دورية أكاديمية

Phase 1b dose-finding study of rituximab, lenalidomide, and ibrutinib (R2I) in patients with relapsed/refractory mantle cell lymphoma.

التفاصيل البيبلوغرافية
العنوان: Phase 1b dose-finding study of rituximab, lenalidomide, and ibrutinib (R2I) in patients with relapsed/refractory mantle cell lymphoma.
المؤلفون: Ip, Andrew, Petrillo, Alessandra, Pia, Alexandra Della, Lee, Geeny G., Gill, Sarvarinder, Varughese, Tony, Zenreich, Joshua, Gutierrez, Martin, Zhang, Jiayu, Ahn, Jaeil, Bharani, Vishnu, Nejad, Ava S., Pascual, Lauren, Feldman, Tatyana A., Leslie, Lori A., Goy, Andre H.
المصدر: Leukemia & Lymphoma; Dec2023, Vol. 64 Issue 14, p2225-2235, 11p
مصطلحات موضوعية: LENALIDOMIDE, RITUXIMAB, NON-Hodgkin's lymphoma, EXANTHEMA
مستخلص: 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 560mg (days 1–28) of 28-day cycles. The MTD for lenalidomide was 20mg; 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 36.92months (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. [ABSTRACT FROM AUTHOR]
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قاعدة البيانات: Complementary Index
الوصف
تدمد:10428194
DOI:10.1080/10428194.2023.2259528