Non Hodgkin Lymphoma Clinical Trial
VELCADE,Rituximab,Cyclophosphamide and Decadron
Summary
Overall response rate and Time to disease progression using this regimen in patients with low-grade B-Cell Non-Hodgkin's Lymphoma.
Full Description
This is a phase II open label study that is looking at the VRCD combination regimen in patients with previously untreated low-grade Non-Hodgkin's Lymphoma. Treatment will start by combining oral dexamethasone and cyclophosphamide with intravenous VELCADE, rituximab. Chemotherapy cycles will be given as outlined below every 35-days and will continue until two cycles beyond complete remission (CR), toxicity, patient's withdrawal, disease progression, or a maximum of 8 cycles.
Eligibility Criteria
Inclusion Criteria:
Small Lymphocytic Lymphoma
Follicular Cell Lymphoma (grades I and II)
Mantle Cell Lymphoma patients that are not considered eligible for high-dose therapy and stem cell transplant
Lymphoplasmacytic lymphoma including Waldenstrom's Macroglobulinemia
Marginal Zone Lymphoma
MALT Lymphoma that has ONLY failed antibiotic therapy or involved field radiation.
Adequate bone marrow function, renal function, and hepatic function as outlined in details below.
ECOG performance status of 0, 1, or 2
Able to read, understand, and sign an IRB approved informed consent
Exclusion Criteria:
Known HIV positive status
Known CNS involvement
Prior therapy for lymphoma EXCLUDING antibiotic treatment for MALT-Type NHL.
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There are 2 Locations for this study
Niles Illinois, 60714, United States
Park Ridge Illinois, 60068, United States
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