Real-world clinical outcomes in patients with CLL previously treated with covalent BTKi and BCL2i regimens

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Authors: Jennifer Prescott, Christina M. Parrinello, Ahmed Sawas, Enrico De Nigris, Jing Yang, Erik W. Bloomquist, Indu Shrivastava, Changxia Shao, Xinyue Liu, Mohammed Z.H. Farooqui, Sameer Ashok Parikh
Cited by: 1
References: 24

Abstract

Patients with chronic lymphocytic leukemia (CLL) who are double-exposed (DE) or double-refractory (DR) to covalent Bruton tyrosine kinase inhibitors (cBTKi) and B-cell lymphoma 2 inhibitors (BCL2i) have limited treatment options and poor outcomes. We evaluated real-world treatment patterns, response, and time-to-event (TTE) outcomes in patients with DE CLL (N = 264), and among the DE-only (ie, DE but not DR; n =157) and DR (n = 107) subcohorts, using the Flatiron Health Research Database. The DE cohort included patients who started first-line therapy for CLL on/after 1 January 2011, had a line of therapy (LOT) for CLL after being DE and on/before 30 November 2022, and met other inclusion criteria. Real-world response rate (rwRR) and TTE outcomes (duration of response [rwDOR], progression-free survival [rwPFS], time to next treatment [rwTTNT], and overall survival [rwOS]), were evaluated. Most patients were retreated with a cBTKi- and/or a BCL2i-based therapy (DE, 69%; DE only, 75%; DR, 54%) as their first index LOT. rwRR was similar between groups (DE, 39%; DE only, 41%; DR, 36%), but median TTE outcomes were shorter in the DR subcohort (DR vs DE vs DE only: rwDOR, 11.5 vs 20.3 vs 26.2 months; rwPFS, 5.0 vs 8.8 vs 11.3 months; rwTTNT, 8.0 vs 13.8 vs 22.1 months; rwOS, 14.7 vs 25.2 vs 38.2 months) and shorter with each subsequent index LOT. Our results suggest an unmet need among patients with DR CLL. Future studies should continue to evaluate response durability with different treatments in DE and DR CLL populations.

Fields of Study & Subjects

Chronic Lymphocytic Leukemia Research Celiac Disease Research and Management Glycogen Storage Diseases and Myoclonus

Publication details

Journal / source
Blood Neoplasia
Publisher
Elsevier BV
Volume
3
Issue
3
Pages
100237–100237
Publication date
20 April 2026
Language
EN