Department of Medicine, University of Chicago Medicine, Chicago, Illinois, USA.
Curr Opin Cardiol. 2019 May;34(3):283-288. doi: 10.1097/HCO.0000000000000619.
The purpose of this review is to discuss the clinical and treatment-related factors that increase the risk of cardiotoxicity with anthracyclines and human epidermal growth factor 2 receptor inhibitors.
Age and preexisting left ventricular dysfunction have been identified most consistently as being associated with the development of clinical heart failure or a worsening of left ventricular function with chemotherapy. Other cardiovascular conditions, including hypertension, diabetes, and coronary artery disease, are also associated with the risk of cardiotoxicity. There is growing evidence that Blacks are at a higher risk of developing cardiotoxicity than Whites, even after adjusting for known confounders. Pharmacogenomics is also emerging as a potential tool to help identify patients who are at higher risk for cardiotoxicity. Treatment-related risk factors include the dose of anthracycline or its formulation, whether the patient is receiving additional chemotherapeutic agents or radiation.
Several clinical and treatment-related risk factors are associated with cardiotoxicity. Further study is needed to determine whether optimization of modifiable risk factors prior to treatment can reduce the risk of cardiotoxicity.
本文旨在讨论增加蒽环类药物和人表皮生长因子 2 受体抑制剂相关心脏毒性风险的临床和治疗相关因素。
年龄和预先存在的左心室功能障碍与化疗后临床心力衰竭或左心室功能恶化的发生最一致相关。其他心血管疾病,包括高血压、糖尿病和冠状动脉疾病,也与心脏毒性的风险相关。越来越多的证据表明,黑人患心脏毒性的风险高于白人,即使在调整了已知的混杂因素后也是如此。药物基因组学也正在成为一种潜在的工具,可以帮助识别心脏毒性风险较高的患者。治疗相关的危险因素包括蒽环类药物的剂量或其制剂,患者是否正在接受其他化疗药物或放疗。
几个临床和治疗相关的危险因素与心脏毒性相关。需要进一步研究,以确定在治疗前是否可以通过优化可改变的危险因素来降低心脏毒性的风险。