Non Hodgkin Lymphoma Clinical Trial

A Study to Evaluate Lenalidomide Combined With Dexamethasone in Relapsed or Refractory Diffuse Large B-Cell Lymphoma

Summary

To evaluate the safety and efficacy of lenalidomide (Revlimid ®) in combination with dexamethasone in subjects with relapsed or refractory diffuse large B-cell lymphoma.

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Full Description

Non-Hodgkin's lymphoma (NHL) can be divided into two general prognostic groups: the indolent lymphomas and the aggressive lymphomas. Indolent lymphomas have a relatively good prognosis, with median survival time as long as 10 years, but they are not usually curable in advanced stages. Aggressive NHL constitutes about half of all cases of NHL in North America and Western Europe. Of the aggressive lymphomas, diffuse large B-cell lymphoma (DLBCL) is the most common type, accounting for up to 30 percent of newly diagnosed cases. The aggressive type of NHL has a shorter natural history; approximately 50-60% of these subjects can be cured with combination chemotherapy regimens. Even with recent advances, many patients with advanced stage DLBCL are not cured with conventional therapy. This leaves a subset of subjects who will eventually relapse or who are refractory to treatment.

Due to the variation in the clinical behavior of the different types of aggressive NHL, it is important to test lenalidomide in DLBCL. Other studies are addressing the activity of lenalidomide in the other types of aggressive lymphomas, as well as in indolent NHL. It is important to test lenalidomide in combination therapy. This study is focused on treating subjects with relapsed or refractory DLBCL using oral lenalidomide in combination with oral dexamethasone.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Biopsy-proven diffuse large B-cell non-Hodgkin's lymphoma
Relapsed or refractory to previous therapy for non-Hodgkin's lymphoma
Measurable disease on cross sectional imaging that is at least 2 cm in the longest diameter
ECOG performance score of 0,1 or 2
Willing to follow the pregnancy precautions

Exclusion Criteria:

Any of the following laboratory abnormalities.
Absolute neutrophil count (ANC) < 1,500 cells/mm3 (1.5 x 109/L).
Platelet count < 60,000/mm3 (60 x 109/L).
Serum SGOT/AST or SGPT/ALT 5.0 x upper limit of normal (ULN).
Serum total bilirubin > 2.0 mg/dL (34 µmol/L).
Subjects who are candidates for and willing to undergo an autologous stem cell transplant.
History of active CNS lymphoma within the previous 3 months
Subjects not willing or unable to take DVT prophylaxis
History of other malignancies within the past year
Positive HIV or active Hepatitis B or C

Study is for people with:

Non Hodgkin Lymphoma

Phase:

Phase 2

Estimated Enrollment:

26

Study ID:

NCT00474188

Recruitment Status:

Terminated

Sponsor:

Celgene Corporation

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There are 23 Locations for this study

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Palo Verde Hematology/Oncology, Ltd.
Glendale Arizona, 85304, United States
Tower Cancer Research Foundation
Beverly Hills California, 90211, United States
Advanced Medical Specialties
Miami Florida, 33176, United States
Hematology/Oncology Associates of Treasure Coast
Port St. Lucie Florida, 34952, United States
Northwest Georgia Oncology Centers
Marietta Georgia, 30060, United States
Cancer Care & Hematology Specialists of Chicagoland
Arlington Heights Illinois, 60005, United States
Northwestern University, Feinberg School of Medicine
Chicago Illinois, 60611, United States
Rush University Medical Center
Chicago Illinois, 60612, United States
University of Kentucky
Lexington Kentucky, 40536, United States
Southwest Oncology Associates
Lafayette Louisiana, 70503, United States
Washington County Hospital, The Center for Clinical Research
Hagerstown Maryland, 21742, United States
Kalamazoo Hematology & Oncology
Kalamazoo Michigan, 49048, United States
Oncology & Hematology Specialists, PA
Denville New Jersey, 07834, United States
Hackensack University Medical Center
Hackensack New Jersey, 07601, United States
Northwestern Carolina, Oncology and Hematology PA
Hickory North Carolina, 28602, United States
New Bern Cancer Care
New Bern North Carolina, 28562, United States
James Cancer Hospital
Columbus Ohio, 43210, United States
SouthWest Regional Cancer Center
Austin Texas, 78705, United States
Northern Utah Associates
Ogden Utah, 84403, United States
The Alfred Hospital
Melbourne Victoria, VIC30, Australia
Frankston Hospital
Frankston , VIC 3, Australia
HOCA
South Brisbane , QLD 4, Australia
Border Medical Oncology
Wodonga , VIC 3, Australia
Cross Cancer Institute
Edmonton Alberta, T6G 1, Canada

How clear is this clinincal trial information?

Study is for people with:

Non Hodgkin Lymphoma

Phase:

Phase 2

Estimated Enrollment:

26

Study ID:

NCT00474188

Recruitment Status:

Terminated

Sponsor:


Celgene Corporation

How clear is this clinincal trial information?

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