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Brief Title: A Study to Evaluate Lenalidomide Combined With Dexamethasone in Relapsed or Refractory Diffuse Large B-Cell Lymphoma
Official Title: A Phase II, Multicenter, Single-Arm, Open-Label Study to Evaluate the Safety and Efficacy of Lenalidomide (Revlimid ®) in Combination With Dexamethasone in Subjects With Relapsed or Refractory Diffuse Large B-Cell Lymphoma
Study ID: NCT00474188
Brief 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.
Detailed 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.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Palo Verde Hematology/Oncology, Ltd., Glendale, Arizona, United States
Tower Cancer Research Foundation, Beverly Hills, California, United States
Advanced Medical Specialties, Miami, Florida, United States
Hematology/Oncology Associates of Treasure Coast, Port St. Lucie, Florida, United States
Northwest Georgia Oncology Centers, Marietta, Georgia, United States
Cancer Care & Hematology Specialists of Chicagoland, Arlington Heights, Illinois, United States
Northwestern University, Feinberg School of Medicine, Chicago, Illinois, United States
Rush University Medical Center, Chicago, Illinois, United States
University of Kentucky, Lexington, Kentucky, United States
Southwest Oncology Associates, Lafayette, Louisiana, United States
Washington County Hospital, The Center for Clinical Research, Hagerstown, Maryland, United States
Kalamazoo Hematology & Oncology, Kalamazoo, Michigan, United States
Oncology & Hematology Specialists, PA, Denville, New Jersey, United States
Hackensack University Medical Center, Hackensack, New Jersey, United States
Northwestern Carolina, Oncology and Hematology PA, Hickory, North Carolina, United States
New Bern Cancer Care, New Bern, North Carolina, United States
James Cancer Hospital, Columbus, Ohio, United States
SouthWest Regional Cancer Center, Austin, Texas, United States
Northern Utah Associates, Ogden, Utah, United States
The Alfred Hospital, Melbourne, Victoria, Australia
Frankston Hospital, Frankston, , Australia
HOCA, South Brisbane, , Australia
Border Medical Oncology, Wodonga, , Australia
Cross Cancer Institute, Edmonton, Alberta, Canada
Name: Andrew Spencer, MD
Affiliation: The Alfred
Role: PRINCIPAL_INVESTIGATOR