SWOG-9704 Chemoradiotherapy and Peripheral Stem Cell Transplantation Compared With Combination Chemotherapy in Treating Patients With Non-Hodgkin's Lymphoma
NCT00004031 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 397
Last updated 2021-02-02
Summary
RATIONALE: Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die. Radiation therapy uses high-energy x-rays to damage cancer cells. Peripheral stem cell transplantation may allow the doctor to give higher doses of chemotherapy and radiation and kill more cancer cells. It is not yet known whether chemoradiotherapy plus peripheral stem cell transplantation is more effective than combination chemotherapy alone in treating non-Hodgkin's lymphoma.
PURPOSE: This randomized phase III trial is studying chemoradiotherapy and peripheral stem cell transplantation to see how well they work compared to combination chemotherapy in treating patients with stage II, stage III, or stage IV non-Hodgkin's lymphoma.
Conditions
Interventions
- BIOLOGICAL
-
375 mg/m2 IV every 21 days
- DRUG
-
CHOP regimen
- DRUG
-
carmustine
- DRUG
- DRUG
-
doxorubicin hydrochloride
- DRUG
-
etoposide
- DRUG
- DRUG
-
vincristine sulfate
- PROCEDURE
-
bone marrow ablation with stem cell support
- PROCEDURE
-
peripheral blood stem cell transplantation
- RADIATION
-
radiation therapy
Sponsors & Collaborators
-
National Cancer Institute (NCI)
collaborator NIH -
Cancer and Leukemia Group B
collaborator NETWORK -
Eastern Cooperative Oncology Group
collaborator NETWORK -
NCIC Clinical Trials Group
collaborator NETWORK -
SWOG Cancer Research Network
lead NETWORK
Principal Investigators
-
Patrick J. Stiff, MD · Loyola University
-
Thomas C. Shea, MD · UNC Lineberger Comprehensive Cancer Center
-
David P. Schenkein, MD · Tufts Medical Center Cancer Center
-
Stephen Couban, MD · Cancer Care Nova Scotia
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 15 Years
- Max Age
- 65 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 1997-07-31
- Primary Completion
- 2008-06-01
- Completion
- 2013-10-31
Countries
- United States
- Canada
Study Locations
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