Overview

S0019 Combination Chemotherapy With or Without Rituximab in Treating Patients With Relapsed or Refractory Non-Hodgkin's Lymphoma

Status:
Terminated
Trial end date:
2006-11-01
Target enrollment:
0
Participant gender:
All
Summary
RATIONALE: Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die. Monoclonal antibodies such as rituximab can locate cancer cells and either kill them or deliver cancer-killing substances to them without harming normal cells. It is not yet known whether combination chemotherapy is more effective with or without rituximab for non-Hodgkin's lymphoma. PURPOSE: Randomized phase III trial to compare the effectiveness of combination chemotherapy with or without rituximab in treating patients who have relapsed or refractory non-Hodgkin's lymphoma.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Southwest Oncology Group
Collaborator:
National Cancer Institute (NCI)
Treatments:
Carboplatin
Etoposide
Etoposide phosphate
Ifosfamide
Isophosphamide mustard
Lenograstim
Rituximab
Criteria
DISEASE CHARACTERISTICS: Histologically proven aggressive B-cell non-Hodgkin's lymphoma
that has failed prior combination chemotherapy with an anthracycline-containing regimen
Eligible histologies: Diffuse large cell Small non-cleaved cell/Burkitt's lymphoma No
lymphoblastic or mantle cell lymphoma First relapse or primary refractory disease
Ineligible for or refused treatment with salvage chemotherapy followed by high-dose therapy
and autologous stem cell rescue Documented CD20 antigen expression Measurable disease No
clinical evidence of CNS involvement by lymphoma

PATIENT CHARACTERISTICS: Age: Over 18 Performance status: Zubrod 0-2 Life expectancy: Not
specified Hematopoietic: Not specified Hepatic: Bilirubin no greater than 2 times upper
limit of normal Renal: Creatinine no greater than 1.5 mg/dL OR Creatinine clearance greater
than 60 mL/min Other: HIV negative Not pregnant or nursing Fertile patients must use
effective contraception No other malignancy within the past 5 years except adequately
treated basal cell or squamous cell skin cancer or carcinoma in situ of the cervix

PRIOR CONCURRENT THERAPY: Biologic therapy: See Disease Characteristics No prior rituximab
Chemotherapy: See Disease Characteristics Endocrine therapy: Not specified Radiotherapy:
Not specified Surgery: Not specified Other: Recovered from toxic effects of all prior
therapy No other concurrent therapy unless disease progression occurs