Al-Otaibi Talal Khalid, Weitzman Benjamin, Tahir Usman A, Asnani Aarti
CardioVascular Institute, Beth Israel Deaconess Medical Center, Boston, MA, United States.
Front Cardiovasc Med. 2022 Apr 21;9:867873. doi: 10.3389/fcvm.2022.867873. eCollection 2022.
Anthracyclines are a major component of chemotherapies used in many pediatric and adult malignancies. Anthracycline-associated cardiotoxicity (ACT) is a dose-dependent adverse effect that has substantial impact on morbidity and mortality. Therefore, the identification of genetic variants associated with increased risk of ACT has the potential for significant clinical impact to improve patient care. The goal of this review is to summarize the current evidence supporting genetic variants associated with ACT, identify gaps and limitations in current knowledge, and propose future directions for incorporating genetics into clinical practice for patients treated with anthracyclines. We will discuss mechanisms of ACT that could be illuminated by genetics and discuss clinical applications for the cardiologist/cardio-oncologist.
蒽环类药物是许多儿科和成人恶性肿瘤化疗方案的主要组成部分。蒽环类药物相关心脏毒性(ACT)是一种剂量依赖性不良反应,对发病率和死亡率有重大影响。因此,识别与ACT风险增加相关的基因变异可能对改善患者护理产生重大临床影响。本综述的目的是总结支持与ACT相关基因变异的现有证据,识别当前知识中的差距和局限性,并提出将遗传学纳入接受蒽环类药物治疗患者临床实践的未来方向。我们将讨论遗传学可能阐明的ACT机制,并讨论心脏病专家/心脏肿瘤学家的临床应用。