Genetics of Anthracycline Cardiomyopathy in Cancer Survivors JACC: CardioOncology State-of-the-Art Review

被引:65
作者
Bhatia, Smita [1 ]
机构
[1] Univ Alabama Birmingham, Inst Canc Outcomes & Survivorship, 1600 7th Ave South,Lowder 500, Birmingham, AL 35233 USA
来源
JACC: CARDIOONCOLOGY | 2020年 / 2卷 / 04期
基金
美国国家卫生研究院;
关键词
anthracycline chemotherapy; cardiomyopathy; heart failure; genomics; metabolomics; prediction; GENOME-WIDE ASSOCIATION; INDUCED CARDIOTOXICITY; LONG-TERM; CHILDHOOD-CANCER; RISK-FACTORS; HEART-FAILURE; DOXORUBICIN CARDIOTOXICITY; CARDIAC DYSFUNCTION; MTDNA LESIONS; POLYMORPHISMS;
D O I
10.1016/j.jaccao.2020.09.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Anthracyclines are an integral part of chemotherapy regimens used to treat a variety of childhood-onset and adult-onset cancers. However, the development of cardiac dysfunction and heart failure often compromises the clinical utility of anthracyclines. The risk of cardiac dysfunction increases with anthracycline dose. This anthracycline-cardiac dysfunction association is modified by several demographic and clinical factors, such as age at anthracycline exposure (<4 years and >= 65 years); female sex; chest radiation; presence of cardiovascular risk factors (diabetes, hypertension); and concurrent use of cyclophosphamide, paclitaxel, and trastuzumab. However, the clinical variables alone yield modest predictive power in detecting cardiac dysfunction. Recently, attention has focused on the molecular basis of anthracycline-related cardiac dysfunction, providing an initial understanding of the mechanism of anthracycline-related cardiomyopathy. This review describes the current state of knowledge with respect to the pathogenesis of anthracycline-related cardiomyopathy and identifies the critical next steps to mitigate this problem. (C) 2020 The Author. Published by Elsevier on behalf of the American College of Cardiology Foundation.
引用
收藏
页码:539 / 552
页数:14
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