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International consensus statement on the management of cardiovascular risk of Bruton’s tyrosine kinase inhibitors in CLL
Bruton’s tyrosine kinase inhibitors (BTKis) have altered the treatment landscape for chronic lymphocytic leukemia (CLL) by offering effective and well-tolerated therapeutic options. However, since the approval of ibrutinib, concern has risen regarding the risk of cardiovascular (CV) adverse events,...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Hematology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9631706/ https://www.ncbi.nlm.nih.gov/pubmed/35790105 http://dx.doi.org/10.1182/bloodadvances.2022007938 |
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author | Awan, Farrukh T. Addison, Daniel Alfraih, Feras Baratta, Sergio J. Campos, Rodrigo Noronha Cugliari, María Silvana Goh, Yeow Tee Ionin, Valery Alexandrovich Mundnich, Stefanie Sverdlov, Aaron L. Tam, Constantine Ysebaert, Loïc |
author_facet | Awan, Farrukh T. Addison, Daniel Alfraih, Feras Baratta, Sergio J. Campos, Rodrigo Noronha Cugliari, María Silvana Goh, Yeow Tee Ionin, Valery Alexandrovich Mundnich, Stefanie Sverdlov, Aaron L. Tam, Constantine Ysebaert, Loïc |
author_sort | Awan, Farrukh T. |
collection | PubMed |
description | Bruton’s tyrosine kinase inhibitors (BTKis) have altered the treatment landscape for chronic lymphocytic leukemia (CLL) by offering effective and well-tolerated therapeutic options. However, since the approval of ibrutinib, concern has risen regarding the risk of cardiovascular (CV) adverse events, including atrial fibrillation (AF), hypertension, and heart failure. Newer BTKis appear to have lower CV risks, but data are limited. It is important to understand the risks posed by BTKis and how those risks interact with individual patients, and we convened a panel of physicians with expertise in CLL and CV toxicities in oncology to develop evidence-based consensus recommendations for community hematologists and oncologists. Care providers should thoroughly assess a patient’s CV risk level before treatment initiation, including established CV diseases and risk factors, and perform investigations dependent on preexisting diseases and risk factors, including an electrocardiogram (ECG). For patients with high CV risk, BTKi treatment is often appropriate in consultation with a multidisciplinary team (MDT), and more selective BTKis, including acalabrutinib and zanubrutinib, are preferred. BTKi treatment should generally be avoided in patients with a history of heart failure. Ibrutinib should be avoided in patients with a history of ventricular arrhythmias, but the risk of newer drugs is not yet known. Finally, an MDT is crucial to help manage emerging toxicities with the goal of maintaining BTKi therapy, if possible. Optimizing heart failure, arrhythmia, and hypertension control will likely improve tolerance and maintenance of BTKi therapy. However, additional studies are needed to identify the most optimal strategy for these drugs. |
format | Online Article Text |
id | pubmed-9631706 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society of Hematology |
record_format | MEDLINE/PubMed |
spelling | pubmed-96317062022-11-04 International consensus statement on the management of cardiovascular risk of Bruton’s tyrosine kinase inhibitors in CLL Awan, Farrukh T. Addison, Daniel Alfraih, Feras Baratta, Sergio J. Campos, Rodrigo Noronha Cugliari, María Silvana Goh, Yeow Tee Ionin, Valery Alexandrovich Mundnich, Stefanie Sverdlov, Aaron L. Tam, Constantine Ysebaert, Loïc Blood Adv Review Article Bruton’s tyrosine kinase inhibitors (BTKis) have altered the treatment landscape for chronic lymphocytic leukemia (CLL) by offering effective and well-tolerated therapeutic options. However, since the approval of ibrutinib, concern has risen regarding the risk of cardiovascular (CV) adverse events, including atrial fibrillation (AF), hypertension, and heart failure. Newer BTKis appear to have lower CV risks, but data are limited. It is important to understand the risks posed by BTKis and how those risks interact with individual patients, and we convened a panel of physicians with expertise in CLL and CV toxicities in oncology to develop evidence-based consensus recommendations for community hematologists and oncologists. Care providers should thoroughly assess a patient’s CV risk level before treatment initiation, including established CV diseases and risk factors, and perform investigations dependent on preexisting diseases and risk factors, including an electrocardiogram (ECG). For patients with high CV risk, BTKi treatment is often appropriate in consultation with a multidisciplinary team (MDT), and more selective BTKis, including acalabrutinib and zanubrutinib, are preferred. BTKi treatment should generally be avoided in patients with a history of heart failure. Ibrutinib should be avoided in patients with a history of ventricular arrhythmias, but the risk of newer drugs is not yet known. Finally, an MDT is crucial to help manage emerging toxicities with the goal of maintaining BTKi therapy, if possible. Optimizing heart failure, arrhythmia, and hypertension control will likely improve tolerance and maintenance of BTKi therapy. However, additional studies are needed to identify the most optimal strategy for these drugs. American Society of Hematology 2022-09-27 /pmc/articles/PMC9631706/ /pubmed/35790105 http://dx.doi.org/10.1182/bloodadvances.2022007938 Text en © 2022 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved. |
spellingShingle | Review Article Awan, Farrukh T. Addison, Daniel Alfraih, Feras Baratta, Sergio J. Campos, Rodrigo Noronha Cugliari, María Silvana Goh, Yeow Tee Ionin, Valery Alexandrovich Mundnich, Stefanie Sverdlov, Aaron L. Tam, Constantine Ysebaert, Loïc International consensus statement on the management of cardiovascular risk of Bruton’s tyrosine kinase inhibitors in CLL |
title | International consensus statement on the management of cardiovascular risk of Bruton’s tyrosine kinase inhibitors in CLL |
title_full | International consensus statement on the management of cardiovascular risk of Bruton’s tyrosine kinase inhibitors in CLL |
title_fullStr | International consensus statement on the management of cardiovascular risk of Bruton’s tyrosine kinase inhibitors in CLL |
title_full_unstemmed | International consensus statement on the management of cardiovascular risk of Bruton’s tyrosine kinase inhibitors in CLL |
title_short | International consensus statement on the management of cardiovascular risk of Bruton’s tyrosine kinase inhibitors in CLL |
title_sort | international consensus statement on the management of cardiovascular risk of bruton’s tyrosine kinase inhibitors in cll |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9631706/ https://www.ncbi.nlm.nih.gov/pubmed/35790105 http://dx.doi.org/10.1182/bloodadvances.2022007938 |
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