Department of Internal Medicine, William Beaumont Hospital, Royal Oak, Michigan, USA.
Department of Hematology and Medical Oncology, William Beaumont Hospital, Royal Oak, Michigan, USA.
Curr Cardiol Rev. 2023;19(3):e310522205428. doi: 10.2174/1573403X18666220531094800.
Cardiotoxicity from chemotherapy regimens has been long reported. However, the understanding of cardiac side effects of biological therapies is rapidly evolving. With cancer patients achieving higher life expectancy due to the use of personalized medicine and novel targeted anticancer agents, the occurrence of cardiotoxicity is becoming more significant. Novel biological therapies include anti-HER2 antibodies, tyrosine kinase inhibitors, bruton kinase inhibitors, antivascular endothelial growth factors, proteasome inhibitors, immunomodulator drugs, and immune checkpoint inhibitors. Potential cardiovascular toxicities linked to these anticancer agents include hypertension, arrhythmias, QT prolongation, myocardial ischemia and infarction, left ventricular dysfunction, congestive heart failure, and thromboembolism. Cardiac biomarkers, electrocardiography, echocardiography and magnetic resonance imaging are common diagnostic modalities used for early detection of these complications and timely intervention. This review discusses the various types of cardiotoxicities caused by novel anticancer biologic agents, their molecular and pathophysiological mechanisms, risk factors, and diagnostic and management strategies that can be used to prevent, minimize, and treat them.
化疗方案引起的心脏毒性已被长期报道。然而,人们对生物疗法的心脏副作用的认识正在迅速发展。由于采用了个性化医学和新型靶向抗癌药物,癌症患者的预期寿命延长,因此心脏毒性的发生变得更加重要。新型生物疗法包括抗 HER2 抗体、酪氨酸激酶抑制剂、布鲁顿酪氨酸激酶抑制剂、抗血管内皮生长因子、蛋白酶体抑制剂、免疫调节剂药物和免疫检查点抑制剂。这些抗癌药物相关的潜在心血管毒性包括高血压、心律失常、QT 间期延长、心肌缺血和梗死、左心室功能障碍、充血性心力衰竭和血栓栓塞。心脏生物标志物、心电图、超声心动图和磁共振成像常用于早期检测这些并发症,并及时进行干预。本文讨论了新型抗癌生物制剂引起的各种类型的心脏毒性、其分子和病理生理机制、危险因素以及可用于预防、最小化和治疗这些毒性的诊断和管理策略。