Prevention of Cardiotoxicities With Traditional and Novel Chemotherapeutic Agents

被引:6
|
作者
Sharalaya Z. [1 ]
Collier P. [1 ]
机构
[1] Robert and Suzanne Tomsich Department of Cardiovascular Medicine, Sydell and Arnold Miller Family Heart and Vascular Institute, The Cleveland Clinic Foundation, 9500 Euclid Avenue, Desk J1-5, Cleveland, 44195, OH
关键词
Anthracycline; Cardiomyopathy; Cardiotoxicity; Chemotherapy; Heart failure; Novel chemotherapeutics; Prevention;
D O I
10.1007/s11897-018-0400-1
中图分类号
学科分类号
摘要
Purpose of Review: This review will discuss strategies to prevent cardiotoxicity associated with chemotherapeutics. Forty years ago, investigators identified dose-dependent cardiotoxicity related to anthracycline-based regimens. Over recent decades, the development of more selective, mechanism-based chemotherapeutics has been associated with both on-target and off-target adverse cardiovascular sequelae. Recent Findings: Strategies to prevent or attenuate cardiotoxicities include limitation of anthracycline dose, appropriate patient selection, referral/access to cardio-oncology programs, early recognition of cardiac side effects, active cardio-surveillance, cardio-protective medical therapy, treatment-specific concerns, and follow-up. The importance of accurate diagnosis of cardiotoxicity is important as false-positive testing may result in inappropriate holding or stopping potentially life-saving chemotherapy. Data to support use of cardio-protective medical therapy to prevent chemotherapy-related cardiotoxicity is modest at best, limited by marginal effect size, small patient numbers, and short follow-up. Summary: The rapid growth in cardio-oncology clinics may facilitate larger multi-center randomized controlled trials in this area. © 2018, Springer Science+Business Media, LLC, part of Springer Nature.
引用
收藏
页码:260 / 269
页数:9
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