About this trial
This randomized phase I/II trial studies the best dose and side effects of durvalumab and to see how well it works with or without lenalidomide in treating patients with cutaneous or peripheral T cell lymphoma that has come back and does not respond to treatment. Monoclonal antibodies, such as durvalumab, may interfere with the ability of cancer cells to grow and spread. Drugs used in chemotherapy, such as lenalidomide, work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving durvalumab and lenalidomide may work better in treating patients with cutaneous or peripheral T cell lymphoma.
Eligibility criteria
Qualifiers
Documented informed consent of the participant and/or legally authorized representative
Registered into Revlimid REMS program
Eastern Cooperative Oncology Group (ECOG) performance status of 0-2
Fully recovered from acute toxicities (except alopecia) of all prior therapies to Common Terminology Criteria for Adverse Events (CTCAE) =< grade 1
Disqualifiers
Immunotherapy with immune checkpoint inhibitors, cell-based therapies, or cancer vaccines
Lenalidomide, thalidomide or other immunomodulatory drugs (IMiDs)
Monoclonal antibody within 5 half-lives of the antibody prior to initiating protocol therapy
Any systemic therapy, including monoclonal antibody within 28 days or 5 half-lives (whichever is shorter) of initiating protocol therapy
Trial design
Treatments tested in this trial
- Durvalumab
- Laboratory Biomarker Analysis
- Lenalidomide
Treatment groups
Sponsors and collaborators
City of Hope Medical Center
Lead sponsor
National Cancer Institute (NCI)
Collaborator