Overview

A Study of MabThera/Rituxan (Rituximab) Alone and in Combination With Roferon-A in Patients With Follicular or Other CD20+ Low-Grade (Indolent) Lymphoma

Status:
Completed
Trial end date:
2011-07-01
Target enrollment:
0
Participant gender:
All
Summary
This randomized, open-label study will compare the efficacy and safety of MabThera/Rituxan (rituximab) alone, and in combination with Roferon-A (interferon alfa-2a) in patients with follicular or other CD20+ low-grade lymphoma. Patients will be randomized to receive either MabThera/Rituxan 375 mg/m2 intravenously weekly for 4 weeks or Roferon-A 3 MIU/day subcutaneously in Week 1 followed by 4.5 MIU/day sc in Weeks 2-5 plus MabThera/Rituxan 375 mg/m2 weekly iv in Weeks 3-6. Patients who have a response will receive an additional cycle of treatment. The anticipated time on study treatment is up to 6 months.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Hoffmann-La Roche
Collaborator:
Nordic Lymphoma Group
Treatments:
Interferon alpha-2
Interferon-alpha
Interferons
Rituximab
Criteria
Inclusion Criteria:

- Adult patients >18 years of age

- CD20+ low-grade (indolent) lymphoma of follicular and marginal zone type, small
lymphocytic lymphoma without a B-CLL phenotype, or indolent lymphoma not otherwise
specified

- Stage II (with bulky disease), III, or IV lymphoma

- No previous chemotherapy or a maximum of 6 months chlorambucil or cyclophosphamide

- Indication for treatment: symptomatic enlarged lymph nodes, spleen or other lymphoma
manifestations, progression >6 months of lymphadenopathy or splenomegaly, anemia or
thrombocytopenia or decreased hemoglobin or platelets due to lymphoma, general
symptoms (weight loss, night sweats or fever)

- WHO performance status 0-2

Exclusion Criteria:

- Prior treatment with rituximab or an interferon

- B-CLL, mantle cell lymphoma, lymphoplasmacytic lymphoma (Waldenstroem's disease), or
central nervous system lymphoma

- Indolent lymphoma transformed into aggressive lymphoma

- Indolent lymphoma with bulky tumor requiring urgent therapy

- Prior malignancies, except non-melanoma skin tumors, in situ cervical cancer, or
curative surgery >5 years ago

- Positive for HIV infection

- Uncontrolled asthma or allergy requiring corticosteroids