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Ibrutinib-Associated Cardiotoxicity: From the Pharmaceutical to the Clinical

Ibrutinib is the first-in-class Bruton tyrosine kinase (BTK) inhibitor that has revolutionized the treatment of B cell malignancies. Unfortunately, increased incidences of cardiotoxicity have limited its use. Despite over a decade of research, the biological mechanisms underlying ibrutinib cardiotox...

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Detalles Bibliográficos
Autores principales: Dong, Rong, Yan, Youyou, Zeng, Xiaokang, Lin, Nengming, Tan, Biqin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9508996/
https://www.ncbi.nlm.nih.gov/pubmed/36164415
http://dx.doi.org/10.2147/DDDT.S377697
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author Dong, Rong
Yan, Youyou
Zeng, Xiaokang
Lin, Nengming
Tan, Biqin
author_facet Dong, Rong
Yan, Youyou
Zeng, Xiaokang
Lin, Nengming
Tan, Biqin
author_sort Dong, Rong
collection PubMed
description Ibrutinib is the first-in-class Bruton tyrosine kinase (BTK) inhibitor that has revolutionized the treatment of B cell malignancies. Unfortunately, increased incidences of cardiotoxicity have limited its use. Despite over a decade of research, the biological mechanisms underlying ibrutinib cardiotoxicity remain unclear. In this review, we discuss the pharmacological properties of ibrutinib, the incidence and mechanisms of ibrutinib-induced cardiotoxicity, and practical management to prevent and treat this condition. We also synopsize and discuss the cardiovascular adverse effects related to other more selective BTK inhibitors, which may guide the selection of appropriate BTK inhibitors.
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spelling pubmed-95089962022-09-25 Ibrutinib-Associated Cardiotoxicity: From the Pharmaceutical to the Clinical Dong, Rong Yan, Youyou Zeng, Xiaokang Lin, Nengming Tan, Biqin Drug Des Devel Ther Review Ibrutinib is the first-in-class Bruton tyrosine kinase (BTK) inhibitor that has revolutionized the treatment of B cell malignancies. Unfortunately, increased incidences of cardiotoxicity have limited its use. Despite over a decade of research, the biological mechanisms underlying ibrutinib cardiotoxicity remain unclear. In this review, we discuss the pharmacological properties of ibrutinib, the incidence and mechanisms of ibrutinib-induced cardiotoxicity, and practical management to prevent and treat this condition. We also synopsize and discuss the cardiovascular adverse effects related to other more selective BTK inhibitors, which may guide the selection of appropriate BTK inhibitors. Dove 2022-09-20 /pmc/articles/PMC9508996/ /pubmed/36164415 http://dx.doi.org/10.2147/DDDT.S377697 Text en © 2022 Dong et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Review
Dong, Rong
Yan, Youyou
Zeng, Xiaokang
Lin, Nengming
Tan, Biqin
Ibrutinib-Associated Cardiotoxicity: From the Pharmaceutical to the Clinical
title Ibrutinib-Associated Cardiotoxicity: From the Pharmaceutical to the Clinical
title_full Ibrutinib-Associated Cardiotoxicity: From the Pharmaceutical to the Clinical
title_fullStr Ibrutinib-Associated Cardiotoxicity: From the Pharmaceutical to the Clinical
title_full_unstemmed Ibrutinib-Associated Cardiotoxicity: From the Pharmaceutical to the Clinical
title_short Ibrutinib-Associated Cardiotoxicity: From the Pharmaceutical to the Clinical
title_sort ibrutinib-associated cardiotoxicity: from the pharmaceutical to the clinical
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9508996/
https://www.ncbi.nlm.nih.gov/pubmed/36164415
http://dx.doi.org/10.2147/DDDT.S377697
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