Overview

Rituximab Plus Fludarabine in Treating Patients With Waldenstrom's Macroglobulinemia

Status:
Completed
Trial end date:
1969-12-31
Target enrollment:
0
Participant gender:
All
Summary
RATIONALE: Monoclonal antibodies such as rituximab can locate cancer cells and either kill them or deliver cancer-killing substances to them without harming normal cells. Drugs used in chemotherapy use different way to stop cancer cells from dividing so they stop growing or die. Combining monoclonal antibody therapy with chemotherapy may kill more cancer cells. PURPOSE: Phase II trial to study the effectiveness of rituximab plus fludarabine in treating patients who have Waldenstrom's macroglobulinemia.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Jonsson Comprehensive Cancer Center
Collaborator:
National Cancer Institute (NCI)
Treatments:
Fludarabine
Fludarabine phosphate
Rituximab
Vidarabine
Criteria
DISEASE CHARACTERISTICS:

- Diagnosis of Waldenstrom's macroglobulinemia

- CD20 positive by bone marrow immunohistochemistry or flow cytometry

- Presence of monoclonal paraprotein

- IgM level at least 2 times upper limit of normal (ULN)

PATIENT CHARACTERISTICS:

Age:

- Over 18

Performance status:

- ECOG 0-2

Life expectancy:

- At least 6 months

Hematopoietic:

- Absolute neutrophil count greater than 1,000/mm^3

- Platelet count greater than 25,000/mm^3

Hepatic:

- Bilirubin less than 2.5 times ULN

- SGOT less than 2.5 times ULN

Renal:

- Creatinine less than 2.5 mg/dL

Other:

- Not pregnant or nursing

- Fertile patients must use effective contraception during and for 6 months after study

- No serious comorbid disease

- No uncontrolled bacterial, fungal, or viral infection

- No other active malignancy

PRIOR CONCURRENT THERAPY:

Biologic therapy:

- No prior rituximab

- No prior nucleoside analogue therapy

Chemotherapy:

- At least 30 days since prior chemotherapy

Endocrine therapy:

- At least 30 days since prior steroid therapy

- No concurrent corticosteroids

Radiotherapy:

- At least 30 days since prior radiotherapy

Surgery:

- Not specified

Other:

- No more than 2 prior courses of therapy