VELCADE,Rituximab,Cyclophosphamide and Decadron
Status: | Terminated |
---|---|
Conditions: | Lymphoma, Lymphoma |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - 90 |
Updated: | 9/21/2018 |
Start Date: | August 2006 |
End Date: | January 2011 |
Phase II Study Investigating the Efficacy of VELCADE®, Rituximab, Cyclophosphamide and Decadron (VRCD Regimen) in Front-line Therapy of Patients With Low-grade Non-Hodgkin's Lymphoma
Overall response rate and Time to disease progression using this regimen in patients with
low-grade B-Cell Non-Hodgkin's Lymphoma.
low-grade B-Cell Non-Hodgkin's Lymphoma.
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.
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.
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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