Cardiac toxicity with anti-HER-2 therapies-what have we learned so far?

被引:93
作者
de Azambuja, Evandro [1 ,2 ]
Bedard, Philippe L. [1 ]
Suter, Thomas [3 ]
Piccart-Gebhart, Martine [1 ,2 ]
机构
[1] Inst Jules Bordet, B-1000 Brussels, Belgium
[2] Univ Libre Bruxelles, Brussels, Belgium
[3] Univ Hosp Bern, Swiss Cardiovasc Ctr, CH-3010 Bern, Switzerland
关键词
Breast cancer; Anti-HER-2; therapies; Cardiotoxicity; Trastuzumab; Lapatinib; HER2-POSITIVE BREAST-CANCER; BETA-ADRENERGIC ACTIVITY; ADJUVANT CHEMOTHERAPY; PARASYMPATHETIC ACTIVITY; MUSCARINIC MODULATION; LAPATINIB GW572016; TYROSINE KINASES; CLINICAL-TRIALS; FOLLOW-UP; TRASTUZUMAB;
D O I
10.1007/s11523-009-0112-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Trastuzumab, a monoclonal antibody that blocks HER-2 receptor, improves the survival of women with HER-2-positive early and advanced breast cancer when given with chemotherapy. Lapatinib, a dual tyrosine kinase inhibitor of EGFR and HER-2, is approved for the treatment of metastatic breast cancer patients after failure of prior anthracycline, taxanes and trastuzumab therapies in combination with capecitabine. Importantly, cardiac toxicity, manifested as symptomatic congestive heart failure or asymptomatic left ventricular ejection fraction decline, has been reported in some of the patients receiving these novel anti-HER-2 therapies, particularly when these drugs are used following anthracyclines, whose cardiotoxic potential has been recognized for decades. This review will focus on the incidence, natural history, underlying mechanisms, management, and areas of uncertainty regarding trastuzumab-and lapatinib-induced cardiotoxicity.
引用
收藏
页码:77 / 88
页数:12
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