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Editorial
. 2024 Sep 5;144(10):1029-1031.
doi: 10.1182/blood.2024025237.

A fresh look at covalent BTK inhibitor resistance

Affiliations
Editorial

A fresh look at covalent BTK inhibitor resistance

Lindsey E Roeker. Blood. .
No abstract available

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Conflict of interest statement

Conflict-of-interest disclosure: L.E.R. has served as a consultant for AbbVie, Ascentage, AstraZeneca, Beigene, Janssen, Loxo Oncology, Pharmacyclics, Pfizer, TG Therapeutics; is a member of a data safety monitoring committee for Ascentage; served as a Continuing Medical Education speaker for DAVA, Curio, Medscape, and PeerView; holds minority ownership interest in Abbott Laboratories; received travel support from Loxo Oncology; and has received research funding (paid to the institution) from Adaptive Biotechnologies, AstraZeneca, Genentech, AbbVie, Pfizer, Loxo Oncology, Aptose Biosciences, Dren Bio, and Qilu Puget Sound Biotherapeutics.

Figures

None
In this study, mutational profiling was performed on paired samples from patients with relapsed or refractory CLL who were treated with covalent BTKis (ibrutinib or acalabrutinib) in the ELEVATE-RR study. Here we can see the distribution of BTK and B-cell receptor pathway mutations that developed during treatment with ibrutinib or acalabrutinib.

Comment on

References

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    1. Mato AR, Woyach JA, Brown JR, et al. Pirtobrutinib after a covalent BTK inhibitor in chronic lymphocytic leukemia. N Engl J Med. 2023;389(1):33–44. - PubMed

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