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Acalabrutinib-Related Cardiac Toxicities in Patients with Chronic Lymphocytic Leukemia: A Meta-Analysis of Randomized Controlled Trials

Acalabrutinib, a second-generation and more selective Bruton's tyrosine kinase inhibitor, was developed to potentiate efficacy while minimizing ibrutinib-associated side effects. We undertook a systematic review and meta-analysis of randomized clinical trials to determine the risks of acalabrut...

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Autores principales: Htut, Thura Win, Han, Myat Min, Thein, Kyaw Zin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Innovative Healthcare Institute 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9153250/
https://www.ncbi.nlm.nih.gov/pubmed/35664088
http://dx.doi.org/10.36401/JIPO-21-12
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author Htut, Thura Win
Han, Myat Min
Thein, Kyaw Zin
author_facet Htut, Thura Win
Han, Myat Min
Thein, Kyaw Zin
author_sort Htut, Thura Win
collection PubMed
description Acalabrutinib, a second-generation and more selective Bruton's tyrosine kinase inhibitor, was developed to potentiate efficacy while minimizing ibrutinib-associated side effects. We undertook a systematic review and meta-analysis of randomized clinical trials to determine the risks of acalabrutinib-related cardiac toxicities in patients with chronic lymphocytic leukemia. Patients on acalabrutinib experienced higher risk of any-grade cardiac events (risk ratio, 1.75; p = 0.01) while there was a considerable trend toward statistical significance in the risk of any-grade atrial fibrillation (risk ratio, 2.56; p = 0.05). There was no significant increase in the risk of hypertension or high-grade cardiac events or atrial fibrillation in the acalabrutinib group.
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spelling pubmed-91532502022-06-04 Acalabrutinib-Related Cardiac Toxicities in Patients with Chronic Lymphocytic Leukemia: A Meta-Analysis of Randomized Controlled Trials Htut, Thura Win Han, Myat Min Thein, Kyaw Zin J Immunother Precis Oncol Review Article Acalabrutinib, a second-generation and more selective Bruton's tyrosine kinase inhibitor, was developed to potentiate efficacy while minimizing ibrutinib-associated side effects. We undertook a systematic review and meta-analysis of randomized clinical trials to determine the risks of acalabrutinib-related cardiac toxicities in patients with chronic lymphocytic leukemia. Patients on acalabrutinib experienced higher risk of any-grade cardiac events (risk ratio, 1.75; p = 0.01) while there was a considerable trend toward statistical significance in the risk of any-grade atrial fibrillation (risk ratio, 2.56; p = 0.05). There was no significant increase in the risk of hypertension or high-grade cardiac events or atrial fibrillation in the acalabrutinib group. Innovative Healthcare Institute 2021-11-04 /pmc/articles/PMC9153250/ /pubmed/35664088 http://dx.doi.org/10.36401/JIPO-21-12 Text en © 2022 https://creativecommons.org/licenses/by-nc-nd/4.0/This work is published under a CC-BY-NC-ND 4.0 International License.
spellingShingle Review Article
Htut, Thura Win
Han, Myat Min
Thein, Kyaw Zin
Acalabrutinib-Related Cardiac Toxicities in Patients with Chronic Lymphocytic Leukemia: A Meta-Analysis of Randomized Controlled Trials
title Acalabrutinib-Related Cardiac Toxicities in Patients with Chronic Lymphocytic Leukemia: A Meta-Analysis of Randomized Controlled Trials
title_full Acalabrutinib-Related Cardiac Toxicities in Patients with Chronic Lymphocytic Leukemia: A Meta-Analysis of Randomized Controlled Trials
title_fullStr Acalabrutinib-Related Cardiac Toxicities in Patients with Chronic Lymphocytic Leukemia: A Meta-Analysis of Randomized Controlled Trials
title_full_unstemmed Acalabrutinib-Related Cardiac Toxicities in Patients with Chronic Lymphocytic Leukemia: A Meta-Analysis of Randomized Controlled Trials
title_short Acalabrutinib-Related Cardiac Toxicities in Patients with Chronic Lymphocytic Leukemia: A Meta-Analysis of Randomized Controlled Trials
title_sort acalabrutinib-related cardiac toxicities in patients with chronic lymphocytic leukemia: a meta-analysis of randomized controlled trials
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9153250/
https://www.ncbi.nlm.nih.gov/pubmed/35664088
http://dx.doi.org/10.36401/JIPO-21-12
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