TY - JOUR
T1 - International consensus statement on the management of cardiovascular risk of Bruton’s tyrosine kinase inhibitors in CLL
AU - Awan, Farrukh T.
AU - Addison, Daniel
AU - Alfraih, Feras
AU - Baratta, Sergio J.
AU - Campos, Rodrigo Noronha
AU - Cugliari, María Silvana
AU - Goh, Yeow Tee
AU - Ionin, Valery Alexandrovich
AU - Mundnich, Stefanie
AU - Sverdlov, Aaron L.
AU - Tam, Constantine
AU - Ysebaert, Loïc
N1 - Funding Information:
Cellectar Biosciences, and received research funding from Pharma-cyclics. F.A. has received payment for speaking, expert testimony, and travel support from AstraZeneca, Janssen, and Sobi and is an unpaid board member for the Saudi Society for Blood Disorders. R.N.C. has received consulting fees and speaking honoraria from AstraZeneca, Boehringer Ingelheim, and Novartis, as well as honoraria from Servier and Sankyo; travel support for attending meetings from Bayer, Boehringer Ingelheim, and Torrent; and has been paid for participating in advisory boards for AstraZeneca and Boehringer Ingelheim. M.S.C. has received honoraria for educational activities and conferences from AstraZeneca, AbbVie, Bristol Myers Squibb, Takeda, Raffo, Roche, and Sandoz; support for attending meetings from AstraZeneca, AbbVie, Tuteur, and Roche; has advised AbbVie, AstraZeneca, Sanofi, Takeda, and Raffo; and is an unpaid member of the Argentinian Society of Hematology, CLL, and Lymphoma Subcommittee. Y.T.G. has received speaking compensation through his institution from AstraZeneca, Johnson & Johnson, AbbVie, and Roche. A.L.S. receives funding for research and education from the National Heart Foundation of Australia, the New South Wales Ministry of Health (Australia), Race Oncology Pty Ltd., Celgene Pty Ltd., Bristol-Myers Squibb Australia Pty Ltd., Hunter Cancer Research Alliance, Vifor Pharma, Entrepreneurs’ Programme/Biotronik Australia, Royal Australasian College of Physicians Foundation/Foundation
Publisher Copyright:
© 2022 by The American Society of Hematology.
PY - 2022/9/27
Y1 - 2022/9/27
N2 - 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.
AB - 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.
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U2 - 10.1182/bloodadvances.2022007938
DO - 10.1182/bloodadvances.2022007938
M3 - Review article
C2 - 35790105
AN - SCOPUS:85141401507
SN - 2473-9529
VL - 6
SP - 5516
EP - 5525
JO - Blood advances
JF - Blood advances
IS - 18
ER -