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Brief Title: Combination Chemotherapy in Treating Young Male Patients With Hodgkin's Lymphoma
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
Study ID: NCT00398554
Brief Summary: 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.
Detailed Description: 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.
Minimum Age:
Eligible Ages: CHILD, ADULT
Sex: MALE
Healthy Volunteers: No
Klinikum Augsburg, Augsburg, , Germany
Charite University Medical Center of Berlin, Berlin, , Germany
Medizinische Universitaetsklinik I at the University of Cologne, Cologne, , Germany
Universitaets - Kinderklinik, Erlangen, , Germany
Universitaetsfrauenklinik Frankfurt, Frankfurt, , Germany
Universitaetsklinikum Halle, Halle, , Germany
Medizinische Hochschule Hannover, Hannover, , Germany
Universitaets - Kinderklinik, Leipzig, , Germany
Medizinische Klinik und Poliklinik A - Universitaetsklinikum Muenster, Muenster, , Germany
Kinderklinik d. TU / Schwabing, Munich, , Germany
Klinikum Oldenburg, Oldenburg, , Germany
University Children's Hospital, Zurich, , Switzerland
Name: Dieter Koerholz, MD
Affiliation: Martin-Luther-Universität Halle-Wittenberg
Role: STUDY_CHAIR