Difference between revisions of "Osteosarcoma - historical"

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m (Text replacement - "As a general rule, this includes the inferior arm(s) of a randomized study, unless said regimens continue to be recommended by trustworthy sources such as the [http://www.nccn.org/professionals/physician_gls/f_guidelines.asp NCCN Guidelines]. " to "")
 
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[[#top|Back to Top]]
 
[[#top|Back to Top]]
 
</div>
 
</div>
The purpose of this page is to provide references to regimens that are obsolete, outdated, or of historical interest only. As a general rule, this includes the inferior arm(s) of a randomized study, unless said regimens continue to be recommended by trustworthy sources such as the [http://www.nccn.org/professionals/physician_gls/f_guidelines.asp NCCN Guidelines]. Is there a regimen missing from this list? See the [[Osteosarcoma|main osteosarcoma page]] for current regimens.
+
The purpose of this page is to provide references to regimens that are obsolete, outdated, or of historical interest only. Is there a regimen missing from this list? See the [[Osteosarcoma|main osteosarcoma page]] for current regimens.
 
{| class="wikitable" style="float:right; margin-right: 5px;"
 
{| class="wikitable" style="float:right; margin-right: 5px;"
 
|-
 
|-
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==MA-BCD {{#subobject:f7c8d9|Regimen=1}}==
 
==MA-BCD {{#subobject:f7c8d9|Regimen=1}}==
 
MA-BCD: High-dose '''<u>M</u>'''ethotrexate, '''<u>A</u>'''driamycin (Doxorubicin), '''<u>B</u>'''leomycin, '''<u>C</u>'''yclophosphamide, '''<u>D</u>'''actinomycin
 
MA-BCD: High-dose '''<u>M</u>'''ethotrexate, '''<u>A</u>'''driamycin (Doxorubicin), '''<u>B</u>'''leomycin, '''<u>C</u>'''yclophosphamide, '''<u>D</u>'''actinomycin
<div class="toccolours" style="background-color:#eeeeee">
+
<div class="toccolours" style="background-color:#ee6b6e">
 
===Regimen {{#subobject:fe9985|Variant=1}}===
 
===Regimen {{#subobject:fe9985|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
Line 49: Line 49:
 
**Cycles 2 to 4: 0.45 mg/m<sup>2</sup> IV bolus once per day on days 43 & 44
 
**Cycles 2 to 4: 0.45 mg/m<sup>2</sup> IV bolus once per day on days 43 & 44
 
====Supportive therapy====
 
====Supportive therapy====
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> PO every 6 hours x 12 hours once per day, starting 24 hours after the completion of each methotrexate infusion; additional leucovorin used for delayed methotrexate elimination
+
*[[Leucovorin (Folinic acid)]] 15 mg/m<sup>2</sup> PO every 6 hours x 12 hours once per day, starting 24 hours after the completion of each 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
 
*[[Normal saline]] 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
 
*[[Normal saline]] 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
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==M-BCD {{#subobject:6f3563|Regimen=1}}==
 
==M-BCD {{#subobject:6f3563|Regimen=1}}==
 
M-BCD: High-dose '''<u>M</u>'''ethotrexate, '''<u>B</u>'''leomycin, '''<u>C</u>'''yclophosphamide, '''<u>D</u>'''actinomycin
 
M-BCD: High-dose '''<u>M</u>'''ethotrexate, '''<u>B</u>'''leomycin, '''<u>C</u>'''yclophosphamide, '''<u>D</u>'''actinomycin
<div class="toccolours" style="background-color:#eeeeee">
+
<div class="toccolours" style="background-color:#ee6b6e">
 
===Regimen {{#subobject:8ea4f8|Variant=1}}===
 
===Regimen {{#subobject:8ea4f8|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
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*[[Dactinomycin (Cosmegen)]] 0.6 mg/m<sup>2</sup> IV bolus once per day on days 1 & 2
 
*[[Dactinomycin (Cosmegen)]] 0.6 mg/m<sup>2</sup> IV bolus once per day on days 1 & 2
 
====Supportive therapy====
 
====Supportive therapy====
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> PO every 6 hours x 12 hours once per day on days 16 & 23, starting 24 hours after the completion of methotrexate infusion; additional leucovorin used for delayed methotrexate elimination
+
*[[Leucovorin (Folinic acid)]] 15 mg/m<sup>2</sup> PO every 6 hours x 12 hours once per day on days 16 & 23, 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
 
*[[Normal saline]] 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
 
*[[Normal saline]] 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
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=Adjuvant therapy=
 
=Adjuvant therapy=
 
==Doxorubicin monotherapy {{#subobject:681e0f|Regimen=1}}==
 
==Doxorubicin monotherapy {{#subobject:681e0f|Regimen=1}}==
<div class="toccolours" style="background-color:#eeeeee">
+
<div class="toccolours" style="background-color:#ee6b6e">
 
===Regimen {{#subobject:81ee7b|Variant=1}}===
 
===Regimen {{#subobject:81ee7b|Variant=1}}===
 
{| class="wikitable" style="width: 40%; text-align:center;"  
 
{| class="wikitable" style="width: 40%; text-align:center;"  
Line 122: Line 122:
 
==IP-BCD {{#subobject:b45a8a|Regimen=1}}==
 
==IP-BCD {{#subobject:b45a8a|Regimen=1}}==
 
IP-BCD: '''<u>I</u>'''fosfamide, '''<u>P</u>'''latinol (Cisplatin), '''<u>B</u>'''leomycin, '''<u>C</u>'''yclophosphamide, '''<u>D</u>'''actinomycin
 
IP-BCD: '''<u>I</u>'''fosfamide, '''<u>P</u>'''latinol (Cisplatin), '''<u>B</u>'''leomycin, '''<u>C</u>'''yclophosphamide, '''<u>D</u>'''actinomycin
<div class="toccolours" style="background-color:#eeeeee">
+
<div class="toccolours" style="background-color:#ee6b6e">
 
===Regimen {{#subobject:c70abe|Variant=1}}===
 
===Regimen {{#subobject:c70abe|Variant=1}}===
 
{| class="wikitable sortable" style="width: 60%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 60%; text-align:center;"  
Line 136: Line 136:
 
<div class="toccolours" style="background-color:#cbd5e8">
 
<div class="toccolours" style="background-color:#cbd5e8">
 
====Preceding treatment====
 
====Preceding treatment====
*[[Osteosarcoma#MAP|Neoadjuvant MAP]], then [[Surgery#Surgical_resection|surgery]], with poor response
+
*Neoadjuvant [[Osteosarcoma#MAP|MAP]], then [[Surgery#Surgical_resection|surgery]], with poor response
 
</div>
 
</div>
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
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==MA-BCD/AP {{#subobject:2ce305|Regimen=1}}==
 
==MA-BCD/AP {{#subobject:2ce305|Regimen=1}}==
 
MA-BCD/AP: High-dose '''<u>M</u>'''ethotrexate, '''<u>A</u>'''driamycin (Doxorubicin), '''<u>B</u>'''leomycin, '''<u>C</u>'''yclophosphamide, '''<u>D</u>'''actinomycin alternating with '''<u>A</u>'''driamycin (Doxorubicin) & '''<u>P</u>'''latinol (Cisplatin)
 
MA-BCD/AP: High-dose '''<u>M</u>'''ethotrexate, '''<u>A</u>'''driamycin (Doxorubicin), '''<u>B</u>'''leomycin, '''<u>C</u>'''yclophosphamide, '''<u>D</u>'''actinomycin alternating with '''<u>A</u>'''driamycin (Doxorubicin) & '''<u>P</u>'''latinol (Cisplatin)
<div class="toccolours" style="background-color:#eeeeee">
+
<div class="toccolours" style="background-color:#ee6b6e">
 
===Regimen {{#subobject:59841a|Variant=1}}===
 
===Regimen {{#subobject:59841a|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
Line 190: Line 190:
 
==M-BCD {{#subobject:67c944|Regimen=1}}==
 
==M-BCD {{#subobject:67c944|Regimen=1}}==
 
M-BCD: High-dose '''<u>M</u>'''ethotrexate, '''<u>B</u>'''leomycin, '''<u>C</u>'''yclophosphamide, '''<u>D</u>'''actinomycin
 
M-BCD: High-dose '''<u>M</u>'''ethotrexate, '''<u>B</u>'''leomycin, '''<u>C</u>'''yclophosphamide, '''<u>D</u>'''actinomycin
<div class="toccolours" style="background-color:#eeeeee">
+
<div class="toccolours" style="background-color:#ee6b6e">
 
===Regimen {{#subobject:3696a1|Variant=1}}===
 
===Regimen {{#subobject:3696a1|Variant=1}}===
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
 
{| class="wikitable sortable" style="width: 100%; text-align:center;"  
Line 215: Line 215:
 
<div class="toccolours" style="background-color:#cbd5e8">
 
<div class="toccolours" style="background-color:#cbd5e8">
 
====Preceding treatment====
 
====Preceding treatment====
*[[#M-BCD|Neoadjuvant M-BCD]], then [[Surgery#Surgical_resection|surgery]], with good response
+
*Neoadjuvant [[#M-BCD|M-BCD]], then [[Surgery#Surgical_resection|surgery]], with good response
 
</div>
 
</div>
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
Line 225: Line 225:
 
*[[Dactinomycin (Cosmegen)]] 0.6 mg/m<sup>2</sup> IV bolus once per day on days 1 & 2
 
*[[Dactinomycin (Cosmegen)]] 0.6 mg/m<sup>2</sup> IV bolus once per day on days 1 & 2
 
====Supportive therapy====
 
====Supportive therapy====
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> PO every 6 hours x 12 hours once per day on days 16 & 23, starting 24 hours after the completion of methotrexate infusion; additional leucovorin used for delayed methotrexate elimination
+
*[[Leucovorin (Folinic acid)]] 15 mg/m<sup>2</sup> PO every 6 hours x 12 hours once per day on days 16 & 23, 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
 
*[[Normal saline]] 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
 
*[[Normal saline]] 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
Line 235: Line 235:
 
# '''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]
 
# '''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]
 
==Methotrexate & Vincristine {{#subobject:606364|Regimen=1}}==
 
==Methotrexate & Vincristine {{#subobject:606364|Regimen=1}}==
<div class="toccolours" style="background-color:#eeeeee">
+
<div class="toccolours" style="background-color:#ee6b6e">
 
===Regimen {{#subobject:8f64e5|Variant=1}}===
 
===Regimen {{#subobject:8f64e5|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/10.1056/NEJM197411072911902 Jaffe et al. 1974]
 
|[https://doi.org/10.1056/NEJM197411072911902 Jaffe et al. 1974]
 +
|1972-06 to NR
 
|style="background-color:#91cf61"|Non-randomized
 
|style="background-color:#91cf61"|Non-randomized
 
|-
 
|-
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<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
 
====Chemotherapy====
 
====Chemotherapy====
*[[Methotrexate (MTX)]]
+
*[[Methotrexate (MTX)]] 1500 mg/m<sup>2</sup> IV over 6 hours once on day 1
*[[Vincristine (Oncovin)]]
+
*[[Vincristine (Oncovin)]] 2 mg/m<sup>2</sup> IV once on day 1, '''given 30 minutes prior to methotrexate'''
 
====Supportive therapy====
 
====Supportive therapy====
*[[Folinic acid (Leucovorin)]]
+
*[[Leucovorin (Folinic acid)]]
'''21-day cycle for up to 35 cycles (2 years)'''
+
'''14-day cycle until therapeutic goal achieved, then 21-day cycle for up to 33 cycles (2 years total)'''
 
</div></div>
 
</div></div>
 
===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://doi.org/10.1056/NEJM197411072911902 link to original article] [https://pubmed.ncbi.nlm.nih.gov/4606174/ PubMed]
+
# 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://doi.org/10.1056/NEJM197411072911902 link to original article] '''contains dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/4606174/ PubMed]
 +
 
 
=Relapsed, refractory, or metastatic=
 
=Relapsed, refractory, or metastatic=
 
==Doxorubicin monotherapy {{#subobject:8a4535|Regimen=1}}==
 
==Doxorubicin monotherapy {{#subobject:8a4535|Regimen=1}}==
<div class="toccolours" style="background-color:#eeeeee">
+
<div class="toccolours" style="background-color:#ee6b6e">
 
===Regimen {{#subobject:dc69eb|Variant=1}}===
 
===Regimen {{#subobject:dc69eb|Variant=1}}===
 
{| class="wikitable" style="width: 40%; text-align:center;"  
 
{| class="wikitable" style="width: 40%; text-align:center;"  
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|-
 
|-
 
|[https://jamanetwork.com/journals/jama/article-abstract/344236 Cortes et al. 1972]
 
|[https://jamanetwork.com/journals/jama/article-abstract/344236 Cortes et al. 1972]
| style="background-color:#ffffbe" |Non-randomized, <20 pts
+
| style="background-color:#ffffbe" |Non-randomized, fewer than 20 pts
 
|-
 
|-
 
|}
 
|}
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==MAPifn [COG AOST0331]==
 
==MAPifn [COG AOST0331]==
 
<div class="toccolours" style="background-color:#c8a2c8">
 
<div class="toccolours" style="background-color:#c8a2c8">
 +
{| class="wikitable sortable" style="width: 60%; text-align:center;"
 +
!style="width: 33%"|Study
 +
!style="width: 33%"|Dates of enrollment
 +
!style="width: 33%"|[[Levels_of_Evidence#Evidence|Evidence]]
 +
|-
 +
|[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5052459/ Marina et al. 2019 (COG AOST0331)]
 +
|2005-04-14 to 2011-06-30
 +
| style="background-color:#91cf61" |Non-randomized part of phase 3 RCT
 +
|-
 +
|}
 
''Note: Induction is received by all patients and consists of 2 cycles of MAP. The remainder of this protocol is for good responders.''
 
''Note: Induction is received by all patients and consists of 2 cycles of MAP. The remainder of this protocol is for good responders.''
<div class="toccolours" style="background-color:#eeeeee">
+
<div class="toccolours" style="background-color:#ee6b6e">
 
===Induction===
 
===Induction===
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
Line 288: Line 301:
 
*[[Methotrexate (MTX)]] 12,000 mg/m<sup>2</sup> (maximum dose of 20,000 mg) IV over 4 hours once on day 1 of weeks 4, 5, 9, and 10.  
 
*[[Methotrexate (MTX)]] 12,000 mg/m<sup>2</sup> (maximum dose of 20,000 mg) IV over 4 hours once on day 1 of weeks 4, 5, 9, and 10.  
 
====Supportive therapy====
 
====Supportive therapy====
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> PO or IV every 6 hours beginning 24 hours after the beginning of the methotrexate infusion and continuing until the serum methotrexate level is less than 0.1 μM.
+
*[[Leucovorin (Folinic acid)]] 15 mg/m<sup>2</sup> PO or IV every 6 hours beginning 24 hours after the beginning of the methotrexate infusion and continuing until the serum methotrexate level is less than 0.1 μM.
'''10 Week course'''
+
'''10-week course'''
 
</div></div><br>
 
</div></div><br>
<div class="toccolours" style="background-color:#eeeeee">
+
<div class="toccolours" style="background-color:#ee6b6e">
 
===Consolidation, Cycles 3-4===
 
===Consolidation, Cycles 3-4===
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
Line 299: Line 312:
 
*[[Methotrexate (MTX)]] 12,000 mg/m<sup>2</sup> (maximum dose of 20,000 mg) IV over 4 hours once on day 1 of weeks 15, 16, 20, and 21.  
 
*[[Methotrexate (MTX)]] 12,000 mg/m<sup>2</sup> (maximum dose of 20,000 mg) IV over 4 hours once on day 1 of weeks 15, 16, 20, and 21.  
 
====Supportive therapy====
 
====Supportive therapy====
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> PO or IV every 6 hours beginning 24 hours after the beginning of the methotrexate infusion and continuing until the serum methotrexate level is less than 0.1 μM.
+
*[[Leucovorin (Folinic acid)]] 15 mg/m<sup>2</sup> PO or IV every 6 hours beginning 24 hours after the beginning of the methotrexate infusion and continuing until the serum methotrexate level is less than 0.1 μM.
'''10 Week course'''
+
'''10-week course'''
 
</div></div><br>
 
</div></div><br>
<div class="toccolours" style="background-color:#eeeeee">
+
<div class="toccolours" style="background-color:#ee6b6e">
 
===Consolidation, Cycles 5-6===
 
===Consolidation, Cycles 5-6===
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
Line 309: Line 322:
 
*[[Methotrexate (MTX)]] 12,000 mg/m<sup>2</sup> (maximum dose of 20,000 mg) IV over 4 hours once on day 1 of weeks 24, 25, 28, and 29
 
*[[Methotrexate (MTX)]] 12,000 mg/m<sup>2</sup> (maximum dose of 20,000 mg) IV over 4 hours once on day 1 of weeks 24, 25, 28, and 29
 
====Supportive therapy====
 
====Supportive therapy====
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> PO or IV every 6 hours beginning 24 hours after the beginning of the methotrexate infusion and continuing until the serum methotrexate level is less than 0.1 μM.
+
*[[Leucovorin (Folinic acid)]] 15 mg/m<sup>2</sup> PO or IV every 6 hours beginning 24 hours after the beginning of the methotrexate infusion and continuing until the serum methotrexate level is less than 0.1 μM.
'''10 Week course'''
+
'''10-week course'''
 
</div></div><br>
 
</div></div><br>
<div class="toccolours" style="background-color:#eeeeee">
+
<div class="toccolours" style="background-color:#ee6b6e">
 
===Maintenance, Weeks 30-104===
 
===Maintenance, Weeks 30-104===
 +
''Note: Peginterferon alfa-2b dose is increased only if the starting dose is well tolerated.''
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
 
====Immunotherapy====
 
====Immunotherapy====
*[[Peginterferon alfa-2b (Sylatron)]] 0.5 mcg/kg/day (MAX DOSE = 50 mcg) subcutaneously on day 1 of Weeks 30, 31, 32, and 33.
+
*[[Peginterferon alfa-2b (Sylatron)]] as follows:
**If well tolerated during first 4 weeks of therapy, escalate dose.
+
**Cycles 1 to 4: 0.5 mcg/kg (maximum dose of 50 mcg) SC once on day 1
*[[Peginterferon alfa-2b (Sylatron)]] 1 mcg/kg/day (MAX DOSE = 100 mcg) subcutaneously on day 1 of Weeks 34 through 104.
+
**Cycles 5 to 75: 1 mcg/kg (maximum dose of 100 mcg) SC once on day 1
'''75 Week course'''
+
'''7-day cycle for 75 cycles'''
 
</div></div></div>
 
</div></div></div>
 
===References===
 
===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 dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/27569442/ PubMed] [https://clinicaltrials.gov/study/NCT00134030 Clinical Trials Registry]
+
# '''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]
 +
 
 
==MAPIE [COG AOST0331]==
 
==MAPIE [COG AOST0331]==
 
<div class="toccolours" style="background-color:#c8a2c8">
 
<div class="toccolours" style="background-color:#c8a2c8">
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|}
 
|}
 
''Note: Induction is received by all patients and consists of 2 cycles of MAP; subsequent treatments in this protocol are for poor responders.''
 
''Note: Induction is received by all patients and consists of 2 cycles of MAP; subsequent treatments in this protocol are for poor responders.''
<div class="toccolours" style="background-color:#eeeeee">
+
<div class="toccolours" style="background-color:#ee6b6e">
 
===Induction===
 
===Induction===
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
Line 348: Line 363:
 
*[[Methotrexate (MTX)]] 12,000 mg/m<sup>2</sup> (maximum dose of 20,000 mg) IV over 4 hours once on day 1 of weeks 4, 5, 9, and 10.  
 
*[[Methotrexate (MTX)]] 12,000 mg/m<sup>2</sup> (maximum dose of 20,000 mg) IV over 4 hours once on day 1 of weeks 4, 5, 9, and 10.  
 
====Supportive therapy====
 
====Supportive therapy====
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> PO or IV every 6 hours beginning 24 hours after the beginning of the methotrexate infusion and continuing until the serum methotrexate level is less than 0.1 μM.
+
*[[Leucovorin (Folinic acid)]] 15 mg/m<sup>2</sup> PO or IV every 6 hours beginning 24 hours after the beginning of the methotrexate infusion and continuing until the serum methotrexate level is less than 0.1 μM.
 
'''10 Week course'''
 
'''10 Week course'''
 
</div></div><br>
 
</div></div><br>
<div class="toccolours" style="background-color:#eeeeee">
+
<div class="toccolours" style="background-color:#ee6b6e">
 
===Consolidation, MAPIE Cycles 3 and 7===
 
===Consolidation, MAPIE Cycles 3 and 7===
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
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*[[Methotrexate (MTX)]] 12,000 mg/m<sup>2</sup> (maximum dose of 20,000 mg) IV over 4 hours once on day 1 of weeks 15 and 31.  
 
*[[Methotrexate (MTX)]] 12,000 mg/m<sup>2</sup> (maximum dose of 20,000 mg) IV over 4 hours once on day 1 of weeks 15 and 31.  
 
====Supportive therapy====
 
====Supportive therapy====
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> PO or IV every 6 hours beginning 24 hours after the beginning of the methotrexate infusion and continuing until the serum methotrexate level is less than 0.1 μM.
+
*[[Leucovorin (Folinic acid)]] 15 mg/m<sup>2</sup> PO or IV every 6 hours beginning 24 hours after the beginning of the methotrexate infusion and continuing until the serum methotrexate level is less than 0.1 μM.
 
'''5-Week Courses'''
 
'''5-Week Courses'''
 
</div></div><br>
 
</div></div><br>
<div class="toccolours" style="background-color:#eeeeee">
+
<div class="toccolours" style="background-color:#ee6b6e">
 
===Consolidation, MAP Cycles 4, 6, and 8===
 
===Consolidation, MAP Cycles 4, 6, and 8===
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
Line 371: Line 386:
 
====Supportive therapy====
 
====Supportive therapy====
 
*[[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.
 
*[[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.
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> PO or IV every 6 hours beginning 24 hours after the beginning of the methotrexate infusion and continuing until the serum methotrexate level is less than 0.1 μM.
+
*[[Leucovorin (Folinic acid)]] 15 mg/m<sup>2</sup> PO or IV every 6 hours beginning 24 hours after the beginning of the methotrexate infusion and continuing until the serum methotrexate level is less than 0.1 μM.
 
'''5-Week Courses'''
 
'''5-Week Courses'''
 
</div></div><br>
 
</div></div><br>
<div class="toccolours" style="background-color:#eeeeee">
+
<div class="toccolours" style="background-color:#ee6b6e">
 
===Consolidation, MAP Cycle 5===
 
===Consolidation, MAP Cycle 5===
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
Line 383: Line 398:
 
====Supportive therapy====
 
====Supportive therapy====
 
*[[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.
 
*[[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.
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> PO or IV every 6 hours beginning 24 hours after the beginning of the methotrexate infusion and continuing until the serum methotrexate level is less than 0.1 μM.
+
*[[Leucovorin (Folinic acid)]] 15 mg/m<sup>2</sup> PO or IV every 6 hours beginning 24 hours after the beginning of the methotrexate infusion and continuing until the serum methotrexate level is less than 0.1 μM.
 
'''5-Week Courses'''
 
'''5-Week Courses'''
 
</div></div><br>
 
</div></div><br>
<div class="toccolours" style="background-color:#eeeeee">
+
<div class="toccolours" style="background-color:#ee6b6e">
 
===Consolidation, MAP Cycle 9===
 
===Consolidation, MAP Cycle 9===
 
<div class="toccolours" style="background-color:#b3e2cd">
 
<div class="toccolours" style="background-color:#b3e2cd">
Line 395: Line 410:
 
====Supportive therapy====
 
====Supportive therapy====
 
*[[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.
 
*[[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.
*[[Folinic acid (Leucovorin)]] 15 mg/m<sup>2</sup> PO or IV every 6 hours beginning 24 hours after the beginning of the methotrexate infusion and continuing until the serum methotrexate level is less than 0.1 μM.
+
*[[Leucovorin (Folinic acid)]] 15 mg/m<sup>2</sup> PO or IV every 6 hours beginning 24 hours after the beginning of the methotrexate infusion and continuing until the serum methotrexate level is less than 0.1 μM.
 
'''5-Week Courses'''
 
'''5-Week Courses'''
 
</div></div></div>
 
</div></div></div>
 
===References===
 
===References===
#'''EURAMOS-1 poor response:''' 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 dosing details in manuscript''' [https://pubmed.ncbi.nlm.nih.gov/27569442/ PubMed] [https://clinicaltrials.gov/study/NCT00134030 Clinical Trials Registry]
+
# '''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]
 
[[Category:Osteosarcoma regimens]]
 
[[Category:Osteosarcoma regimens]]
 
[[Category:Historical regimens]]
 
[[Category:Historical regimens]]

Latest revision as of 11:39, 13 May 2024

The purpose of this page is to provide references to regimens that are obsolete, outdated, or of historical interest only. Is there a regimen missing from this list? See the main osteosarcoma page for current regimens.

8 regimens on this page
8 variants on this page


Neoadjuvant therapy

MA-BCD

MA-BCD: High-dose Methotrexate, Adriamycin (Doxorubicin), Bleomycin, Cyclophosphamide, Dactinomycin

Regimen

Study Dates of enrollment Evidence Comparator Comparative Efficacy
Winkler et al. 1984 (COSS-80) 1979-1982 Phase 3 (C) MAP 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

  • 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)
  • 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 22 & 29
    • 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
  • Bleomycin (Blenoxane) as follows:
    • Cycle 1: 12 mg/m2 IV bolus once per day on days 36 & 37
    • Cycles 2 to 4: 12 mg/m2 IV bolus once per day on days 43 & 44
  • Cyclophosphamide (Cytoxan) as follows:
    • Cycle 1: 600 mg/m2 IV bolus once per day on days 36 & 37
    • Cycles 2 to 4: 600 mg/m2 IV bolus once per day on days 43 & 44
  • Dactinomycin (Cosmegen) as follows:
    • Cycle 1: 0.45 mg/m2 IV bolus once per day on days 36 & 37
    • Cycles 2 to 4: 0.45 mg/m2 IV bolus once per day on days 43 & 44

Supportive therapy

  • Leucovorin (Folinic acid) 15 mg/m2 PO every 6 hours x 12 hours once per day, starting 24 hours after the completion of each methotrexate infusion; additional leucovorin used for delayed methotrexate elimination
  • Sodium bicarbonate urine alkalinization prior to high-dose methotrexate
  • Normal saline 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

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

M-BCD

M-BCD: High-dose Methotrexate, Bleomycin, Cyclophosphamide, Dactinomycin

Regimen

Study Dates of enrollment Evidence Comparator Comparative Efficacy
Winkler et al. 1988 (COSS-82) 1982-1984 Phase 3 (C) MAP Inferior 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.

Chemotherapy

Supportive therapy

  • Leucovorin (Folinic acid) 15 mg/m2 PO every 6 hours x 12 hours once per day on days 16 & 23, 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
  • Normal saline 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

35-day cycle for 2 cycles

Subsequent treatment

  • Surgery, then risk-adapted treatment:
    • COSS-82, patients who had a good response: Adjuvant M-BCD
    • COSS-82, patients who had a poor response: Adjuvant AP

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

Adjuvant therapy

Doxorubicin monotherapy

Regimen

Study Evidence
Cortes et al. 1974 Non-randomized

Preceding treatment

Chemotherapy

4- to 6-week cycle for 6 cycles

References

  1. 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. link to original article contains dosing details in abstract PubMed

IP-BCD

IP-BCD: Ifosfamide, Platinol (Cisplatin), Bleomycin, Cyclophosphamide, Dactinomycin

Regimen

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

Preceding treatment

Chemotherapy

Supportive therapy

  • Mesna (Mesnex) 2000 mg/m2 IV over 23.5 hours once per day on days 1 to 5, given second, with ifosfamide, then 2000 mg/m2/day IV continuous infusion over 48 hours, started on day 6 (total dose: 14,000 mg/m2)
  • Mannitol given with cisplatin; no further details provided

35-day cycle for 3 cycles

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

MA-BCD/AP

MA-BCD/AP: High-dose Methotrexate, Adriamycin (Doxorubicin), Bleomycin, Cyclophosphamide, Dactinomycin alternating with Adriamycin (Doxorubicin) & Platinol (Cisplatin)

Regimen

Study Dates of enrollment Evidence Comparator Comparative Efficacy
Link et al. 1986 1982-1984 Phase 3 (E-esc) No further treatment Superior RFS

Preceding treatment

References

  1. Link MP, Goorin AM, Miser AW, Green AA, Pratt CB, Belasco JB, Pritchard J, Malpas JS, Baker AR, Kirkpatrick JA, Ayala AG, Shuster JJ, Abelson HT, Simone JV, Vietti TJ. The effect of adjuvant chemotherapy on relapse-free survival in patients with osteosarcoma of the extremity. N Engl J Med. 1986 Jun 19;314(25):1600-6. link to original article PubMed

M-BCD

M-BCD: High-dose Methotrexate, Bleomycin, Cyclophosphamide, Dactinomycin

Regimen

Study Dates of enrollment Evidence Comparator Comparative Efficacy
Eilber et al. 1987 1981-1984 Randomized (E-esc) Observation Seems to have superior OS
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 references; schedule of doses is primarily extrapolated from Figure 1 of Winkler et al. 1988, which does not contain clear delineations in time.

Preceding treatment

Chemotherapy

Supportive therapy

  • Leucovorin (Folinic acid) 15 mg/m2 PO every 6 hours x 12 hours once per day on days 16 & 23, 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
  • Normal saline 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

35-day cycle for 2 cycles

References

  1. Eilber F, Giuliano A, Eckardt J, Patterson K, Moseley S, Goodnight J. Adjuvant chemotherapy for osteosarcoma: a randomized prospective trial. J Clin Oncol. 1987 Jan;5(1):21-6. link to original article PubMed
    1. Update: Bernthal NM, Federman N, Eilber FR, Nelson SD, Eckardt JJ, Eilber FC, Tap WD. Long-term results (>25 years) of a randomized, prospective clinical trial evaluating chemotherapy in patients with high-grade, operable osteosarcoma. Cancer. 2012 Dec 1;118(23):5888-93. Epub 2012 May 30. link to original article 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

Methotrexate & Vincristine

Regimen

Study Dates of enrollment Evidence
Jaffe et al. 1974 1972-06 to NR Non-randomized

Preceding treatment

Chemotherapy

Supportive therapy

14-day cycle until therapeutic goal achieved, then 21-day cycle for up to 33 cycles (2 years total)

References

  1. 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. link to original article contains dosing details in manuscript PubMed

Relapsed, refractory, or metastatic

Doxorubicin monotherapy

Regimen

Study Evidence
Cortes et al. 1972 Non-randomized, fewer than 20 pts

References

  1. Cortes EP, Holland JF, Wang JJ, Sinks LF. Doxorubicin in disseminated osteosarcoma. JAMA. 1972 Sep 4;221(10):1132-8. link to original article PubMed

MAPifn [COG AOST0331]

Study Dates of enrollment Evidence
Marina et al. 2019 (COG AOST0331) 2005-04-14 to 2011-06-30 Non-randomized part of phase 3 RCT

Note: Induction is received by all patients and consists of 2 cycles of MAP. The remainder of this protocol is for good responders.

Induction

Chemotherapy

  • Cisplatin (Platinol) 60 mg/m2 IV infusion over 4 hours, started on day 1 of weeks 1 and 6
  • Doxorubicin (Adriamycin) 37.5 mg/m2/day (total dose is 75 mg/m2 given as a 48 hour infusion) on days 1 to 2 of Weeks 1 and 6
  • Methotrexate (MTX) 12,000 mg/m2 (maximum dose of 20,000 mg) IV over 4 hours once on day 1 of weeks 4, 5, 9, and 10.

Supportive therapy

  • Leucovorin (Folinic acid) 15 mg/m2 PO or IV every 6 hours beginning 24 hours after the beginning of the methotrexate infusion and continuing until the serum methotrexate level is less than 0.1 μM.

10-week course


Consolidation, Cycles 3-4

Chemotherapy

  • Cisplatin (Platinol) 60 mg/m2 IV infusion over 4 hours, started on day 1 of weeks 12 and 17
  • Doxorubicin (Adriamycin) 37.5 mg/m2/day (total dose is 75 mg/m2 given as a 48 hour infusion) on days 1 to 2 of Weeks 12 and 17.
  • Methotrexate (MTX) 12,000 mg/m2 (maximum dose of 20,000 mg) IV over 4 hours once on day 1 of weeks 15, 16, 20, and 21.

Supportive therapy

  • Leucovorin (Folinic acid) 15 mg/m2 PO or IV every 6 hours beginning 24 hours after the beginning of the methotrexate infusion and continuing until the serum methotrexate level is less than 0.1 μM.

10-week course


Consolidation, Cycles 5-6

Chemotherapy

  • Doxorubicin (Adriamycin) 37.5 mg/m2/day (total dose is 75 mg/m2 given as a 48 hour infusion) on days 1 to 2 of Weeks 22 and 26.
  • Methotrexate (MTX) 12,000 mg/m2 (maximum dose of 20,000 mg) IV over 4 hours once on day 1 of weeks 24, 25, 28, and 29

Supportive therapy

  • Leucovorin (Folinic acid) 15 mg/m2 PO or IV every 6 hours beginning 24 hours after the beginning of the methotrexate infusion and continuing until the serum methotrexate level is less than 0.1 μM.

10-week course


Maintenance, Weeks 30-104

Note: Peginterferon alfa-2b dose is increased only if the starting dose is well tolerated.

Immunotherapy

  • Peginterferon alfa-2b (Sylatron) as follows:
    • Cycles 1 to 4: 0.5 mcg/kg (maximum dose of 50 mcg) SC once on day 1
    • Cycles 5 to 75: 1 mcg/kg (maximum dose of 100 mcg) SC once on day 1

7-day cycle for 75 cycles

References

  1. 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

MAPIE [COG AOST0331]

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

Note: Induction is received by all patients and consists of 2 cycles of MAP; subsequent treatments in this protocol are for poor responders.

Induction

Chemotherapy

  • Cisplatin (Platinol) 60 mg/m2 IV infusion over 4 hours, started on day 1 of weeks 1 and 6
  • Doxorubicin (Adriamycin) 37.5 mg/m2/day (total dose is 75 mg/m2 given as a 48 hour infusion) on days 1 to 2 of Weeks 1 and 6
  • Methotrexate (MTX) 12,000 mg/m2 (maximum dose of 20,000 mg) IV over 4 hours once on day 1 of weeks 4, 5, 9, and 10.

Supportive therapy

  • Leucovorin (Folinic acid) 15 mg/m2 PO or IV every 6 hours beginning 24 hours after the beginning of the methotrexate infusion and continuing until the serum methotrexate level is less than 0.1 μM.

10 Week course


Consolidation, MAPIE Cycles 3 and 7

Chemotherapy

  • Cisplatin (Platinol) 60 mg/m2 IV infusion over 4 hours, started on day 1 of weeks 12 and 28
  • Doxorubicin (Adriamycin) 37.5 mg/m2/day (total dose is 75 mg/m2 given as a 48 hour infusion) on days 1 to 2 of Weeks 12 and 28.
  • Methotrexate (MTX) 12,000 mg/m2 (maximum dose of 20,000 mg) IV over 4 hours once on day 1 of weeks 15 and 31.

Supportive therapy

  • Leucovorin (Folinic acid) 15 mg/m2 PO or IV every 6 hours beginning 24 hours after the beginning of the methotrexate infusion and continuing until the serum methotrexate level is less than 0.1 μM.

5-Week Courses


Consolidation, MAP Cycles 4, 6, and 8

Chemotherapy

  • Ifosfamide (Ifex) 2.8 g/m2/dose IV over 4 hours once per day on days 1 through 5 of weeks 16, 24, and 32.
  • Etoposide (Vepesid) 100 mg/m2/dose IV over 60 minutes once per day on days 1 through 5 of weeks 16, 24, and 32.
  • Methotrexate (MTX) 12,000 mg/m2 (maximum dose of 20,000 mg) IV over 4 hours once on day 1 of weeks 19, 27, and 35.

Supportive therapy

  • Mesna (Mesnex) 2.8 g/m2/24 hours IV continuous infusion over 24 hours on days 1 through 5 of weeks 16, 24, and 32.
  • Leucovorin (Folinic acid) 15 mg/m2 PO or IV every 6 hours beginning 24 hours after the beginning of the methotrexate infusion and continuing until the serum methotrexate level is less than 0.1 μM.

5-Week Courses


Consolidation, MAP Cycle 5

Chemotherapy

  • Doxorubicin (Adriamycin) 37.5 mg/m2/day (total dose is 75 mg/m2 given as a 48 hour infusion) on days 1 to 2 of Week 20.
  • Ifosfamide (Ifex) 3 g/m2/dose IV over 4 hours once per day on days 1, 2, and 3 of weeks 20.
  • Methotrexate (MTX) 12,000 mg/m2 (maximum dose of 20,000 mg) IV over 4 hours once on day 1 of weeks 23.

Supportive therapy

  • Mesna (Mesnex) 3 g/m2/24 hours IV continuous infusion over 24 hours on days 1, 2, and 3 of weeks 20.
  • Leucovorin (Folinic acid) 15 mg/m2 PO or IV every 6 hours beginning 24 hours after the beginning of the methotrexate infusion and continuing until the serum methotrexate level is less than 0.1 μM.

5-Week Courses


Consolidation, MAP Cycle 9

Chemotherapy

  • Doxorubicin (Adriamycin) 37.5 mg/m2/day (total dose is 75 mg/m2 given as a 48 hour infusion) on days 1 to 2 of Week 36.
  • Ifosfamide (Ifex) 3 g/m2/dose IV over 4 hours once per day on days 1, 2, and 3 of weeks 36.
  • Methotrexate (MTX) 12,000 mg/m2 (maximum dose of 20,000 mg) IV over 4 hours once on day 1 of weeks 39 and 40.

Supportive therapy

  • Mesna (Mesnex) 3 g/m2/24 hours IV continuous infusion over 24 hours on days 1, 2, and 3 of weeks 36.
  • Leucovorin (Folinic acid) 15 mg/m2 PO or IV every 6 hours beginning 24 hours after the beginning of the methotrexate infusion and continuing until the serum methotrexate level is less than 0.1 μM.

5-Week Courses

References

  1. 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