A multicenter study of venetoclax-based treatment for patients with Richter transformation of chronic lymphocytic leukemia

Author:

Hampel Paul J.1ORCID,Swaminathan Mahesh2,Rogers Kerry A.3,Parry Erin M.4ORCID,Burger Jan A.2ORCID,Davids Matthew S.4,Ding Wei1,Ferrajoli Alessandra2,Hyak Jonathan M.3ORCID,Jain Nitin2,Kenderian Saad S.1,Wang Yucai1ORCID,Wierda William G.2,Woyach Jennifer A.3,Parikh Sameer A.1ORCID,Thompson Philip A.2ORCID

Affiliation:

1. 1Division of Hematology, Department of Medicine, Mayo Clinic, Rochester, MN

2. 2Department of Leukemia, The University of Texas M.D. Anderson Cancer Center, Houston, TX

3. 3Division of Hematology, The Ohio State University, Columbus, OH

4. 4Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA

Abstract

Abstract Patients with chronic lymphocytic leukemia (CLL) who develop Richter transformation (RT) have a poor prognosis when treated with chemoimmunotherapy regimens used for de novo diffuse large B-cell lymphoma. Venetoclax, a BCL2 inhibitor, has single-agent efficacy in patients with RT and is potentially synergistic with chemoimmunotherapy. In this multicenter, retrospective study, we evaluated 62 patients with RT who received venetoclax-based treatment outside of a clinical trial, in combination with a Bruton tyrosine kinase inhibitor (BTKi; n=28), rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone (R-CHOP) (n=13), or intensive chemoimmunotherapy other than R-CHOP (n=21). The best overall and complete response rates were 36%/25%, 54%/46%, and 52%/38%, respectively. The median progression-free and overall survival estimates for the same treatment groups were 4.9/14.3 months, 14.9 months/not reached, and 3.3/9 months, respectively. CLL with del(17p) was associated with a lower complete response rate in the total cohort (odds ratio [OR] 0.15; 95% confidence interval [CI] 0.04-0.6; p=0.01) and venetoclax-naïve subgroup (OR 0.13; 95%CI 0.02-0.66; p=0.01). TP53 mutated CLL was associated with a lower complete response rate (OR 0.15; 95%CI 0.03-0.74; p=0.02) and shorter progression-free survival (hazard ratio 3.1; 95%CI 1.21-7.95; p=0.02) only in venetoclax-naïve subgroup. No other clinical or baseline characteristics, including prior venetoclax treatment for CLL, showed statistically significant association with outcomes. Grade 3-4 neutropenia and thrombocytopenia events were most frequent with intensive chemoimmunotherapy + venetoclax; grade 3-4 infection rates were similar across treatment groups. In this difficult-to-treat RT patient population, venetoclax-based combination regimens achieved high response rates, with durable remission and survival observed in a subset of patients.

Publisher

American Society of Hematology

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