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非蒽环类抗癌药物的心脏和心血管毒性

Cardiac and cardiovascular toxicity of nonanthracycline anticancer drugs.

作者信息

Jones Robin L, Ewer Michael S

机构信息

Royal Marsden Hospital, Department of Medicine, Fulham Road, London SW3 6JJ, UK.

出版信息

Expert Rev Anticancer Ther. 2006 Sep;6(9):1249-69. doi: 10.1586/14737140.6.9.1249.

Abstract

Anthracyclines are a well-known cause of cardiotoxicity, but a number of other drugs used to treat cancer can also result in cardiac and cardiovascular adverse effects. Cardiotoxicity can result in the alteration of cardiac rhythm, changes in blood pressure and ischemia, and can also alter the ability of the heart to contract and/or relax. The clinical spectrum of these toxicities can range from subclinical abnormalities to catastrophic life-threatening, and sometimes fatal, sequelae. These events may occur acutely or may only become apparent months or years following completion of oncological treatment. Ischemia and rhythm abnormalities are treated symptomatically in most cases. Knowledge of these toxicities can aid clinicians to choose the optimal and least toxic regimen suitable for an individual patient.

摘要

蒽环类药物是众所周知的心脏毒性原因,但用于治疗癌症的许多其他药物也可能导致心脏和心血管不良反应。心脏毒性可导致心律改变、血压变化和缺血,还可改变心脏收缩和/或舒张的能力。这些毒性的临床范围可从亚临床异常到灾难性的危及生命甚至有时致命的后遗症。这些事件可能急性发生,也可能在肿瘤治疗完成数月或数年之后才显现出来。在大多数情况下,缺血和心律异常会进行对症治疗。了解这些毒性有助于临床医生为个体患者选择最佳且毒性最小的治疗方案。

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