Non-Hodgkin lymphoma, pediatric
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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
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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
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COPADM: Cyclophosphamide, Oncovin (Vincristine), Prednisone, ADriamycin (Doxorubicin), Methotrexate
Protocol
Study | Years of enrollment | Evidence |
---|---|---|
Patte et al. 2007 (FAB/LMB96) | 1996-2001 | Non-randomized portion of phase 3 RCT |
Note: It is not clear from the manuscript 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 inducation; reduced-dose versus COPADM second inducation; 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