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癌症治疗的常见血管毒性。

Common Vascular Toxicities of Cancer Therapies.

机构信息

Department of Cardiovascular Diseases, Mayo Clinic, 200 First Street SW, Rochester, MN 55902, USA.

出版信息

Cardiol Clin. 2019 Nov;37(4):365-384. doi: 10.1016/j.ccl.2019.07.003. Epub 2019 Aug 26.

DOI:10.1016/j.ccl.2019.07.003
PMID:31587779
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6995033/
Abstract

The introduction of targeted agents into modern cancer therapy pursued the goal of molecularly more specific, and thereby more effective and safer, therapies. Paradoxically, however, several toxicities were brought to greater attention, among these not only cardiac but also vascular toxicities. The latter reach far beyond venous thromboembolism and include a broad spectrum of presentations based on the vascular territories and pathomechanisms involved, including abnormal vascular reactivity, acute thrombosis, or accelerated atherosclerosis. This article provides an overview of the most common presentations and their management strategies.

摘要

靶向药物在现代癌症治疗中的引入旨在追求更具分子特异性的治疗方法,从而实现更有效和更安全的治疗效果。然而,具有讽刺意味的是,一些毒性作用引起了更多的关注,其中不仅包括心脏毒性,还包括血管毒性。后者的范围远远超出了静脉血栓栓塞症,包括基于所涉及的血管区域和病理机制的广泛表现形式,包括血管反应异常、急性血栓形成或加速动脉粥样硬化。本文概述了最常见的表现形式及其管理策略。

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本文引用的文献

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Arterial events in cancer patients-the case of acute coronary thrombosis.癌症患者的动脉事件——以急性冠状动脉血栓形成为例
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Acute coronary syndromes in patients with active hematologic malignancies - Incidence, management, and outcomes.活动性血液恶性肿瘤患者的急性冠状动脉综合征:发生率、处理和结局。
Int J Cardiol. 2019 Jan 15;275:6-12. doi: 10.1016/j.ijcard.2018.10.008. Epub 2018 Oct 5.
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Fourth Universal Definition of Myocardial Infarction (2018).心肌梗死的第四次全球定义(2018年)。
J Am Coll Cardiol. 2018 Oct 30;72(18):2231-2264. doi: 10.1016/j.jacc.2018.08.1038. Epub 2018 Aug 25.
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Role of direct oral anticoagulants in the treatment of cancer-associated venous thromboembolism: guidance from the SSC of the ISTH.直接口服抗凝剂在癌症相关静脉血栓栓塞治疗中的作用:国际血栓与止血学会科学与标准化委员会的指南
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5-fluorouracil and cardiotoxicity: a review.5-氟尿嘧啶与心脏毒性:综述
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The BCR-ABL1 Inhibitors Imatinib and Ponatinib Decrease Plasma Cholesterol and Atherosclerosis, and Nilotinib and Ponatinib Activate Coagulation in a Translational Mouse Model.在一个转化小鼠模型中,BCR-ABL1抑制剂伊马替尼和波纳替尼可降低血浆胆固醇水平并减轻动脉粥样硬化,而尼罗替尼和波纳替尼会激活凝血。
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