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卡培他滨致心脏毒性:病例报告及文献复习。

Capecitabine-induced cardiotoxicity: case report and review of the literature.

机构信息

Department of Oncology, McGill University Health Centre, Montreal, QC.

出版信息

Curr Oncol. 2010 Feb;17(1):59-63. doi: 10.3747/co.v17i1.437.

Abstract

Capecitabine, an oral prodrug of 5-fluorouracil (5FU), has been integrated into the management of multiple cancer types because of convenience of administration and efficacy comparable with 5fu. Cardiotoxicity induced by 5FU-in particular angina-has been well described in the literature, but reports of adverse cardiac events with capecitabine are also emerging. The mechanism underlying 5FU cardiotoxicity has long been thought to result from coronary vasospasm, but animal-model studies and patient echocardiographic findings both suggest a cardiomyopathic picture. Although 5FU cardiotoxicity is often reversible and can be managed supportively, presentations that are more severe-including arrhythmias, acute ischemic events, and cardiogenic shock-have been documented. In this report, we describe the case of a patient who ultimately required a pacemaker after developing symptomatic bradycardia and sinus arrest while receiving capecitabine for colon cancer.

摘要

卡培他滨是 5-氟尿嘧啶(5FU)的口服前体药物,由于其给药方便且疗效与 5FU 相当,已被纳入多种癌症的治疗方案中。5FU 引起的心脏毒性(尤其是心绞痛)在文献中已有详细描述,但卡培他滨引起的不良心脏事件的报告也在不断出现。长期以来,人们一直认为 5FU 心脏毒性是由于冠状动脉痉挛引起的,但动物模型研究和患者超声心动图结果均提示存在心肌病样改变。尽管 5FU 心脏毒性通常是可逆的且可以支持治疗,但也有更严重的表现,包括心律失常、急性缺血事件和心源性休克。在本报告中,我们描述了 1 例结肠癌患者在接受卡培他滨治疗时出现症状性心动过缓和窦性停搏,最终需要安装起搏器的病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01a8/2826779/cb283e658a02/conc17-1-59f1.jpg

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