Navigating cancer therapy induced cardiotoxicity: From pathophysiology to treatment innovations

被引:0
|
作者
Tetterton-Kellner, Jessica [1 ]
Jensen, Brian C. [2 ,3 ]
Nguyen, Juliane [1 ,2 ]
机构
[1] Univ N Carolina, Eshelman Sch Pharm, Div Pharmacoengn & Mol Pharmaceut, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, McAllister Heart Inst, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Dept Med, Div Cardiol, Chapel Hill, NC 27599 USA
关键词
Cardiotoxicity; Chemotherapy induced cardiotoxicity; Anthracycline induced cardiotoxicity; Dilated cardiomyopathy; ANTHRACYCLINE CARDIOTOXICITY; CARDIOVASCULAR TOXICITY; INDUCED CARDIOMYOPATHY; LIPOSOMAL DOXORUBICIN; TEI INDEX; TRASTUZUMAB; EXERCISE; CHEMOTHERAPY; DEXRAZOXANE; DYSFUNCTION;
D O I
10.1016/j.addr.2024.115361
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Every year, more than a million people in the United States undergo chemotherapy or radiation therapy for cancer, as estimated by the CDC. While chemotherapy has been an instrumental tool for treating cancer, it also causes severe adverse effects. The more commonly acknowledged adverse effects include hair loss, fatigue, and nausea, but a more severe and longer lasting side effect is cardiotoxicity. Cardiotoxicity, or heart damage, is a common complication of cancer treatments. It can range from mild to severe, and it can affect some patients temporarily or others permanently, even after they are cured of cancer. Dexrazoxane is the only FDA-approved drug for treating anthracycline induced cardiotoxicity, but it also has drawbacks and adverse effects. There is no other type of chemotherapy induced cardiotoxicity that has an approved treatment option. In this review, we discuss the pathophysiology of chemotherapeutic-induced cardiotoxicity, methods and guidelines of diagnosis, methods of treatment and mitigation, and current drug delivery approaches in therapeutic development.
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页数:14
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