| Literature DB >> 33856277 |
Wyndham H Wilson1, Tycel Phillips2, Leslie Popplewell3, Sven de Vos4, Saurabh Chhabra5, Amy S Kimball6, Darrin Beaupre7, Da Wei Huang1, George Wright1, Kevin Kwei8, Jerry Ping9, Jutta K Neuenburg10, Louis M Staudt11.
Abstract
Relapsed/refractory diffuse large B-cell lymphoma (DLBCL) is difficult to cure; non-germinal center B-cell-like (non-GCB) and activated B-cell-like (ABC) DLBCL have worse outcomes than GCB DLBCL. Ibrutinib and lenalidomide are synergistic in vitro in ABC DLBCL and may augment salvage chemotherapy. In part 1 of this phase 1b/2 study (NCT02142049), patients with relapsed/refractory DLBCL received ibrutinib 560 mg and escalating doses of lenalidomide on Days 1-7 with DA-EPOCH-R (Days 1-5) in 21-day cycles. In part 1 (N = 15), the maximum tolerated dose was not reached with lenalidomide 25 mg (recommended part 2 dose [RP2D]); most common grade ≥3 adverse events were anemia (73%) and febrile neutropenia (47%); the overall response rate (ORR) was 40%. At the RP2D (n = 26), ORR was 71% in non-GCB and 64% in ABC. Ibrutinib and lenalidomide with DA-EPOCH-R had a manageable safety profile and antitumor activity in relapsed/refractory DLBCL, especially the non-GCB subtype.Entities:
Keywords: Ibrutinib; activated B-cell-like; diffuse large B-cell lymphoma; dose-adjusted EPOCH-R; germinal center B-cell-like; lenalidomide
Year: 2021 PMID: 33856277 DOI: 10.1080/10428194.2021.1907371
Source DB: PubMed Journal: Leuk Lymphoma ISSN: 1026-8022