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Rituximab in Treating Patients With Non-Hodgkin's Lymphoma or Hodgkin's Disease

Phase 2
Completed
Conditions
Lymphoma
Interventions
Biological: rituximab
Registration Number
NCT00003849
Lead Sponsor
Alliance for Clinical Trials in Oncology
Brief Summary

RATIONALE: Monoclonal antibodies can locate cancer cells and either kill them or deliver cancer-killing substances to them.

PURPOSE: Phase II trial to study the effectiveness of rituximab in treating patients who have non-Hodgkin's lymphoma or Hodgkin's disease.

Detailed Description

OBJECTIVES: I. Determine the response rate (complete or partial) to rituximab in previously untreated patients with stage III or IV CD20+ B-cell follicular small cleaved cell non-Hodgkin's lymphoma. II. Determine the response rate (complete or partial) to rituximab in patients with relapsed CD20+ Hodgkin's disease. III. Determine the time to progression and time to chemotherapy in these patients after treatment with rituximab.

OUTLINE: Patients are stratified according to disease (follicular small cleaved cell non-Hodgkin's lymphoma vs relapsed Hodgkin's disease). Patients receive rituximab IV over 4-6 hours on day 1 weekly for 4 weeks. Patients are followed at 1, 3, 6, 9, and 12 months, then every 6 months for 3 years, then annually thereafter.

PROJECTED ACCRUAL: A total of 21-32 patients will be accrued for each arm of this study within 7-10.5 months.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
39
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
rituximabrituximabPatients receive rituximab IV over 4-6 hours on day 1 weekly for 4 weeks. Patients are followed at 1, 3, 6, 9, and 12 months, then every 6 months for 3 years, then annually thereafter.
Primary Outcome Measures
NameTimeMethod
response rateUp to 5 years
Secondary Outcome Measures
NameTimeMethod
time to progressionUp to 5 years

Trial Locations

Locations (21)

Siouxland Hematology-Oncology

πŸ‡ΊπŸ‡Έ

Sioux City, Iowa, United States

CentraCare Clinic

πŸ‡ΊπŸ‡Έ

Saint Cloud, Minnesota, United States

CCOP - Scottsdale Oncology Program

πŸ‡ΊπŸ‡Έ

Scottsdale, Arizona, United States

CCOP - Illinois Oncology Research Association

πŸ‡ΊπŸ‡Έ

Peoria, Illinois, United States

CCOP - Cedar Rapids Oncology Project

πŸ‡ΊπŸ‡Έ

Cedar Rapids, Iowa, United States

CCOP - Iowa Oncology Research Association

πŸ‡ΊπŸ‡Έ

Des Moines, Iowa, United States

CCOP - Wichita

πŸ‡ΊπŸ‡Έ

Wichita, Kansas, United States

CCOP - Duluth

πŸ‡ΊπŸ‡Έ

Duluth, Minnesota, United States

CCOP - Metro-Minnesota

πŸ‡ΊπŸ‡Έ

Saint Louis Park, Minnesota, United States

Quain & Ramstad Clinic, P.C.

πŸ‡ΊπŸ‡Έ

Bismarck, North Dakota, United States

CCOP - Merit Care Hospital

πŸ‡ΊπŸ‡Έ

Fargo, North Dakota, United States

Altru Health Systems

πŸ‡ΊπŸ‡Έ

Grand Forks, North Dakota, United States

CCOP - Toledo Community Hospital Oncology Program

πŸ‡ΊπŸ‡Έ

Toledo, Ohio, United States

Rapid City Regional Hospital

πŸ‡ΊπŸ‡Έ

Rapid City, South Dakota, United States

CCOP - Sioux Community Cancer Consortium

πŸ‡ΊπŸ‡Έ

Sioux Falls, South Dakota, United States

Saskatchewan Cancer Agency

πŸ‡¨πŸ‡¦

Regina, Saskatchewan, Canada

CCOP - Carle Cancer Center

πŸ‡ΊπŸ‡Έ

Urbana, Illinois, United States

CCOP - Ochsner

πŸ‡ΊπŸ‡Έ

New Orleans, Louisiana, United States

CCOP - Ann Arbor Regional

πŸ‡ΊπŸ‡Έ

Ann Arbor, Michigan, United States

Mayo Clinic Cancer Center

πŸ‡ΊπŸ‡Έ

Rochester, Minnesota, United States

CCOP - Missouri Valley Cancer Consortium

πŸ‡ΊπŸ‡Έ

Omaha, Nebraska, United States

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