VH, Burgers M, Sneath R, Souhami R, van Oosterom AT, Voûte PA, Rouesse J, Spooner D, Craft AW, Somers R, Pringle J, Malcolm AJ, van der Eiiken J, Thomas D, Uscinska B, Machin D, van Glabbeke M; European Osteosarcoma Intergroup. A comparison of two short intensive adjuvant chemotherapy regimens in operable osteosarcoma of limbs in children and young adults: the first study of the European Osteosarcoma Intergroup. J Clin Oncol. 1992 Oct;10(10):1579-91. [https://doi.org/10.1200/jco.1992.10.10.1579 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/1403038/ PubMed]
# Souhami RL, Craft AW, Van der Eijken JW, Nooij M, Spooner D, Bramwell VH, Wierzbicki R, Malcolm AJ, Kirkpatrick A, Uscinska BM, Van Glabbeke M, Machin D; European Osteosarcoma Intergroup. Randomised trial of two regimens of chemotherapy in operable osteosarcoma: a study of the European Osteosarcoma Intergroup. Lancet. 1997 Sep 27;350(9082):911-7. [https://www.thelancet.com/journals/lancet/article/PIIS0140-6736%2897%2902307-6/fulltext link to original article] [https://pubmed.ncbi.nlm.nih.gov/9314869 PubMed]
+
# Souhami RL, Craft AW, Van der Eijken JW, Nooij M, Spooner D, Bramwell VH, Wierzbicki R, Malcolm AJ, Kirkpatrick A, Uscinska BM, Van Glabbeke M, Machin D; European Osteosarcoma Intergroup. Randomised trial of two regimens of chemotherapy in operable osteosarcoma: a study of the European Osteosarcoma Intergroup. Lancet. 1997 Sep 27;350(9082):911-7. [https://doi.org/10.1016/S0140-6736(97)02307-6 link to original article] [https://pubmed.ncbi.nlm.nih.gov/9314869/ PubMed]
# '''EORTC 80931:''' Lewis IJ, Nooij MA, Whelan J, Sydes MR, Grimer R, Hogendoorn PC, Memon MA, Weeden S, Uscinska BM, van Glabbeke M, Kirkpatrick A, Hauben EI, Craft AW, Taminiau AH; MRC BO06 and EORTC 80931 collaborators; European Osteosarcoma Intergroup. Improvement in histologic response but not survival in osteosarcoma patients treated with intensified chemotherapy: a randomized phase III trial of the European Osteosarcoma Intergroup. J Natl Cancer Inst. 2007 Jan 17;99(2):112-28. [http://jnci.oxfordjournals.org/content/99/2/112.full link to original article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/17227995 PubMed] NCT00002539
+
# '''EORTC 80931:''' Lewis IJ, Nooij MA, Whelan J, Sydes MR, Grimer R, Hogendoorn PC, Memon MA, Weeden S, Uscinska BM, van Glabbeke M, Kirkpatrick A, Hauben EI, Craft AW, Taminiau AH; MRC BO06 and EORTC 80931 collaborators; European Osteosarcoma Intergroup. Improvement in histologic response but not survival in osteosarcoma patients treated with intensified chemotherapy: a randomized phase III trial of the European Osteosarcoma Intergroup. J Natl Cancer Inst. 2007 Jan 17;99(2):112-28. [http://jnci.oxfordjournals.org/content/99/2/112.full link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/17227995/ PubMed] [https://clinicaltrials.gov/study/NCT00002539 NCT00002539]
# '''SFOP OS94:''' Le Deley MC, Guinebretière JM, Gentet JC, Pacquement H, Pichon F, Marec-Bérard P, Entz-Werlé N, Schmitt C, Brugières L, Vanel D, Dupoüy N, Tabone MD, Kalifa C; Société Française d'Oncologie Pédiatrique (SFOP). SFOP OS94: a randomised trial comparing preoperative high-dose methotrexate plus doxorubicin to high-dose methotrexate plus etoposide and ifosfamide in osteosarcoma patients. Eur J Cancer. 2007 Mar;43(4):752-61. Epub 2007 Jan 30. [https://www.ejcancer.com/article/S0959-8049(06)01072-0/abstract link to original article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/17267204 PubMed] NCT00180908
+
# '''SFOP OS94:''' Le Deley MC, Guinebretière JM, Gentet JC, Pacquement H, Pichon F, Marec-Bérard P, Entz-Werlé N, Schmitt C, Brugières L, Vanel D, Dupoüy N, Tabone MD, Kalifa C; Société Française d'Oncologie Pédiatrique (SFOP). SFOP OS94: a randomised trial comparing preoperative high-dose methotrexate plus doxorubicin to high-dose methotrexate plus etoposide and ifosfamide in osteosarcoma patients. Eur J Cancer. 2007 Mar;43(4):752-61. Epub 2007 Jan 30. [https://doi.org/10.1016/j.ejca.2006.10.023 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/17267204/ PubMed] [https://clinicaltrials.gov/study/NCT00180908 NCT00180908]
 
 
 
==Cisplatin, Epirubicin, Ifosfamide {{#subobject:cd0e26|Regimen=1}}==
 
==Cisplatin, Epirubicin, Ifosfamide {{#subobject:cd0e26|Regimen=1}}==
{| class="wikitable" style="float:right; margin-left: 5px;"
+
<div class="toccolours" style="background-color:#eeeeee">
|-
 
|[[#top|back to top]]
 
|}
 
 
===Regimen {{#subobject:320a96|Variant=1}}===
 
===Regimen {{#subobject:320a96|Variant=1}}===
 
{| class="wikitable" style="width: 40%; text-align:center;"  
 
{| class="wikitable" style="width: 40%; text-align:center;"  
Line 752: Line 565:
 
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|-
|[http://content.karger.com/produktedb/produkte.asp?DOI=10.1159/000113017 Basaran et al. 2007]
+
|[https://doi.org/10.1159/000113017 Basaran et al. 2007]
|style="background-color:#91cf61"|Phase II
+
|style="background-color:#91cf61"|Phase 2
 
|-
 
|-
 
|}
 
|}
 +
<div class="toccolours" style="background-color:#cbd5e8">
 
====Preceding treatment====
 
====Preceding treatment====
*[[#Cisplatin.2C_Epirubicin.2C_Ifosfamide|Neoadjuvant cisplatin, epirubicin, ifosfamide]], then [[Surgery#Surgical_resection|surgery]]
+
*Neoadjuvant [[#Cisplatin.2C_Epirubicin.2C_Ifosfamide|cisplatin, epirubicin, ifosfamide]], then [[Surgery#Surgical_resection|surgery]]
 +
</div>
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
*[[Cisplatin (Platinol)]] 100 mg/m<sup>2</sup> IV over 2 hours
+
*[[Cisplatin (Platinol)]] 100 mg/m<sup>2</sup> IV over 2 hours once on day 1
 
*[[Epirubicin (Ellence)]] 90 mg/m<sup>2</sup> IV over 15 minutes once on day 1
 
*[[Epirubicin (Ellence)]] 90 mg/m<sup>2</sup> IV over 15 minutes once on day 1
*[[Ifosfamide (Ifex)]] 2000 mg/m<sup>2</sup> IV over 4 hours once per day on days 2 to 4, '''given with [[Mesna (Mesnex)]]'''
+
*[[Ifosfamide (Ifex)]] 2000 mg/m<sup>2</sup> IV over 4 hours once per day on days 2 to 4, '''given with mesna'''
 
+
====Supportive therapy====
====Supportive medications====
+
*[[Mesna (Mesnex)]] 2000 mg/m<sup>2</sup> IV over 4 hours once per day on days 2 to 4, '''given with ifosfamide'''
*[[Mesna (Mesnex)]] 2000 mg/m<sup>2</sup> IV over 4 hours once per day on days 2 to 4, '''given with [[Ifosfamide (Ifex)]]'''
+
*Pre- and post-[[:Category:Hydration|hydration]] with mannitol diuresis for cisplatin
*Prehydration and posthydration with mannitol diuresis for [[Cisplatin (Platinol)]]
 
 
 
 
'''28-day cycle for 3 cycles'''
 
'''28-day cycle for 3 cycles'''
 
+
</div></div>
 
===References===
 
===References===
# Basaran M, Bavbek ES, Saglam S, Eralp L, Sakar B, Atalar AC, Bilgic B, Ozger H, Onat H. A phase II study of cisplatin, ifosfamide and epirubicin combination chemotherapy in adults with nonmetastatic and extremity osteosarcomas. Oncology. 2007;72(3-4):255-60. Epub 2008 Jan 10. [http://content.karger.com/produktedb/produkte.asp?DOI=10.1159/000113017 link to original article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/18185020 PubMed]
+
# Basaran M, Bavbek ES, Saglam S, Eralp L, Sakar B, Atalar AC, Bilgic B, Ozger H, Onat H. A phase II study of cisplatin, ifosfamide and epirubicin combination chemotherapy in adults with nonmetastatic and extremity osteosarcomas. Oncology. 2007;72(3-4):255-60. Epub 2008 Jan 10. [https://doi.org/10.1159/000113017 link to original article] '''contains dosing details in abstract''' [https://pubmed.ncbi.nlm.nih.gov/18185020/ PubMed]
 
 
==Doxorubicin monotherapy {{#subobject:681e0f|Regimen=1}}==
 
{| class="wikitable" style="float:right; margin-left: 5px;"
 
|-
 
|[[#top|back to top]]
 
|}
 
===Regimen {{#subobject:81ee7b|Variant=1}}===
 
{| class="wikitable" style="width: 40%; text-align:center;"
 
!style="width: 25%"|Study
 
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|[https://www.nejm.org/doi/full/10.1056/NEJM197411072911903 Cortes et al. 1974]
 
|style="background-color:#91cf61"|Non-randomized
 
|-
 
|}
 
''Of historic interest.''
 
====Preceding treatment====
 
*[[Surgery#Surgical_resection|Surgery]]
 
====Chemotherapy====
 
*[[Doxorubicin (Adriamycin)]] 30 mg/m<sup>2</sup> IV once per day on days 1 to 3
 
 
 
'''4- to 6-week cycle for 6 cycles'''
 
===References===
 
# Cortes EP, Holland JF, Wang JJ, Sinks LF, Blom J, Senn H, Bank A, Glidewell O. Amputation and adriamycin in primary osteosarcoma. N Engl J Med. 1974 Nov 7;291(19):998-1000. [https://www.nejm.org/doi/full/10.1056/NEJM197411072911903 link to original article] '''contains protocol''' [https://pubmed.ncbi.nlm.nih.gov/4528415 PubMed]
 
 
 
 
==IE {{#subobject:777bc8|Regimen=1}}==
 
==IE {{#subobject:777bc8|Regimen=1}}==
{| class="wikitable" style="float:right; margin-left: 5px;"
 
|-
 
|[[#top|back to top]]
 
|}
 
 
IE: '''<u>I</u>'''fosfamide, '''<u>E</u>'''toposide
 
IE: '''<u>I</u>'''fosfamide, '''<u>E</u>'''toposide
 
+
<div class="toccolours" style="background-color:#eeeeee">
 
===Regimen {{#subobject:7d60b5|Variant=1}}===
 
===Regimen {{#subobject:7d60b5|Variant=1}}===
{| class="wikitable" style="width: 40%; text-align:center;"  
+
{| class="wikitable sortable" style="width: 60%; text-align:center;"  
!style="width: 25%"|Study
+
!style="width: 33%"|Study
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
+
!style="width: 33%"|Dates of enrollment
 +
!style="width: 33%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|-
|[https://www.ejcancer.com/article/S0959-8049(06)01072-0/abstract Le Deley et al. 2007 (SFOP OS94)]
+
|[https://doi.org/10.1016/j.ejca.2006.10.023 Le Deley et al. 2007 (SFOP OS94)]
|style="background-color:#91cf61"|Non-randomized portion of RCT
+
|1994-2001
 +
|style="background-color:#91cf61"|Non-randomized part of phase 3 RCT
 
|-
 
|-
 
|}
 
|}
 
''Details were not listed about the length of each cycle. Other regimens have used 21 to 28-day cycles.''
 
''Details were not listed about the length of each cycle. Other regimens have used 21 to 28-day cycles.''
 +
<div class="toccolours" style="background-color:#cbd5e8">
 
====Preceding treatment====
 
====Preceding treatment====
*[[#MA|Neoadjuvant MA]], then [[Surgery#Surgical_resection|surgery]], with poor response
+
*Neoadjuvant [[#MA|MA]], then [[Surgery#Surgical_resection|surgery]], with poor response
 +
</div>
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
*[[Ifosfamide (Ifex)]] 3000 mg/m<sup>2</sup> IV over 3 hours once per day on days 1 to 4, '''given during [[Mesna (Mesnex)]] infusion'''
+
*[[Ifosfamide (Ifex)]] 3000 mg/m<sup>2</sup> IV over 3 hours once per day on days 1 to 4, '''given during mesna infusion'''
 
**Given in NS 250 to 500 mL
 
**Given in NS 250 to 500 mL
 
*[[Etoposide (Vepesid)]] 75 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1 to 4
 
*[[Etoposide (Vepesid)]] 75 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1 to 4
 
**Given in NS 250 to 500 mL
 
**Given in NS 250 to 500 mL
 
+
====Supportive therapy====
====Supportive medications====
 
 
*[[Mesna (Mesnex)]] 3600 mg/m<sup>2</sup>/day IV continuous infusion over 96 hours, started on day 1 (total dose: 14,400 mg/m<sup>2</sup>)
 
*[[Mesna (Mesnex)]] 3600 mg/m<sup>2</sup>/day IV continuous infusion over 96 hours, started on day 1 (total dose: 14,400 mg/m<sup>2</sup>)
 
*Up to 2 L/day hydration with ifosfamide & mesna
 
*Up to 2 L/day hydration with ifosfamide & mesna
 
 
'''5 cycles'''
 
'''5 cycles'''
 
+
</div></div>
 
===References===
 
===References===
# '''SFOP OS94:''' Le Deley MC, Guinebretière JM, Gentet JC, Pacquement H, Pichon F, Marec-Bérard P, Entz-Werlé N, Schmitt C, Brugières L, Vanel D, Dupoüy N, Tabone MD, Kalifa C; Société Française d'Oncologie Pédiatrique (SFOP). SFOP OS94: a randomised trial comparing preoperative high-dose methotrexate plus doxorubicin to high-dose methotrexate plus etoposide and ifosfamide in osteosarcoma patients. Eur J Cancer. 2007 Mar;43(4):752-61. Epub 2007 Jan 30. [https://www.ejcancer.com/article/S0959-8049(06)01072-0/abstract link to original article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/17267204 PubMed] NCT00180908
+
# '''SFOP OS94:''' Le Deley MC, Guinebretière JM, Gentet JC, Pacquement H, Pichon F, Marec-Bérard P, Entz-Werlé N, Schmitt C, Brugières L, Vanel D, Dupoüy N, Tabone MD, Kalifa C; Société Française d'Oncologie Pédiatrique (SFOP). SFOP OS94: a randomised trial comparing preoperative high-dose methotrexate plus doxorubicin to high-dose methotrexate plus etoposide and ifosfamide in osteosarcoma patients. Eur J Cancer. 2007 Mar;43(4):752-61. Epub 2007 Jan 30. [https://doi.org/10.1016/j.ejca.2006.10.023 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/17267204/ PubMed] [https://clinicaltrials.gov/study/NCT00180908 NCT00180908]
 
 
 
==MA {{#subobject:cf86ac|Regimen=1}}==
 
==MA {{#subobject:cf86ac|Regimen=1}}==
{| class="wikitable" style="float:right; margin-left: 5px;"
 
|-
 
|[[#top|back to top]]
 
|}
 
 
MA: High-dose '''<u>M</u>'''ethotrexate, '''<u>A</u>'''driamycin (Doxorubicin)
 
MA: High-dose '''<u>M</u>'''ethotrexate, '''<u>A</u>'''driamycin (Doxorubicin)
 
+
<div class="toccolours" style="background-color:#eeeeee">
===Protocol {{#subobject:243248|Variant=1}}===
+
===Regimen {{#subobject:243248|Variant=1}}===
{| class="wikitable" style="width: 40%; text-align:center;"  
+
{| class="wikitable sortable" style="width: 60%; text-align:center;"  
!style="width: 25%"|Study
+
!style="width: 33%"|Study
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
+
!style="width: 33%"|Dates of enrollment
 +
!style="width: 33%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|-
|[https://www.ejcancer.com/article/S0959-8049(06)01072-0/abstract Le Deley et al. 2007 (SFOP OS94)]
+
|[https://doi.org/10.1016/j.ejca.2006.10.023 Le Deley et al. 2007 (SFOP OS94)]
|style="background-color:#91cf61"|Non-randomized portion of RCT
+
|1994-2001
 +
|style="background-color:#91cf61"|Non-randomized part of phase 3 RCT
 
|-
 
|-
 
|}
 
|}
 +
<div class="toccolours" style="background-color:#cbd5e8">
 
====Preceding treatment====
 
====Preceding treatment====
*[[#MA|Neoadjuvant MA]], then [[Surgery#Surgical_resection|surgery]], with good response
+
*Neoadjuvant [[#MA|MA]], then [[Surgery#Surgical_resection|surgery]], with good response
====Chemotherapy, part 1====
+
</div>
 +
<div class="toccolours" style="background-color:#b3e2cd">
 +
====Chemotherapy====
 
*[[Methotrexate (MTX)]] 12,000 mg/m<sup>2</sup> IV over 4 hours once per day on days 1, 8, 15
 
*[[Methotrexate (MTX)]] 12,000 mg/m<sup>2</sup> IV over 4 hours once per day on days 1, 8, 15
 
**Given in D5W 1L with sodium bicarbonate 1 mEq/kg
 
**Given in D5W 1L with sodium bicarbonate 1 mEq/kg
*[[Doxorubicin (Adriamycin)]] 70 mg/m<sup>2</sup> IV over 6 hours once on day 22
+
*[[Doxorubicin (Adriamycin)]] as follows:
 
+
**Cycles 1 to 3: 70 mg/m<sup>2</sup> IV over 6 hours once on day 22
====Supportive medications====
+
====Supportive therapy====
*[[Folinic acid (Leucovorin)]] 15 mg PO every 6 hours for up to 11 doses, starting on days 1, 8, 15, starting 20 hours after the completion of [[Methotrexate (MTX)]] infusion
+
*[[Leucovorin (Folinic acid)]] 15 mg PO every 6 hours for up to 11 doses, starting on days 1, 8, 15, starting 20 hours after the completion of methotrexate infusion
 
*For methotrexate: hydration & urine alkalinization by PO and IV routes to maintain 1.6 L/m<sup>2</sup> urine output over the first 24 hours and 2 L/m<sup>2</sup> on days 2 & 3, with urine pH greater than 7
 
*For methotrexate: hydration & urine alkalinization by PO and IV routes to maintain 1.6 L/m<sup>2</sup> urine output over the first 24 hours and 2 L/m<sup>2</sup> on days 2 & 3, with urine pH greater than 7
 
*Daily monitoring of methotrexate levels and creatinine
 
*Daily monitoring of methotrexate levels and creatinine
 
+
'''28-day cycle for 4 cycles'''
'''28-day cycle for 3 cycles, followed by:'''
+
</div></div>
====Chemotherapy, part 2====
 
*[[Methotrexate (MTX)]] 12,000 mg/m<sup>2</sup> IV over 4 hours once per day on days 1, 8, 15
 
**Given in D5W 1L with sodium bicarbonate 1 mEq/kg
 
 
 
====Supportive medications====
 
*[[Folinic acid (Leucovorin)]] 15 mg PO every 6 hours for up to 11 doses, starting on days 1, 8, 15, starting 20 hours after the completion of [[Methotrexate (MTX)]] infusion
 
*For methotrexate: hydration & urine alkalinization by PO and IV routes to maintain 1.6 L/m<sup>2</sup> urine output over the first 24 hours and 2 L/m<sup>2</sup> on days 2 & 3, with urine pH greater than 7
 
*Daily monitoring of methotrexate levels and creatinine
 
 
 
'''21-day course'''
 
 
 
 
===References===
 
===References===
# '''SFOP OS94:''' Le Deley MC, Guinebretière JM, Gentet JC, Pacquement H, Pichon F, Marec-Bérard P, Entz-Werlé N, Schmitt C, Brugières L, Vanel D, Dupoüy N, Tabone MD, Kalifa C; Société Française d'Oncologie Pédiatrique (SFOP). SFOP OS94: a randomised trial comparing preoperative high-dose methotrexate plus doxorubicin to high-dose methotrexate plus etoposide and ifosfamide in osteosarcoma patients. Eur J Cancer. 2007 Mar;43(4):752-61. Epub 2007 Jan 30. [https://www.ejcancer.com/article/S0959-8049(06)01072-0/abstract link to original article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/17267204 PubMed] NCT00180908
+
# '''SFOP OS94:''' Le Deley MC, Guinebretière JM, Gentet JC, Pacquement H, Pichon F, Marec-Bérard P, Entz-Werlé N, Schmitt C, Brugières L, Vanel D, Dupoüy N, Tabone MD, Kalifa C; Société Française d'Oncologie Pédiatrique (SFOP). SFOP OS94: a randomised trial comparing preoperative high-dose methotrexate plus doxorubicin to high-dose methotrexate plus etoposide and ifosfamide in osteosarcoma patients. Eur J Cancer. 2007 Mar;43(4):752-61. Epub 2007 Jan 30. [https://doi.org/10.1016/j.ejca.2006.10.023 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/17267204/ PubMed] [https://clinicaltrials.gov/study/NCT00180908 NCT00180908]
  
 
==MAP {{#subobject:3b095e|Regimen=1}}==
 
==MAP {{#subobject:3b095e|Regimen=1}}==
{| class="wikitable" style="float:right; margin-left: 5px;"
 
|-
 
|[[#top|back to top]]
 
|}
 
 
MAP: High-dose '''<u>M</u>'''ethotrexate, '''<u>A</u>'''driamycin (Doxorubicin), '''<u>P</u>'''latinol (Cisplatin)
 
MAP: High-dose '''<u>M</u>'''ethotrexate, '''<u>A</u>'''driamycin (Doxorubicin), '''<u>P</u>'''latinol (Cisplatin)
 
+
<div class="toccolours" style="background-color:#eeeeee">
 
===Regimen variant #1, 8000/75/100 {{#subobject:6db034|Variant=1}}===
 
===Regimen variant #1, 8000/75/100 {{#subobject:6db034|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
!style="width: 20%"|Years of enrollment
+
!style="width: 20%"|Dates of enrollment
 
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|Comparator
 
!style="width: 20%"|Comparator
Line 890: Line 663:
 
|[https://doi.org/10.1200/jco.1992.10.10.1579 Bramwell et al. 1992]
 
|[https://doi.org/10.1200/jco.1992.10.10.1579 Bramwell et al. 1992]
 
|1983-1986
 
|1983-1986
|style="background-color:#1a9851"|Phase III (E-esc)
+
|style="background-color:#1a9851"|Phase 3 (E-esc)
 
|[[#Cisplatin_.26_Doxorubicin_2|Cisplatin & Doxorubicin]]
 
|[[#Cisplatin_.26_Doxorubicin_2|Cisplatin & Doxorubicin]]
 
|style="background-color:#fc8d59"|Seems to have inferior DFS
 
|style="background-color:#fc8d59"|Seems to have inferior DFS
Line 896: Line 669:
 
|}
 
|}
 
''Note: The body of Bramwell et al. 1992 says that methotrexate is given over 4 hours, whereas Bramwell et al. 1992 figure 1's text says that methotrexate is given over 6 hours.''
 
''Note: The body of Bramwell et al. 1992 says that methotrexate is given over 4 hours, whereas Bramwell et al. 1992 figure 1's text says that methotrexate is given over 6 hours.''
 +
<div class="toccolours" style="background-color:#cbd5e8">
 
====Preceding treatment====
 
====Preceding treatment====
*[[#MAP|Neoadjuvant MAP]], then [[Surgery#Surgical_resection|surgery]]
+
*Neoadjuvant [[#MAP|MAP]], then [[Surgery#Surgical_resection|surgery]]
 +
</div>
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
 
*[[Methotrexate (MTX)]] 8000 mg/m<sup>2</sup> IV over 4 to 6 hours once on day 1
 
*[[Methotrexate (MTX)]] 8000 mg/m<sup>2</sup> IV over 4 to 6 hours once on day 1
 
*[[Doxorubicin (Adriamycin)]] 25 mg/m<sup>2</sup> IV bolus once per day on days 11 to 13
 
*[[Doxorubicin (Adriamycin)]] 25 mg/m<sup>2</sup> IV bolus once per day on days 11 to 13
 
*[[Cisplatin (Platinol)]] 100 mg/m<sup>2</sup> IV continuous infusion over 24 hours, started on day 11
 
*[[Cisplatin (Platinol)]] 100 mg/m<sup>2</sup> IV continuous infusion over 24 hours, started on day 11
 
+
====Supportive therapy====
====Supportive medications====
+
*[[Leucovorin (Folinic acid)]] 12 mg/m<sup>2</sup> IV every 6 hours x 10 doses or 15 mg/m<sup>2</sup> PO every 6 hours x 10 doses, starting 24 hours after the start of methotrexate infusion
*[[Folinic acid (Leucovorin)]] 12 mg/m<sup>2</sup> IV every 6 hours x 10 doses or 15 mg/m<sup>2</sup> PO every 6 hours x 10 doses, starting 24 hours after the start of methotrexate infusion
 
 
**Monitor methotrexate level at "24 hours and 48 hours"--it is unclear in the reference if this is time after the start/end of methotrexate, beginning of leucovorin, or something else
 
**Monitor methotrexate level at "24 hours and 48 hours"--it is unclear in the reference if this is time after the start/end of methotrexate, beginning of leucovorin, or something else
 
**Methotrexate levels higher than 100 nmol/L at 48 hours required additional leucovorin rescue
 
**Methotrexate levels higher than 100 nmol/L at 48 hours required additional leucovorin rescue
Line 911: Line 686:
 
*Posthydration for methotrexate: Alternating liters of D5W and NS 3000 mL/m<sup>2</sup> over 24 hours, with KCl 60 mEq/L.
 
*Posthydration for methotrexate: Alternating liters of D5W and NS 3000 mL/m<sup>2</sup> over 24 hours, with KCl 60 mEq/L.
 
*Sodium bicarbonate 3 g PO Q6H, starting 12 hours before methotrexate, and sodium bicarbonate 167 mmol/L IV until serum methotrexate level is less than 8000 to 10,000 nmol/L. Note: the reference is not clear about when/if PO sodium bicarbonate is stopped, when IV sodium bicarbonate is started, or the administration rate of IV sodium bicarbonate.
 
*Sodium bicarbonate 3 g PO Q6H, starting 12 hours before methotrexate, and sodium bicarbonate 167 mmol/L IV until serum methotrexate level is less than 8000 to 10,000 nmol/L. Note: the reference is not clear about when/if PO sodium bicarbonate is stopped, when IV sodium bicarbonate is started, or the administration rate of IV sodium bicarbonate.
*Prehydration for cisplatin: normal saline 400 mL/m<sup>2</sup> and D5W 400 mL/m<sup>2</sup> over 2 hours--the reference did not clarify if these two solutions are given at the same time
+
*Prehydration for cisplatin: normal saline 400 mL/m<sup>2</sup> and D5W 400 mL/m<sup>2</sup> IV over 2 hours--the reference did not clarify if these two solutions are given at the same time
 
*The volume of fluid for cisplatin continuous infusion is 2400 mL/m<sup>2</sup> NS, with KCl 80 mEq/L and mannitol 32,000 mg/m<sup>2</sup>
 
*The volume of fluid for cisplatin continuous infusion is 2400 mL/m<sup>2</sup> NS, with KCl 80 mEq/L and mannitol 32,000 mg/m<sup>2</sup>
 
*Posthydration for cisplatin: D5W 600 mL/m<sup>2</sup> over 6 hours, with KCl 20 mEq/L and mannitol 8000 mg/m<sup>2</sup>; and NS 600 mL/m<sup>2</sup> over 6 hours, with KCl 20 mEq/L, magnesium sulfate 2 mmol/L, and calcium gluconate 0.6 mmol/L--the reference did not clarify if these two solutions are given at the same time. Then D5W 600 mL/m<sup>2</sup> over 12 hours, with KCl 20 mEq/L and mannitol 8000 mg/m<sup>2</sup>.
 
*Posthydration for cisplatin: D5W 600 mL/m<sup>2</sup> over 6 hours, with KCl 20 mEq/L and mannitol 8000 mg/m<sup>2</sup>; and NS 600 mL/m<sup>2</sup> over 6 hours, with KCl 20 mEq/L, magnesium sulfate 2 mmol/L, and calcium gluconate 0.6 mmol/L--the reference did not clarify if these two solutions are given at the same time. Then D5W 600 mL/m<sup>2</sup> over 12 hours, with KCl 20 mEq/L and mannitol 8000 mg/m<sup>2</sup>.
 
*With cisplatin, [[Furosemide (Lasix)]] 20 to 40 mg IV if urine output is less than 400 mL/m<sup>2</sup> over 6 hours
 
*With cisplatin, [[Furosemide (Lasix)]] 20 to 40 mg IV if urine output is less than 400 mL/m<sup>2</sup> over 6 hours
 
 
'''21-day cycle for 2 cycles'''
 
'''21-day cycle for 2 cycles'''
 
+
</div></div><br>
===Protocol variant #2, 8000/90/120 {{#subobject:85bced|Variant=1}}===
+
<div class="toccolours" style="background-color:#eeeeee">
 +
===Regimen variant #2, 8000/90/120 {{#subobject:85bced|Variant=1}}===
 
{| class="wikitable" style="width: 40%; text-align:center;"  
 
{| class="wikitable" style="width: 40%; text-align:center;"  
 
!style="width: 25%"|Study
 
!style="width: 25%"|Study
 
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|-
|[https://onlinelibrary.wiley.com/doi/10.1002/1097-0142(19931201)72:11%3C3227::AID-CNCR2820721116%3E3.0.CO;2-C/abstract Bacci et al. 1993 (IOR/OS-2)]
+
|[https://doi.org/10.1002/1097-0142(19931201)72:11%3C3227::AID-CNCR2820721116%3E3.0.CO;2-C Bacci et al. 1993 (IOR/OS-2)]
|style="background-color:#91cf61"|Phase II
+
|style="background-color:#91cf61"|Phase 2
 
|-
 
|-
 
|}
 
|}
 +
''Note: Figure 1 of Bacci et al. 2000 actually depicted the first cycle as being 47 days, and cycles 2 & 3 being 48 days.''
 +
<div class="toccolours" style="background-color:#cbd5e8">
 
====Preceding treatment====
 
====Preceding treatment====
*[[#MAP|Neoadjuvant MAP]], then [[Surgery#Surgical_resection|surgery]], with at least 90% tumor necrosis in the surgically removed specimen
+
*Neoadjuvant [[#MAP|MAP]], then [[Surgery#Surgical_resection|surgery]], with at least 90% tumor necrosis in the surgically removed specimen
====Chemotherapy, part 1====
+
</div>
*[[Methotrexate (MTX)]] 8000 mg/m<sup>2</sup> IV over 6 hours once on day 21
+
<div class="toccolours" style="background-color:#b3e2cd">
*[[Doxorubicin (Adriamycin)]] 45 mg/m<sup>2</sup> IV over 4 hours once per day on days 1 & 2
+
====Chemotherapy====
*[[Cisplatin (Platinol)]] 40 mg/m<sup>2</sup>/day IV continuous infusion over 72 hours, started on day 27 (total dose per cycle: 120 mg/m<sup>2</sup>)
+
*[[Methotrexate (MTX)]] as follows:
 
+
**Cycles 1 to 3: 8000 mg/m<sup>2</sup> IV over 6 hours once on day 21
====Supportive medications====
 
*[[Folinic acid (Leucovorin)]] 15 mg IV every 6 hours x 11 doses on days 22 to 24, starting 24 hours after the start of [[Methotrexate (MTX)]] infusion
 
*Hydration during and after [[Methotrexate (MTX)]] infusion
 
 
 
'''48-day cycle for 3 cycles, then'''--note: Figure 1 of Bacci et al. 2000 actually depicted the first cycle as being 47 days, and cycles 2 & 3 being 48 days.
 
 
 
====Chemotherapy, part 2====
 
 
*[[Doxorubicin (Adriamycin)]] 45 mg/m<sup>2</sup> IV over 4 hours once per day on days 1 & 2
 
*[[Doxorubicin (Adriamycin)]] 45 mg/m<sup>2</sup> IV over 4 hours once per day on days 1 & 2
 
+
*[[Cisplatin (Platinol)]] as follows:
'''Given once after cycle 3'''
+
**Cycles 1 to 3: 40 mg/m<sup>2</sup>/day IV continuous infusion over 72 hours, started on day 27 (total dose per cycle: 120 mg/m<sup>2</sup>)
 +
====Supportive therapy====
 +
*[[Leucovorin (Folinic acid)]] as follows:
 +
**Cycles 1 to 3: 15 mg IV every 6 hours x 11 doses on days 22 to 24, starting 24 hours after the start of methotrexate infusion
 +
*Hydration during and after methotrexate infusion
 +
'''48-day cycle for 4 cycles'''
 +
</div></div><br>
 +
<div class="toccolours" style="background-color:#eeeeee">
  
 
===Regimen variant #3, 12,000/60/90 {{#subobject:03bb56|Variant=1}}===
 
===Regimen variant #3, 12,000/60/90 {{#subobject:03bb56|Variant=1}}===
{| class="wikitable" style="width: 40%; text-align:center;"  
+
{| class="wikitable sortable" style="width: 60%; text-align:center;"  
!style="width: 25%"|Study
+
!style="width: 33%"|Study
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
+
!style="width: 33%"|Dates of enrollment
 +
!style="width: 33%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|-
 
|[https://doi.org/10.1200/jco.1988.6.2.329 Winkler et al. 1988 (COSS-82)]
 
|[https://doi.org/10.1200/jco.1988.6.2.329 Winkler et al. 1988 (COSS-82)]
|style="background-color:#91cf61"|Non-randomized portion of RCT
+
|1982-1984
 +
|style="background-color:#91cf61"|Non-randomized part of phase 3 RCT
 
|-
 
|-
 
|}
 
|}
 +
<div class="toccolours" style="background-color:#cbd5e8">
 
====Preceding treatment====
 
====Preceding treatment====
*[[#MAP|Neoadjuvant MAP]], then [[Surgery#Surgical_resection|surgery]], with good response
+
*Neoadjuvant [[#MAP|MAP]], then [[Surgery#Surgical_resection|surgery]], with good response
 +
</div>
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
 
*[[Methotrexate (MTX)]] 12,000 mg/m<sup>2</sup> (maximum dose of 20,000 mg) IV over 4 hours once per day on days 22 & 29
 
*[[Methotrexate (MTX)]] 12,000 mg/m<sup>2</sup> (maximum dose of 20,000 mg) IV over 4 hours once per day on days 22 & 29
Line 961: Line 743:
 
*[[Doxorubicin (Adriamycin)]] 30 mg/m<sup>2</sup> IV bolus once per day on days 1 & 2
 
*[[Doxorubicin (Adriamycin)]] 30 mg/m<sup>2</sup> IV bolus once per day on days 1 & 2
 
*[[Cisplatin (Platinol)]] 90 mg/m<sup>2</sup> IV over 4 hours once on day 3
 
*[[Cisplatin (Platinol)]] 90 mg/m<sup>2</sup> IV over 4 hours once on day 3
 
+
====Supportive therapy====
====Supportive medications====
+
*[[Leucovorin (Folinic acid)]] 15 mg/m<sup>2</sup> PO every 6 hours x 12 hours once per day on days 23 & 30, starting 24 hours after the completion of methotrexate infusion; additional leucovorin used for delayed methotrexate elimination
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> PO every 6 hours x 12 hours once per day on days 23 & 30, starting 24 hours after the completion of methotrexate infusion; additional leucovorin used for delayed methotrexate elimination
 
 
*Sodium bicarbonate urine alkalinization prior to high-dose methotrexate
 
*Sodium bicarbonate urine alkalinization prior to high-dose methotrexate
 
*NS 4.5 L/m<sup>2</sup> on day 1 after methotrexate; NS 3 L/m<sup>2</sup> on day 2, with adjustments made to keep urine pH greater than 7.4
 
*NS 4.5 L/m<sup>2</sup> on day 1 after methotrexate; NS 3 L/m<sup>2</sup> on day 2, with adjustments made to keep urine pH greater than 7.4
 
*12 hours of hydration prior to cisplatin & 20 hours of hydration after cisplatin; total amount of fluid given over 36hours of prehydration, cisplatin, and posthydration is NS 6 L/m<sup>2</sup> with mannitol 8 g/L and potassium 20 mval/L.
 
*12 hours of hydration prior to cisplatin & 20 hours of hydration after cisplatin; total amount of fluid given over 36hours of prehydration, cisplatin, and posthydration is NS 6 L/m<sup>2</sup> with mannitol 8 g/L and potassium 20 mval/L.
 
*Magnesium 180 mg/m<sup>2</sup> PO "per day throughout the whole chemotherapy time"--as described in COSS-80
 
*Magnesium 180 mg/m<sup>2</sup> PO "per day throughout the whole chemotherapy time"--as described in COSS-80
 
 
'''35-day cycle for 2 cycles'''
 
'''35-day cycle for 2 cycles'''
 
+
</div></div><br>
 +
<div class="toccolours" style="background-color:#eeeeee">
 
===Regimen variant #4, 12,000/75/120 {{#subobject:11a698|Variant=1}}===
 
===Regimen variant #4, 12,000/75/120 {{#subobject:11a698|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
!style="width: 20%"|Years of enrollment
+
!style="width: 20%"|Dates of enrollment
 
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|Comparator
 
!style="width: 20%"|Comparator
Line 981: Line 762:
 
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052459/ Marina et al. 2016 (EURAMOS-1 poor response)]
 
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052459/ Marina et al. 2016 (EURAMOS-1 poor response)]
 
|2005-2011
 
|2005-2011
|style="background-color:#1a9851"|Phase III (C)
+
|style="background-color:#1a9851"|Phase 3 (C)
 
|[[#MAPIE|MAPIE]]
 
|[[#MAPIE|MAPIE]]
 
| style="background-color:#ffffbf" |Did not meet primary endpoint of EFS
 
| style="background-color:#ffffbf" |Did not meet primary endpoint of EFS
 
|-
 
|-
 
|}
 
|}
 +
<div class="toccolours" style="background-color:#cbd5e8">
 
====Preceding treatment====
 
====Preceding treatment====
*[[#MAP|Neoadjuvant MAP]] x 2, then [[Surgery#Surgical_resection|surgery]]
+
*Neoadjuvant [[#MAP|MAP]] x 2, then [[Surgery#Surgical_resection|surgery]]
 +
</div>
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
*[[Methotrexate (MTX)]] as follows:
+
*[[Methotrexate (MTX)]] by the following site-based criteria:
 
**Non-COG sites: 12,000 mg/m<sup>2</sup> IV over 4 hours once per day on days 22 & 29
 
**Non-COG sites: 12,000 mg/m<sup>2</sup> IV over 4 hours once per day on days 22 & 29
 
**COG sites: 12,000 mg/m<sup>2</sup> (maximum dose of 20,000 mg) IV over 4 hours once per day on days 22 & 29
 
**COG sites: 12,000 mg/m<sup>2</sup> (maximum dose of 20,000 mg) IV over 4 hours once per day on days 22 & 29
 
*[[Doxorubicin (Adriamycin)]] 37.5 mg/m<sup>2</sup> IV once per day on days 1 & 2
 
*[[Doxorubicin (Adriamycin)]] 37.5 mg/m<sup>2</sup> IV once per day on days 1 & 2
*[[Cisplatin (Platinol)]] 40 mg/m<sup>2</sup>/day IV continuous infusion over 72 hours, started on day 1 (total dose per cycle: 120 mg/m<sup>2</sup>)
+
*[[Cisplatin (Platinol)]] by the following site-based criteria:
 +
**Non-COG sites: 40 mg/m<sup>2</sup>/day IV continuous infusion over 72 hours, started on day 1 (total dose per cycle: 120 mg/m<sup>2</sup>)
 
**COG sites: 60 mg/m<sup>2</sup> IV once per day on days 1 & 2
 
**COG sites: 60 mg/m<sup>2</sup> IV once per day on days 1 & 2
 
+
====Supportive therapy====
====Supportive medications====
+
*[[Leucovorin (Folinic acid)]] 15 mg/m<sup>2</sup> (route/schedule not specified), starting 24 to 48 hours after methotrexate infusion, continued until MTX level less than 100 nmol/L
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> (route/schedule not specified), starting 24 to 48 hours after [[Methotrexate (MTX)]] infusion, continued until MTX level less than 100 nmol/L
 
 
 
 
'''35-day cycle for 2 cycles'''
 
'''35-day cycle for 2 cycles'''
 +
</div>
 +
<div class="toccolours" style="background-color:#cbd5e7">
 
====Subsequent treatment====
 
====Subsequent treatment====
*[[#MA_2|MA]] x 2
+
*Adjuvant [[#MA_2|MA]] x 2
 
+
</div></div>
 
===References===
 
===References===
# '''COSS-82:''' Winkler K, Beron G, Delling G, Heise U, Kabisch H, Purfürst C, Berger J, Ritter J, Jürgens H, Gerein V, Graf N, Russe W, Gruemayer ER, Ertelt W, Kotz R, Preuzzer P, Prindull G, Brandeis W, Landbeck G. Neoadjuvant chemotherapy of osteosarcoma: results of a randomized cooperative trial (COSS-82) with salvage chemotherapy based on histological tumor response. J Clin Oncol. 1988 Feb;6(2):329-37. [https://doi.org/10.1200/jco.1988.6.2.329 link to original article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/2448428 PubMed]
+
# '''COSS-82:''' Winkler K, Beron G, Delling G, Heise U, Kabisch H, Purfürst C, Berger J, Ritter J, Jürgens H, Gerein V, Graf N, Russe W, Gruemayer ER, Ertelt W, Kotz R, Preuzzer P, Prindull G, Brandeis W, Landbeck G. Neoadjuvant chemotherapy of osteosarcoma: results of a randomized cooperative trial (COSS-82) with salvage chemotherapy based on histological tumor response. J Clin Oncol. 1988 Feb;6(2):329-37. [https://doi.org/10.1200/jco.1988.6.2.329 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/2448428/ PubMed]
# Bramwell VH, Burgers M, Sneath R, Souhami R, van Oosterom AT, Voûte PA, Rouesse J, Spooner D, Craft AW, Somers R, Pringle J, Malcolm AJ, van der Eiiken J, Thomas D, Uscinska B, Machin D, van Glabbeke M; European Osteosarcoma Intergroup. A comparison of two short intensive adjuvant chemotherapy regimens in operable osteosarcoma of limbs in children and young adults: the first study of the European Osteosarcoma Intergroup. J Clin Oncol. 1992 Oct;10(10):1579-91. [https://doi.org/10.1200/jco.1992.10.10.1579 link to original article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/1403038 PubMed]
+
# Bramwell VH, Burgers M, Sneath R, Souhami R, van Oosterom AT, Voûte PA, Rouesse J, Spooner D, Craft AW, Somers R, Pringle J, Malcolm AJ, van der Eiiken J, Thomas D, Uscinska B, Machin D, van Glabbeke M; European Osteosarcoma Intergroup. A comparison of two short intensive adjuvant chemotherapy regimens in operable osteosarcoma of limbs in children and young adults: the first study of the European Osteosarcoma Intergroup. J Clin Oncol. 1992 Oct;10(10):1579-91. [https://doi.org/10.1200/jco.1992.10.10.1579 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/1403038/ PubMed]
# '''IOR/OS-2:''' Bacci G, Picci P, Ferrari S, Ruggieri P, Casadei R, Tienghi A, Brach del Prever A, Gherlinzoni F, Mercuri M, Monti C. Primary chemotherapy and delayed surgery for nonmetastatic osteosarcoma of the extremities: results in 164 patients preoperatively treated with high doses of methotrexate followed by cisplatin and doxorubicin. Cancer. 1993 Dec 1;72(11):3227-38. [https://onlinelibrary.wiley.com/doi/10.1002/1097-0142(19931201)72:11%3C3227::AID-CNCR2820721116%3E3.0.CO;2-C/abstract link to original article] [https://pubmed.ncbi.nlm.nih.gov/8242546 PubMed]
+
# '''IOR/OS-2:''' Bacci G, Picci P, Ferrari S, Ruggieri P, Casadei R, Tienghi A, Brach del Prever A, Gherlinzoni F, Mercuri M, Monti C. Primary chemotherapy and delayed surgery for nonmetastatic osteosarcoma of the extremities: results in 164 patients preoperatively treated with high doses of methotrexate followed by cisplatin and doxorubicin. Cancer. 1993 Dec 1;72(11):3227-38. [https://doi.org/10.1002/1097-0142(19931201)72:11%3C3227::AID-CNCR2820721116%3E3.0.CO;2-C link to original article] [https://pubmed.ncbi.nlm.nih.gov/8242546/ PubMed]
## '''Update:''' Bacci G, Ferrari S, Bertoni F, Ruggieri P, Picci P, Longhi A, Casadei R, Fabbri N, Forni C, Versari M, Campanacci M. Long-term outcome for patients with nonmetastatic osteosarcoma of the extremity treated at the Istituto Ortopedico Rizzoli according to the Istituto Ortopedico Rizzoli/Osteosarcoma-2 protocol: an updated report. J Clin Oncol. 2000 Dec 15;18(24):4016-27. [https://doi.org/10.1200/jco.2000.18.24.4016 link to original article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/11118462 PubMed]
+
## '''Update:''' Bacci G, Ferrari S, Bertoni F, Ruggieri P, Picci P, Longhi A, Casadei R, Fabbri N, Forni C, Versari M, Campanacci M. Long-term outcome for patients with nonmetastatic osteosarcoma of the extremity treated at the Istituto Ortopedico Rizzoli according to the Istituto Ortopedico Rizzoli/Osteosarcoma-2 protocol: an updated report. J Clin Oncol. 2000 Dec 15;18(24):4016-27. [https://doi.org/10.1200/jco.2000.18.24.4016 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/11118462/ PubMed]
# '''EURAMOS-1 good response:''' Bielack SS, Smeland S, Whelan JS, Marina N, Jovic G, Hook JM, Krailo MD, Gebhardt M, Pápai Z, Meyer J, Nadel H, Randall RL, Deffenbaugh C, Nagarajan R, Brennan B, Letson GD, Teot LA, Goorin A, Baumhoer D, Kager L, Werner M, Lau CC, Sundby Hall K, Gelderblom H, Meyers P, Gorlick R, Windhager R, Helmke K, Eriksson M, Hoogerbrugge PM, Schomberg P, Tunn PU, Kühne T, Jürgens H, van den Berg H, Böhling T, Picton S, Renard M, Reichardt P, Gerss J, Butterfass-Bahloul T, Morris C, Hogendoorn PC, Seddon B, Calaminus G, Michelagnoli M, Dhooge C, Sydes MR, Bernstein M; EURAMOS-1 investigators. Methotrexate, doxorubicin, and cisplatin (MAP) plus maintenance pegylated interferon alfa-2b versus MAP alone in patients with resectable high-grade osteosarcoma and good histologic response to preoperative map: first results of the EURAMOS-1 good response randomized controlled trial. J Clin Oncol. 2015 Jul 10;33(20):2279-87. Epub 2015 Jun 1. [https://doi.org/10.1200/JCO.2014.60.0734 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4486345/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/26033801 PubMed]
+
# '''EURAMOS-1 good response:''' Bielack SS, Smeland S, Whelan JS, Marina N, Jovic G, Hook JM, Krailo MD, Gebhardt M, Pápai Z, Meyer J, Nadel H, Randall RL, Deffenbaugh C, Nagarajan R, Brennan B, Letson GD, Teot LA, Goorin A, Baumhoer D, Kager L, Werner M, Lau CC, Sundby Hall K, Gelderblom H, Meyers P, Gorlick R, Windhager R, Helmke K, Eriksson M, Hoogerbrugge PM, Schomberg P, Tunn PU, Kühne T, Jürgens H, van den Berg H, Böhling T, Picton S, Renard M, Reichardt P, Gerss J, Butterfass-Bahloul T, Morris C, Hogendoorn PC, Seddon B, Calaminus G, Michelagnoli M, Dhooge C, Sydes MR, Bernstein M; EURAMOS-1 investigators. Methotrexate, doxorubicin, and cisplatin (MAP) plus maintenance pegylated interferon alfa-2b versus MAP alone in patients with resectable high-grade osteosarcoma and good histologic response to preoperative map: first results of the EURAMOS-1 good response randomized controlled trial. J Clin Oncol. 2015 Jul 10;33(20):2279-87. Epub 2015 Jun 1. [https://doi.org/10.1200/JCO.2014.60.0734 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4486345/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/26033801/ PubMed]
# '''EURAMOS-1 poor response:''' Marina NM, Smeland S, Bielack SS, Bernstein M, Jovic G, Krailo MD, Hook JM, Arndt C, van den Berg H, Brennan B, Brichard B, Brown KL, Butterfass-Bahloul T, Calaminus G, Daldrup-Link HE, Eriksson M, Gebhardt MC, Gelderblom H, Gerss J, Goldsby R, Goorin A, Gorlick R, Grier HE, Hale JP, Hall KS, Hardes J, Hawkins DS, Helmke K, Hogendoorn PC, Isakoff MS, Janeway KA, Jürgens H, Kager L, Kühne T, Lau CC, Leavey PJ, Lessnick SL, Mascarenhas L, Meyers PA, Mottl H, Nathrath M, Papai Z, Randall RL, Reichardt P, Renard M, Safwat AA, Schwartz CL, Stevens MC, Strauss SJ, Teot L, Werner M, Sydes MR, Whelan JS. Comparison of MAPIE versus MAP in patients with a poor response to preoperative chemotherapy for newly diagnosed high-grade osteosarcoma (EURAMOS-1): an open-label, international, randomised controlled trial. Lancet Oncol. 2016 Oct;17(10):1396-1408. Epub 2016 Aug 25. [https://www.thelancet.com/journals/lanonc/article/PIIS1470-2045(16)30214-5/fulltext link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052459/ link to PMC article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/27569442 PubMed] NCT00134030
+
# '''EURAMOS-1 poor response:''' Marina NM, Smeland S, Bielack SS, Bernstein M, Jovic G, Krailo MD, Hook JM, Arndt C, van den Berg H, Brennan B, Brichard B, Brown KL, Butterfass-Bahloul T, Calaminus G, Daldrup-Link HE, Eriksson M, Gebhardt MC, Gelderblom H, Gerss J, Goldsby R, Goorin A, Gorlick R, Grier HE, Hale JP, Hall KS, Hardes J, Hawkins DS, Helmke K, Hogendoorn PC, Isakoff MS, Janeway KA, Jürgens H, Kager L, Kühne T, Lau CC, Leavey PJ, Lessnick SL, Mascarenhas L, Meyers PA, Mottl H, Nathrath M, Papai Z, Randall RL, Reichardt P, Renard M, Safwat AA, Schwartz CL, Stevens MC, Strauss SJ, Teot L, Werner M, Sydes MR, Whelan JS. Comparison of MAPIE versus MAP in patients with a poor response to preoperative chemotherapy for newly diagnosed high-grade osteosarcoma (EURAMOS-1): an open-label, international, randomised controlled trial. Lancet Oncol. 2016 Oct;17(10):1396-1408. Epub 2016 Aug 25. [https://doi.org/10.1016/S1470-2045(16)30214-5 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052459/ link to PMC article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/27569442/ PubMed] [https://clinicaltrials.gov/study/NCT00134030 NCT00134030]
 
 
 
==MAPI {{#subobject:909a14|Regimen=1}}==
 
==MAPI {{#subobject:909a14|Regimen=1}}==
{| class="wikitable" style="float:right; margin-left: 5px;"
 
|-
 
|[[#top|back to top]]
 
|}
 
 
MAPI: High-dose '''<u>M</u>'''ethotrexate, '''<u>A</u>'''driamycin (Doxorubicin), '''<u>P</u>'''latinol (Cisplatin), '''<u>I</u>'''fosfamide
 
MAPI: High-dose '''<u>M</u>'''ethotrexate, '''<u>A</u>'''driamycin (Doxorubicin), '''<u>P</u>'''latinol (Cisplatin), '''<u>I</u>'''fosfamide
 +
<div class="toccolours" style="background-color:#eeeeee">
 
===Regimen {{#subobject:61db3e|Variant=1}}===
 
===Regimen {{#subobject:61db3e|Variant=1}}===
 
{| class="wikitable" style="width: 40%; text-align:center;"  
 
{| class="wikitable" style="width: 40%; text-align:center;"  
Line 1,023: Line 804:
 
|-
 
|-
 
|[https://doi.org/10.1093/annonc/mdg286 Bacci et al. 2003]
 
|[https://doi.org/10.1093/annonc/mdg286 Bacci et al. 2003]
|style="background-color:#91cf61"|Phase II
+
|style="background-color:#91cf61"|Phase 2
 
|-
 
|-
 
|}
 
|}
 +
<div class="toccolours" style="background-color:#cbd5e8">
 
====Preceding treatment====
 
====Preceding treatment====
*[[#MAPI|Neoadjuvant MAPI]], then [[Surgery#Surgical_resection|surgery]]
+
*Neoadjuvant [[#MAPI|MAPI]], then [[Surgery#Surgical_resection|surgery]]
 +
</div>
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
 
*[[Methotrexate (MTX)]] 12,000 mg/m<sup>2</sup> IV over 4 hours once on day 36
 
*[[Methotrexate (MTX)]] 12,000 mg/m<sup>2</sup> IV over 4 hours once on day 36
**If 4-hour methotrexate level is less than 10,000 nmol/L, the next cycle's dose is increased by 2000 mg/m<sup>2</sup>
 
 
*[[Doxorubicin (Adriamycin)]] 90 mg/m<sup>2</sup> IV continuous infusion over 24 hours, started on day 1
 
*[[Doxorubicin (Adriamycin)]] 90 mg/m<sup>2</sup> IV continuous infusion over 24 hours, started on day 1
 
*[[Cisplatin (Platinol)]] 60 mg/m<sup>2</sup>/day IV continuous infusion over 48 hours, started on day 43 (total dose per cycle: 120 mg/m<sup>2</sup>)  
 
*[[Cisplatin (Platinol)]] 60 mg/m<sup>2</sup>/day IV continuous infusion over 48 hours, started on day 43 (total dose per cycle: 120 mg/m<sup>2</sup>)  
*[[Ifosfamide (Ifex)]] 3000 mg/m<sup>2</sup>/day IV continuous infusion over 120 hours, started on day 22, '''given with [[Mesna (Mesnex)]]''' (total dose per cycle: 15,000 mg/m<sup>2</sup>)
+
*[[Ifosfamide (Ifex)]] 3000 mg/m<sup>2</sup>/day IV continuous infusion over 120 hours, started on day 22, '''given with mesna''' (total dose per cycle: 15,000 mg/m<sup>2</sup>)
 
+
====Supportive therapy====
====Supportive medications====
+
*[[Mesna (Mesnex)]] 3000 mg/m<sup>2</sup>/day IV continuous infusion over 120 hours, started on day 22, '''given with ifosfamide''' (total dose per cycle: 15,000 mg/m<sup>2</sup>)
*[[Mesna (Mesnex)]] 3000 mg/m<sup>2</sup>/day IV continuous infusion over 120 hours, started on day 22, '''given with [[Ifosfamide (Ifex)]]''' (total dose per cycle: 15,000 mg/m<sup>2</sup>)
+
*[[Leucovorin (Folinic acid)]] 15 mg (route not specified) every 6 hours x 11 doses, starting day 36, 24 hours after the start of methotrexate
*[[Folinic acid (Leucovorin)]] 15 mg (route not specified) every 6 hours x 11 doses, starting day 36, 24 hours after the start of [[Methotrexate (MTX)]]
+
*Hydration during and after methotrexate as described by: Rosen G, Nirenberg A. Chemotherapy for osteogenic sarcoma: an investigative method, not a recipe. Cancer Treat Rep. 1982 Sep;66(9):1687-97. [https://pubmed.ncbi.nlm.nih.gov/6981454/ PubMed]
*Hydration during and after [[Methotrexate (MTX)]] as described by: Rosen G, Nirenberg A. Chemotherapy for osteogenic sarcoma: an investigative method, not a recipe. Cancer Treat Rep. 1982 Sep;66(9):1687-97. [https://pubmed.ncbi.nlm.nih.gov/6981454 PubMed]
 
 
 
 
'''9-week cycle for 3 cycles'''
 
'''9-week cycle for 3 cycles'''
 
+
</div>
 +
<div class="toccolours" style="background-color:#fff2ae">
 +
====Dose and schedule modifications====
 +
*If 4-hour methotrexate level is less than 10,000 nmol/L, the next cycle's methotrexate dose is increased by 2000 mg/m<sup>2</sup>
 +
</div></div>
 
===References===
 
===References===
# Bacci G, Briccoli A, Rocca M, Ferrari S, Donati D, Longhi A, Bertoni F, Bacchini P, Giacomini S, Forni C, Manfrini M, Galletti S. Neoadjuvant chemotherapy for osteosarcoma of the extremities with metastases at presentation: recent experience at the Rizzoli Institute in 57 patients treated with cisplatin, doxorubicin, and a high dose of methotrexate and ifosfamide. Ann Oncol. 2003 Jul;14(7):1126-34. [https://doi.org/10.1093/annonc/mdg286 link to original article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/12853357 PubMed]
+
# Bacci G, Briccoli A, Rocca M, Ferrari S, Donati D, Longhi A, Bertoni F, Bacchini P, Giacomini S, Forni C, Manfrini M, Galletti S. Neoadjuvant chemotherapy for osteosarcoma of the extremities with metastases at presentation: recent experience at the Rizzoli Institute in 57 patients treated with cisplatin, doxorubicin, and a high dose of methotrexate and ifosfamide. Ann Oncol. 2003 Jul;14(7):1126-34. [https://doi.org/10.1093/annonc/mdg286 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/12853357/ PubMed]
 
 
 
==MAPIE {{#subobject:d9962f|Regimen=1}}==
 
==MAPIE {{#subobject:d9962f|Regimen=1}}==
{| class="wikitable" style="float:right; margin-left: 5px;"
 
|-
 
|[[#top|back to top]]
 
|}
 
 
MAPIE: High-dose '''<u>M</u>'''ethotrexate, '''<u>A</u>'''driamycin (Doxorubicin), '''<u>P</u>'''latinol (Cisplatin), '''<u>I</u>'''fosfamide, '''<u>E</u>'''toposide
 
MAPIE: High-dose '''<u>M</u>'''ethotrexate, '''<u>A</u>'''driamycin (Doxorubicin), '''<u>P</u>'''latinol (Cisplatin), '''<u>I</u>'''fosfamide, '''<u>E</u>'''toposide
 
+
<div class="toccolours" style="background-color:#eeeeee">
===Protocol {{#subobject:97ec7e|Variant=1}}===
+
===Regimen {{#subobject:97ec7e|Variant=1}}===
 
{| class="wikitable" style="width: 40%; text-align:center;"  
 
{| class="wikitable" style="width: 40%; text-align:center;"  
 
!style="width: 25%"|Study
 
!style="width: 25%"|Study
 
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|-
|[https://onlinelibrary.wiley.com/doi/10.1002/1097-0142(19931201)72:11%3C3227::AID-CNCR2820721116%3E3.0.CO;2-C/abstract Bacci et al. 1993 (IOR/OS-2)]
+
|[https://doi.org/10.1002/1097-0142(19931201)72:11%3C3227::AID-CNCR2820721116%3E3.0.CO;2-C Bacci et al. 1993 (IOR/OS-2)]
|style="background-color:#91cf61"|Phase II
+
|style="background-color:#91cf61"|Phase 2
 
|-
 
|-
 
|}
 
|}
 +
''Note: Figure 1 of Bacci et al. 2000 actually depicted the first cycle as being 68 days, and cycles 2 & 3 being 69 days.''
 +
<div class="toccolours" style="background-color:#cbd5e8">
 
====Preceding treatment====
 
====Preceding treatment====
*[[#MAP|Neoadjuvant MAP]], then [[Surgery#Surgical_resection|surgery]], with less than 90% tumor necrosis in the surgically removed specimen
+
*Neoadjuvant [[#MAP|MAP]], then [[Surgery#Surgical_resection|surgery]], with less than 90% tumor necrosis in the surgically removed specimen
====Chemotherapy, part 1====
+
</div>
*[[Methotrexate (MTX)]] 8000 mg/m<sup>2</sup> IV over 6 hours once on day 42
+
<div class="toccolours" style="background-color:#b3e2cd">
 +
====Chemotherapy====
 +
*[[Methotrexate (MTX)]] as follows:
 +
**Cycles 1 to 3: 8000 mg/m<sup>2</sup> IV over 6 hours once on day 42
 
*[[Doxorubicin (Adriamycin)]] 45 mg/m<sup>2</sup> IV over 4 hours once per day on days 1 & 2
 
*[[Doxorubicin (Adriamycin)]] 45 mg/m<sup>2</sup> IV over 4 hours once per day on days 1 & 2
*[[Cisplatin (Platinol)]] 40 mg/m<sup>2</sup>/day IV continuous infusion over 72 hours, started on day 48 (total dose per cycle: 120 mg/m<sup>2</sup>)
+
*[[Cisplatin (Platinol)]] as follows:
*[[Ifosfamide (Ifex)]] 2000 mg/m<sup>2</sup> IV over 90 minutes once per day on days 21 to 25
+
**Cycles 1 to 3: 40 mg/m<sup>2</sup>/day IV continuous infusion over 72 hours, started on day 48 (total dose per cycle: 120 mg/m<sup>2</sup>)
*[[Etoposide (Vepesid)]] 120 mg/m<sup>2</sup> IV over 60 minutes once per day on days 48 to 50
+
*[[Ifosfamide (Ifex)]] as follows:
 
+
**Cycles 1 to 3: 2000 mg/m<sup>2</sup> IV over 90 minutes once per day on days 21 to 25, with mesna
====Supportive medications====
+
*[[Etoposide (Vepesid)]] as follows:
*[[Mesna (Mesnex)]] with [[Ifosfamide (Ifex)]]; no actual dose is listed in the reference
+
**Cycles 1 to 3: 120 mg/m<sup>2</sup> IV over 60 minutes once per day on days 48 to 50
*[[Folinic acid (Leucovorin)]] 15 mg IV every 6 hours x 11 doses on days 43 to 45, starting 24 hours after the start of [[Methotrexate (MTX)]] infusion
+
====Supportive therapy====
*Hydration during and after [[Methotrexate (MTX)]] infusion
+
*[[Mesna (Mesnex)]] as follows:
 
+
**Cycles 1 to 3: with ifosfamide; no actual dose is listed in the reference
'''69-day cycle for 3 cycles, then'''--note: Figure 1 of Bacci et al. 2000 actually depicted the first cycle as being 68 days, and cycles 2 & 3 being 69 days.
+
*[[Leucovorin (Folinic acid)]] as follows:
 
+
**Cycles 1 to 3: 15 mg IV every 6 hours x 11 doses on days 43 to 45, starting 24 hours after the start of methotrexate infusion
====Chemotherapy, part 2====
+
*Hydration during and after methotrexate infusion
*[[Doxorubicin (Adriamycin)]] 45 mg/m<sup>2</sup> IV over 4 hours once per day on days 1 & 2
+
'''69-day cycle for 4 cycles'''  
 
+
</div></div>
'''Given once after postoperative chemotherapy cycle 3'''
 
 
 
 
===References===
 
===References===
# '''IOR/OS-2:''' Bacci G, Picci P, Ferrari S, Ruggieri P, Casadei R, Tienghi A, Brach del Prever A, Gherlinzoni F, Mercuri M, Monti C. Primary chemotherapy and delayed surgery for nonmetastatic osteosarcoma of the extremities: results in 164 patients preoperatively treated with high doses of methotrexate followed by cisplatin and doxorubicin. Cancer. 1993 Dec 1;72(11):3227-38. [https://onlinelibrary.wiley.com/doi/10.1002/1097-0142(19931201)72:11%3C3227::AID-CNCR2820721116%3E3.0.CO;2-C/abstract link to original article] [https://pubmed.ncbi.nlm.nih.gov/8242546 PubMed]
+
# '''IOR/OS-2:''' Bacci G, Picci P, Ferrari S, Ruggieri P, Casadei R, Tienghi A, Brach del Prever A, Gherlinzoni F, Mercuri M, Monti C. Primary chemotherapy and delayed surgery for nonmetastatic osteosarcoma of the extremities: results in 164 patients preoperatively treated with high doses of methotrexate followed by cisplatin and doxorubicin. Cancer. 1993 Dec 1;72(11):3227-38. [https://doi.org/10.1002/1097-0142(19931201)72:11%3C3227::AID-CNCR2820721116%3E3.0.CO;2-C link to original article] [https://pubmed.ncbi.nlm.nih.gov/8242546/ PubMed]
## '''Update:''' Bacci G, Ferrari S, Bertoni F, Ruggieri P, Picci P, Longhi A, Casadei R, Fabbri N, Forni C, Versari M, Campanacci M. Long-term outcome for patients with nonmetastatic osteosarcoma of the extremity treated at the Istituto Ortopedico Rizzoli according to the Istituto Ortopedico Rizzoli/Osteosarcoma-2 protocol: an updated report. J Clin Oncol. 2000 Dec 15;18(24):4016-27. [https://doi.org/10.1200/jco.2000.18.24.4016 link to original article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/11118462 PubMed]
+
## '''Update:''' Bacci G, Ferrari S, Bertoni F, Ruggieri P, Picci P, Longhi A, Casadei R, Fabbri N, Forni C, Versari M, Campanacci M. Long-term outcome for patients with nonmetastatic osteosarcoma of the extremity treated at the Istituto Ortopedico Rizzoli according to the Istituto Ortopedico Rizzoli/Osteosarcoma-2 protocol: an updated report. J Clin Oncol. 2000 Dec 15;18(24):4016-27. [https://doi.org/10.1200/jco.2000.18.24.4016 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/11118462/ PubMed]
# '''EURAMOS-1 poor response:''' Marina NM, Smeland S, Bielack SS, Bernstein M, Jovic G, Krailo MD, Hook JM, Arndt C, van den Berg H, Brennan B, Brichard B, Brown KL, Butterfass-Bahloul T, Calaminus G, Daldrup-Link HE, Eriksson M, Gebhardt MC, Gelderblom H, Gerss J, Goldsby R, Goorin A, Gorlick R, Grier HE, Hale JP, Hall KS, Hardes J, Hawkins DS, Helmke K, Hogendoorn PC, Isakoff MS, Janeway KA, Jürgens H, Kager L, Kühne T, Lau CC, Leavey PJ, Lessnick SL, Mascarenhas L, Meyers PA, Mottl H, Nathrath M, Papai Z, Randall RL, Reichardt P, Renard M, Safwat AA, Schwartz CL, Stevens MC, Strauss SJ, Teot L, Werner M, Sydes MR, Whelan JS. Comparison of MAPIE versus MAP in patients with a poor response to preoperative chemotherapy for newly diagnosed high-grade osteosarcoma (EURAMOS-1): an open-label, international, randomised controlled trial. Lancet Oncol. 2016 Oct;17(10):1396-1408. Epub 2016 Aug 25. [https://www.thelancet.com/journals/lanonc/article/PIIS1470-2045(16)30214-5/fulltext link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052459/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/27569442 PubMed] NCT00134030
+
# '''EURAMOS-1 poor response:''' Marina NM, Smeland S, Bielack SS, Bernstein M, Jovic G, Krailo MD, Hook JM, Arndt C, van den Berg H, Brennan B, Brichard B, Brown KL, Butterfass-Bahloul T, Calaminus G, Daldrup-Link HE, Eriksson M, Gebhardt MC, Gelderblom H, Gerss J, Goldsby R, Goorin A, Gorlick R, Grier HE, Hale JP, Hall KS, Hardes J, Hawkins DS, Helmke K, Hogendoorn PC, Isakoff MS, Janeway KA, Jürgens H, Kager L, Kühne T, Lau CC, Leavey PJ, Lessnick SL, Mascarenhas L, Meyers PA, Mottl H, Nathrath M, Papai Z, Randall RL, Reichardt P, Renard M, Safwat AA, Schwartz CL, Stevens MC, Strauss SJ, Teot L, Werner M, Sydes MR, Whelan JS. Comparison of MAPIE versus MAP in patients with a poor response to preoperative chemotherapy for newly diagnosed high-grade osteosarcoma (EURAMOS-1): an open-label, international, randomised controlled trial. Lancet Oncol. 2016 Oct;17(10):1396-1408. Epub 2016 Aug 25. [https://doi.org/10.1016/S1470-2045(16)30214-5 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052459/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/27569442/ PubMed] [https://clinicaltrials.gov/study/NCT00134030 NCT00134030]
  
 
==M-EI {{#subobject:79b8f9|Regimen=1}}==
 
==M-EI {{#subobject:79b8f9|Regimen=1}}==
{| class="wikitable" style="float:right; margin-left: 5px;"
 
|-
 
|[[#top|back to top]]
 
|}
 
 
M-EI: '''<u>M</u>'''ethotrexate, '''<u>E</u>'''toposide, '''<u>I</u>'''fosfamide
 
M-EI: '''<u>M</u>'''ethotrexate, '''<u>E</u>'''toposide, '''<u>I</u>'''fosfamide
===Protocol {{#subobject:7fc4e3|Variant=1}}===
+
<div class="toccolours" style="background-color:#eeeeee">
{| class="wikitable" style="width: 40%; text-align:center;"  
+
===Regimen {{#subobject:7fc4e3|Variant=1}}===
!style="width: 25%"|Study
+
{| class="wikitable sortable" style="width: 60%; text-align:center;"  
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
+
!style="width: 33%"|Study
 +
!style="width: 33%"|Dates of enrollment
 +
!style="width: 33%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|-
|[https://www.ejcancer.com/article/S0959-8049(06)01072-0/abstract Le Deley et al. 2007 (SFOP OS94)]
+
|[https://doi.org/10.1016/j.ejca.2006.10.023 Le Deley et al. 2007 (SFOP OS94)]
|style="background-color:#91cf61"|Non-randomized portion of RCT
+
|1994-2001
 +
|style="background-color:#91cf61"|Non-randomized part of phase 3 RCT
 
|-
 
|-
 
|}
 
|}
 +
<div class="toccolours" style="background-color:#cbd5e8">
 
====Preceding treatment====
 
====Preceding treatment====
*[[#M-EI|Neoadjuvant M-EI]], then [[Surgery#Surgical_resection|surgery]], with good response
+
*Neoadjuvant [[#M-EI|M-EI]], then [[Surgery#Surgical_resection|surgery]], with good response
====Chemotherapy, part 1====
+
</div>
 +
<div class="toccolours" style="background-color:#b3e2cd">
 +
====Chemotherapy====
 
*[[Methotrexate (MTX)]] 12,000 mg/m<sup>2</sup> IV over 4 hours once per day on days 1, 8, 15
 
*[[Methotrexate (MTX)]] 12,000 mg/m<sup>2</sup> IV over 4 hours once per day on days 1, 8, 15
 
**Given in D5W 1L with sodium bicarbonate 1 mEq/kg
 
**Given in D5W 1L with sodium bicarbonate 1 mEq/kg
*[[Etoposide (Vepesid)]] 75 mg/m<sup>2</sup> IV over 60 minutes once per day on days 22 to 25 (week 4)
+
*[[Etoposide (Vepesid)]] as follows:
**Given in NS 250 to 500 mL
+
**Cycles 1 to 3: 75 mg/m<sup>2</sup> IV over 60 minutes once per day on days 22 to 25 (week 4)
*[[Ifosfamide (Ifex)]] 3000 mg/m<sup>2</sup> IV over 3 hours once per day on days 22 to 25 (week 4), '''given during [[Mesna (Mesnex)]] infusion''' (total dose per cycle: 12,000 mg/m<sup>2</sup>)
+
***Given in NS 250 to 500 mL
**Given in NS 250 to 500 mL
+
*[[Ifosfamide (Ifex)]] as follows:
 
+
**Cycles 1 to 3: 3000 mg/m<sup>2</sup> IV over 3 hours once per day on days 22 to 25 (week 4), '''given during mesna infusion''' (total dose per cycle: 12,000 mg/m<sup>2</sup>)
====Supportive medications====
+
***Given in NS 250 to 500 mL
*[[Folinic acid (Leucovorin)]] 15 mg PO every 6 hours for up to 11 doses, starting on days 1, 8, 15, starting 20 hours after the completion of [[Methotrexate (MTX)]] infusion
+
====Supportive therapy====
 +
*[[Leucovorin (Folinic acid)]] 15 mg PO every 6 hours for up to 11 doses, starting on days 1, 8, 15, starting 20 hours after the completion of methotrexate infusion
 
*For methotrexate: hydration & urine alkalinization by PO and IV routes to maintain 1.6 L/m<sup>2</sup> urine output over the first 24 hours and 2 L/m<sup>2</sup> on days 2 & 3, with urine pH greater than 7
 
*For methotrexate: hydration & urine alkalinization by PO and IV routes to maintain 1.6 L/m<sup>2</sup> urine output over the first 24 hours and 2 L/m<sup>2</sup> on days 2 & 3, with urine pH greater than 7
 
*Daily monitoring of methotrexate levels and creatinine
 
*Daily monitoring of methotrexate levels and creatinine
*[[Mesna (Mesnex)]] 3600 mg/m<sup>2</sup>/day IV continuous infusion over 96 hours, started on day 22 (week 4) (total dose per cycle: 14,400 mg/m<sup>2</sup>)
+
*[[Mesna (Mesnex)]] as follows:
 +
**Cycles 1 to 3: 3600 mg/m<sup>2</sup>/day IV continuous infusion over 96 hours, started on day 22 (week 4) (total dose per cycle: 14,400 mg/m<sup>2</sup>)
 
*Up to 2 L/day hydration with ifosfamide & mesna
 
*Up to 2 L/day hydration with ifosfamide & mesna
 
+
'''28-day cycle for 4 cycles'''
'''28-day cycle for 3 cycles, followed by:'''
+
</div></div>
 
 
====Chemotherapy, part 2====
 
*[[Methotrexate (MTX)]] 12,000 mg/m<sup>2</sup> IV over 4 hours once per day on days 1, 8, 15
 
**Given in D5W 1L with sodium bicarbonate 1 mEq/kg
 
 
 
====Supportive medications====
 
*[[Folinic acid (Leucovorin)]] 15 mg PO every 6 hours for up to 11 doses, starting on days 1, 8, 15, starting 20 hours after the completion of [[Methotrexate (MTX)]] infusion
 
*For methotrexate: hydration & urine alkalinization by PO and IV routes to maintain 1.6 L/m<sup>2</sup> urine output over the first 24 hours and 2 L/m<sup>2</sup> on days 2 & 3, with urine pH greater than 7
 
*Daily monitoring of methotrexate levels and creatinine
 
 
 
'''21-day course'''
 
 
 
===References===
 
# '''SFOP OS94:''' Le Deley MC, Guinebretière JM, Gentet JC, Pacquement H, Pichon F, Marec-Bérard P, Entz-Werlé N, Schmitt C, Brugières L, Vanel D, Dupoüy N, Tabone MD, Kalifa C; Société Française d'Oncologie Pédiatrique (SFOP). SFOP OS94: a randomised trial comparing preoperative high-dose methotrexate plus doxorubicin to high-dose methotrexate plus etoposide and ifosfamide in osteosarcoma patients. Eur J Cancer. 2007 Mar;43(4):752-61. Epub 2007 Jan 30. [https://www.ejcancer.com/article/S0959-8049(06)01072-0/abstract link to original article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/17267204 PubMed] NCT00180908
 
# '''OS2006:''' Piperno-Neumann S, Le Deley MC, Rédini F, Pacquement H, Marec-Bérard P, Petit P, Brisse H, Lervat C, Gentet JC, Entz-Werlé N, Italiano A, Corradini N, Bompas E, Penel N, Tabone MD, Gomez-Brouchet A, Guinebretière JM, Mascard E, Gouin F, Chevance A, Bonnet N, Blay JY, Brugières L; Sarcoma Group of UNICANCER; SFCE; GSF-GETO. Zoledronate in combination with chemotherapy and surgery to treat osteosarcoma (OS2006): a randomised, multicentre, open-label, phase 3 trial. Lancet Oncol. 2016 Aug;17(8):1070-1080. Epub 2016 Jun 17. [https://www.thelancet.com/journals/lanonc/article/PIIS1470-2045(16)30096-1/fulltext link to original article] [https://pubmed.ncbi.nlm.nih.gov/27324280 PubMed] NCT00470223
 
## '''Update:''' Gaspar N, Occean BV, Pacquement H, Bompas E, Bouvier C, Brisse HJ, Castex MP, Cheurfa N, Corradini N, Delaye J, Entz-Werlé N, Gentet JC, Italiano A, Lervat C, Marec-Berard P, Mascard E, Redini F, Saumet L, Schmitt C, Tabone MD, Verite-Goulard C, Le Deley MC, Piperno-Neumann S, Brugieres L; SFCE; GSF-GETO; UNICANCER sarcoma group. Results of methotrexate-etoposide-ifosfamide based regimen (M-EI) in osteosarcoma patients included in the French OS2006/sarcome-09 study. Eur J Cancer. 2018 Jan;88:57-66. Epub 2017 Nov 28. [https://www.ejcancer.com/article/S0959-8049(17)31339-4/fulltext link to original article] [https://pubmed.ncbi.nlm.nih.gov/29190507 PubMed]
 
 
 
==Methotrexate & Vincristine {{#subobject:606364|Regimen=1}}==
 
{| class="wikitable" style="float:right; margin-left: 5px;"
 
|-
 
|[[#top|back to top]]
 
|}
 
===Regimen {{#subobject:8f64e5|Variant=1}}===
 
{| class="wikitable" style="width: 40%; text-align:center;"
 
!style="width: 25%"|Study
 
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|[https://www.nejm.org/doi/full/10.1056/NEJM197411072911902 Jaffe et al. 1974]
 
|style="background-color:#91cf61"|Non-randomized
 
|-
 
|}
 
''Of historic interest.''
 
====Preceding treatment====
 
*[[Surgery#Surgical_resection|Surgery]]
 
====Chemotherapy====
 
*[[Methotrexate (MTX)]]
 
*[[Vincristine (Oncovin)]]
 
 
 
====Supportive medications====
 
*[[Folinic acid (Leucovorin)]]
 
 
 
'''21-day cycle for up to 35 cycles (2 years)'''
 
 
===References===
 
===References===
# Jaffe N, Frei E 3rd, Traggis D, Bishop Y. Adjuvant methotrexate and citrovorum-factor treatment of osteogenic sarcoma. N Engl J Med. 1974 Nov 7;291(19):994-7. [https://www.nejm.org/doi/full/10.1056/NEJM197411072911902 link to original article] [https://pubmed.ncbi.nlm.nih.gov/4606174 PubMed]
+
# '''SFOP OS94:''' Le Deley MC, Guinebretière JM, Gentet JC, Pacquement H, Pichon F, Marec-Bérard P, Entz-Werlé N, Schmitt C, Brugières L, Vanel D, Dupoüy N, Tabone MD, Kalifa C; Société Française d'Oncologie Pédiatrique (SFOP). SFOP OS94: a randomised trial comparing preoperative high-dose methotrexate plus doxorubicin to high-dose methotrexate plus etoposide and ifosfamide in osteosarcoma patients. Eur J Cancer. 2007 Mar;43(4):752-61. Epub 2007 Jan 30. [https://doi.org/10.1016/j.ejca.2006.10.023 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/17267204/ PubMed] [https://clinicaltrials.gov/study/NCT00180908 NCT00180908]
 +
# '''OS2006:''' Piperno-Neumann S, Le Deley MC, Rédini F, Pacquement H, Marec-Bérard P, Petit P, Brisse H, Lervat C, Gentet JC, Entz-Werlé N, Italiano A, Corradini N, Bompas E, Penel N, Tabone MD, Gomez-Brouchet A, Guinebretière JM, Mascard E, Gouin F, Chevance A, Bonnet N, Blay JY, Brugières L; Sarcoma Group of UNICANCER; SFCE; GSF-GETO. Zoledronate in combination with chemotherapy and surgery to treat osteosarcoma (OS2006): a randomised, multicentre, open-label, phase 3 trial. Lancet Oncol. 2016 Aug;17(8):1070-1080. Epub 2016 Jun 17. [https://doi.org/10.1016/S1470-2045(16)30096-1 link to original article] [https://pubmed.ncbi.nlm.nih.gov/27324280/ PubMed] [https://clinicaltrials.gov/study/NCT00470223 NCT00470223]
 +
## '''Update:''' Gaspar N, Occean BV, Pacquement H, Bompas E, Bouvier C, Brisse HJ, Castex MP, Cheurfa N, Corradini N, Delaye J, Entz-Werlé N, Gentet JC, Italiano A, Lervat C, Marec-Berard P, Mascard E, Redini F, Saumet L, Schmitt C, Tabone MD, Verite-Goulard C, Le Deley MC, Piperno-Neumann S, Brugieres L; SFCE; GSF-GETO; UNICANCER sarcoma group. Results of methotrexate-etoposide-ifosfamide based regimen (M-EI) in osteosarcoma patients included in the French OS2006/sarcome-09 study. Eur J Cancer. 2018 Jan;88:57-66. Epub 2017 Nov 28. [https://doi.org/10.1016/j.ejca.2017.09.036 link to original article] [https://pubmed.ncbi.nlm.nih.gov/29190507/ PubMed]
  
 
=Relapsed, refractory, or metastatic, first-line=
 
=Relapsed, refractory, or metastatic, first-line=
 
 
==Cisplatin & Doxorubicin {{#subobject:418c69|Regimen=1}}==
 
==Cisplatin & Doxorubicin {{#subobject:418c69|Regimen=1}}==
{| class="wikitable" style="float:right; margin-left: 5px;"
 
|-
 
|[[#top|back to top]]
 
|}
 
 
AP: '''<u>A</u>'''driamycin (Doxorubicin) & '''<u>P</u>'''latinol (Cisplatin)
 
AP: '''<u>A</u>'''driamycin (Doxorubicin) & '''<u>P</u>'''latinol (Cisplatin)
 +
<div class="toccolours" style="background-color:#eeeeee">
 
===Regimen {{#subobject:60d18a|Variant=1}}===
 
===Regimen {{#subobject:60d18a|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
!style="width: 20%"|Years of enrollment
+
!style="width: 20%"|Dates of enrollment
 
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|Comparator
 
!style="width: 20%"|Comparator
Line 1,183: Line 926:
 
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2395371/ Bramwell et al. 1997 (EOI 80831/MRC B002)]
 
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2395371/ Bramwell et al. 1997 (EOI 80831/MRC B002)]
 
|1983-1986
 
|1983-1986
|style="background-color:#1a9851"|Phase III (E-de-esc)
+
|style="background-color:#1a9851"|Phase 3 (E-de-esc)
 
|[[#MAP_3|MAP]]
 
|[[#MAP_3|MAP]]
 
|style="background-color:#d73027"|Inferior OS
 
|style="background-color:#d73027"|Inferior OS
Line 1,189: Line 932:
 
|}
 
|}
 
''Note: the authors state that "[i]t is likely that random bias in the population..accounts for the difference in outcome favoring the three-drug treatment in patients with metastatic disease."''
 
''Note: the authors state that "[i]t is likely that random bias in the population..accounts for the difference in outcome favoring the three-drug treatment in patients with metastatic disease."''
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
 
*[[Cisplatin (Platinol)]] 100 mg/m<sup>2</sup> IV continuous infusion over 24 hours, started on day 1
 
*[[Cisplatin (Platinol)]] 100 mg/m<sup>2</sup> IV continuous infusion over 24 hours, started on day 1
 
*[[Doxorubicin (Adriamycin)]] 25 mg/m<sup>2</sup> IV bolus once per day on days 1 to 3
 
*[[Doxorubicin (Adriamycin)]] 25 mg/m<sup>2</sup> IV bolus once per day on days 1 to 3
 
+
====Supportive therapy====
====Supportive medications====
+
*Prehydration: normal saline 400 mL/m<sup>2</sup> and D5W 400 mL/m<sup>2</sup> IV over 2 hours--the reference did not clarify if these two solutions are given at the same time
*Prehydration: normal saline 400 mL/m<sup>2</sup> and D5W 400 mL/m<sup>2</sup> over 2 hours--the reference did not clarify if these two solutions are given at the same time
 
 
*The volume of fluid for cisplatin continuous infusion is 2400 mL/m<sup>2</sup> NS, with KCl 80 mEq/L and mannitol 32,000 mg/m<sup>2</sup>
 
*The volume of fluid for cisplatin continuous infusion is 2400 mL/m<sup>2</sup> NS, with KCl 80 mEq/L and mannitol 32,000 mg/m<sup>2</sup>
 
*Posthydration: D5W 600 mL/m<sup>2</sup> over 6 hours, with KCl 20 mEq/L and mannitol 8000 mg/m<sup>2</sup>; and NS 600 mL/m<sup>2</sup> over 6 hours, with KCl 20 mEq/L, magnesium sulfate 2 mmol/L, and calcium gluconate 0.6 mmol/L--the reference did not clarify if these two solutions are given at the same time. Then D5W 600 mL/m<sup>2</sup> over 12 hours, with KCl 20 mEq/L and mannitol 8000 mg/m<sup>2</sup>.
 
*Posthydration: D5W 600 mL/m<sup>2</sup> over 6 hours, with KCl 20 mEq/L and mannitol 8000 mg/m<sup>2</sup>; and NS 600 mL/m<sup>2</sup> over 6 hours, with KCl 20 mEq/L, magnesium sulfate 2 mmol/L, and calcium gluconate 0.6 mmol/L--the reference did not clarify if these two solutions are given at the same time. Then D5W 600 mL/m<sup>2</sup> over 12 hours, with KCl 20 mEq/L and mannitol 8000 mg/m<sup>2</sup>.
 
*[[Furosemide (Lasix)]] 20 to 40 mg IV if urine output is less than 400 mL/m<sup>2</sup> over 6 hours
 
*[[Furosemide (Lasix)]] 20 to 40 mg IV if urine output is less than 400 mL/m<sup>2</sup> over 6 hours
 
 
'''21-day cycle for 6 cycles'''
 
'''21-day cycle for 6 cycles'''
 
+
</div></div>
 
===References===
 
===References===
# '''EOI 80831/MRC B002:''' Bramwell VH, Burgers MV, Souhami RL, Taminiau AH, Van Der Eijken JW, Craft AW, Malcolm AJ, Uscinska B, Kirkpatrick AL, Machin D, Van Glabbeke MM; European Osteosarcoma Intergroup. A randomized comparison of two short intensive chemotherapy regimens in children and young adults with osteosarcoma: results in patients with metastases: a study of the European Osteosarcoma Intergroup. Sarcoma. 1997;1(3-4):155-60. [https://doi.org/10.1080/13577149778245 link to original article] '''contains verified partial protocol''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2395371/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/18521218 PubMed]
+
# '''EOI 80831/MRC B002:''' Bramwell VH, Burgers MV, Souhami RL, Taminiau AH, Van Der Eijken JW, Craft AW, Malcolm AJ, Uscinska B, Kirkpatrick AL, Machin D, Van Glabbeke MM; European Osteosarcoma Intergroup. A randomized comparison of two short intensive chemotherapy regimens in children and young adults with osteosarcoma: results in patients with metastases: a study of the European Osteosarcoma Intergroup. Sarcoma. 1997;1(3-4):155-60. [https://doi.org/10.1080/13577149778245 link to original article] '''contains dosing details in manuscript''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2395371/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/18521218/ PubMed]
 
 
==Doxorubicin monotherapy {{#subobject:8a4535|Regimen=1}}==
 
{| class="wikitable" style="float:right; margin-left: 5px;"
 
|-
 
|[[#top|back to top]]
 
|}
 
===Regimen {{#subobject:dc69eb|Variant=1}}===
 
{| class="wikitable" style="width: 40%; text-align:center;"
 
!style="width: 25%"|Study
 
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|[https://jamanetwork.com/journals/jama/article-abstract/344236 Cores et al. 1972]
 
| style="background-color:#ffffbe" |Non-randomized, <20 pts
 
|-
 
|}
 
''Of historic interest.''
 
====Chemotherapy====
 
*[[Doxorubicin (Adriamycin)]]
 
===References===
 
# Cores EP, Holland JF, Wang JJ, Sinks LF. Doxorubicin in disseminated osteosarcoma. JAMA. 1972 Sep 4;221(10):1132-8. [https://jamanetwork.com/journals/jama/article-abstract/344236 link to original article] [https://pubmed.ncbi.nlm.nih.gov/4512088 PubMed]
 
 
 
 
==MAP {{#subobject:ed2dcf|Regimen=1}}==
 
==MAP {{#subobject:ed2dcf|Regimen=1}}==
{| class="wikitable" style="float:right; margin-left: 5px;"
 
|-
 
|[[#top|back to top]]
 
|}
 
 
MAP: High-dose '''<u>M</u>'''ethotrexate, '''<u>A</u>'''driamycin (Doxorubicin), '''<u>P</u>'''latinol (Cisplatin)
 
MAP: High-dose '''<u>M</u>'''ethotrexate, '''<u>A</u>'''driamycin (Doxorubicin), '''<u>P</u>'''latinol (Cisplatin)
 +
<div class="toccolours" style="background-color:#eeeeee">
 
===Regimen {{#subobject:d359c6|Variant=1}}===
 
===Regimen {{#subobject:d359c6|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
!style="width: 20%"|Years of enrollment
+
!style="width: 20%"|Dates of enrollment
 
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|Comparator
 
!style="width: 20%"|Comparator
Line 1,240: Line 958:
 
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2395371/ Bramwell et al. 1997 (EOI 80831/MRC B002)]
 
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2395371/ Bramwell et al. 1997 (EOI 80831/MRC B002)]
 
|1983-1986
 
|1983-1986
|style="background-color:#1a9851"|Phase III (E-esc)
+
|style="background-color:#1a9851"|Phase 3 (E-esc)
 
|[[#Cisplatin_.26_Doxorubicin_3|Cisplatin & Doxorubicin]]
 
|[[#Cisplatin_.26_Doxorubicin_3|Cisplatin & Doxorubicin]]
 
|style="background-color:#1a9850"|Superior OS
 
|style="background-color:#1a9850"|Superior OS
Line 1,246: Line 964:
 
|}
 
|}
 
''Note: the authors state that "[i]t is likely that random bias in the population..accounts for the difference in outcome favoring the three-drug treatment in patients with metastatic disease."''
 
''Note: the authors state that "[i]t is likely that random bias in the population..accounts for the difference in outcome favoring the three-drug treatment in patients with metastatic disease."''
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
 
*[[Methotrexate (MTX)]] 8000 mg/m<sup>2</sup> IV over 4 hours once on day 1
 
*[[Methotrexate (MTX)]] 8000 mg/m<sup>2</sup> IV over 4 hours once on day 1
 
*[[Doxorubicin (Adriamycin)]] 25 mg/m<sup>2</sup> IV bolus once per day on days 11 to 13
 
*[[Doxorubicin (Adriamycin)]] 25 mg/m<sup>2</sup> IV bolus once per day on days 11 to 13
 
*[[Cisplatin (Platinol)]] 100 mg/m<sup>2</sup> IV continuous infusion over 24 hours, started on day 11
 
*[[Cisplatin (Platinol)]] 100 mg/m<sup>2</sup> IV continuous infusion over 24 hours, started on day 11
 
+
====Supportive therapy====
====Supportive medications====
+
*[[Leucovorin (Folinic acid)]] 12 mg/m<sup>2</sup> IV every 6 hours x 10 doses or 15 mg/m<sup>2</sup> PO every 6 hours x 10 doses, starting 24 hours after the start of methotrexate infusion
*[[Folinic acid (Leucovorin)]] 12 mg/m<sup>2</sup> IV every 6 hours x 10 doses or 15 mg/m<sup>2</sup> PO every 6 hours x 10 doses, starting 24 hours after the start of methotrexate infusion
 
 
**Monitor methotrexate level at "24 hours and 48 hours"--it is unclear in the reference if this is time after the start/end of methotrexate, beginning of leucovorin, or something else
 
**Monitor methotrexate level at "24 hours and 48 hours"--it is unclear in the reference if this is time after the start/end of methotrexate, beginning of leucovorin, or something else
 
**Methotrexate levels higher than 100 nmol/L at 48 hours required additional leucovorin rescue
 
**Methotrexate levels higher than 100 nmol/L at 48 hours required additional leucovorin rescue
Line 1,259: Line 977:
 
*Posthydration for methotrexate: Alternating liters of D5W and NS 3000 mL/m<sup>2</sup> over 24 hours, with KCl 60 mEq/L.
 
*Posthydration for methotrexate: Alternating liters of D5W and NS 3000 mL/m<sup>2</sup> over 24 hours, with KCl 60 mEq/L.
 
*Sodium bicarbonate 3 g PO Q6H, starting 12 hours before methotrexate, and sodium bicarbonate 167 mmol/L IV until serum methotrexate level is less than 8000 to 10,000 nmol/L. Note: the reference is not clear about when/if PO sodium bicarbonate is stopped, when IV sodium bicarbonate is started, or the administration rate of IV sodium bicarbonate.
 
*Sodium bicarbonate 3 g PO Q6H, starting 12 hours before methotrexate, and sodium bicarbonate 167 mmol/L IV until serum methotrexate level is less than 8000 to 10,000 nmol/L. Note: the reference is not clear about when/if PO sodium bicarbonate is stopped, when IV sodium bicarbonate is started, or the administration rate of IV sodium bicarbonate.
*Prehydration for cisplatin: normal saline 400 mL/m<sup>2</sup> and D5W 400 mL/m<sup>2</sup> over 2 hours--the reference did not clarify if these two solutions are given at the same time
+
*Prehydration for cisplatin: normal saline 400 mL/m<sup>2</sup> and D5W 400 mL/m<sup>2</sup> IV over 2 hours--the reference did not clarify if these two solutions are given at the same time
 
*The volume of fluid for cisplatin continuous infusion is 2400 mL/m<sup>2</sup> NS, with KCl 80 mEq/L and mannitol 32,000 mg/m<sup>2</sup>
 
*The volume of fluid for cisplatin continuous infusion is 2400 mL/m<sup>2</sup> NS, with KCl 80 mEq/L and mannitol 32,000 mg/m<sup>2</sup>
 
*Posthydration for cisplatin: D5W 600 mL/m<sup>2</sup> over 6 hours, with KCl 20 mEq/L and mannitol 8000 mg/m<sup>2</sup>; and NS 600 mL/m<sup>2</sup> over 6 hours, with KCl 20 mEq/L, magnesium sulfate 2 mmol/L, and calcium gluconate 0.6 mmol/L--the reference did not clarify if these two solutions are given at the same time. Then D5W 600 mL/m<sup>2</sup> over 12 hours, with KCl 20 mEq/L and mannitol 8000 mg/m<sup>2</sup>.
 
*Posthydration for cisplatin: D5W 600 mL/m<sup>2</sup> over 6 hours, with KCl 20 mEq/L and mannitol 8000 mg/m<sup>2</sup>; and NS 600 mL/m<sup>2</sup> over 6 hours, with KCl 20 mEq/L, magnesium sulfate 2 mmol/L, and calcium gluconate 0.6 mmol/L--the reference did not clarify if these two solutions are given at the same time. Then D5W 600 mL/m<sup>2</sup> over 12 hours, with KCl 20 mEq/L and mannitol 8000 mg/m<sup>2</sup>.
 
*With cisplatin, [[Furosemide (Lasix)]] 20 to 40 mg IV if urine output is less than 400 mL/m<sup>2</sup> over 6 hours
 
*With cisplatin, [[Furosemide (Lasix)]] 20 to 40 mg IV if urine output is less than 400 mL/m<sup>2</sup> over 6 hours
 
 
'''21-day cycle for 4 cycles'''
 
'''21-day cycle for 4 cycles'''
 
+
</div></div>
 
===References===
 
===References===
# '''EOI 80831/MRC B002:''' Bramwell VH, Burgers MV, Souhami RL, Taminiau AH, Van Der Eijken JW, Craft AW, Malcolm AJ, Uscinska B, Kirkpatrick AL, Machin D, Van Glabbeke MM; European Osteosarcoma Intergroup. A randomized comparison of two short intensive chemotherapy regimens in children and young adults with osteosarcoma: results in patients with metastases: a study of the European Osteosarcoma Intergroup. Sarcoma. 1997;1(3-4):155-60. [https://doi.org/10.1080/13577149778245 link to original article] '''contains verified partial protocol''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2395371/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/18521218 PubMed]
+
# '''EOI 80831/MRC B002:''' Bramwell VH, Burgers MV, Souhami RL, Taminiau AH, Van Der Eijken JW, Craft AW, Malcolm AJ, Uscinska B, Kirkpatrick AL, Machin D, Van Glabbeke MM; European Osteosarcoma Intergroup. A randomized comparison of two short intensive chemotherapy regimens in children and young adults with osteosarcoma: results in patients with metastases: a study of the European Osteosarcoma Intergroup. Sarcoma. 1997;1(3-4):155-60. [https://doi.org/10.1080/13577149778245 link to original article] '''contains dosing details in manuscript''' [https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2395371/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/18521218/ PubMed]
 
 
 
=Relapsed, refractory, or metastatic, subsequent lines=
 
=Relapsed, refractory, or metastatic, subsequent lines=
 
==Cabozantinib monotherapy {{#subobject:s9nxm1|Regimen=1}}==
 
==Cabozantinib monotherapy {{#subobject:s9nxm1|Regimen=1}}==
{| class="wikitable" style="float:right; margin-left: 5px;"
+
<div class="toccolours" style="background-color:#eeeeee">
|-
 
|[[#top|back to top]]
 
|}
 
 
===Regimen variant #1, adult dosing {{#subobject:8c0u8g|Variant=1}}===
 
===Regimen variant #1, adult dosing {{#subobject:8c0u8g|Variant=1}}===
 
{| class="wikitable sortable" style="width: 60%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 60%; text-align:center;"  
 
!style="width: 33%"|Study
 
!style="width: 33%"|Study
!style="width: 33%"|Years of enrollment
+
!style="width: 33%"|Dates of enrollment
 
!style="width: 33%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 33%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|-
|[https://doi.org/10.1016/s1470-2045(19)30825-3 Italiano et al. 2020 (CABONE)]
+
|[https://www.ncbi.nlm.nih.gov/pmc/articles/pmc8763616/ Italiano et al. 2020 (CABONE)]
 
|2015-2018
 
|2015-2018
| style="background-color:#91cf61" |Phase II
+
| style="background-color:#91cf61" |Phase 2
 
|-
 
|-
 
|}
 
|}
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Targeted therapy====
 
====Targeted therapy====
*[[Cabozantinib (Cometriq)]] 60 mg PO once per day
+
*[[Cabozantinib (Cometriq)]] 60 mg PO once per day on day 1 to 28
 
 
 
'''28-day cycles'''
 
'''28-day cycles'''
 
+
</div></div><br>
 +
<div class="toccolours" style="background-color:#eeeeee">
 
===Regimen variant #2, pediatric dosing {{#subobject:yr1u8g|Variant=1}}===
 
===Regimen variant #2, pediatric dosing {{#subobject:yr1u8g|Variant=1}}===
 
{| class="wikitable sortable" style="width: 60%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 60%; text-align:center;"  
 
!style="width: 33%"|Study
 
!style="width: 33%"|Study
!style="width: 33%"|Years of enrollment
+
!style="width: 33%"|Dates of enrollment
 
!style="width: 33%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 33%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|-
|[https://doi.org/10.1016/s1470-2045(19)30825-3 Italiano et al. 2020 (CABONE)]
+
|[https://www.ncbi.nlm.nih.gov/pmc/articles/pmc8763616/ Italiano et al. 2020 (CABONE)]
 
|2015-2018
 
|2015-2018
| style="background-color:#91cf61" |Phase II
+
| style="background-color:#91cf61" |Phase 2
 
|-
 
|-
 
|}
 
|}
 
''Note: this dosing was for children aged less than 16 years.''
 
''Note: this dosing was for children aged less than 16 years.''
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Targeted therapy====
 
====Targeted therapy====
*[[Cabozantinib (Cometriq)]] 40 mg/m<sup>2</sup> PO once per day
+
*[[Cabozantinib (Cometriq)]] 40 mg/m<sup>2</sup> PO once per day on days 1 to 28
 
 
 
'''28-day cycles'''
 
'''28-day cycles'''
 
+
</div></div>
 
===References===
 
===References===
#'''CABONE:''' Italiano A, Mir O, Mathoulin-Pelissier S, Penel N, Piperno-Neumann S, Bompas E, Chevreau C, Duffaud F, Entz-Werlé N, Saada E, Ray-Coquard I, Lervat C, Gaspar N, Marec-Berard P, Pacquement H, Wright J, Toulmonde M, Bessede A, Crombe A, Kind M, Bellera C, Blay JY. Cabozantinib in patients with advanced Ewing sarcoma or osteosarcoma (CABONE): a multicentre, single-arm, phase 2 trial. Lancet Oncol. 2020 Mar;21(3):446-455. Epub 2020 Feb 17. [https://doi.org/10.1016/s1470-2045(19)30825-3 link to original article] '''contains protocol''' [https://pubmed.ncbi.nlm.nih.gov/32078813/ PubMed] NCT02243605
+
#'''CABONE:''' Italiano A, Mir O, Mathoulin-Pelissier S, Penel N, Piperno-Neumann S, Bompas E, Chevreau C, Duffaud F, Entz-Werlé N, Saada E, Ray-Coquard I, Lervat C, Gaspar N, Marec-Berard P, Pacquement H, Wright J, Toulmonde M, Bessede A, Crombe A, Kind M, Bellera C, Blay JY. Cabozantinib in patients with advanced Ewing sarcoma or osteosarcoma (CABONE): a multicentre, single-arm, phase 2 trial. Lancet Oncol. 2020 Mar;21(3):446-455. Epub 2020 Feb 17. [https://doi.org/10.1016/s1470-2045(19)30825-3 link to original article] '''contains dosing details in abstract''' [https://www.ncbi.nlm.nih.gov/pmc/articles/pmc8763616/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/32078813/ PubMed] [https://clinicaltrials.gov/study/NCT02243605 NCT02243605]
 
 
 
==Cyclophosphamide & Etoposide {{#subobject:7bb7cb|Regimen=1}}==
 
==Cyclophosphamide & Etoposide {{#subobject:7bb7cb|Regimen=1}}==
{| class="wikitable" style="float:right; margin-left: 5px;"
+
<div class="toccolours" style="background-color:#eeeeee">
|-
 
|[[#top|back to top]]
 
|}
 
 
===Regimen {{#subobject:1d31a0|Variant=1}}===
 
===Regimen {{#subobject:1d31a0|Variant=1}}===
{| class="wikitable" style="width: 40%; text-align:center;"  
+
{| class="wikitable sortable" style="width: 60%; text-align:center;"  
!style="width: 25%"|Study
+
!style="width: 33%"|Study
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
+
!style="width: 33%"|Dates of enrollment
 +
!style="width: 33%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|-
|[https://onlinelibrary.wiley.com/doi/10.1002/cncr.24368/full Berger et al. 2009]
+
|[https://doi.org/10.1002/cncr.24368 Berger et al. 2009]
|style="background-color:#91cf61"|Phase II
+
|2002-07 to 2006-09
 +
|style="background-color:#91cf61"|Phase 2
 
|-
 
|-
 
|}
 
|}
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
 
*[[Cyclophosphamide (Cytoxan)]] 4000 mg/m<sup>2</sup> IV over 3 hours once on day 1
 
*[[Cyclophosphamide (Cytoxan)]] 4000 mg/m<sup>2</sup> IV over 3 hours once on day 1
 
*[[Etoposide (Vepesid)]] 100 mg/m<sup>2</sup> IV over 60 minutes twice per day on days 2 to 4 (total dose: 600 mg/m<sup>2</sup>)
 
*[[Etoposide (Vepesid)]] 100 mg/m<sup>2</sup> IV over 60 minutes twice per day on days 2 to 4 (total dose: 600 mg/m<sup>2</sup>)
 
+
====Supportive therapy====
====Supportive medications====
+
*[[Mesna (Mesnex)]] 1400 mg/m<sup>2</sup> IV three times per day on day 1, given prior to, 4 hours after, and 8 hours after cyclophosphamide
*[[Mesna (Mesnex)]] 1400 mg/m<sup>2</sup> IV three times per day on day 1, given prior to, 4 hours after, and 8 hours after [[Cyclophosphamide (Cytoxan)]]
 
 
**With mesna, 3000 mL/m<sup>2</sup> hydration
 
**With mesna, 3000 mL/m<sup>2</sup> hydration
 
 
'''At least 21-day cycle for 2 cycles, then restaging'''
 
'''At least 21-day cycle for 2 cycles, then restaging'''
 
+
</div>
 +
<div class="toccolours" style="background-color:#cbd5e7">
 
====Subsequent treatment====
 
====Subsequent treatment====
 
*Patients with no progression received an experimental protocol with:
 
*Patients with no progression received an experimental protocol with:
Line 1,340: Line 1,052:
 
**Progression-free patients received reduced intensity stem cell transplant (preferably from a matched sibling donor (MSD))
 
**Progression-free patients received reduced intensity stem cell transplant (preferably from a matched sibling donor (MSD))
 
**Patients with no MSD received IL-2 maintenance, 5 days a week every 2 weeks x 12 cycles (reference did not specify if a cycle was 2 weeks, 4 weeks, or another length)
 
**Patients with no MSD received IL-2 maintenance, 5 days a week every 2 weeks x 12 cycles (reference did not specify if a cycle was 2 weeks, 4 weeks, or another length)
 
+
</div></div>
 
===References===
 
===References===
# Berger M, Grignani G, Ferrari S, Biasin E, Brach del Prever A, Aliberti S, Saglio F, Aglietta M, Fagioli F. Phase 2 trial of two courses of cyclophosphamide and etoposide for relapsed high-risk osteosarcoma patients. Cancer. 2009 Jul 1;115(13):2980-7. [https://onlinelibrary.wiley.com/doi/10.1002/cncr.24368/full link to original article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/19452540 PubMed]
+
# Berger M, Grignani G, Ferrari S, Biasin E, Brach del Prever A, Aliberti S, Saglio F, Aglietta M, Fagioli F. Phase 2 trial of two courses of cyclophosphamide and etoposide for relapsed high-risk osteosarcoma patients. Cancer. 2009 Jul 1;115(13):2980-7. [https://doi.org/10.1002/cncr.24368 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/19452540/ PubMed]
  
 
==Cyclophosphamide & Topotecan {{#subobject:533aef|Regimen=1}}==
 
==Cyclophosphamide & Topotecan {{#subobject:533aef|Regimen=1}}==
{| class="wikitable" style="float:right; margin-left: 5px;"
+
<div class="toccolours" style="background-color:#eeeeee">
|-
 
|[[#top|back to top]]
 
|}
 
 
===Regimen {{#subobject:950899|Variant=1}}===
 
===Regimen {{#subobject:950899|Variant=1}}===
 
{| class="wikitable" style="width: 40%; text-align:center;"  
 
{| class="wikitable" style="width: 40%; text-align:center;"  
Line 1,355: Line 1,064:
 
|-
 
|-
 
|[https://doi.org/10.1200/jco.2001.19.15.3463 Saylors et al. 2001]
 
|[https://doi.org/10.1200/jco.2001.19.15.3463 Saylors et al. 2001]
|style="background-color:#91cf61"|Phase II
+
|style="background-color:#91cf61"|Phase 2
 
|-
 
|-
 
|}
 
|}
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
 
*[[Cyclophosphamide (Cytoxan)]] 250 mg/m<sup>2</sup> IV over 30 minutes once per day on days 1 to 5, '''given first'''
 
*[[Cyclophosphamide (Cytoxan)]] 250 mg/m<sup>2</sup> IV over 30 minutes once per day on days 1 to 5, '''given first'''
 
*[[Topotecan (Hycamtin)]] 0.75 mg/m<sup>2</sup> IV over 30 minutes once per day on days 1 to 5, '''given second'''
 
*[[Topotecan (Hycamtin)]] 0.75 mg/m<sup>2</sup> IV over 30 minutes once per day on days 1 to 5, '''given second'''
 
+
====Supportive therapy====
====Supportive medications====
 
 
*500 mL/m/2 fluids IV or PO once per day on days 1 to 5; 2 to 4 hours prior to chemotherapy
 
*500 mL/m/2 fluids IV or PO once per day on days 1 to 5; 2 to 4 hours prior to chemotherapy
 
*[[:Category:Emesis_prevention|Antiemetics]] once per day on days 1 to 5, prior to chemotherapy
 
*[[:Category:Emesis_prevention|Antiemetics]] once per day on days 1 to 5, prior to chemotherapy
 
*3 liters/m<sup>2</sup> fluids IV or PO over 24 hours after chemotherapy
 
*3 liters/m<sup>2</sup> fluids IV or PO over 24 hours after chemotherapy
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day, starting on day 6, to continue until post-nadir ANC is at least 1500/uL
+
*[[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day, starting on day 6, to continue until post-nadir ANC is at least 1500/μL
 
 
 
'''21-day cycle for 12 to 14 cycles'''
 
'''21-day cycle for 12 to 14 cycles'''
 
+
</div></div>
 
===References===
 
===References===
# Saylors RL 3rd, Stine KC, Sullivan J, Kepner JL, Wall DA, Bernstein ML, Harris MB, Hayashi R, Vietti TJ; Pediatric Oncology Group. Cyclophosphamide plus topotecan in children with recurrent or refractory solid tumors: a Pediatric Oncology Group phase II study. J Clin Oncol. 2001 Aug 1;19(15):3463-9. [https://doi.org/10.1200/jco.2001.19.15.3463 link to original article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/11481351 PubMed]
+
# Saylors RL 3rd, Stine KC, Sullivan J, Kepner JL, Wall DA, Bernstein ML, Harris MB, Hayashi R, Vietti TJ; Pediatric Oncology Group. Cyclophosphamide plus topotecan in children with recurrent or refractory solid tumors: a Pediatric Oncology Group phase II study. J Clin Oncol. 2001 Aug 1;19(15):3463-9. [https://doi.org/10.1200/jco.2001.19.15.3463 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/11481351/ PubMed]
 
 
 
==Docetaxel & Gemcitabine {{#subobject:55d598|Regimen=1}}==
 
==Docetaxel & Gemcitabine {{#subobject:55d598|Regimen=1}}==
{| class="wikitable" style="float:right; margin-left: 5px;"
+
<div class="toccolours" style="background-color:#eeeeee">
|-
 
|[[#top|back to top]]
 
|}
 
 
===Regimen {{#subobject:c3c88e|Variant=1}}===
 
===Regimen {{#subobject:c3c88e|Variant=1}}===
 
{| class="wikitable" style="width: 40%; text-align:center;"  
 
{| class="wikitable" style="width: 40%; text-align:center;"  
Line 1,383: Line 1,087:
 
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|-
|[https://onlinelibrary.wiley.com/doi/10.1002/cncr.23586/full Navid et al. 2008]
+
|[https://doi.org/10.1002/cncr.23586 Navid et al. 2008]
 
|style="background-color:#ffffbe"|Retrospective
 
|style="background-color:#ffffbe"|Retrospective
 
|-
 
|-
 
|}
 
|}
''17 of the 22 patients in this retrospective review had osteosarcoma.''
+
''Note: 17 of the 22 patients in this retrospective review had osteosarcoma.''
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
 
*[[Docetaxel (Taxotere)]] 75 to 100 mg/m<sup>2</sup> IV over 60 minutes once on day 8, '''given second'''
 
*[[Docetaxel (Taxotere)]] 75 to 100 mg/m<sup>2</sup> IV over 60 minutes once on day 8, '''given second'''
 
*[[Gemcitabine (Gemzar)]] 675 mg/m<sup>2</sup> IV over 90 minutes once per day on days 1 & 8, '''given first'''
 
*[[Gemcitabine (Gemzar)]] 675 mg/m<sup>2</sup> IV over 90 minutes once per day on days 1 & 8, '''given first'''
 
+
====Supportive therapy====
====Supportive medications====
 
 
*[[Ondansetron (Zofran)]] (dose/route not specified) once per day on days 1 & 8, prior to chemotherapy
 
*[[Ondansetron (Zofran)]] (dose/route not specified) once per day on days 1 & 8, prior to chemotherapy
*[[Dexamethasone (Decadron)]] starting either the day before or the day of [[Docetaxel (Taxotere)]], and continued for 2 days after [[Docetaxel (Taxotere)]]
+
*[[Dexamethasone (Decadron)]] starting either the day before or the day of docetaxel, and continued for 2 days after docetaxel
 
*Per physician discretion: H1 or H2 blockers such as [[Diphenhydramine (Benadryl)]] and [[Ranitidine (Zantac)]] once per day on days 1 & 8  
 
*Per physician discretion: H1 or H2 blockers such as [[Diphenhydramine (Benadryl)]] and [[Ranitidine (Zantac)]] once per day on days 1 & 8  
 
*Some patients received [[Filgrastim (Neupogen)]] starting on day 9
 
*Some patients received [[Filgrastim (Neupogen)]] starting on day 9
 
 
'''21-day cycles'''
 
'''21-day cycles'''
 
+
</div></div>
 
===References===
 
===References===
# '''Retrospective:''' Navid F, Willert JR, McCarville MB, Furman W, Watkins A, Roberts W, Daw NC. Combination of gemcitabine and docetaxel in the treatment of children and young adults with refractory bone sarcoma. Cancer. 2008 Jul 15;113(2):419-25. [https://onlinelibrary.wiley.com/doi/10.1002/cncr.23586/full link to original article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/18484657 PubMed]
+
# '''Retrospective:''' Navid F, Willert JR, McCarville MB, Furman W, Watkins A, Roberts W, Daw NC. Combination of gemcitabine and docetaxel in the treatment of children and young adults with refractory bone sarcoma. Cancer. 2008 Jul 15;113(2):419-25. [https://doi.org/10.1002/cncr.23586 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/18484657/ PubMed]
 
 
 
==Gemcitabine monotherapy {{#subobject:2a9006|Regimen=1}}==
 
==Gemcitabine monotherapy {{#subobject:2a9006|Regimen=1}}==
{| class="wikitable" style="float:right; margin-left: 5px;"
+
<div class="toccolours" style="background-color:#eeeeee">
|-
 
|[[#top|back to top]]
 
|}
 
 
===Regimen {{#subobject:fb0d84|Variant=1}}===
 
===Regimen {{#subobject:fb0d84|Variant=1}}===
 
{| class="wikitable" style="width: 40%; text-align:center;"  
 
{| class="wikitable" style="width: 40%; text-align:center;"  
Line 1,414: Line 1,113:
 
|-
 
|-
 
|[https://doi.org/10.1007/s002800050027 Merimsky et al. 2000]
 
|[https://doi.org/10.1007/s002800050027 Merimsky et al. 2000]
|style="background-color:#91cf61"|Phase II
+
|style="background-color:#91cf61"|Phase 2
 
|-
 
|-
 
|}
 
|}
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
 
*[[Gemcitabine (Gemzar)]] as follows:
 
*[[Gemcitabine (Gemzar)]] as follows:
 
**Cycle 1: 1000 mg/m<sup>2</sup> IV once per day on days 1, 8, 15, 22
 
**Cycle 1: 1000 mg/m<sup>2</sup> IV once per day on days 1, 8, 15, 22
**Cycle 2 onwards: [[Gemcitabine (Gemzar)]] 1000 mg/m<sup>2</sup> IV once per day on days 1, 8, 15
+
**Cycle 2 onwards: 1000 mg/m<sup>2</sup> IV once per day on days 1, 8, 15
 
 
 
'''28-day cycles'''
 
'''28-day cycles'''
 
+
</div></div>
 
===References===
 
===References===
# Merimsky O, Meller I, Flusser G, Kollender Y, Issakov J, Weil-Ben-Arush M, Fenig E, Neuman G, Sapir D, Ariad S, Inbar M. Gemcitabine in soft tissue or bone sarcoma resistant to standard chemotherapy: a phase II study. Cancer Chemother Pharmacol. 2000;45(2):177-81. [https://doi.org/10.1007/s002800050027 link to original article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/10663634 PubMed]
+
# Merimsky O, Meller I, Flusser G, Kollender Y, Issakov J, Weil-Ben-Arush M, Fenig E, Neuman G, Sapir D, Ariad S, Inbar M. Gemcitabine in soft tissue or bone sarcoma resistant to standard chemotherapy: a phase II study. Cancer Chemother Pharmacol. 2000;45(2):177-81. [https://doi.org/10.1007/s002800050027 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/10663634/ PubMed]
 
 
 
==ICE {{#subobject:3fe1fa|Regimen=1}}==
 
==ICE {{#subobject:3fe1fa|Regimen=1}}==
{| class="wikitable" style="float:right; margin-left: 5px;"
 
|-
 
|[[#top|back to top]]
 
|}
 
 
ICE: '''<u>I</u>'''fosfamide, '''<u>C</u>'''arboplatin, '''<u>E</u>'''toposide
 
ICE: '''<u>I</u>'''fosfamide, '''<u>C</u>'''arboplatin, '''<u>E</u>'''toposide
 +
<div class="toccolours" style="background-color:#eeeeee">
 
===Regimen {{#subobject:61c68a|Variant=1}}===
 
===Regimen {{#subobject:61c68a|Variant=1}}===
 
{| class="wikitable" style="width: 40%; text-align:center;"  
 
{| class="wikitable" style="width: 40%; text-align:center;"  
Line 1,438: Line 1,133:
 
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|-
|[https://onlinelibrary.wiley.com/doi/10.1002/pbc.20227/abstract Van Winkle et al. 2005]
+
|[https://doi.org/10.1002/pbc.20227 Van Winkle et al. 2005]
|style="background-color:#91cf61"|Phase II
+
|style="background-color:#91cf61"|Phase 2
 
|-
 
|-
 
|}
 
|}
 
''Note: the reference did not mention [[Mesna (Mesnex)]] being used.''
 
''Note: the reference did not mention [[Mesna (Mesnex)]] being used.''
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
 
*[[Ifosfamide (Ifex)]] 1800 mg/m<sup>2</sup> IV once per day on days 1 to 5
 
*[[Ifosfamide (Ifex)]] 1800 mg/m<sup>2</sup> IV once per day on days 1 to 5
Line 1,448: Line 1,144:
 
**Note: the reference did not explicitly say which 2 days carboplatin should be given on
 
**Note: the reference did not explicitly say which 2 days carboplatin should be given on
 
*[[Etoposide (Vepesid)]] 100 mg/m<sup>2</sup> IV once per day on days 1 to 5
 
*[[Etoposide (Vepesid)]] 100 mg/m<sup>2</sup> IV once per day on days 1 to 5
 
+
====Supportive therapy====
====Supportive medications====
 
 
*Depending on the study the patients were enrolled on, they received one of the following:
 
*Depending on the study the patients were enrolled on, they received one of the following:
**CCG-0894: [[Filgrastim (Neupogen)]] 5 or 10 mcg/kg SC once per day, starting 24 hours after completing ICE, and to continue until day 18 if ANC is at least 1000/uL, or until ANC is at least 1000/uL above nadir, whichever comes later
+
**CCG-0894: [[Filgrastim (Neupogen)]] 5 or 10 mcg/kg SC once per day, starting 24 hours after completing ICE, and to continue until day 18 if ANC is at least 1000/μL, or until ANC is at least 1000/μL above nadir, whichever comes later
**CCG-0924: PIXY 321 at doses of 500/750/1000 mcg/m<sup>2</sup> SC once per day or 500 mcg/m<sup>2</sup> SC twice per day, starting on day 5 and to continue until day 18 unless ANC reached 20,000/uL or platelet count is at least 900 x 10<sup>9</sup>/L for 2 days between days 13 to 18, or until ANC is at least 1000/uL and platelet count is at least 100 x 10<sup>9</sup>/L, whichever comes later
+
**CCG-0924: PIXY 321 at doses of 500/750/1000 mcg/m<sup>2</sup> SC once per day or 500 mcg/m<sup>2</sup> SC twice per day, starting on day 5 and to continue until day 18 unless ANC reached 20,000/μL or platelet count is at least 900 x 10<sup>9</sup>/L for 2 days between days 13 to 18, or until ANC is at least 1000/μL and platelet count is at least 100 x 10<sup>9</sup>/L, whichever comes later
**CCG-0931: [[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day and IL-6 at 2.5, 3.75, or 5 mcg/kg SC twice per day, starting 24 hours after completing ICE. Filgrastim is continued until ANC is at least 1000/uL, and IL-6 is continued until platelets are at least 100 x 10<sup>9</sup>/L for 2 consecutive days or until day 35, whichever comes sooner.
+
**CCG-0931: [[Filgrastim (Neupogen)]] 5 mcg/kg SC once per day and IL-6 at 2.5, 3.75, or 5 mcg/kg SC twice per day, starting 24 hours after completing ICE. Filgrastim is continued until ANC is at least 1000/μL, and IL-6 is continued until platelets are at least 100 x 10<sup>9</sup>/L for 2 consecutive days or until day 35, whichever comes sooner.
 
+
'''21-day cycles''', with next cycle starting as soon as ANC is at least 1000/μL and platelet count is at least 100 x 10<sup>9</sup>/L
'''21-day cycles''', with next cycle starting as soon as ANC is at least 1000/uL and platelet count is at least 100 x 10<sup>9</sup>/L
+
</div>
 +
<div class="toccolours" style="background-color:#cbd5e7">
 
====Subsequent treatment====
 
====Subsequent treatment====
 
*Resection of disease was allowed after 4 cycles based on patient's response to ICE
 
*Resection of disease was allowed after 4 cycles based on patient's response to ICE
 
+
</div></div>
 
===References===
 
===References===
# Van Winkle P, Angiolillo A, Krailo M, Cheung YK, Anderson B, Davenport V, Reaman G, Cairo MS; Children's Cancer Group. Ifosfamide, carboplatin, and etoposide (ICE) reinduction chemotherapy in a large cohort of children and adolescents with recurrent/refractory sarcoma: the Children's Cancer Group (CCG) experience. Pediatr Blood Cancer. 2005 Apr;44(4):338-47. [https://onlinelibrary.wiley.com/doi/10.1002/pbc.20227/abstract link to original article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/15503297 PubMed]
+
# Van Winkle P, Angiolillo A, Krailo M, Cheung YK, Anderson B, Davenport V, Reaman G, Cairo MS; Children's Cancer Group. Ifosfamide, carboplatin, and etoposide (ICE) reinduction chemotherapy in a large cohort of children and adolescents with recurrent/refractory sarcoma: the Children's Cancer Group (CCG) experience. Pediatr Blood Cancer. 2005 Apr;44(4):338-47. [https://doi.org/10.1002/pbc.20227 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/15503297/ PubMed]
 
 
 
==IE {{#subobject:29f233|Regimen=1}}==
 
==IE {{#subobject:29f233|Regimen=1}}==
{| class="wikitable" style="float:right; margin-left: 5px;"
 
|-
 
|[[#top|back to top]]
 
|}
 
 
IE: '''<u>I</u>'''fosfamide & '''<u>E</u>'''toposide
 
IE: '''<u>I</u>'''fosfamide & '''<u>E</u>'''toposide
 +
<div class="toccolours" style="background-color:#eeeeee">
 
===Regimen {{#subobject:659e8c|Variant=1}}===
 
===Regimen {{#subobject:659e8c|Variant=1}}===
{| class="wikitable" style="width: 40%; text-align:center;"  
+
{| class="wikitable sortable" style="width: 60%; text-align:center;"  
!style="width: 25%"|Study
+
!style="width: 33%"|Study
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
+
!style="width: 33%"|Dates of enrollment
 +
!style="width: 33%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|-
|[https://www.ejcancer.com/article/S0959-8049(96)00439-X/abstract Gentet et al. 1997]
+
|[https://doi.org/10.1016/s0959-8049(96)00439-x Gentet et al. 1997]
|style="background-color:#91cf61"|Phase II
+
|1992-01 to 1995-01
 +
|style="background-color:#91cf61"|Phase 2
 
|-
 
|-
 
|}
 
|}
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
 
*[[Ifosfamide (Ifex)]] 3000 mg/m<sup>2</sup> IV over 3 hours once per day on days 1 to 4
 
*[[Ifosfamide (Ifex)]] 3000 mg/m<sup>2</sup> IV over 3 hours once per day on days 1 to 4
Line 1,482: Line 1,177:
 
*[[Etoposide (Vepesid)]] 75 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1 to 4
 
*[[Etoposide (Vepesid)]] 75 mg/m<sup>2</sup> IV over 60 minutes once per day on days 1 to 4
 
**Given in D5W 250 to 500 mL
 
**Given in D5W 250 to 500 mL
 
+
====Supportive therapy====
====Supportive medications====
 
 
*[[Mesna (Mesnex)]] 3600 mg/m<sup>2</sup>/day IV continuous infusion over 96 hours, started on day 1 (total dose per cycle: 14,400 mg/m<sup>2</sup>)
 
*[[Mesna (Mesnex)]] 3600 mg/m<sup>2</sup>/day IV continuous infusion over 96 hours, started on day 1 (total dose per cycle: 14,400 mg/m<sup>2</sup>)
 
*At least 2000 mL/m<sup>2</sup>/day of hydration with chemotherapy
 
*At least 2000 mL/m<sup>2</sup>/day of hydration with chemotherapy
 
+
'''21- to 28-day cycle for 2 cycles; next cycle starting when ANC greater than 1500/μL and platelet count greater than 100 x 10<sup>9</sup>/L'''
'''21- to 28-day cycle for 2 cycles, with next cycle starting when ANC greater than 1500/uL and platelet count greater than 100 x 10<sup>9</sup>/L'''
+
</div></div>
 
 
 
===References===
 
===References===
# Gentet JC, Brunat-Mentigny M, Demaille MC, Pein F, Avet-Loiseau H, Berger C, De Lumley L, Pacquement H, Schmitt C, Sariban E, Pillon P, Bernard JL, Kalifa C. Ifosfamide and etoposide in childhood osteosarcoma: a phase II study of the French Society of Paediatric Oncology. Eur J Cancer. 1997 Feb;33(2):232-7. [https://www.ejcancer.com/article/S0959-8049(96)00439-X/abstract link to original article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/9135494 PubMed]
+
# Gentet JC, Brunat-Mentigny M, Demaille MC, Pein F, Avet-Loiseau H, Berger C, De Lumley L, Pacquement H, Schmitt C, Sariban E, Pillon P, Bernard JL, Kalifa C. Ifosfamide and etoposide in childhood osteosarcoma: a phase II study of the French Society of Paediatric Oncology. Eur J Cancer. 1997 Feb;33(2):232-7. [https://doi.org/10.1016/s0959-8049(96)00439-x link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/9135494/ PubMed]
  
 
==Regorafenib monotherapy {{#subobject:267gu1|Regimen=1}}==
 
==Regorafenib monotherapy {{#subobject:267gu1|Regimen=1}}==
{| class="wikitable" style="float:right; margin-left: 5px;"
+
<div class="toccolours" style="background-color:#eeeeee">
|-
 
|[[#top|back to top]]
 
|}
 
 
===Regimen {{#subobject:8c0b71|Variant=1}}===
 
===Regimen {{#subobject:8c0b71|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
!style="width: 20%"|Study
 
!style="width: 20%"|Study
!style="width: 20%"|Years of enrollment
+
!style="width: 20%"|Dates of enrollment
 
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
!style="width: 20%"|Comparator
 
!style="width: 20%"|Comparator
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
!style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]]
 
|-
 
|-
|[http://www.ncbi.nlm.nih.gov/pmc/articles/pmc7799443/ Davis et al. 2019 (SARC024)]
+
|[https://www.ncbi.nlm.nih.gov/pmc/articles/pmc7799443/ Davis et al. 2019 (SARC024)]
 
|2014-2018
 
|2014-2018
| style="background-color:#1a9851" |Randomized Phase II (E-esc)
+
| style="background-color:#1a9851" |Randomized Phase 2 (E-esc)
|Placebo
+
|[[Osteosarcoma_-_null_regimens#Placebo|Placebo]]
| style="background-color:#1a9850" |Superior PFS<br>Median PFS: 3.6 vs 1.7 mo<br>(HR 0.42, 95% CI 0.21-0.85)
+
| style="background-color:#1a9850" |Superior PFS (primary endpoint)<br>Median PFS: 3.6 vs 1.7 mo<br>(HR 0.42, 95% CI 0.21-0.85)
 
|-
 
|-
 
|}
 
|}
 +
<div class="toccolours" style="background-color:#b3e2cd">
 
====Targeted therapy====
 
====Targeted therapy====
*[[Regorafenib (Stivarga)]] 160 mg PO once per day
+
*[[Regorafenib (Stivarga)]] 160 mg PO once per day on days 1 to 28
 
 
 
'''28-day cycles'''
 
'''28-day cycles'''
 
+
</div></div>
 
===References===
 
===References===
#'''SARC024:''' Davis LE, Bolejack V, Ryan CW, Ganjoo KN, Loggers ET, Chawla S, Agulnik M, Livingston MB, Reed D, Keedy V, Rushing D, Okuno S, Reinke DK, Riedel RF, Attia S, Mascarenhas L, Maki RG. Randomized Double-Blind Phase II Study of Regorafenib in Patients With Metastatic Osteosarcoma. J Clin Oncol. 2019 Jun 1;37(16):1424-1431. Epub 2019 Apr 23. [https://doi.org/10.1200/jco.18.02374 link to original article] [http://www.ncbi.nlm.nih.gov/pmc/articles/pmc7799443/ link to PMC article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/31013172/ PubMed] NCT02048371
+
#'''SARC024:''' Davis LE, Bolejack V, Ryan CW, Ganjoo KN, Loggers ET, Chawla S, Agulnik M, Livingston MB, Reed D, Keedy V, Rushing D, Okuno S, Reinke DK, Riedel RF, Attia S, Mascarenhas L, Maki RG. Randomized Double-Blind Phase II Study of Regorafenib in Patients With Metastatic Osteosarcoma. J Clin Oncol. 2019 Jun 1;37(16):1424-1431. Epub 2019 Apr 23. [https://doi.org/10.1200/jco.18.02374 link to original article] [https://www.ncbi.nlm.nih.gov/pmc/articles/pmc7799443/ link to PMC article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/31013172/ PubMed] [https://clinicaltrials.gov/study/NCT02048371 NCT02048371]
  
 
==Samarium-153 with stem cell support {{#subobject:26224a|Regimen=1}}==
 
==Samarium-153 with stem cell support {{#subobject:26224a|Regimen=1}}==
{| class="wikitable" style="float:right; margin-left: 5px;"
+
<div class="toccolours" style="background-color:#eeeeee">
|-
 
|[[#top|back to top]]
 
|}
 
 
===Regimen {{#subobject:8c0a7f|Variant=1}}===
 
===Regimen {{#subobject:8c0a7f|Variant=1}}===
{| class="wikitable" style="width: 40%; text-align:center;"  
+
{| class="wikitable sortable" style="width: 60%; text-align:center;"  
!style="width: 25%"|Study
+
!style="width: 33%"|Study
!style="width: 25%"|[[Levels_of_Evidence#Evidence|Evidence]]
+
!style="width: 33%"|Dates of enrollment
 +
!style="width: 33%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
|-
 
|-
 
|[https://doi.org/10.1200/jco.2002.20.1.189 Anderson et al. 2002]
 
|[https://doi.org/10.1200/jco.2002.20.1.189 Anderson et al. 2002]
|style="background-color:#ffffbe"|Phase I
+
|NR
 +
|style="background-color:#ffffbe"|Phase 1
 
|-
 
|-
 
|}
 
|}
 
+
*Peripheral blood progenitor cell (PBPC) or bone marrow harvest and cryopreservation of at least 2 x 10<sup>6</sup> CD34+ cells/kg
*Peripheral blood progenetor cell (PBPC) or bone marrow harvest and cryopreservation of at least 2 x 10<sup>6</sup> CD34+ cells/kg
+
<div class="toccolours" style="background-color:#b3e2cd">
 
====Radiotherapy====
 
====Radiotherapy====
 
*[[Samarium-153 (Quadramet)]] 30 mCi/kg IV once on day 0
 
*[[Samarium-153 (Quadramet)]] 30 mCi/kg IV once on day 0
 
+
====Supportive therapy====
====Supportive medications====
+
*[[Autologous stem cells]] (peripheral blood progenitor cell (PBPC) or bone marrow cells) re-infused on day +14
*Growth factor support with ONE of the following started when ANC less than 1000/uL:
+
*Growth factor support with ONE of the following started when ANC less than 1000/μL:
 
**[[Filgrastim (Neupogen)]]
 
**[[Filgrastim (Neupogen)]]
 
**[[Sargramostim (Leukine)]]  
 
**[[Sargramostim (Leukine)]]  
 
+
'''One course'''
'''On day +14, infuse peripheral blood progenetor cell (PBPC) or bone marrow cells'''
+
</div></div>
 
 
 
===References===
 
===References===
# '''Phase 1:''' Anderson PM, Wiseman GA, Dispenzieri A, Arndt CA, Hartmann LC, Smithson WA, Mullan BP, Bruland OS. High-dose samarium-153 ethylene diamine tetramethylene phosphonate: low toxicity of skeletal irradiation in patients with osteosarcoma and bone metastases. J Clin Oncol. 2002 Jan 1;20(1):189-96. [https://doi.org/10.1200/jco.2002.20.1.189 link to original article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/11773169 PubMed]
+
# '''Phase 1:''' Anderson PM, Wiseman GA, Dispenzieri A, Arndt CA, Hartmann LC, Smithson WA, Mullan BP, Bruland OS. High-dose samarium-153 ethylene diamine tetramethylene phosphonate: low toxicity of skeletal irradiation in patients with osteosarcoma and bone metastases. J Clin Oncol. 2002 Jan 1;20(1):189-96. [https://doi.org/10.1200/jco.2002.20.1.189 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/11773169/ PubMed]
  
 
==Sorafenib monotherapy {{#subobject:s9ggu1|Regimen=1}}==
 
==Sorafenib monotherapy {{#subobject:s9ggu1|Regimen=1}}==
{| class="wikitable" style="float:right; margin-left: 5px;"
+
<div class="toccolours" style="background-color:#eeeeee">
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===Regimen {{#subobject:8c0hcs|Variant=1}}===
 
===Regimen {{#subobject:8c0hcs|Variant=1}}===
 
{| class="wikitable sortable" style="width: 60%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 60%; text-align:center;"  
 
!style="width: 33%"|Study
 
!style="width: 33%"|Study
!style="width: 33%"|Years of enrollment
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!style="width: 33%"|Dates of enrollment
 
!style="width: 33%"|[[Levels_of_Evidence#Evidence|Evidence]]
 
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|[https://doi.org/10.1093/annonc/mdr151 Grignani et al. 2011]
 
|[https://doi.org/10.1093/annonc/mdr151 Grignani et al. 2011]
 
|2008-2009
 
|2008-2009
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====Targeted therapy====
 
====Targeted therapy====
*[[Sorafenib (Nexavar)]] 400 mg PO twice per day
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*[[Sorafenib (Nexavar)]] 400 mg PO twice per day on days 1 to 28
 
 
 
'''28-day cycles'''
 
'''28-day cycles'''
 
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===References===
 
===References===
# Grignani G, Palmerini E, Dileo P, Asaftei SD, D'Ambrosio L, Pignochino Y, Mercuri M, Picci P, Fagioli F, Casali PG, Ferrari S, Aglietta M. A phase II trial of sorafenib in relapsed and unresectable high-grade osteosarcoma after failure of standard multimodal therapy: an Italian Sarcoma Group study. Ann Oncol. 2012 Feb;23(2):508-16. Epub 2011 Apr 28. [https://doi.org/10.1093/annonc/mdr151 link to original article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/21527590/ PubMed] EudraCT 2007-004396-19
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# Grignani G, Palmerini E, Dileo P, Asaftei SD, D'Ambrosio L, Pignochino Y, Mercuri M, Picci P, Fagioli F, Casali PG, Ferrari S, Aglietta M. A phase II trial of sorafenib in relapsed and unresectable high-grade osteosarcoma after failure of standard multimodal therapy: an Italian Sarcoma Group study. Ann Oncol. 2012 Feb;23(2):508-16. Epub 2011 Apr 28. [https://doi.org/10.1093/annonc/mdr151 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/21527590/ PubMed] EudraCT 2007-004396-19
 
 
 
[[Category:Osteosarcoma regimens]]
 
[[Category:Osteosarcoma regimens]]
 
[[Category:Disease-specific pages]]
 
[[Category:Disease-specific pages]]
 
[[Category:Bone sarcomas]]
 
[[Category:Bone sarcomas]]
[[Category:Pediatric solid tumors]]
 

Latest revision as of 19:27, 23 June 2024

Section editor
Elizabethdavis2.jpg
Elizabeth J. Davis, MD
Vanderbilt University
Nashville, TN, USA

Are you looking for a regimen but can't find it here? It is possible that we've moved it to the historical regimens page. For placebo or observational studies in this condition, please visit this page. If you still can't find it, please let us know so we can add it!

26 regimens on this page
37 variants on this page


Guidelines

Given the rapid change in evidence in many areas of hematology/oncology, readers are encouraged to consider any guideline published 5+ years ago to be for historical purposes, only.

ESMO

NCCN

Neoadjuvant therapy

Cisplatin & Doxorubicin

AP: Adriamycin (Doxorubicin) & Platinol (Cisplatin)

Regimen variant #1

Study Dates of enrollment Evidence Comparator Comparative Efficacy
Bramwell et al. 1992 1983-1986 Phase 3 (E-switch-ic) MAP Seems to have superior DFS
Souhami et al. 1997 1986-1991 Phase 3 (E-de-esc) Multi-drug T10 protocol Did not meet co-primary endpoints of PFS/OS

Chemotherapy

Supportive therapy

  • Prehydration: normal saline 400 mL/m2 and D5W 400 mL/m2 IV over 2 hours--the reference did not clarify if these two solutions are given at the same time
  • The volume of fluid for cisplatin continuous infusion is 2400 mL/m2 NS, with KCl 80 mEq/L and mannitol 32,000 mg/m2
  • Posthydration: D5W 600 mL/m2 over 6 hours, with KCl 20 mEq/L and mannitol 8000 mg/m2; and NS 600 mL/m2 over 6 hours, with KCl 20 mEq/L, magnesium sulfate 2 mmol/L, and calcium gluconate 0.6 mmol/L--the reference did not clarify if these two solutions are given at the same time. Then D5W 600 mL/m2 over 12 hours, with KCl 20 mEq/L and mannitol 8000 mg/m2.
  • Furosemide (Lasix) 20 to 40 mg IV if urine output is less than 400 mL/m2 over 6 hours

21-day cycle for 3 cycles

Subsequent treatment

  • Definitive surgery on week 9, then adjuvant AP that starts 14 to 28 days after surgery


Regimen variant #2

Study Dates of enrollment Evidence Comparator Comparative Efficacy
Lewis et al. 2007 (EORTC 80931) 1993-2002 Phase 3 (C) Cisplatin & Doxorubicin; dose-intense Did not meet primary endpoint of OS

Chemotherapy

Supportive therapy

  • 4 hours of prehydration prior to cisplatin
  • 24 hours of posthydration & mannitol after cisplatin
  • Recommended that fluid for cisplatin is isotonic saline with potassium chloride and mannitol

21-day cycle for 2 cycles

Subsequent treatment

  • Definitive surgery in a 14-day window between cycles 2 & 3, then adjuvant AP

References

  1. Bramwell VH, Burgers M, Sneath R, Souhami R, van Oosterom AT, Voûte PA, Rouesse J, Spooner D, Craft AW, Somers R, Pringle J, Malcolm AJ, van der Eiiken J, Thomas D, Uscinska B, Machin D, van Glabbeke M; European Osteosarcoma Intergroup. A comparison of two short intensive adjuvant chemotherapy regimens in operable osteosarcoma of limbs in children and young adults: the first study of the European Osteosarcoma Intergroup. J Clin Oncol. 1992 Oct;10(10):1579-91. link to original article contains dosing details in manuscript PubMed
  2. Souhami RL, Craft AW, Van der Eijken JW, Nooij M, Spooner D, Bramwell VH, Wierzbicki R, Malcolm AJ, Kirkpatrick A, Uscinska BM, Van Glabbeke M, Machin D; European Osteosarcoma Intergroup. Randomised trial of two regimens of chemotherapy in operable osteosarcoma: a study of the European Osteosarcoma Intergroup. Lancet. 1997 Sep 27;350(9082):911-7. link to original article PubMed
  3. EORTC 80931: Lewis IJ, Nooij MA, Whelan J, Sydes MR, Grimer R, Hogendoorn PC, Memon MA, Weeden S, Uscinska BM, van Glabbeke M, Kirkpatrick A, Hauben EI, Craft AW, Taminiau AH; MRC BO06 and EORTC 80931 collaborators; European Osteosarcoma Intergroup. Improvement in histologic response but not survival in osteosarcoma patients treated with intensified chemotherapy: a randomized phase III trial of the European Osteosarcoma Intergroup. J Natl Cancer Inst. 2007 Jan 17;99(2):112-28. link to original article contains dosing details in manuscript PubMed NCT00002539

Cisplatin, Epirubicin, Ifosfamide

Regimen

Study Evidence
Basaran et al. 2007 Phase 2

Chemotherapy

Supportive therapy

  • Mesna (Mesnex) 2000 mg/m2 IV over 4 hours once per day on days 2 to 4, given with ifosfamide
  • Pre- and post-hydration with mannitol diuresis for cisplatin

21-day cycle for 3 cycles

Subsequent treatment

References

  1. Basaran M, Bavbek ES, Saglam S, Eralp L, Sakar B, Atalar AC, Bilgic B, Ozger H, Onat H. A phase II study of cisplatin, ifosfamide and epirubicin combination chemotherapy in adults with nonmetastatic and extremity osteosarcomas. Oncology. 2007;72(3-4):255-60. Epub 2008 Jan 10. link to original article contains dosing details in manuscript PubMed

MA

MA: High-dose Methotrexate, Adriamycin (Doxorubicin)

Regimen

Study Dates of enrollment Evidence Comparator Comparative Efficacy
Le Deley et al. 2007 (SFOP OS94) 1994-2001 Phase 3 (C) M-EI Might have inferior EFS

Chemotherapy

  • Methotrexate (MTX) as follows:
    • Cycles 1, 2, 3, 6, 7, 10, 11: 12,000 mg/m2 IV over 4 hours once on day 1
      • Given in D5W 1L with sodium bicarbonate 1 mEq/kg
  • Doxorubicin (Adriamycin) as follows:
    • Cycles 4 & 8: 70 mg/m2 IV over 6 hours once on day 1

Supportive therapy

  • Leucovorin (Folinic acid) 15 mg PO every 6 hours for up to 11 doses on weeks 1, 2, 3, 6, 7, 10, 11, starting 20 hours after the completion of methotrexate infusion
  • For methotrexate: hydration & urine alkalinization by PO and IV routes to maintain 1.6 L/m2 urine output over the first 24 hours and 2 L/m2 on days 2 & 3, with urine pH greater than 7
  • Daily monitoring of methotrexate levels and creatinine

7-day cycle for 11 cycles

Subsequent treatment

  • Surgery occurs during week 12, with risk-adapted treatment by the following response-based criteria:
    • SFOP OS94, patients with good response: Adjuvant MA
    • SFOP OS94, patients with poor response: Adjuvant IE

References

  1. SFOP OS94: Le Deley MC, Guinebretière JM, Gentet JC, Pacquement H, Pichon F, Marec-Bérard P, Entz-Werlé N, Schmitt C, Brugières L, Vanel D, Dupoüy N, Tabone MD, Kalifa C; Société Française d'Oncologie Pédiatrique (SFOP). SFOP OS94: a randomised trial comparing preoperative high-dose methotrexate plus doxorubicin to high-dose methotrexate plus etoposide and ifosfamide in osteosarcoma patients. Eur J Cancer. 2007 Mar;43(4):752-61. Epub 2007 Jan 30. link to original article contains dosing details in manuscript PubMed NCT00180908

MAP

MAP: High-dose Methotrexate, Adriamycin (Doxorubicin), Platinol (Cisplatin)

Regimen variant #1

Study Dates of enrollment Evidence Comparator Comparative Efficacy
Bramwell et al. 1992 1983-1986 Phase 3 (E-esc) Cisplatin & Doxorubicin Seems to have inferior DFS

Note: The body of Bramwell et al. 1992 says that methotrexate is given over 4 hours, whereas Bramwell et al. 1992 figure 1's text says that methotrexate is given over 6 hours.

Chemotherapy

Supportive therapy

  • Leucovorin (Folinic acid) 12 mg/m2 IV every 6 hours x 10 doses or 15 mg/m2 PO every 6 hours x 10 doses, starting 24 hours after the start of methotrexate infusion
    • Monitor methotrexate level at "24 hours and 48 hours"--it is unclear in the reference if this is time after the start/end of methotrexate, beginning of leucovorin, or something else
    • Methotrexate levels higher than 100 nmol/L at 48 hours required additional leucovorin rescue
  • Prehydration for methotrexate: "0.9 NaCl:D5W"--unclear if this means either normal saline or D5W can be used--750 mL/m2 over 6 hours, with KCl 20 mEq/L
  • The volume of fluid for methotrexate is D5W 1000 mL, to be given over 6 hours
  • Posthydration for methotrexate: Alternating liters of D5W and NS 3000 mL/m2 over 24 hours, with KCl 60 mEq/L.
  • Sodium bicarbonate 3 g PO Q6H, starting 12 hours before methotrexate, and sodium bicarbonate 167 mmol/L IV until serum methotrexate level is less than 8000 to 10,000 nmol/L. Note: the reference is not clear about when/if PO sodium bicarbonate is stopped, when IV sodium bicarbonate is started, or the administration rate of IV sodium bicarbonate.
  • Prehydration for cisplatin: normal saline 400 mL/m2 and D5W 400 mL/m2 IV over 2 hours--the reference did not clarify if these two solutions are given at the same time
  • The volume of fluid for cisplatin continuous infusion is 2400 mL/m2 NS, with KCl 80 mEq/L and mannitol 32,000 mg/m2
  • Posthydration for cisplatin: D5W 600 mL/m2 over 6 hours, with KCl 20 mEq/L and mannitol 8000 mg/m2; and NS 600 mL/m2 over 6 hours, with KCl 20 mEq/L, magnesium sulfate 2 mmol/L, and calcium gluconate 0.6 mmol/L--the reference did not clarify if these two solutions are given at the same time. Then D5W 600 mL/m2 over 12 hours, with KCl 20 mEq/L and mannitol 8000 mg/m2.
  • Furosemide (Lasix) 20 to 40 mg IV if urine output is less than 400 mL/m2 over 6 hours during cisplatin

21-day cycle for 2 cycles

Subsequent treatment

  • Definitive surgery on week 9, then adjuvant MAP that starts 14 to 28 days after surgery


Regimen variant #2

Study Evidence
Bacci et al. 1993 (IOR/OS-2) Phase 2

Chemotherapy

Supportive therapy

  • Leucovorin (Folinic acid) 15 mg IV every 6 hours x 11 doses on days 2 to 4, starting 24 hours after the start of methotrexate infusion
  • Hydration during and after methotrexate infusion

27-day cycle for 2 cycles

Subsequent treatment

  • Definitive surgery, then risk-adapted therapy. Amputated patients restart chemotherapy 3 to 5 days after surgery; patients who undergo limb salvage or rotation plasty restart chemotherapy 10 to 21 days after surgery.
    • IOR/OS-2, at least 90% tumor necrosis in the surgically removed specimen: Adjuvant MAP
    • IOR/OS-2, less than 90% tumor necrosis in the surgically removed specimen: Adjuvant MAPIE


Regimen variant #3

Study Dates of enrollment Evidence Comparator Comparative Efficacy
Winkler et al. 1988 (COSS-82) 1982-1984 Phase 3 (E-switch-ic) M-BCD Superior ORR

Note: The exact schedule is unclear based on limited information in the reference, as schedule of doses is primarily extrapolated from Figure 1, which does not contain clear delineations in time. The dose/schedule of cisplatin reflects the protocol amendment that was done because of nephrotoxicity.

Chemotherapy

  • Methotrexate (MTX) 12,000 mg/m2 (maximum dose of 20,000 mg) IV over 4 hours once per day on days 22 & 29
    • MTX is dissolved at a concentration of 20,000 mg/L in a solution containing 5% glucose
  • Doxorubicin (Adriamycin) 30 mg/m2 IV bolus once per day on days 1 & 2
  • Cisplatin (Platinol) 90 mg/m2 IV over 4 hours once on day 3

Supportive therapy

  • Leucovorin (Folinic acid) 15 mg/m2 PO every 6 hours x 12 hours once per day on days 23 & 30, starting 24 hours after the completion of methotrexate infusion; additional leucovorin used for delayed methotrexate elimination
  • Sodium bicarbonate urine alkalinization prior to high-dose methotrexate
  • NS 4.5 L/m2 on day 1 after methotrexate; NS 3 L/m2 on day 2, with adjustments made to keep urine pH greater than 7.4
  • 12 hours of hydration prior to cisplatin & 20 hours of hydration after cisplatin; total amount of fluid given over 36hours of prehydration, cisplatin, and posthydration is NS 6 L/m2 with mannitol 8 g/L and potassium 20 mval/L.
  • Magnesium 180 mg/m2 PO "per day throughout the whole chemotherapy time"--as described in COSS-80

35-day cycle for 2 cycles

Subsequent treatment

  • Surgery, then risk-adapted treatment:
    • COSS-82, good response: Adjuvant MAP
    • COSS-82, poor response: Adjuvant IP-BCD


Regimen variant #4

Study Dates of enrollment Evidence Comparator Comparative Efficacy
Winkler et al. 1984 (COSS-80) 1979-1982 Phase 3 (E-switch-ic) MA-BCD Did not meet primary endpoint of CDF rate

Note: The exact schedule is unclear based on limited/conflicting information in the reference. For example, Figure 1 appears to depict high-dose methotrexate starting 2 weeks after adriamycin, but the text says that methotrexate begins after a 3-week rest period. Additionally, the diagram in Figure 1 implies that the later therapies are given 4 times (once, then repeated x 3 cycles), but based on the cumulative doses listed, they are only given for a total of 3 cycles. The optional interferon arm is omitted given lack of benefit seen in the study.

Chemotherapy

  • Methotrexate (MTX) as follows:
    • Cycle 1: 12,000 mg/m2 (maximum dose of 20,000 mg) IV over 4 hours once per day on days 29 & 36
    • Cycles 2 to 4: 12,000 mg/m2 (maximum dose of 20,000 mg) IV over 4 hours once per day on days 1, 8, 29, 36
    • MTX is dissolved at a concentration of 20,000 mg/L in a solution containing 5% glucose
  • Doxorubicin (Adriamycin) as follows:
    • Cycles 1, 3, 4: 45 mg/m2 IV bolus once per day on days 1 & 2
    • Cycle 2: 45 mg/m2 IV bolus once per day on days 15 & 16 (delayed during cycle 2 until after surgery)
  • Cisplatin (Platinol) 120 mg/m2 IV over 5 hours once on day 43

Supportive therapy

  • Leucovorin (Folinic acid) 15 mg/m2 PO every 6 hours x 12 hours once per day on days 2, 9, 30, 37, starting 24 hours after the completion of methotrexate infusion; additional leucovorin used for delayed methotrexate elimination
  • Sodium bicarbonate urine alkalinization prior to high-dose methotrexate
  • NS 4.5 L/m2 on day 1 after methotrexate; NS 3 L/m2 on day 2, with adjustments made to keep urine pH greater than 7.4
  • 3 hours of hydration prior to cisplatin & 3 hours of hydration after cisplatin; total amount of fluid given over 11 hours of prehydration, cisplatin, and posthydration is NS 2.5 L/m2 with mannitol 8 g/L and potassium 20 mval/L.
  • Magnesium 180 mg/m2 PO "per day throughout the whole chemotherapy time" with cisplatin

8-week cycle for 4 cycles, with surgery done during cycle 2 before doxorubicin; surgery is done 9 to 18 weeks after the start of chemotherapy

References

  1. COSS-80: Winkler K, Beron G, Kotz R, Salzer-Kuntschik M, Beck J, Beck W, Brandeis W, Ebell W, Erttmann R, Göbel U, Havers W, Henze G, Hinderfeld L, Höcker P, Jobke A, Jürgens H, Kabisch H, Preusser P, Prindull G, Ramach W, Ritter J, Sekera J, Treuner J, Wist G, Landbeck G. Neoadjuvant chemotherapy for osteogenic sarcoma: results of a Cooperative German/Austrian study. J Clin Oncol. 1984 Jun;2(6):617-24. link to original article contains dosing details in manuscript PubMed
  2. COSS-82: Winkler K, Beron G, Delling G, Heise U, Kabisch H, Purfürst C, Berger J, Ritter J, Jürgens H, Gerein V, Graf N, Russe W, Gruemayer ER, Ertelt W, Kotz R, Preuzzer P, Prindull G, Brandeis W, Landbeck G. Neoadjuvant chemotherapy of osteosarcoma: results of a randomized cooperative trial (COSS-82) with salvage chemotherapy based on histological tumor response. J Clin Oncol. 1988 Feb;6(2):329-37. link to original article contains dosing details in manuscript PubMed
  3. Bramwell VH, Burgers M, Sneath R, Souhami R, van Oosterom AT, Voûte PA, Rouesse J, Spooner D, Craft AW, Somers R, Pringle J, Malcolm AJ, van der Eiiken J, Thomas D, Uscinska B, Machin D, van Glabbeke M; European Osteosarcoma Intergroup. A comparison of two short intensive adjuvant chemotherapy regimens in operable osteosarcoma of limbs in children and young adults: the first study of the European Osteosarcoma Intergroup. J Clin Oncol. 1992 Oct;10(10):1579-91. link to original article contains dosing details in manuscript PubMed content property of HemOnc.org
  4. IOR/OS-2: Bacci G, Picci P, Ferrari S, Ruggieri P, Casadei R, Tienghi A, Brach del Prever A, Gherlinzoni F, Mercuri M, Monti C. Primary chemotherapy and delayed surgery for nonmetastatic osteosarcoma of the extremities: results in 164 patients preoperatively treated with high doses of methotrexate followed by cisplatin and doxorubicin. Cancer. 1993 Dec 1;72(11):3227-38. link to original article PubMed
    1. Update: Bacci G, Ferrari S, Bertoni F, Ruggieri P, Picci P, Longhi A, Casadei R, Fabbri N, Forni C, Versari M, Campanacci M. Long-term outcome for patients with nonmetastatic osteosarcoma of the extremity treated at the Istituto Ortopedico Rizzoli according to the Istituto Ortopedico Rizzoli/Osteosarcoma-2 protocol: an updated report. J Clin Oncol. 2000 Dec 15;18(24):4016-27. link to original article contains dosing details in manuscript PubMed

MAPI

MAPI: High-dose Methotrexate, Adriamycin (Doxorubicin), Platinol (Cisplatin), Ifosfamide

Regimen

Study Evidence
Bacci et al. 2003 Phase 2

Chemotherapy

  • Methotrexate (MTX) 12,000 mg/m2 IV over 4 hours once on day 1
  • Cisplatin (Platinol) 60 mg/m2/day IV continuous infusion over 48 hours, started on day 8 (total dose per cycle: 120 mg/m2)
  • Doxorubicin (Adriamycin) 75 mg/m2 IV continuous infusion over 24 hours, started on day 10
  • Ifosfamide (Ifex) 3000 mg/m2/day IV continuous infusion over 120 hours, started on day 29, given with mesna (total dose per cycle: 15,000 mg/m2)

Supportive therapy

  • Leucovorin (Folinic acid) 15 mg (route not specified) every 6 hours x 11 doses (note: the reference says "11 cycles," but it is assumed this is the intended meaning), starting day 2, 24 hours after the start of methotrexate
  • Hydration during and after methotrexate as described by: Rosen G, Nirenberg A. Chemotherapy for osteogenic sarcoma: an investigative method, not a recipe. Cancer Treat Rep. 1982 Sep;66(9):1687-97. PubMed
  • Mesna (Mesnex) 3000 mg/m2/day IV continuous infusion over 120 hours, started on day 29, given with ifosfamide (total dose: 15,000 mg/m2)

42-day cycle for 2 cycles

Subsequent treatment

Dose and schedule modifications

  • If 4-hour methotrexate level is less than 10,000 nmol/L, the next cycle's methotrexate dose is increased by 2000 mg/m2

References

  1. Bacci G, Briccoli A, Rocca M, Ferrari S, Donati D, Longhi A, Bertoni F, Bacchini P, Giacomini S, Forni C, Manfrini M, Galletti S. Neoadjuvant chemotherapy for osteosarcoma of the extremities with metastases at presentation: recent experience at the Rizzoli Institute in 57 patients treated with cisplatin, doxorubicin, and a high dose of methotrexate and ifosfamide. Ann Oncol. 2003 Jul;14(7):1126-34. link to original article contains dosing details in manuscript PubMed

M-EI

M-EI: Methotrexate, Etoposide, Ifosfamide

Regimen

Study Dates of enrollment Evidence Comparator Comparative Efficacy
Le Deley et al. 2007 (SFOP OS94) 1994-2001 Phase 3 (E-switch-ic) MA Might have superior EFS
Piperno-Neumann et al. 2016 (OS2006) 2007-2014 Phase 3 (C) M-EI & Zoledronic acid Might have superior EFS
EFS36: 63.4% vs 57.1%
(HR 0.74, 95% CI 0.51-1.05)

Note: this regimen information is from SFOP OS94.

Chemotherapy

  • Methotrexate (MTX) as follows:
    • Cycles 1, 2, 3, 7, 8, 12, 13: 12,000 mg/m2 IV over 4 hours once on day 1
      • Given in D5W 1L with sodium bicarbonate 1 mEq/kg
  • Etoposide (Vepesid) as follows:
    • Cycles 4 & 9: 75 mg/m2 IV over 60 minutes once per day on days 1 to 4
      • Given in NS 250 to 500 mL
  • Ifosfamide (Ifex) as follows:
    • Cycles 4 & 9: 3000 mg/m2 IV over 3 hours once per day on days 1 to 4, given with mesna
      • Given in NS 250 to 500 mL

Supportive therapy

  • Leucovorin (Folinic acid) 15 mg PO every 6 hours for up to 11 doses on weeks 1, 2, 3, 7, 8, 12, 13, starting 20 hours after the completion of methotrexate infusion
  • For methotrexate: hydration & urine alkalinization by PO and IV routes to maintain 1.6 L/m2 urine output over the first 24 hours and 2 L/m2 on days 2 & 3, with urine pH greater than 7
  • Daily monitoring of methotrexate levels and creatinine
  • Mesna (Mesnex) 3600 mg/m2/day IV continuous infusion over 96 hours, started on day 22 (week 4) and 57 (week 9), given with ifosfamide (total dose: 14,400 mg/m2)
  • Up to 2 L/day hydration with ifosfamide & mesna

7-day cycle for 13 cycles

Subsequent treatment

  • Surgery occurs during week 14, with further treatment based on pathologic response:
    • SFOP OS94, patients with good response: Adjuvant M-EI
    • SFOP OS94, patients with poor response: Adjuvant AP

References

  1. SFOP OS94: Le Deley MC, Guinebretière JM, Gentet JC, Pacquement H, Pichon F, Marec-Bérard P, Entz-Werlé N, Schmitt C, Brugières L, Vanel D, Dupoüy N, Tabone MD, Kalifa C; Société Française d'Oncologie Pédiatrique (SFOP). SFOP OS94: a randomised trial comparing preoperative high-dose methotrexate plus doxorubicin to high-dose methotrexate plus etoposide and ifosfamide in osteosarcoma patients. Eur J Cancer. 2007 Mar;43(4):752-61. Epub 2007 Jan 30. link to original article contains dosing details in manuscript PubMed NCT00180908
  2. OS2006: Piperno-Neumann S, Le Deley MC, Rédini F, Pacquement H, Marec-Bérard P, Petit P, Brisse H, Lervat C, Gentet JC, Entz-Werlé N, Italiano A, Corradini N, Bompas E, Penel N, Tabone MD, Gomez-Brouchet A, Guinebretière JM, Mascard E, Gouin F, Chevance A, Bonnet N, Blay JY, Brugières L; Sarcoma Group of UNICANCER; SFCE; GSF-GETO. Zoledronate in combination with chemotherapy and surgery to treat osteosarcoma (OS2006): a randomised, multicentre, open-label, phase 3 trial. Lancet Oncol. 2016 Aug;17(8):1070-1080. Epub 2016 Jun 17. link to original article PubMed NCT00470223
    1. Update: Gaspar N, Occean BV, Pacquement H, Bompas E, Bouvier C, Brisse HJ, Castex MP, Cheurfa N, Corradini N, Delaye J, Entz-Werlé N, Gentet JC, Italiano A, Lervat C, Marec-Berard P, Mascard E, Redini F, Saumet L, Schmitt C, Tabone MD, Verite-Goulard C, Le Deley MC, Piperno-Neumann S, Brugieres L; SFCE; GSF-GETO; UNICANCER sarcoma group. Results of methotrexate-etoposide-ifosfamide based regimen (M-EI) in osteosarcoma patients included in the French OS2006/sarcome-09 study. Eur J Cancer. 2018 Jan;88:57-66. Epub 2017 Nov 28. link to original article PubMed

Adjuvant therapy

Cisplatin & Doxorubicin

AP: Adriamycin (Doxorubicin) & Platinol (Cisplatin)

Regimen variant #1

Study Dates of enrollment Evidence Comparator Comparative Efficacy
Bramwell et al. 1992 1983-1986 Phase 3 (E-esc) MAP Seems to have superior DFS
Souhami et al. 1997 1986-1991 Phase 3 (E-de-esc) Multi-drug T10 protocol Did not meet co-primary endpoints of PFS/OS

Preceding treatment

Chemotherapy

Supportive therapy

  • Prehydration: normal saline 400 mL/m2 and D5W 400 mL/m2 IV over 2 hours--the reference did not clarify if these two solutions are given at the same time
  • The volume of fluid for cisplatin continuous infusion is 2400 mL/m2 NS, with KCl 80 mEq/L and mannitol 32,000 mg/m2
  • Posthydration: D5W 600 mL/m2 over 6 hours, with KCl 20 mEq/L and mannitol 8000 mg/m2; and NS 600 mL/m2 over 6 hours, with KCl 20 mEq/L, magnesium sulfate 2 mmol/L, and calcium gluconate 0.6 mmol/L--the reference did not clarify if these two solutions are given at the same time. Then D5W 600 mL/m2 over 12 hours, with KCl 20 mEq/L and mannitol 8000 mg/m2.
  • Furosemide (Lasix) 20 to 40 mg IV if urine output is less than 400 mL/m2 over 6 hours

21-day cycle for 3 cycles


Regimen variant #2

Study Dates of enrollment Evidence Comparator Comparative Efficacy
Lewis et al. 2007 (EORTC 80931) 1993-2002 Phase 3 (C) Cisplatin & Doxorubicin; dose-intense Did not meet primary endpoint of OS

Preceding treatment

Chemotherapy

Supportive therapy

  • 4 hours of prehydration prior to cisplatin
  • 24 hours of posthydration & mannitol after cisplatin
  • Recommended that fluid for cisplatin is isotonic saline with potassium chloride and mannitol

21-day cycle for 4 cycles


Regimen variant #3, dose intense

Study Dates of enrollment Evidence Comparator Comparative Efficacy
Lewis et al. 2007 (EORTC 80931) 1993-2002 Phase 3 (E-esc) Cisplatin & Doxorubicin; conventional Did not meet primary endpoint of OS

Preceding treatment

Chemotherapy

Supportive therapy

  • Growth factor suppor with ONE of the following:
  • 4 hours of prehydration prior to cisplatin
  • 24 hours of posthydration & mannitol after cisplatin
  • Recommended that fluid for cisplatin is isotonic saline with potassium chloride and mannitol

14-day cycle for 3 cycles


Regimen variant #4

Study Dates of enrollment Evidence
Winkler et al. 1988 (COSS-82) 1982-1984 Non-randomized part of phase 3 RCT

Note: The exact schedule is unclear based on limited information in the reference, as schedule of doses is primarily extrapolated from Figure 1, which does not contain clear delineations in time.

Preceding treatment

Chemotherapy

Supportive therapy

  • 12 hours of hydration prior to cisplatin & 20 hours of hydration after cisplatin; total amount of fluid given over 36hours of prehydration, cisplatin, and posthydration is NS 6 L/m2 with mannitol 8 g/L and potassium 20 mval/L.
  • Magnesium 180 mg/m2 PO "per day throughout the whole chemotherapy time"--as described in COSS-80

21-day cycle for 6 cycles


Regimen variant #5

Study Dates of enrollment Evidence
Le Deley et al. 2007 (SFOP OS94) 1994-2001 Non-randomized part of phase 3 RCT

Details were not listed about the precise schedule. Other regimens have used both medications both on day 1, with 21-day cycles.

Preceding treatment

Chemotherapy

5 cycles (length not specified)

References

  1. COSS-82: Winkler K, Beron G, Delling G, Heise U, Kabisch H, Purfürst C, Berger J, Ritter J, Jürgens H, Gerein V, Graf N, Russe W, Gruemayer ER, Ertelt W, Kotz R, Preuzzer P, Prindull G, Brandeis W, Landbeck G. Neoadjuvant chemotherapy of osteosarcoma: results of a randomized cooperative trial (COSS-82) with salvage chemotherapy based on histological tumor response. J Clin Oncol. 1988 Feb;6(2):329-37. link to original article contains dosing details in manuscript PubMed
  2. Bramwell VH, Burgers M, Sneath R, Souhami R, van Oosterom AT, Voûte PA, Rouesse J, Spooner D, Craft AW, Somers R, Pringle J, Malcolm AJ, van der Eiiken J, Thomas D, Uscinska B, Machin D, van Glabbeke M; European Osteosarcoma Intergroup. A comparison of two short intensive adjuvant chemotherapy regimens in operable osteosarcoma of limbs in children and young adults: the first study of the European Osteosarcoma Intergroup. J Clin Oncol. 1992 Oct;10(10):1579-91. link to original article contains dosing details in manuscript PubMed
  3. Souhami RL, Craft AW, Van der Eijken JW, Nooij M, Spooner D, Bramwell VH, Wierzbicki R, Malcolm AJ, Kirkpatrick A, Uscinska BM, Van Glabbeke M, Machin D; European Osteosarcoma Intergroup. Randomised trial of two regimens of chemotherapy in operable osteosarcoma: a study of the European Osteosarcoma Intergroup. Lancet. 1997 Sep 27;350(9082):911-7. link to original article PubMed
  4. EORTC 80931: Lewis IJ, Nooij MA, Whelan J, Sydes MR, Grimer R, Hogendoorn PC, Memon MA, Weeden S, Uscinska BM, van Glabbeke M, Kirkpatrick A, Hauben EI, Craft AW, Taminiau AH; MRC BO06 and EORTC 80931 collaborators; European Osteosarcoma Intergroup. Improvement in histologic response but not survival in osteosarcoma patients treated with intensified chemotherapy: a randomized phase III trial of the European Osteosarcoma Intergroup. J Natl Cancer Inst. 2007 Jan 17;99(2):112-28. link to original article contains dosing details in manuscript PubMed NCT00002539
  5. SFOP OS94: Le Deley MC, Guinebretière JM, Gentet JC, Pacquement H, Pichon F, Marec-Bérard P, Entz-Werlé N, Schmitt C, Brugières L, Vanel D, Dupoüy N, Tabone MD, Kalifa C; Société Française d'Oncologie Pédiatrique (SFOP). SFOP OS94: a randomised trial comparing preoperative high-dose methotrexate plus doxorubicin to high-dose methotrexate plus etoposide and ifosfamide in osteosarcoma patients. Eur J Cancer. 2007 Mar;43(4):752-61. Epub 2007 Jan 30. link to original article contains dosing details in manuscript PubMed NCT00180908

Cisplatin, Epirubicin, Ifosfamide

Regimen

Study Evidence
Basaran et al. 2007 Phase 2

Preceding treatment

Chemotherapy

Supportive therapy

  • Mesna (Mesnex) 2000 mg/m2 IV over 4 hours once per day on days 2 to 4, given with ifosfamide
  • Pre- and post-hydration with mannitol diuresis for cisplatin

28-day cycle for 3 cycles

References

  1. Basaran M, Bavbek ES, Saglam S, Eralp L, Sakar B, Atalar AC, Bilgic B, Ozger H, Onat H. A phase II study of cisplatin, ifosfamide and epirubicin combination chemotherapy in adults with nonmetastatic and extremity osteosarcomas. Oncology. 2007;72(3-4):255-60. Epub 2008 Jan 10. link to original article contains dosing details in abstract PubMed

IE

IE: Ifosfamide, Etoposide

Regimen

Study Dates of enrollment Evidence
Le Deley et al. 2007 (SFOP OS94) 1994-2001 Non-randomized part of phase 3 RCT

Details were not listed about the length of each cycle. Other regimens have used 21 to 28-day cycles.

Preceding treatment

  • Neoadjuvant MA, then surgery, with poor response

Chemotherapy

  • Ifosfamide (Ifex) 3000 mg/m2 IV over 3 hours once per day on days 1 to 4, given during mesna infusion
    • Given in NS 250 to 500 mL
  • Etoposide (Vepesid) 75 mg/m2 IV over 60 minutes once per day on days 1 to 4
    • Given in NS 250 to 500 mL

Supportive therapy

  • Mesna (Mesnex) 3600 mg/m2/day IV continuous infusion over 96 hours, started on day 1 (total dose: 14,400 mg/m2)
  • Up to 2 L/day hydration with ifosfamide & mesna

5 cycles

References

  1. SFOP OS94: Le Deley MC, Guinebretière JM, Gentet JC, Pacquement H, Pichon F, Marec-Bérard P, Entz-Werlé N, Schmitt C, Brugières L, Vanel D, Dupoüy N, Tabone MD, Kalifa C; Société Française d'Oncologie Pédiatrique (SFOP). SFOP OS94: a randomised trial comparing preoperative high-dose methotrexate plus doxorubicin to high-dose methotrexate plus etoposide and ifosfamide in osteosarcoma patients. Eur J Cancer. 2007 Mar;43(4):752-61. Epub 2007 Jan 30. link to original article contains dosing details in manuscript PubMed NCT00180908

MA

MA: High-dose Methotrexate, Adriamycin (Doxorubicin)

Regimen

Study Dates of enrollment Evidence
Le Deley et al. 2007 (SFOP OS94) 1994-2001 Non-randomized part of phase 3 RCT

Preceding treatment

  • Neoadjuvant MA, then surgery, with good response

Chemotherapy

  • Methotrexate (MTX) 12,000 mg/m2 IV over 4 hours once per day on days 1, 8, 15
    • Given in D5W 1L with sodium bicarbonate 1 mEq/kg
  • Doxorubicin (Adriamycin) as follows:
    • Cycles 1 to 3: 70 mg/m2 IV over 6 hours once on day 22

Supportive therapy

  • Leucovorin (Folinic acid) 15 mg PO every 6 hours for up to 11 doses, starting on days 1, 8, 15, starting 20 hours after the completion of methotrexate infusion
  • For methotrexate: hydration & urine alkalinization by PO and IV routes to maintain 1.6 L/m2 urine output over the first 24 hours and 2 L/m2 on days 2 & 3, with urine pH greater than 7
  • Daily monitoring of methotrexate levels and creatinine

28-day cycle for 4 cycles

References

  1. SFOP OS94: Le Deley MC, Guinebretière JM, Gentet JC, Pacquement H, Pichon F, Marec-Bérard P, Entz-Werlé N, Schmitt C, Brugières L, Vanel D, Dupoüy N, Tabone MD, Kalifa C; Société Française d'Oncologie Pédiatrique (SFOP). SFOP OS94: a randomised trial comparing preoperative high-dose methotrexate plus doxorubicin to high-dose methotrexate plus etoposide and ifosfamide in osteosarcoma patients. Eur J Cancer. 2007 Mar;43(4):752-61. Epub 2007 Jan 30. link to original article contains dosing details in manuscript PubMed NCT00180908

MAP

MAP: High-dose Methotrexate, Adriamycin (Doxorubicin), Platinol (Cisplatin)

Regimen variant #1, 8000/75/100

Study Dates of enrollment Evidence Comparator Comparative Efficacy
Bramwell et al. 1992 1983-1986 Phase 3 (E-esc) Cisplatin & Doxorubicin Seems to have inferior DFS

Note: The body of Bramwell et al. 1992 says that methotrexate is given over 4 hours, whereas Bramwell et al. 1992 figure 1's text says that methotrexate is given over 6 hours.

Preceding treatment

Chemotherapy

Supportive therapy

  • Leucovorin (Folinic acid) 12 mg/m2 IV every 6 hours x 10 doses or 15 mg/m2 PO every 6 hours x 10 doses, starting 24 hours after the start of methotrexate infusion
    • Monitor methotrexate level at "24 hours and 48 hours"--it is unclear in the reference if this is time after the start/end of methotrexate, beginning of leucovorin, or something else
    • Methotrexate levels higher than 100 nmol/L at 48 hours required additional leucovorin rescue
  • Prehydration for methotrexate: "0.9 NaCl:D5W"--unclear if this means either normal saline or D5W can be used--750 mL/m2 over 6 hours, with KCl 20 mEq/L
  • The volume of fluid for methotrexate is D5W 1000 mL, to be given over 6 hours
  • Posthydration for methotrexate: Alternating liters of D5W and NS 3000 mL/m2 over 24 hours, with KCl 60 mEq/L.
  • Sodium bicarbonate 3 g PO Q6H, starting 12 hours before methotrexate, and sodium bicarbonate 167 mmol/L IV until serum methotrexate level is less than 8000 to 10,000 nmol/L. Note: the reference is not clear about when/if PO sodium bicarbonate is stopped, when IV sodium bicarbonate is started, or the administration rate of IV sodium bicarbonate.
  • Prehydration for cisplatin: normal saline 400 mL/m2 and D5W 400 mL/m2 IV over 2 hours--the reference did not clarify if these two solutions are given at the same time
  • The volume of fluid for cisplatin continuous infusion is 2400 mL/m2 NS, with KCl 80 mEq/L and mannitol 32,000 mg/m2
  • Posthydration for cisplatin: D5W 600 mL/m2 over 6 hours, with KCl 20 mEq/L and mannitol 8000 mg/m2; and NS 600 mL/m2 over 6 hours, with KCl 20 mEq/L, magnesium sulfate 2 mmol/L, and calcium gluconate 0.6 mmol/L--the reference did not clarify if these two solutions are given at the same time. Then D5W 600 mL/m2 over 12 hours, with KCl 20 mEq/L and mannitol 8000 mg/m2.
  • With cisplatin, Furosemide (Lasix) 20 to 40 mg IV if urine output is less than 400 mL/m2 over 6 hours

21-day cycle for 2 cycles


Regimen variant #2, 8000/90/120

Study Evidence
Bacci et al. 1993 (IOR/OS-2) Phase 2

Note: Figure 1 of Bacci et al. 2000 actually depicted the first cycle as being 47 days, and cycles 2 & 3 being 48 days.

Preceding treatment

  • Neoadjuvant MAP, then surgery, with at least 90% tumor necrosis in the surgically removed specimen

Chemotherapy

  • Methotrexate (MTX) as follows:
    • Cycles 1 to 3: 8000 mg/m2 IV over 6 hours once on day 21
  • Doxorubicin (Adriamycin) 45 mg/m2 IV over 4 hours once per day on days 1 & 2
  • Cisplatin (Platinol) as follows:
    • Cycles 1 to 3: 40 mg/m2/day IV continuous infusion over 72 hours, started on day 27 (total dose per cycle: 120 mg/m2)

Supportive therapy

  • Leucovorin (Folinic acid) as follows:
    • Cycles 1 to 3: 15 mg IV every 6 hours x 11 doses on days 22 to 24, starting 24 hours after the start of methotrexate infusion
  • Hydration during and after methotrexate infusion

48-day cycle for 4 cycles


Regimen variant #3, 12,000/60/90

Study Dates of enrollment Evidence
Winkler et al. 1988 (COSS-82) 1982-1984 Non-randomized part of phase 3 RCT

Preceding treatment

Chemotherapy

  • Methotrexate (MTX) 12,000 mg/m2 (maximum dose of 20,000 mg) IV over 4 hours once per day on days 22 & 29
    • MTX is dissolved at a concentration of 20,000 mg/L in a solution containing 5% glucose
  • Doxorubicin (Adriamycin) 30 mg/m2 IV bolus once per day on days 1 & 2
  • Cisplatin (Platinol) 90 mg/m2 IV over 4 hours once on day 3

Supportive therapy

  • Leucovorin (Folinic acid) 15 mg/m2 PO every 6 hours x 12 hours once per day on days 23 & 30, starting 24 hours after the completion of methotrexate infusion; additional leucovorin used for delayed methotrexate elimination
  • Sodium bicarbonate urine alkalinization prior to high-dose methotrexate
  • NS 4.5 L/m2 on day 1 after methotrexate; NS 3 L/m2 on day 2, with adjustments made to keep urine pH greater than 7.4
  • 12 hours of hydration prior to cisplatin & 20 hours of hydration after cisplatin; total amount of fluid given over 36hours of prehydration, cisplatin, and posthydration is NS 6 L/m2 with mannitol 8 g/L and potassium 20 mval/L.
  • Magnesium 180 mg/m2 PO "per day throughout the whole chemotherapy time"--as described in COSS-80

35-day cycle for 2 cycles


Regimen variant #4, 12,000/75/120

Study Dates of enrollment Evidence Comparator Comparative Efficacy
Marina et al. 2016 (EURAMOS-1 poor response) 2005-2011 Phase 3 (C) MAPIE Did not meet primary endpoint of EFS

Preceding treatment

Chemotherapy

  • Methotrexate (MTX) by the following site-based criteria:
    • Non-COG sites: 12,000 mg/m2 IV over 4 hours once per day on days 22 & 29
    • COG sites: 12,000 mg/m2 (maximum dose of 20,000 mg) IV over 4 hours once per day on days 22 & 29
  • Doxorubicin (Adriamycin) 37.5 mg/m2 IV once per day on days 1 & 2
  • Cisplatin (Platinol) by the following site-based criteria:
    • Non-COG sites: 40 mg/m2/day IV continuous infusion over 72 hours, started on day 1 (total dose per cycle: 120 mg/m2)
    • COG sites: 60 mg/m2 IV once per day on days 1 & 2

Supportive therapy

  • Leucovorin (Folinic acid) 15 mg/m2 (route/schedule not specified), starting 24 to 48 hours after methotrexate infusion, continued until MTX level less than 100 nmol/L

35-day cycle for 2 cycles

Subsequent treatment

  • Adjuvant MA x 2

References

  1. COSS-82: Winkler K, Beron G, Delling G, Heise U, Kabisch H, Purfürst C, Berger J, Ritter J, Jürgens H, Gerein V, Graf N, Russe W, Gruemayer ER, Ertelt W, Kotz R, Preuzzer P, Prindull G, Brandeis W, Landbeck G. Neoadjuvant chemotherapy of osteosarcoma: results of a randomized cooperative trial (COSS-82) with salvage chemotherapy based on histological tumor response. J Clin Oncol. 1988 Feb;6(2):329-37. link to original article contains dosing details in manuscript PubMed
  2. Bramwell VH, Burgers M, Sneath R, Souhami R, van Oosterom AT, Voûte PA, Rouesse J, Spooner D, Craft AW, Somers R, Pringle J, Malcolm AJ, van der Eiiken J, Thomas D, Uscinska B, Machin D, van Glabbeke M; European Osteosarcoma Intergroup. A comparison of two short intensive adjuvant chemotherapy regimens in operable osteosarcoma of limbs in children and young adults: the first study of the European Osteosarcoma Intergroup. J Clin Oncol. 1992 Oct;10(10):1579-91. link to original article contains dosing details in manuscript PubMed
  3. IOR/OS-2: Bacci G, Picci P, Ferrari S, Ruggieri P, Casadei R, Tienghi A, Brach del Prever A, Gherlinzoni F, Mercuri M, Monti C. Primary chemotherapy and delayed surgery for nonmetastatic osteosarcoma of the extremities: results in 164 patients preoperatively treated with high doses of methotrexate followed by cisplatin and doxorubicin. Cancer. 1993 Dec 1;72(11):3227-38. link to original article PubMed
    1. Update: Bacci G, Ferrari S, Bertoni F, Ruggieri P, Picci P, Longhi A, Casadei R, Fabbri N, Forni C, Versari M, Campanacci M. Long-term outcome for patients with nonmetastatic osteosarcoma of the extremity treated at the Istituto Ortopedico Rizzoli according to the Istituto Ortopedico Rizzoli/Osteosarcoma-2 protocol: an updated report. J Clin Oncol. 2000 Dec 15;18(24):4016-27. link to original article contains dosing details in manuscript PubMed
  4. EURAMOS-1 good response: Bielack SS, Smeland S, Whelan JS, Marina N, Jovic G, Hook JM, Krailo MD, Gebhardt M, Pápai Z, Meyer J, Nadel H, Randall RL, Deffenbaugh C, Nagarajan R, Brennan B, Letson GD, Teot LA, Goorin A, Baumhoer D, Kager L, Werner M, Lau CC, Sundby Hall K, Gelderblom H, Meyers P, Gorlick R, Windhager R, Helmke K, Eriksson M, Hoogerbrugge PM, Schomberg P, Tunn PU, Kühne T, Jürgens H, van den Berg H, Böhling T, Picton S, Renard M, Reichardt P, Gerss J, Butterfass-Bahloul T, Morris C, Hogendoorn PC, Seddon B, Calaminus G, Michelagnoli M, Dhooge C, Sydes MR, Bernstein M; EURAMOS-1 investigators. Methotrexate, doxorubicin, and cisplatin (MAP) plus maintenance pegylated interferon alfa-2b versus MAP alone in patients with resectable high-grade osteosarcoma and good histologic response to preoperative map: first results of the EURAMOS-1 good response randomized controlled trial. J Clin Oncol. 2015 Jul 10;33(20):2279-87. Epub 2015 Jun 1. link to original article link to PMC article PubMed
  5. EURAMOS-1 poor response: Marina NM, Smeland S, Bielack SS, Bernstein M, Jovic G, Krailo MD, Hook JM, Arndt C, van den Berg H, Brennan B, Brichard B, Brown KL, Butterfass-Bahloul T, Calaminus G, Daldrup-Link HE, Eriksson M, Gebhardt MC, Gelderblom H, Gerss J, Goldsby R, Goorin A, Gorlick R, Grier HE, Hale JP, Hall KS, Hardes J, Hawkins DS, Helmke K, Hogendoorn PC, Isakoff MS, Janeway KA, Jürgens H, Kager L, Kühne T, Lau CC, Leavey PJ, Lessnick SL, Mascarenhas L, Meyers PA, Mottl H, Nathrath M, Papai Z, Randall RL, Reichardt P, Renard M, Safwat AA, Schwartz CL, Stevens MC, Strauss SJ, Teot L, Werner M, Sydes MR, Whelan JS. Comparison of MAPIE versus MAP in patients with a poor response to preoperative chemotherapy for newly diagnosed high-grade osteosarcoma (EURAMOS-1): an open-label, international, randomised controlled trial. Lancet Oncol. 2016 Oct;17(10):1396-1408. Epub 2016 Aug 25. link to original article link to PMC article contains dosing details in manuscript PubMed NCT00134030

MAPI

MAPI: High-dose Methotrexate, Adriamycin (Doxorubicin), Platinol (Cisplatin), Ifosfamide

Regimen

Study Evidence
Bacci et al. 2003 Phase 2

Preceding treatment

Chemotherapy

  • Methotrexate (MTX) 12,000 mg/m2 IV over 4 hours once on day 36
  • Doxorubicin (Adriamycin) 90 mg/m2 IV continuous infusion over 24 hours, started on day 1
  • Cisplatin (Platinol) 60 mg/m2/day IV continuous infusion over 48 hours, started on day 43 (total dose per cycle: 120 mg/m2)
  • Ifosfamide (Ifex) 3000 mg/m2/day IV continuous infusion over 120 hours, started on day 22, given with mesna (total dose per cycle: 15,000 mg/m2)

Supportive therapy

  • Mesna (Mesnex) 3000 mg/m2/day IV continuous infusion over 120 hours, started on day 22, given with ifosfamide (total dose per cycle: 15,000 mg/m2)
  • Leucovorin (Folinic acid) 15 mg (route not specified) every 6 hours x 11 doses, starting day 36, 24 hours after the start of methotrexate
  • Hydration during and after methotrexate as described by: Rosen G, Nirenberg A. Chemotherapy for osteogenic sarcoma: an investigative method, not a recipe. Cancer Treat Rep. 1982 Sep;66(9):1687-97. PubMed

9-week cycle for 3 cycles

Dose and schedule modifications

  • If 4-hour methotrexate level is less than 10,000 nmol/L, the next cycle's methotrexate dose is increased by 2000 mg/m2

References

  1. Bacci G, Briccoli A, Rocca M, Ferrari S, Donati D, Longhi A, Bertoni F, Bacchini P, Giacomini S, Forni C, Manfrini M, Galletti S. Neoadjuvant chemotherapy for osteosarcoma of the extremities with metastases at presentation: recent experience at the Rizzoli Institute in 57 patients treated with cisplatin, doxorubicin, and a high dose of methotrexate and ifosfamide. Ann Oncol. 2003 Jul;14(7):1126-34. link to original article contains dosing details in manuscript PubMed

MAPIE

MAPIE: High-dose Methotrexate, Adriamycin (Doxorubicin), Platinol (Cisplatin), Ifosfamide, Etoposide

Regimen

Study Evidence
Bacci et al. 1993 (IOR/OS-2) Phase 2

Note: Figure 1 of Bacci et al. 2000 actually depicted the first cycle as being 68 days, and cycles 2 & 3 being 69 days.

Preceding treatment

  • Neoadjuvant MAP, then surgery, with less than 90% tumor necrosis in the surgically removed specimen

Chemotherapy

  • Methotrexate (MTX) as follows:
    • Cycles 1 to 3: 8000 mg/m2 IV over 6 hours once on day 42
  • Doxorubicin (Adriamycin) 45 mg/m2 IV over 4 hours once per day on days 1 & 2
  • Cisplatin (Platinol) as follows:
    • Cycles 1 to 3: 40 mg/m2/day IV continuous infusion over 72 hours, started on day 48 (total dose per cycle: 120 mg/m2)
  • Ifosfamide (Ifex) as follows:
    • Cycles 1 to 3: 2000 mg/m2 IV over 90 minutes once per day on days 21 to 25, with mesna
  • Etoposide (Vepesid) as follows:
    • Cycles 1 to 3: 120 mg/m2 IV over 60 minutes once per day on days 48 to 50

Supportive therapy

  • Mesna (Mesnex) as follows:
    • Cycles 1 to 3: with ifosfamide; no actual dose is listed in the reference
  • Leucovorin (Folinic acid) as follows:
    • Cycles 1 to 3: 15 mg IV every 6 hours x 11 doses on days 43 to 45, starting 24 hours after the start of methotrexate infusion
  • Hydration during and after methotrexate infusion

69-day cycle for 4 cycles

References

  1. IOR/OS-2: Bacci G, Picci P, Ferrari S, Ruggieri P, Casadei R, Tienghi A, Brach del Prever A, Gherlinzoni F, Mercuri M, Monti C. Primary chemotherapy and delayed surgery for nonmetastatic osteosarcoma of the extremities: results in 164 patients preoperatively treated with high doses of methotrexate followed by cisplatin and doxorubicin. Cancer. 1993 Dec 1;72(11):3227-38. link to original article PubMed
    1. Update: Bacci G, Ferrari S, Bertoni F, Ruggieri P, Picci P, Longhi A, Casadei R, Fabbri N, Forni C, Versari M, Campanacci M. Long-term outcome for patients with nonmetastatic osteosarcoma of the extremity treated at the Istituto Ortopedico Rizzoli according to the Istituto Ortopedico Rizzoli/Osteosarcoma-2 protocol: an updated report. J Clin Oncol. 2000 Dec 15;18(24):4016-27. link to original article contains dosing details in manuscript PubMed
  2. EURAMOS-1 poor response: Marina NM, Smeland S, Bielack SS, Bernstein M, Jovic G, Krailo MD, Hook JM, Arndt C, van den Berg H, Brennan B, Brichard B, Brown KL, Butterfass-Bahloul T, Calaminus G, Daldrup-Link HE, Eriksson M, Gebhardt MC, Gelderblom H, Gerss J, Goldsby R, Goorin A, Gorlick R, Grier HE, Hale JP, Hall KS, Hardes J, Hawkins DS, Helmke K, Hogendoorn PC, Isakoff MS, Janeway KA, Jürgens H, Kager L, Kühne T, Lau CC, Leavey PJ, Lessnick SL, Mascarenhas L, Meyers PA, Mottl H, Nathrath M, Papai Z, Randall RL, Reichardt P, Renard M, Safwat AA, Schwartz CL, Stevens MC, Strauss SJ, Teot L, Werner M, Sydes MR, Whelan JS. Comparison of MAPIE versus MAP in patients with a poor response to preoperative chemotherapy for newly diagnosed high-grade osteosarcoma (EURAMOS-1): an open-label, international, randomised controlled trial. Lancet Oncol. 2016 Oct;17(10):1396-1408. Epub 2016 Aug 25. link to original article link to PMC article PubMed NCT00134030

M-EI

M-EI: Methotrexate, Etoposide, Ifosfamide

Regimen

Study Dates of enrollment Evidence
Le Deley et al. 2007 (SFOP OS94) 1994-2001 Non-randomized part of phase 3 RCT

Preceding treatment

Chemotherapy

  • Methotrexate (MTX) 12,000 mg/m2 IV over 4 hours once per day on days 1, 8, 15
    • Given in D5W 1L with sodium bicarbonate 1 mEq/kg
  • Etoposide (Vepesid) as follows:
    • Cycles 1 to 3: 75 mg/m2 IV over 60 minutes once per day on days 22 to 25 (week 4)
      • Given in NS 250 to 500 mL
  • Ifosfamide (Ifex) as follows:
    • Cycles 1 to 3: 3000 mg/m2 IV over 3 hours once per day on days 22 to 25 (week 4), given during mesna infusion (total dose per cycle: 12,000 mg/m2)
      • Given in NS 250 to 500 mL

Supportive therapy

  • Leucovorin (Folinic acid) 15 mg PO every 6 hours for up to 11 doses, starting on days 1, 8, 15, starting 20 hours after the completion of methotrexate infusion
  • For methotrexate: hydration & urine alkalinization by PO and IV routes to maintain 1.6 L/m2 urine output over the first 24 hours and 2 L/m2 on days 2 & 3, with urine pH greater than 7
  • Daily monitoring of methotrexate levels and creatinine
  • Mesna (Mesnex) as follows:
    • Cycles 1 to 3: 3600 mg/m2/day IV continuous infusion over 96 hours, started on day 22 (week 4) (total dose per cycle: 14,400 mg/m2)
  • Up to 2 L/day hydration with ifosfamide & mesna

28-day cycle for 4 cycles

References

  1. SFOP OS94: Le Deley MC, Guinebretière JM, Gentet JC, Pacquement H, Pichon F, Marec-Bérard P, Entz-Werlé N, Schmitt C, Brugières L, Vanel D, Dupoüy N, Tabone MD, Kalifa C; Société Française d'Oncologie Pédiatrique (SFOP). SFOP OS94: a randomised trial comparing preoperative high-dose methotrexate plus doxorubicin to high-dose methotrexate plus etoposide and ifosfamide in osteosarcoma patients. Eur J Cancer. 2007 Mar;43(4):752-61. Epub 2007 Jan 30. link to original article contains dosing details in manuscript PubMed NCT00180908
  2. OS2006: Piperno-Neumann S, Le Deley MC, Rédini F, Pacquement H, Marec-Bérard P, Petit P, Brisse H, Lervat C, Gentet JC, Entz-Werlé N, Italiano A, Corradini N, Bompas E, Penel N, Tabone MD, Gomez-Brouchet A, Guinebretière JM, Mascard E, Gouin F, Chevance A, Bonnet N, Blay JY, Brugières L; Sarcoma Group of UNICANCER; SFCE; GSF-GETO. Zoledronate in combination with chemotherapy and surgery to treat osteosarcoma (OS2006): a randomised, multicentre, open-label, phase 3 trial. Lancet Oncol. 2016 Aug;17(8):1070-1080. Epub 2016 Jun 17. link to original article PubMed NCT00470223
    1. Update: Gaspar N, Occean BV, Pacquement H, Bompas E, Bouvier C, Brisse HJ, Castex MP, Cheurfa N, Corradini N, Delaye J, Entz-Werlé N, Gentet JC, Italiano A, Lervat C, Marec-Berard P, Mascard E, Redini F, Saumet L, Schmitt C, Tabone MD, Verite-Goulard C, Le Deley MC, Piperno-Neumann S, Brugieres L; SFCE; GSF-GETO; UNICANCER sarcoma group. Results of methotrexate-etoposide-ifosfamide based regimen (M-EI) in osteosarcoma patients included in the French OS2006/sarcome-09 study. Eur J Cancer. 2018 Jan;88:57-66. Epub 2017 Nov 28. link to original article PubMed

Relapsed, refractory, or metastatic, first-line

Cisplatin & Doxorubicin

AP: Adriamycin (Doxorubicin) & Platinol (Cisplatin)

Regimen

Study Dates of enrollment Evidence Comparator Comparative Efficacy
Bramwell et al. 1997 (EOI 80831/MRC B002) 1983-1986 Phase 3 (E-de-esc) MAP Inferior OS

Note: the authors state that "[i]t is likely that random bias in the population..accounts for the difference in outcome favoring the three-drug treatment in patients with metastatic disease."

Chemotherapy

Supportive therapy

  • Prehydration: normal saline 400 mL/m2 and D5W 400 mL/m2 IV over 2 hours--the reference did not clarify if these two solutions are given at the same time
  • The volume of fluid for cisplatin continuous infusion is 2400 mL/m2 NS, with KCl 80 mEq/L and mannitol 32,000 mg/m2
  • Posthydration: D5W 600 mL/m2 over 6 hours, with KCl 20 mEq/L and mannitol 8000 mg/m2; and NS 600 mL/m2 over 6 hours, with KCl 20 mEq/L, magnesium sulfate 2 mmol/L, and calcium gluconate 0.6 mmol/L--the reference did not clarify if these two solutions are given at the same time. Then D5W 600 mL/m2 over 12 hours, with KCl 20 mEq/L and mannitol 8000 mg/m2.
  • Furosemide (Lasix) 20 to 40 mg IV if urine output is less than 400 mL/m2 over 6 hours

21-day cycle for 6 cycles

References

  1. EOI 80831/MRC B002: Bramwell VH, Burgers MV, Souhami RL, Taminiau AH, Van Der Eijken JW, Craft AW, Malcolm AJ, Uscinska B, Kirkpatrick AL, Machin D, Van Glabbeke MM; European Osteosarcoma Intergroup. A randomized comparison of two short intensive chemotherapy regimens in children and young adults with osteosarcoma: results in patients with metastases: a study of the European Osteosarcoma Intergroup. Sarcoma. 1997;1(3-4):155-60. link to original article contains dosing details in manuscript link to PMC article PubMed

MAP

MAP: High-dose Methotrexate, Adriamycin (Doxorubicin), Platinol (Cisplatin)

Regimen

Study Dates of enrollment Evidence Comparator Comparative Efficacy
Bramwell et al. 1997 (EOI 80831/MRC B002) 1983-1986 Phase 3 (E-esc) Cisplatin & Doxorubicin Superior OS

Note: the authors state that "[i]t is likely that random bias in the population..accounts for the difference in outcome favoring the three-drug treatment in patients with metastatic disease."

Chemotherapy

Supportive therapy

  • Leucovorin (Folinic acid) 12 mg/m2 IV every 6 hours x 10 doses or 15 mg/m2 PO every 6 hours x 10 doses, starting 24 hours after the start of methotrexate infusion
    • Monitor methotrexate level at "24 hours and 48 hours"--it is unclear in the reference if this is time after the start/end of methotrexate, beginning of leucovorin, or something else
    • Methotrexate levels higher than 100 nmol/L at 48 hours required additional leucovorin rescue
  • Prehydration for methotrexate: "0.9 NaCl:D5W"--unclear if this means either normal saline or D5W can be used--750 mL/m2 over 6 hours, with KCl 20 mEq/L
  • The volume of fluid for methotrexate is D5W 1000 mL, to be given over 6 hours
  • Posthydration for methotrexate: Alternating liters of D5W and NS 3000 mL/m2 over 24 hours, with KCl 60 mEq/L.
  • Sodium bicarbonate 3 g PO Q6H, starting 12 hours before methotrexate, and sodium bicarbonate 167 mmol/L IV until serum methotrexate level is less than 8000 to 10,000 nmol/L. Note: the reference is not clear about when/if PO sodium bicarbonate is stopped, when IV sodium bicarbonate is started, or the administration rate of IV sodium bicarbonate.
  • Prehydration for cisplatin: normal saline 400 mL/m2 and D5W 400 mL/m2 IV over 2 hours--the reference did not clarify if these two solutions are given at the same time
  • The volume of fluid for cisplatin continuous infusion is 2400 mL/m2 NS, with KCl 80 mEq/L and mannitol 32,000 mg/m2
  • Posthydration for cisplatin: D5W 600 mL/m2 over 6 hours, with KCl 20 mEq/L and mannitol 8000 mg/m2; and NS 600 mL/m2 over 6 hours, with KCl 20 mEq/L, magnesium sulfate 2 mmol/L, and calcium gluconate 0.6 mmol/L--the reference did not clarify if these two solutions are given at the same time. Then D5W 600 mL/m2 over 12 hours, with KCl 20 mEq/L and mannitol 8000 mg/m2.
  • With cisplatin, Furosemide (Lasix) 20 to 40 mg IV if urine output is less than 400 mL/m2 over 6 hours

21-day cycle for 4 cycles

References

  1. EOI 80831/MRC B002: Bramwell VH, Burgers MV, Souhami RL, Taminiau AH, Van Der Eijken JW, Craft AW, Malcolm AJ, Uscinska B, Kirkpatrick AL, Machin D, Van Glabbeke MM; European Osteosarcoma Intergroup. A randomized comparison of two short intensive chemotherapy regimens in children and young adults with osteosarcoma: results in patients with metastases: a study of the European Osteosarcoma Intergroup. Sarcoma. 1997;1(3-4):155-60. link to original article contains dosing details in manuscript link to PMC article PubMed

Relapsed, refractory, or metastatic, subsequent lines

Cabozantinib monotherapy

Regimen variant #1, adult dosing

Study Dates of enrollment Evidence
Italiano et al. 2020 (CABONE) 2015-2018 Phase 2

Targeted therapy

28-day cycles


Regimen variant #2, pediatric dosing

Study Dates of enrollment Evidence
Italiano et al. 2020 (CABONE) 2015-2018 Phase 2

Note: this dosing was for children aged less than 16 years.

Targeted therapy

28-day cycles

References

  1. CABONE: Italiano A, Mir O, Mathoulin-Pelissier S, Penel N, Piperno-Neumann S, Bompas E, Chevreau C, Duffaud F, Entz-Werlé N, Saada E, Ray-Coquard I, Lervat C, Gaspar N, Marec-Berard P, Pacquement H, Wright J, Toulmonde M, Bessede A, Crombe A, Kind M, Bellera C, Blay JY. Cabozantinib in patients with advanced Ewing sarcoma or osteosarcoma (CABONE): a multicentre, single-arm, phase 2 trial. Lancet Oncol. 2020 Mar;21(3):446-455. Epub 2020 Feb 17. link to original article contains dosing details in abstract link to PMC article PubMed NCT02243605

Cyclophosphamide & Etoposide

Regimen

Study Dates of enrollment Evidence
Berger et al. 2009 2002-07 to 2006-09 Phase 2

Chemotherapy

Supportive therapy

  • Mesna (Mesnex) 1400 mg/m2 IV three times per day on day 1, given prior to, 4 hours after, and 8 hours after cyclophosphamide
    • With mesna, 3000 mL/m2 hydration

At least 21-day cycle for 2 cycles, then restaging

Subsequent treatment

  • Patients with no progression received an experimental protocol with:
    • Samarium-153 10 mCi/kg and/or carboplatin & etoposide based on status of bone metastases (no further details about dose/schedule given)
    • Progression-free patients received reduced intensity stem cell transplant (preferably from a matched sibling donor (MSD))
    • Patients with no MSD received IL-2 maintenance, 5 days a week every 2 weeks x 12 cycles (reference did not specify if a cycle was 2 weeks, 4 weeks, or another length)

References

  1. Berger M, Grignani G, Ferrari S, Biasin E, Brach del Prever A, Aliberti S, Saglio F, Aglietta M, Fagioli F. Phase 2 trial of two courses of cyclophosphamide and etoposide for relapsed high-risk osteosarcoma patients. Cancer. 2009 Jul 1;115(13):2980-7. link to original article contains dosing details in manuscript PubMed

Cyclophosphamide & Topotecan

Regimen

Study Evidence
Saylors et al. 2001 Phase 2

Chemotherapy

Supportive therapy

  • 500 mL/m/2 fluids IV or PO once per day on days 1 to 5; 2 to 4 hours prior to chemotherapy
  • Antiemetics once per day on days 1 to 5, prior to chemotherapy
  • 3 liters/m2 fluids IV or PO over 24 hours after chemotherapy
  • Filgrastim (Neupogen) 5 mcg/kg SC once per day, starting on day 6, to continue until post-nadir ANC is at least 1500/μL

21-day cycle for 12 to 14 cycles

References

  1. Saylors RL 3rd, Stine KC, Sullivan J, Kepner JL, Wall DA, Bernstein ML, Harris MB, Hayashi R, Vietti TJ; Pediatric Oncology Group. Cyclophosphamide plus topotecan in children with recurrent or refractory solid tumors: a Pediatric Oncology Group phase II study. J Clin Oncol. 2001 Aug 1;19(15):3463-9. link to original article contains dosing details in manuscript PubMed

Docetaxel & Gemcitabine

Regimen

Study Evidence
Navid et al. 2008 Retrospective

Note: 17 of the 22 patients in this retrospective review had osteosarcoma.

Chemotherapy

Supportive therapy

21-day cycles

References

  1. Retrospective: Navid F, Willert JR, McCarville MB, Furman W, Watkins A, Roberts W, Daw NC. Combination of gemcitabine and docetaxel in the treatment of children and young adults with refractory bone sarcoma. Cancer. 2008 Jul 15;113(2):419-25. link to original article contains dosing details in manuscript PubMed

Gemcitabine monotherapy

Regimen

Study Evidence
Merimsky et al. 2000 Phase 2

Chemotherapy

  • Gemcitabine (Gemzar) as follows:
    • Cycle 1: 1000 mg/m2 IV once per day on days 1, 8, 15, 22
    • Cycle 2 onwards: 1000 mg/m2 IV once per day on days 1, 8, 15

28-day cycles

References

  1. Merimsky O, Meller I, Flusser G, Kollender Y, Issakov J, Weil-Ben-Arush M, Fenig E, Neuman G, Sapir D, Ariad S, Inbar M. Gemcitabine in soft tissue or bone sarcoma resistant to standard chemotherapy: a phase II study. Cancer Chemother Pharmacol. 2000;45(2):177-81. link to original article contains dosing details in manuscript PubMed

ICE

ICE: Ifosfamide, Carboplatin, Etoposide

Regimen

Study Evidence
Van Winkle et al. 2005 Phase 2

Note: the reference did not mention Mesna (Mesnex) being used.

Chemotherapy

Supportive therapy

  • Depending on the study the patients were enrolled on, they received one of the following:
    • CCG-0894: Filgrastim (Neupogen) 5 or 10 mcg/kg SC once per day, starting 24 hours after completing ICE, and to continue until day 18 if ANC is at least 1000/μL, or until ANC is at least 1000/μL above nadir, whichever comes later
    • CCG-0924: PIXY 321 at doses of 500/750/1000 mcg/m2 SC once per day or 500 mcg/m2 SC twice per day, starting on day 5 and to continue until day 18 unless ANC reached 20,000/μL or platelet count is at least 900 x 109/L for 2 days between days 13 to 18, or until ANC is at least 1000/μL and platelet count is at least 100 x 109/L, whichever comes later
    • CCG-0931: Filgrastim (Neupogen) 5 mcg/kg SC once per day and IL-6 at 2.5, 3.75, or 5 mcg/kg SC twice per day, starting 24 hours after completing ICE. Filgrastim is continued until ANC is at least 1000/μL, and IL-6 is continued until platelets are at least 100 x 109/L for 2 consecutive days or until day 35, whichever comes sooner.

21-day cycles, with next cycle starting as soon as ANC is at least 1000/μL and platelet count is at least 100 x 109/L

Subsequent treatment

  • Resection of disease was allowed after 4 cycles based on patient's response to ICE

References

  1. Van Winkle P, Angiolillo A, Krailo M, Cheung YK, Anderson B, Davenport V, Reaman G, Cairo MS; Children's Cancer Group. Ifosfamide, carboplatin, and etoposide (ICE) reinduction chemotherapy in a large cohort of children and adolescents with recurrent/refractory sarcoma: the Children's Cancer Group (CCG) experience. Pediatr Blood Cancer. 2005 Apr;44(4):338-47. link to original article contains dosing details in manuscript PubMed

IE

IE: Ifosfamide & Etoposide

Regimen

Study Dates of enrollment Evidence
Gentet et al. 1997 1992-01 to 1995-01 Phase 2

Chemotherapy

  • Ifosfamide (Ifex) 3000 mg/m2 IV over 3 hours once per day on days 1 to 4
    • Given in D5W 250 to 500 mL
  • Etoposide (Vepesid) 75 mg/m2 IV over 60 minutes once per day on days 1 to 4
    • Given in D5W 250 to 500 mL

Supportive therapy

  • Mesna (Mesnex) 3600 mg/m2/day IV continuous infusion over 96 hours, started on day 1 (total dose per cycle: 14,400 mg/m2)
  • At least 2000 mL/m2/day of hydration with chemotherapy

21- to 28-day cycle for 2 cycles; next cycle starting when ANC greater than 1500/μL and platelet count greater than 100 x 109/L

References

  1. Gentet JC, Brunat-Mentigny M, Demaille MC, Pein F, Avet-Loiseau H, Berger C, De Lumley L, Pacquement H, Schmitt C, Sariban E, Pillon P, Bernard JL, Kalifa C. Ifosfamide and etoposide in childhood osteosarcoma: a phase II study of the French Society of Paediatric Oncology. Eur J Cancer. 1997 Feb;33(2):232-7. link to original article contains dosing details in manuscript PubMed

Regorafenib monotherapy

Regimen

Study Dates of enrollment Evidence Comparator Comparative Efficacy
Davis et al. 2019 (SARC024) 2014-2018 Randomized Phase 2 (E-esc) Placebo Superior PFS (primary endpoint)
Median PFS: 3.6 vs 1.7 mo
(HR 0.42, 95% CI 0.21-0.85)

Targeted therapy

28-day cycles

References

  1. SARC024: Davis LE, Bolejack V, Ryan CW, Ganjoo KN, Loggers ET, Chawla S, Agulnik M, Livingston MB, Reed D, Keedy V, Rushing D, Okuno S, Reinke DK, Riedel RF, Attia S, Mascarenhas L, Maki RG. Randomized Double-Blind Phase II Study of Regorafenib in Patients With Metastatic Osteosarcoma. J Clin Oncol. 2019 Jun 1;37(16):1424-1431. Epub 2019 Apr 23. link to original article link to PMC article contains dosing details in manuscript PubMed NCT02048371

Samarium-153 with stem cell support

Regimen

Study Dates of enrollment Evidence
Anderson et al. 2002 NR Phase 1
  • Peripheral blood progenitor cell (PBPC) or bone marrow harvest and cryopreservation of at least 2 x 106 CD34+ cells/kg

Radiotherapy

Supportive therapy

One course

References

  1. Phase 1: Anderson PM, Wiseman GA, Dispenzieri A, Arndt CA, Hartmann LC, Smithson WA, Mullan BP, Bruland OS. High-dose samarium-153 ethylene diamine tetramethylene phosphonate: low toxicity of skeletal irradiation in patients with osteosarcoma and bone metastases. J Clin Oncol. 2002 Jan 1;20(1):189-96. link to original article contains dosing details in manuscript PubMed

Sorafenib monotherapy

Regimen

Study Dates of enrollment Evidence
Grignani et al. 2011 2008-2009 Phase 2

Targeted therapy

28-day cycles

References

  1. Grignani G, Palmerini E, Dileo P, Asaftei SD, D'Ambrosio L, Pignochino Y, Mercuri M, Picci P, Fagioli F, Casali PG, Ferrari S, Aglietta M. A phase II trial of sorafenib in relapsed and unresectable high-grade osteosarcoma after failure of standard multimodal therapy: an Italian Sarcoma Group study. Ann Oncol. 2012 Feb;23(2):508-16. Epub 2011 Apr 28. link to original article contains dosing details in manuscript PubMed EudraCT 2007-004396-19