Difference between revisions of "Non-Hodgkin lymphoma, pediatric"
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COPADM: '''<u>C</u>'''yclophosphamide, '''<u>O</u>'''ncovin (Vincristine), '''<u>P</u>'''rednisone, '''<u>AD</u>'''riamycin (Doxorubicin), '''<u>M</u>'''ethotrexate | COPADM: '''<u>C</u>'''yclophosphamide, '''<u>O</u>'''ncovin (Vincristine), '''<u>P</u>'''rednisone, '''<u>AD</u>'''riamycin (Doxorubicin), '''<u>M</u>'''ethotrexate | ||
===Protocol {{#subobject:39dc15|Variant=1}}=== | ===Protocol {{#subobject:39dc15|Variant=1}}=== | ||
− | {| class="wikitable sortable" style="width: | + | {| class="wikitable sortable" style="width: 100%; text-align:center;" |
− | !style="width: | + | !style="width: 20%"|Study |
− | !style="width: | + | !style="width: 20%"|Years of enrollment |
− | !style="width: | + | !style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]] |
+ | !style="width: 20%"|Comparator | ||
+ | !style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]] | ||
|- | |- | ||
|[http://www.ncbi.nlm.nih.gov/pmc/articles/pmc1852229/ Patte et al. 2007 (FAB/LMB96)] | |[http://www.ncbi.nlm.nih.gov/pmc/articles/pmc1852229/ Patte et al. 2007 (FAB/LMB96)] | ||
|1996-2001 | |1996-2001 | ||
|style="background-color:#91cf61"|Non-randomized portion of phase 3 RCT | |style="background-color:#91cf61"|Non-randomized portion of phase 3 RCT | ||
+ | | style="background-color:#d3d3d3" | | ||
+ | | style="background-color:#d3d3d3" | | ||
+ | |- | ||
+ | |[http://www.ncbi.nlm.nih.gov/pmc/articles/pmc7720281/ Minard-Colin et al. 2020 (Inter-B-NHL Ritux 2010)] | ||
+ | |2011-2015 | ||
+ | | style="background-color:#1a9851" |Phase III (C) | ||
+ | |[[#R-COPADM|R-COPADM]] | ||
+ | | style="background-color:#d73027" |Inferior OS | ||
|- | |- | ||
|} | |} | ||
− | ''Note: It is not clear from | + | ''Note: It is not clear from Patte et al. 2007 whether the cyclophosphamide was fractionated.'' |
====Preceding treatment==== | ====Preceding treatment==== | ||
*[[#CVP|COP prephase]] | *[[#CVP|COP prephase]] | ||
Line 79: | Line 89: | ||
====Subsequent treatment==== | ====Subsequent treatment==== | ||
− | *[[#COPADM|COPADM second | + | *[[#COPADM|COPADM second induction]]; reduced-dose versus [[#COPADM|COPADM second induction]]; standard-dose |
===References=== | ===References=== | ||
# '''FAB/LMB96:''' Patte C, Auperin A, Gerrard M, Michon J, Pinkerton R, Sposto R, Weston C, Raphael M, Perkins SL, McCarthy K, Cairo MS; FAB/LMB96 International Study Committee. Results of the randomized international FAB/LMB96 trial for intermediate risk B-cell non-Hodgkin lymphoma in children and adolescents: it is possible to reduce treatment for the early responding patients. Blood. 2007 Apr 1;109(7):2773-80. [https://doi.org/10.1182/blood-2006-07-036673 link to original article] [http://www.ncbi.nlm.nih.gov/pmc/articles/pmc1852229/ link to PMC article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/17132719/ PubMed] NCT00002757 | # '''FAB/LMB96:''' Patte C, Auperin A, Gerrard M, Michon J, Pinkerton R, Sposto R, Weston C, Raphael M, Perkins SL, McCarthy K, Cairo MS; FAB/LMB96 International Study Committee. Results of the randomized international FAB/LMB96 trial for intermediate risk B-cell non-Hodgkin lymphoma in children and adolescents: it is possible to reduce treatment for the early responding patients. Blood. 2007 Apr 1;109(7):2773-80. [https://doi.org/10.1182/blood-2006-07-036673 link to original article] [http://www.ncbi.nlm.nih.gov/pmc/articles/pmc1852229/ link to PMC article] '''contains verified protocol''' [https://pubmed.ncbi.nlm.nih.gov/17132719/ PubMed] NCT00002757 | ||
+ | # '''Inter-B-NHL Ritux 2010:''' Minard-Colin V, Aupérin A, Pillon M, Burke GAA, Barkauskas DA, Wheatley K, Delgado RF, Alexander S, Uyttebroeck A, Bollard CM, Zsiros J, Csoka M, Kazanowska B, Chiang AK, Miles RR, Wotherspoon A, Adamson PC, Vassal G, Patte C, Gross TG; European Intergroup for Childhood Non-Hodgkin Lymphoma; Children’s Oncology Group. Rituximab for High-Risk, Mature B-Cell Non-Hodgkin's Lymphoma in Children. N Engl J Med. 2020 Jun 4;382(23):2207-2219. [https://doi.org/10.1056/nejmoa1915315 link to original article] [http://www.ncbi.nlm.nih.gov/pmc/articles/pmc7720281/ link to PMC article] [https://pubmed.ncbi.nlm.nih.gov/32492302/ PubMed] NCT01516580 | ||
+ | |||
+ | ==R-COPADM {{#subobject:bac173|Regimen=1}}== | ||
+ | {| class="wikitable" style="float:right; margin-left: 5px;" | ||
+ | |- | ||
+ | |[[#top|back to top]] | ||
+ | |} | ||
+ | R-COPADM: '''<u>R</u>'''ituximab, '''<u>C</u>'''yclophosphamide, '''<u>O</u>'''ncovin (Vincristine), '''<u>P</u>'''rednisone, '''<u>AD</u>'''riamycin (Doxorubicin), '''<u>M</u>'''ethotrexate | ||
+ | ===Protocol {{#subobject:avdc15|Variant=1}}=== | ||
+ | {| class="wikitable sortable" style="width: 100%; text-align:center;" | ||
+ | !style="width: 20%"|Study | ||
+ | !style="width: 20%"|Years of enrollment | ||
+ | !style="width: 20%"|[[Levels_of_Evidence#Evidence|Evidence]] | ||
+ | !style="width: 20%"|Comparator | ||
+ | !style="width: 20%"|[[Levels_of_Evidence#Comparative_efficacy|Comparative Efficacy]] | ||
+ | |- | ||
+ | |[http://www.ncbi.nlm.nih.gov/pmc/articles/pmc7720281/ Minard-Colin et al. 2020 (Inter-B-NHL Ritux 2010)] | ||
+ | |2011-2015 | ||
+ | | style="background-color:#1a9851" |Phase III (E-RT-esc) | ||
+ | |[[#COPADM|COPADM]] | ||
+ | | style="background-color:#1a9850" |Superior OS<br>OS36: 95.1% vs 87.3%<br>(HR 0.36, 95% CI 0.16-0.82) | ||
+ | |- | ||
+ | |} | ||
+ | ''Note: Only partial dosing information is available in the manuscript/supplement; dosing here is primarily based on FAB/LMB96.'' | ||
+ | ====Preceding treatment==== | ||
+ | *[[#CVP|COP prephase]] | ||
+ | ====Targeted therapy==== | ||
+ | *[[Rituximab (Rituxan)]] 375 mg/m<sup>2</sup> IV once per day on days -2 & 1 | ||
+ | ====Chemotherapy==== | ||
+ | *[[Cyclophosphamide (Cytoxan)]] 250 mg/m<sup>2</sup> IV twice per day on days 2 to 4 (total dose: 1500 mg/m<sup>2</sup>) | ||
+ | *[[Vincristine (Oncovin)]] 2 mg/m<sup>2</sup> IV once on day 1 | ||
+ | *[[Prednisone (Sterapred)]] 60 mg/m<sup>2</sup>/day IV or PO on days 1 to 7 | ||
+ | *[[Doxorubicin (Adriamycin)]] 60 mg/m<sup>2</sup> IV once on day 2 | ||
+ | *[[Methotrexate (MTX)]] 3000 mg/m<sup>2</sup> IV over 3 hours once on day 1 | ||
+ | |||
+ | ====Supportive medications==== | ||
+ | *[[Folinic acid (Leucovorin)]] | ||
+ | |||
+ | ====CNS prophylaxis==== | ||
+ | *[[Methotrexate (MTX)]] (dose not specified) IT once per day on days 2 & 6 | ||
+ | |||
+ | '''One course''' | ||
+ | |||
+ | ====Subsequent treatment==== | ||
+ | *[[#R-COPADM|R-COPADM second induction]] | ||
+ | |||
+ | ===References=== | ||
+ | # '''Inter-B-NHL Ritux 2010:''' Minard-Colin V, Aupérin A, Pillon M, Burke GAA, Barkauskas DA, Wheatley K, Delgado RF, Alexander S, Uyttebroeck A, Bollard CM, Zsiros J, Csoka M, Kazanowska B, Chiang AK, Miles RR, Wotherspoon A, Adamson PC, Vassal G, Patte C, Gross TG; European Intergroup for Childhood Non-Hodgkin Lymphoma; Children’s Oncology Group. Rituximab for High-Risk, Mature B-Cell Non-Hodgkin's Lymphoma in Children. N Engl J Med. 2020 Jun 4;382(23):2207-2219. [https://doi.org/10.1056/nejmoa1915315 link to original article] [http://www.ncbi.nlm.nih.gov/pmc/articles/pmc7720281/ link to PMC article] '''contains partial protocol''' [https://pubmed.ncbi.nlm.nih.gov/32492302/ PubMed] NCT01516580 | ||
[[Category:Non-Hodgkin lymphoma regimens]] | [[Category:Non-Hodgkin lymphoma regimens]] |
Revision as of 23:17, 3 December 2021
Section editor transclusions This page contains studies that were specific to pediatric populations, who are generally treated based on risk-stratification, not on the underlying histology. See individual trials for inclusion criteria.
3 regimens on this page
3 variants on this page
|
Untreated, pre-phase
CVP
back to top |
CVP: Cyclophosphamide, Vincristine, Prednisone
COP: Cyclophosphamide, Oncovin (Vincristine), Prednisone
Regimen
Study | Years of enrollment | Evidence |
---|---|---|
Patte et al. 2007 (FAB/LMB96) | 1996-2001 | Non-randomized portion of phase 3 RCT |
Chemotherapy
- Cyclophosphamide (Cytoxan) 300 mg/m2 IV once on day 1
- Vincristine (Oncovin) 1 mg/m2 IV once on day 1
- Prednisone (Sterapred) 60 mg/m2/day IV or PO on days 1 to 7
CNS prophylaxis
- Methotrexate (MTX) (dose not specified) IT once on day 1
7-day course
Subsequent treatment
References
- FAB/LMB96: Patte C, Auperin A, Gerrard M, Michon J, Pinkerton R, Sposto R, Weston C, Raphael M, Perkins SL, McCarthy K, Cairo MS; FAB/LMB96 International Study Committee. Results of the randomized international FAB/LMB96 trial for intermediate risk B-cell non-Hodgkin lymphoma in children and adolescents: it is possible to reduce treatment for the early responding patients. Blood. 2007 Apr 1;109(7):2773-80. link to original article link to PMC article contains verified protocol PubMed NCT00002757
Untreated, induction
COPADM
back to top |
COPADM: Cyclophosphamide, Oncovin (Vincristine), Prednisone, ADriamycin (Doxorubicin), Methotrexate
Protocol
Study | Years of enrollment | Evidence | Comparator | Comparative Efficacy |
---|---|---|---|---|
Patte et al. 2007 (FAB/LMB96) | 1996-2001 | Non-randomized portion of phase 3 RCT | ||
Minard-Colin et al. 2020 (Inter-B-NHL Ritux 2010) | 2011-2015 | Phase III (C) | R-COPADM | Inferior OS |
Note: It is not clear from Patte et al. 2007 whether the cyclophosphamide was fractionated.
Preceding treatment
Chemotherapy
- Cyclophosphamide (Cytoxan) 250 mg/m2 IV twice per day on days 2 to 4 (total dose: 1500 mg/m2)
- Vincristine (Oncovin) 2 mg/m2 IV once on day 1
- Prednisone (Sterapred) 60 mg/m2/day IV or PO on days 1 to 7
- Doxorubicin (Adriamycin) 60 mg/m2 IV once on day 2
- Methotrexate (MTX) 3000 mg/m2 IV over 3 hours once on day 1
Supportive medications
CNS prophylaxis
- Methotrexate (MTX) (dose not specified) IT once per day on days 2 & 6
One course
Subsequent treatment
- COPADM second induction; reduced-dose versus COPADM second induction; standard-dose
References
- FAB/LMB96: Patte C, Auperin A, Gerrard M, Michon J, Pinkerton R, Sposto R, Weston C, Raphael M, Perkins SL, McCarthy K, Cairo MS; FAB/LMB96 International Study Committee. Results of the randomized international FAB/LMB96 trial for intermediate risk B-cell non-Hodgkin lymphoma in children and adolescents: it is possible to reduce treatment for the early responding patients. Blood. 2007 Apr 1;109(7):2773-80. link to original article link to PMC article contains verified protocol PubMed NCT00002757
- Inter-B-NHL Ritux 2010: Minard-Colin V, Aupérin A, Pillon M, Burke GAA, Barkauskas DA, Wheatley K, Delgado RF, Alexander S, Uyttebroeck A, Bollard CM, Zsiros J, Csoka M, Kazanowska B, Chiang AK, Miles RR, Wotherspoon A, Adamson PC, Vassal G, Patte C, Gross TG; European Intergroup for Childhood Non-Hodgkin Lymphoma; Children’s Oncology Group. Rituximab for High-Risk, Mature B-Cell Non-Hodgkin's Lymphoma in Children. N Engl J Med. 2020 Jun 4;382(23):2207-2219. link to original article link to PMC article PubMed NCT01516580
R-COPADM
back to top |
R-COPADM: Rituximab, Cyclophosphamide, Oncovin (Vincristine), Prednisone, ADriamycin (Doxorubicin), Methotrexate
Protocol
Study | Years of enrollment | Evidence | Comparator | Comparative Efficacy |
---|---|---|---|---|
Minard-Colin et al. 2020 (Inter-B-NHL Ritux 2010) | 2011-2015 | Phase III (E-RT-esc) | COPADM | Superior OS OS36: 95.1% vs 87.3% (HR 0.36, 95% CI 0.16-0.82) |
Note: Only partial dosing information is available in the manuscript/supplement; dosing here is primarily based on FAB/LMB96.
Preceding treatment
Targeted therapy
- Rituximab (Rituxan) 375 mg/m2 IV once per day on days -2 & 1
Chemotherapy
- Cyclophosphamide (Cytoxan) 250 mg/m2 IV twice per day on days 2 to 4 (total dose: 1500 mg/m2)
- Vincristine (Oncovin) 2 mg/m2 IV once on day 1
- Prednisone (Sterapred) 60 mg/m2/day IV or PO on days 1 to 7
- Doxorubicin (Adriamycin) 60 mg/m2 IV once on day 2
- Methotrexate (MTX) 3000 mg/m2 IV over 3 hours once on day 1
Supportive medications
CNS prophylaxis
- Methotrexate (MTX) (dose not specified) IT once per day on days 2 & 6
One course
Subsequent treatment
References
- Inter-B-NHL Ritux 2010: Minard-Colin V, Aupérin A, Pillon M, Burke GAA, Barkauskas DA, Wheatley K, Delgado RF, Alexander S, Uyttebroeck A, Bollard CM, Zsiros J, Csoka M, Kazanowska B, Chiang AK, Miles RR, Wotherspoon A, Adamson PC, Vassal G, Patte C, Gross TG; European Intergroup for Childhood Non-Hodgkin Lymphoma; Children’s Oncology Group. Rituximab for High-Risk, Mature B-Cell Non-Hodgkin's Lymphoma in Children. N Engl J Med. 2020 Jun 4;382(23):2207-2219. link to original article link to PMC article contains partial protocol PubMed NCT01516580