Biomarkers for monitoring chemotherapy-induced cardiotoxicity

被引:24
作者
Cao, Liyun [1 ]
Zhu, Wuqiang [2 ]
Wagar, Elizabeth A. [1 ]
Meng, Qing H. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Unit 37, Dept Lab Med, 1515 Holcombe Blvd, Houston, TX 77030 USA
[2] Univ Alabama Birmingham, Dept Biomed Engn, Birmingham, AL 35294 USA
关键词
Biomarker; chemotherapy; cardiotoxicity; CONGESTIVE-HEART-FAILURE; LEFT-VENTRICULAR DYSFUNCTION; ATRIAL-NATRIURETIC-PEPTIDE; C-REACTIVE PROTEIN; ANTHRACYCLINE-INDUCED CARDIOTOXICITY; HIGH-DOSE CYCLOPHOSPHAMIDE; LONG-TERM SURVIVORS; DOXORUBICIN CARDIOTOXICITY; CANCER-PATIENTS; TROPONIN-T;
D O I
10.1080/10408363.2016.1261270
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Cardiotoxicity, including acute and late-onset cardiotoxicity, is a well-known adverse effect of many types of antitumor agents. Early identification of patients with cardiotoxicity is important to ensure prompt treatment and minimize toxic effects. The etiology of chemotherapy-induced cardiotoxicity is multifactorial. Traditional methods for assessment of chemotherapy-induced cardiotoxicity typically involve serial measurements of cardiac function via multi-modality imaging techniques. Typically, however, significant left ventricular dysfunction has already occurred when cardiotoxicity is detected by imaging techniques. Biomarkers, most importantly cardiac natriuretic peptides and troponins, are promising markers for identifying patients potentially at risk for clinical heart failure symptoms. This review summarizes the recent progress in clinical utilization of biomarkers for early diagnosis of acute cardiotoxicity and for prediction of late-onset cardiotoxicity. We also discuss the conflicting results of different studies and the association of results with study design.
引用
收藏
页码:87 / 101
页数:15
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