Cardiotoxicity of Molecular-targeted Drug Therapy

被引:0
|
作者
Le, Duong L. [1 ]
Huynh Cao [1 ]
Yang, Li-Xi [1 ,2 ]
机构
[1] St Marys Hosp, San Francisco, CA USA
[2] Calif Pacific Med Ctr, Res Inst, Radiobiol Lab, San Francisco, CA 94118 USA
关键词
Cardiotoxicity; molecular-targeted therapy; hypertension; cardiac dysfuntion; VEGF; review; ENDOTHELIAL GROWTH-FACTOR; CONGESTIVE-HEART-FAILURE; CANCER; RISK; HYPERTENSION; ANGIOGENESIS; ANTHRACYCLINE; DYSFUNCTION; INHIBITION; MANAGEMENT;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cardiotoxicity is a well-known side-effect described in patients receiving various antineoplastic agents. With the abundance of clinical research and a heavy focus on drug development over the past decade, there has been a major shift in the use of non-specific cytotoxic drugs to molecular-targeted drug therapy. However, as a result, it has become clear that these drugs have numerous adverse effects, both on-target and off-target. Small-molecule tyrosine kinase inhibitors and other molecular-targeted agents, including monoclonal antibodies, have been the primary agents associated with cardiotoxicity. As more molecular-targeted therapies are developed, early recognition and management of drug-related cardiotoxicity will be extremely important in order to reduce morbidity and mortality. Pretreatment evaluation with a surface electrocardiogram, echocardiography, cardiac history, and comprehensive review of concomitant medications are the current mainstay of treatment. However, much is still unknown about the potential cardiotoxic side-effects of these drug and optimal management. In the present article, we aim to review the cardiovascular implications and related cardiotoxicities associated with molecular target-based chemotherapeutic agents, with special emphasis on hypertension, cardiac dysfunction, and QT prolongation. Their implication, mechanism, and management are discussed where possible.
引用
收藏
页码:3243 / 3249
页数:7
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