| Literature DB >> 34739844 |
Wyndham H Wilson1, George W Wright2, Da Wei Huang1, Brendan Hodkinson3, Sriram Balasubramanian3, Yue Fan3, Jessica Vermeulen3, Martin Shreeve3, Louis M Staudt4.
Abstract
In diffuse large B cell lymphoma (DLBCL), tumors belonging to the ABC but not GCB gene expression subgroup rely upon chronic active B cell receptor signaling for viability, a dependency that is targetable by ibrutinib. A phase III trial ("Phoenix;" ClinicalTrials.gov: NCT01855750) showed a survival benefit of ibrutinib addition to R-CHOP chemotherapy in younger patients with non-GCB DLBCL, but the molecular basis for this benefit was unclear. Analysis of biopsies from Phoenix trial patients revealed three previously characterized genetic subtypes of DLBCL: MCD, BN2, and N1. The 3-year event-free survival of younger patients (age ≤60 years) treated with ibrutinib plus R-CHOP was 100% in the MCD and N1 subtypes while the survival of patients with these subtypes treated with R-CHOP alone was significantly inferior (42.9% and 50%, respectively). This work provides a mechanistic understanding of the benefit of ibrutinib addition to chemotherapy, supporting its use in younger patients with non-GCB DLBCL. Published by Elsevier Inc.Entities:
Keywords: ABC DLBCL; BTK inhibitor; CD79B; MYD88; NOTCH1; cancer genomics; memory B cell; precision medicine
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Year: 2021 PMID: 34739844 PMCID: PMC8722194 DOI: 10.1016/j.ccell.2021.10.006
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743