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新型靶向抗癌疗法诱发的心脏功能障碍:一个新出现的问题。

Cardiac dysfunction induced by novel targeted anticancer therapy: an emerging issue.

作者信息

Chen Ming Hui

机构信息

Department of Cardiology, Children's Hospital Boston, 300 Longwood Avenue, Boston, MA 02115, USA.

出版信息

Curr Cardiol Rep. 2009 May;11(3):167-74. doi: 10.1007/s11886-009-0025-9.

Abstract

Increasing use of targeted anticancer agents that inhibit tyrosine kinase signaling (monoclonal antibodies or tyrosine kinase inhibitors) has dramatically improved the survival of patients with malignancies. However, cardiotoxicity, including heart failure, left ventricular dysfunction, hypertension, myocardial infarction, and thromboembolism, has occurred. Importantly, these cardiotoxicities are at least partially reversible and responsive to medical management. Early recognition of cardiovascular side effects is vital to allow long-term, continuous therapy with these life-prolonging agents. This article reviews potential cardiovascular side effects of frequently used inhibitors of tyrosine kinase activity (eg, trastuzumab, sunitinib) and discusses the diagnosis and management of cardiotoxicity associated with targeted therapy.

摘要

越来越多地使用抑制酪氨酸激酶信号传导的靶向抗癌药物(单克隆抗体或酪氨酸激酶抑制剂)显著提高了恶性肿瘤患者的生存率。然而,已经出现了心脏毒性,包括心力衰竭、左心室功能障碍、高血压、心肌梗死和血栓栓塞。重要的是,这些心脏毒性至少部分是可逆的,并且对药物治疗有反应。早期识别心血管副作用对于长期持续使用这些延长生命的药物进行治疗至关重要。本文综述了常用的酪氨酸激酶活性抑制剂(如曲妥珠单抗、舒尼替尼)潜在的心血管副作用,并讨论了与靶向治疗相关的心脏毒性的诊断和管理。

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