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首页> 外文期刊>Biochimica et biophysica acta. Biomembranes >The concomitant management of cancer therapy and cardiac therapy
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The concomitant management of cancer therapy and cardiac therapy

机译:癌症治疗和心脏治疗的同时管理

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Antitumor drugs have long been known to introduce a measurable risk of cardiovascular events. Cardio-Oncology is the discipline that builds on collaboration between cardiologists and oncologists and aims at screening, preventing or minimizing such a risk. Overt concern about "possible" cardiovascular toxicity might expose cancer patients to the risk of tumor undertreatment and poor oncologic outcome. Careful analysis of risk:benefit balance is therefore central to the management of patients exposed to potentially cardiotoxic drugs. Concomitant or sequential management of cardiac and cancer therapies should also be tailored to the following strengths and weaknesses: i) molecular mechanisms and clinical correlates of cardiotoxicity have been characterized to some extent for anthracyclines but not for other chemotherapeutics or new generation "targeted" drugs, ii) anthracyclines and targeted drugs cause different mechanisms of cardiotoxicity (type I versus type II), and this classification should guide strategies of primary or secondary prevention, iii) with anthracyclines and nonanthracycline chemotherapeutics, cardiovascular events may occur on treatment as well as years or decades after completing chemotherapy, iv) some patients may be predisposed to a higher risk of cardiac events but there is a lack of prospective studies that characterized optimal genetic tests and pharmacologic measures to minimize excess risk, v) clinical toxicity may be preceded by asymptomatic systolic and/or diastolic dysfunction that necessitates innovative mechanism-based pharmacologic treatment, and vi) patient-tailored pharmacologic correction of comorbidities is important for both primary and secondary prevention. Active collaboration of physicians with laboratory scientists is much needed for improving management of cardiovascular sequelae of antitumor therapy. This article is part of a Special Issue entitled: Membrane channels and transporters in cancers. (C) 2015 Elsevier B.V. All rights reserved.
机译:长期以来,已知抗肿瘤药物会带来可测量的心血管事件风险。心脏病学是一门建立在心脏病专家和肿瘤专家之间协作的学科上,旨在筛查,预防或最大程度地降低此类风险。对“可能的”心血管毒性的过分关注可能使癌症患者面临肿瘤治疗不足和肿瘤治疗不良的风险。仔细分析风险:获益平衡对于暴露于潜在心脏毒性药物的患者的管理至关重要。心脏和癌症治疗的伴随或依序管理也应针对以下优点和缺点进行调整:i)蒽环类药物在某种程度上已表征了心脏毒性的分子机制和临床相关性,但其他化学疗法或新一代“靶向”药物则没有, ii)蒽环类药物和靶向药物引起不同的心脏毒性机制(I型与II型),这种分类应指导一级或二级预防策略,iii)蒽环类和非蒽环类化学疗法的治疗,可能在治疗以及年龄,年龄或完成化疗数十年后,iv)一些患者可能易患心脏事件,但缺乏前瞻性研究来表征最佳的遗传学检测和药理学措施,以最大程度地降低过度风险,v)临床毒性可能伴随无症状收缩期和/或未发生舒张功能障碍评估基于机制的创新药物疗法,并且vi)针对合并症的患者量身定制的药理校正对于一级和二级预防都很重要。为了改善抗肿瘤治疗的心血管后遗症的管理,急需医师与实验室科学家的积极合作。本文是《期刊》的特刊的一部分:癌症中的膜通道和转运蛋白。 (C)2015 Elsevier B.V.保留所有权利。

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