Annals of Hematology· 2026Q2
Relapsed/refractory WAldenström macroglobulinemia patients treated by VEnetoclax with or without anti-CD20 antibody: WAVE a retrospective study of the French CLL/WM group (FILO)
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- 2026year
Short summary
Adding anti-CD20 antibody to venetoclax in relapsed/refractory Waldenström macroglobulinemia (WM) patients (n=46) significantly increased deep response rates (56% vs. 24%) and was the only factor associated with deep response in multivariate analysis.
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Key points
- Adding anti-CD20 antibody to venetoclax in R/R WM patients resulted in a 56% deep response rate versus 24% for venetoclax alone (p=0.03).
- Anti-CD20 therapy was the only factor independently associated with deep response rate in multivariate analysis (HR 4.07, p=0.03).
- 2-year PFS was 78% with Ven+anti-CD20 vs. 54% with Ven monotherapy (p=0.25).
- Grade >= 3 adverse events occurred in 68% of patients on Ven+anti-CD20 vs. 33% on Ven monotherapy (p=0.02).
AI-generated from the title and abstract; the full text is not read.
Abstract
Abstract Recently venetoclax (Ven) monotherapy showed promising efficacy for relapsed/refractory (R/R) Waldenström macroglobulinemia (WM), a population with significant medical unmet need. We report the efficacy and safety of Ven associated or not with anti-CD20 therapy, in a real-word cohort of 46 patients with R/R WM treated at 17 French hospitals. The median number of prior lines of treatment was 3, including BTK inhibitor in 89%. Twenty-five patients (54%) received a combination of Ven + anti-CD20. At the time of best response, patients treated with Ven + anti-CD20 had a deep response rate (VGPR + uncertain CR) of 56% vs. 24% with Ven monotherapy ( p = 0.03). Anti-CD20 was the only factor associated with deep response rate in multivariate analysis (hazard ratio 4.07, p = 0.03). The 2-year PFS was 78% (95% CI, 54–90) for patients treated with Ven + anti-CD20 vs. 54% (95% CI, 27–74) with Ven monotherapy ( p = 0.25). AEs of grade ≥ 3 occurred in 17 patients (68%) with Ven + anti-CD20, vs. 7 patients (33%) with Ven ( p = 0.02), including 3 febrile aplasia ( p = 0.24). This is the first report of Ven +/- anti-CD20 in R/R WM, a strategy associated with deep responses and promising PFS, warranting further evaluation in prospective studies.
The authors' abstract, as published at the source. Annals of Hematology, 2026 · DOI ↗
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Field: Genetics (Medicine)
GeneticsMedicine