| Literature DB >> 31101647 |
Anthony R Mato1, Lindsey E Roeker1, Toby A Eyre2, Chadi Nabhan3, Nicole Lamanna4, Brian T Hill5, Danielle M Brander6, Paul M Barr7, Frederick Lansigan8, Bruce D Cheson9, Arun K Singavi10, Maryam Sarraf Yazdy9, Nirav N Shah10, John N Allan11, Erica B Bhavsar11, Joanna Rhodes12, Kaitlin Kennard12, Stephen J Schuster12, AnnaLynn M Williams7, Alan P Skarbnik13, Andre H Goy13, Julie M Goodfriend1, Colleen Dorsey1, Catherine C Coombs14, Hande Tuncer15, Chaitra S Ujjani16, Ryan Jacobs17, Allison M Winter5, John M Pagel18, Neil Bailey18, Anna Schuh2, Mazyar Shadman16, Andrea Sitlinger6, Hanna Weissbrot4, Sivraj Muralikrishnan8, Andrew Zelenetz1, Amy A Kirkwood19, Christopher P Fox20.
Abstract
Venetoclax (VEN) is approved for relapsed/refractory (R/R) chronic lymphocytic leukemia (CLL) as monotherapy (VENmono) or in combination with rituximab. Whether VEN plus anti-CD20 (VENcombo) is superior to VENmono is unknown. We conducted a multicenter, retrospective cohort analysis comparing 321 CLL patients treated with VENmono vs VENcombo across the United States and the United Kingdom. We examined demographics, baseline characteristics, dosing, adverse events, response rates, and outcomes. The primary endpoints were progression-free survival (PFS) and overall survival (OS), estimated by Kaplan-Meier method, in patients treated with VENmono vs VENcombo. Univariate and bivariate analyses were performed with COX regression. Three hundred twenty-one CLL patients were included (3 median prior treatments, 78% prior ibrutinib). The overall response rates (ORRs) were similar (VENmono, 81% ORR, 34% complete remission [CR] vs VENcombo, 84% ORR, 32% CR). With a median follow-up of 13.4 months, no differences in PFS and OS were observed between the groups. In unadjusted analyses, the hazard ratios (HRs) for PFS and OS for VENmono vs VENcombo were HR 1.0 (95% confidence interval [CI], 0.6-1.8; P = .7) and HR 1.2 (95% CI, 0.6-2.3; P = .5), respectively. When adjusting for differences between the cohorts, the addition of an anti-CD20 antibody in combination with VEN did not impact PFS (HR, 1.0; 95% CI, 0.5-2.0; P = .9) or OS (HR, 1.1; 95% CI, 0.4-2.6; P = .8). We demonstrate comparable efficacy between VENmono and VENcombo in a heavily pretreated, high-risk, retrospective cohort, in terms of both response data and survival outcomes. Prospective studies are needed to validate these findings.Entities:
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Year: 2019 PMID: 31101647 PMCID: PMC6538868 DOI: 10.1182/bloodadvances.2019000180
Source DB: PubMed Journal: Blood Adv ISSN: 2473-9529