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Leuk Lymphoma ; 64(14): 2225-2235, 2023 Dec.
Article in English | MEDLINE | ID: mdl-37740588

ABSTRACT

Mantle cell lymphoma (MCL) is a rare non-Hodgkin lymphoma that frequently becomes chemoresistant over time. The distinct mechanisms of ibrutinib and lenalidomide provided a judicious rationale to explore the combination with anti-CD20 immunotherapy. In this phase 1b study (NCT02446236), patients (n = 25) with relapsed/refractory MCL received rituximab with escalating doses of lenalidomide (days 1-21) and ibrutinib 560 mg (days 1-28) of 28-day cycles. The MTD for lenalidomide was 20 mg; most common grade ≥3 adverse events were skin rashes (32%) and neutropenic fever (24%). The best ORR was 88%, CR rate was 83%, and median duration of response (DOR) was 36.92 months (95% CI 33.77, 51.37). Responses were seen even in refractory patients or with high-risk features (e.g. blastoid variant, TP53 mutation, Ki-67 > 30%). R2I was safe and tolerable in patients with R/R MCL.


Subject(s)
Lenalidomide , Lymphoma, Mantle-Cell , Piperidines , Rituximab , Adult , Humans , Antineoplastic Combined Chemotherapy Protocols/adverse effects , Lenalidomide/administration & dosage , Lenalidomide/adverse effects , Lymphoma, Mantle-Cell/drug therapy , Lymphoma, Mantle-Cell/pathology , Piperidines/administration & dosage , Piperidines/adverse effects , Piperidines/therapeutic use , Rituximab/administration & dosage , Rituximab/adverse effects , Treatment Outcome , Dose-Response Relationship, Drug , Recurrence
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