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Spots Global Cancer Trial Database for Combination Chemotherapy in Treating Young Male Patients With Hodgkin's Lymphoma

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Trial Identification

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

Conditions

Lymphoma

Study Description

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.

Eligibility

Minimum Age:

Eligible Ages: CHILD, ADULT

Sex: MALE

Healthy Volunteers: No

Locations

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

Contact Details

Name: Dieter Koerholz, MD

Affiliation: Martin-Luther-Universität Halle-Wittenberg

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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