Lymphoma Clinical Trial
Official title:
Pilot Study for Therapy Optimising for Hodgkin's Lymphoma in Childhood and Adolescence; Optimising Therapy for Boys With Hodgkin's Lymphoma in Intermediate and Advanced Stages. Safety and Efficacy Study for Drug Combination VECOPA
RATIONALE: Drugs used in chemotherapy work in different ways to stop the growth of cancer
cells, either by killing the cells or by stopping them from dividing. Giving combination
chemotherapy may kill more cancer cells.
PURPOSE: This phase II trial is studying the side effects and how well combination
chemotherapy works in treating young male patients with Hodgkin's lymphoma.
OBJECTIVES:
- Determine the safety and efficacy of combination chemotherapy comprising vincristine,
etoposide, cyclophosphamide, vinblastine, prednisone, and doxorubicin hydrochloride
(VECOPA) in pediatric male patients with previously untreated stage II-IV classic
Hodgkin's lymphoma.
- Compare the effects of VECOPA vs cyclophosphamide, vincristine, procarbazine
hydrochloride, and prednisone (COPP) in these patients.
OUTLINE: This is a pilot, multicenter study. Patients are stratified according to disease
stage (IA/B[E], IIA[E], IIB, or IIIA vs IIB[E], IIIA/B[E], IIIB, or IVA/B).
- Stratum 1 (stages IA/B[E], IIA[E], IIB, or IIIA): Patients receive oral prednisone on
days 1-15, vincristine IV on days 1, 8, and 15, doxorubicin hydrochloride IV over 4
hours on days 1 and 15, and etoposide IV over 2 hours on days 2-6 (OEPA). Treatment
repeats every 4 weeks for 2 courses. Beginning at week 9, patients receive VECOPA
chemotherapy comprising oral prednisone on days 1-14 and 21-34, etoposide IV over 2
hours on days 1-3, doxorubicin hydrochloride IV over 2 hours on day 21, vinblastine IV
and cyclophosphamide IV over 1 hour on days 1 and 21, and vincristine IV on days 8 and
29. Patients then undergo radiotherapy.
- Stratum 2 (stages IIB[E], IIIA/B[E], IIIB, or IVA/B): Patients receive 2 courses of OEPA
as in stratum 1 followed by 2 courses of VECOPA (6-week courses). Patients then undergo
radiotherapy.
After completion of study treatment, patients are followed periodically for at least 6 years.
PROJECTED ACCRUAL: A total of 30 patients will be accrued for this study.
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