A Phase 1 Study of Lenalidomide in Combination with EPOCH Chemotherapy for HTLV-Associated Adult T-Cell Leukemia-Lymphoma (ATLL)
Study of Lenalidomide in Combination with Chemotherapy in Patients with HTLV-Associated Adult T-Cell Leukemia-Lymphoma (ATLL)
Sponsor: National Cancer Institute
Enrolling: Male and Female Patients
IRB Number: AAAT9880
U.S. Govt. ID: NCT04301076
Contact: Research Nurse Navigator: 212-342-5162 / cancerclinicaltrials@cumc.columbia.edu
Additional Study Information: This study is being done to determine if a study drug called lenalidomide can be combined with full doses of EPOCH chemotherapy for patients with Adult T-Cell Leukemia-Lymphoma (ATLL), and to define the highest dose and longest duration of lenalidomide that can be given safely in combination with EPOCH. EPOCH chemotherapy is a combination of five chemotherapy drugs that are given over five days: etoposide, prednisone, vincristine, cyclophosphamide, and doxorubicin and has been approved by the FDA for use in patients with ATLL. The study drug, lenalidomide, in combination with EPOCH has not been approved by the FDA for any cancer. This is the first time all of these drugs will be tested together in patients with HTLV associated adult T-cell leukemia-lymphoma (ATLL). The study doctors want to find out if this approach is better or worse than the usual approach for patients with HTLV-associated adult T-cell leukemia-lymphoma. The usual approach is defined as care most people get for HTLV-associated adult T-cell leukemia-lymphoma.
Investigator
Jennifer Amengual, MD
Do You Qualify?
Are you at least 18 years old? Yes No
Have you been diagnosed with HTLV-Associated Adult T-Cell Leukemia-Lymphoma (ATLL)? Yes No
Are you able to make regularly scheduled visits to the clinic for treatment and examinations? Yes No
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For more information, please contact:
Research Nurse Navigator
cancerclinicaltrials@cumc.columbia.edu
212-342-5162