Comparison of Two Combination Chemotherapy Regimens in Treating Patients With Stage III or Stage IV Hodgkin's Lymphoma
NCT00049595 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 552
Last updated 2025-08-05
Summary
RATIONALE: Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die. Combining more than one drug may kill more cancer cells. It is not yet known which combination chemotherapy regimen is more effective in treating stage III or stage IV Hodgkin's lymphoma.
PURPOSE: Randomized phase III trial to compare the effectiveness of two combination chemotherapy regimens in treating patients who have stage III or stage IV Hodgkin's lymphoma.
Conditions
Interventions
- BIOLOGICAL
-
bleomycin sulfate
- BIOLOGICAL
- BIOLOGICAL
- DRUG
-
ABVD regimen
- DRUG
-
BEACOPP regimen
- DRUG
- DRUG
-
dacarbazine
- DRUG
-
doxorubicin hydrochloride
- DRUG
-
etoposide
- DRUG
- DRUG
-
procarbazine hydrochloride
- DRUG
-
vinblastine sulfate
- DRUG
-
vincristine sulfate
Sponsors & Collaborators
-
Lymphoma Trials Office
collaborator OTHER -
Lymphoma Study Association
collaborator OTHER -
Grup per l'Estudi dels Limfomes de Catalunya i Balears
collaborator OTHER -
NCIC Clinical Trials Group
collaborator NETWORK -
Australasian Leukaemia and Lymphoma Group
collaborator OTHER -
Nordic Lymphoma Group
collaborator NETWORK -
European Organisation for Research and Treatment of Cancer - EORTC
lead NETWORK
Principal Investigators
-
Patrice P. Carde, MD · Gustave Roussy, Cancer Campus, Grand Paris
-
David C. Linch · Middlesex Hospital
-
Marine Divine, MD · Centre Hospitalier Universitaire Henri Mondor
-
Anna Sureda · Hospital de la Santa Cruz i Sant Pau
-
Ralph M. Meyer, MD, FRCPC · Margaret and Charles Juravinski Cancer Centre
-
David Ma, MD · St Vincent's Hospital
-
Devinder Gill, MD · Princess Alexandra Hospital
-
Bengt Glimelius, MD · Uppsala University Hospital
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 16 Years
- Max Age
- 60 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2002-08-31
- Primary Completion
- 2010-01-31
Countries
- Australia
- Belgium
- Canada
- Croatia
- Czechia
- France
- Hungary
- Netherlands
- New Zealand
- Poland
- Spain
- Sweden
- United Kingdom
Study Locations
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