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

No results posted yet for this study

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

filgrastim

BIOLOGICAL

pegfilgrastim

DRUG

ABVD regimen

DRUG

BEACOPP regimen

DRUG

dacarbazine

DRUG

doxorubicin hydrochloride

DRUG

etoposide

DRUG

prednisone

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

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00049595 on ClinicalTrials.gov