McGowan John V, Chung Robin, Maulik Angshuman, Piotrowska Izabela, Walker J Malcolm, Yellon Derek M
The Hatter Cardiovascular Institute, University College London, London, WC1E 6HX, UK.
Cardiovasc Drugs Ther. 2017 Feb;31(1):63-75. doi: 10.1007/s10557-016-6711-0.
Anthracycline chemotherapy maintains a prominent role in treating many forms of cancer. Cardiotoxic side effects limit their dosing and improved cancer outcomes expose the cancer survivor to increased cardiovascular morbidity and mortality. The basic mechanisms of cardiotoxicity may involve direct pathways for reactive oxygen species generation and topoisomerase 2 as well as other indirect pathways. Cardioprotective treatments are few and those that have been examined include renin angiotensin system blockade, beta blockers, or the iron chelator dexrazoxane. New treatments exploiting the ErbB or other novel pro-survival pathways, such as conditioning, are on the cardioprotection horizon. Even in the forthcoming era of targeted cancer therapies, the substantial proportion of today's anthracycline-treated cancer patients may become tomorrow's cardiac patient.
蒽环类化疗药物在多种癌症的治疗中仍占据重要地位。心脏毒性副作用限制了其用药剂量,而癌症治疗效果的改善使癌症幸存者面临心血管疾病发病率和死亡率上升的风险。心脏毒性的基本机制可能涉及活性氧生成和拓扑异构酶2的直接途径以及其他间接途径。心脏保护治疗方法较少,已研究的包括肾素血管紧张素系统阻断剂、β受体阻滞剂或铁螯合剂右丙亚胺。利用表皮生长因子受体(ErbB)或其他新型促生存途径(如预处理)的新治疗方法正在研究中。即使在即将到来的靶向癌症治疗时代,如今接受蒽环类治疗的大量癌症患者仍可能在未来成为心脏病患者。