Expired Study
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New York, New York 10021


Primary Objective: Evaluate the clinical activity of the RT-PEPC combination regimen (rituximab, thalidomide, and prednisone, etoposide, procarbazine, cyclophosphamide) in patients with relapsed mantle cell lymphoma. Specifically, response rate (RR) and time to disease progression (TTP) will be assessed. Secondary Objectives: 1. Assess the toxicity profiles of RT-PEPC treatment in patients with relapsed mantle cell lymphoma. 2. Prospectively characterize the angiogenic profile of patients with mantle cell lymphoma during treatment with RT-PEPC. The dynamics of the angiogenic profile will be correlated with clinical response to RT-PEPC therapy. 3. Assess the quality of life of patients receiving RT-PEPC treatment


Inclusion Criteria: - Histologically confirmed diagnosis of mantle cell Non-Hodgkin's Lymphoma with characteristic immunophenotypic profiles: CD5(+),CD23(-), CD19(+) or CD20(+), cyclin D1(+), and CD10(-) - Patient has persistent / recurrent disease after standard chemotherapy - Patient has not received either standard or investigational drugs within the last 3 weeks - Available frozen tumor tissue obtained since completion of last prior therapy (rebiopsy if needed) - Patient has measurable disease as defined by a tumor mass > 1.5 cm in one dimension - Age > 18 years - Absolute granulocyte count > 1000 cells/mm3 - Platelet count > 50,000 cells/mm3 - Creatinine < 2.0 x ULN - Total bilirubin < 2.0 x ULN - Patient has KPS > 50% - Patient agrees to use birth control if of reproductive potential Exclusion Criteria: - Known central nervous system (CNS) involvement by lymphoma - Known HIV disease - Known peripheral neuropathy > grade 2 - Patient is pregnant or nursing - Patient has had major surgery within the last 3 weeks - Patient is receiving other investigational drugs



Primary Contact:

Principal Investigator
John P Leonard, MD
Weill Medical College of Cornell University

Backup Contact:


Location Contact:

New York, New York 10021
United States

There is no listed contact information for this specific location.

Site Status: N/A

Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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