Cardiotoxicity Alerts during Treatment with Trastuzumab in Breast Cancer at Four-year Follow-up

D. Santos, M. Tettamanti, C. Chacon, J. Nadal, V. Costanzo, A. Nervo, Federico Losco, R. Chacón
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引用次数: 2

Abstract

Background: Adjuvant treatment of HER2+ breast cancer includes adriamycin and trastuzumab, a monoclonal antibody that producescardiotoxicity. The actual epidemiologic impact of trastuzumab-related cardiotoxicity in unselected populations in Argentinaremains unknown.Objectives: The aim of this study was to evaluate the impact of trastuzumab-related cardiotoxicity during adjuvant treatment forbreast cancer in an unselected population after >12 months of completing therapy.Methods: Among 888 patients prospectively evaluated for breast cancer, 231 (38%) were HER2+ and received adjuvant therapy withadriamycin and trastuzumab. Left ventricular ejection fraction was evaluated before treatment, after completing adriamycin and thenevery 3 months during follow-up. Cardiotoxicity was defined as a decline in left ventricular ejection fraction >10%, according to the definitionof the American College of Cardiology and was compared with the definitions of the B-31 trial and the MD Anderson Cancer Center.Results: A decline in left ventricular ejection fraction >10% from baseline values occurred in 65% (n=150) of the patients during amean follow-up of 48±12 months. In the per group analysis, patients included in the B-31and MD Anderson Cancer Center vs. theAmerican College of Cardiology definitions presented greater percent fall in left ventricular ejection fraction during treatment: 20%vs. 20% vs. 16%, respectively (p <0.04) and ended treatment with left ventricular ejection fraction <50% in 42% vs. 41% vs. 33% ofcases, respectively (p=0.01).Conclusions: In the population treated with trastuzumab under cardio-oncology surveillance during 48±12 months:1- Left ventricular ejection fraction was significantly decreased in more than 60% of patients.2- Different guidelines show different cardiotoxicity risks which demands continuous cardio-oncological monitoring.
4年随访中曲妥珠单抗治疗乳腺癌期间的心脏毒性警报
背景:HER2+乳腺癌的辅助治疗包括阿霉素和曲妥珠单抗(一种产生心脏毒性的单克隆抗体)。曲妥珠单抗相关心脏毒性在阿根廷未选择人群中的实际流行病学影响仍然未知。目的:本研究的目的是评估在完成治疗>12个月后未选择的乳腺癌辅助治疗期间曲妥珠单抗相关心脏毒性的影响。方法:在888例乳腺癌前瞻性评估患者中,231例(38%)为HER2+,接受了阿霉素和曲妥珠单抗的辅助治疗。治疗前评估左心室射血分数,完成阿霉素治疗后评估左心室射血分数,随访中每3个月评估一次。根据美国心脏病学会的定义,心脏毒性定义为左心室射血分数下降>10%,并与B-31试验和MD安德森癌症中心的定义进行比较。结果:在平均48±12个月的随访期间,65% (n=150)的患者左心室射血分数比基线值下降>10%。在每组分析中,包括在b -31和MD安德森癌症中心的患者与美国心脏病学会定义的患者相比,在治疗期间左室射血分数下降的百分比更高:20%比20%。分别为20% vs. 16% (p <0.04), 42% vs. 41% vs. 33%的病例以左室射血分数<50%结束治疗(p=0.01)。结论:在48±12个月的心脏肿瘤学监测下接受曲妥珠单抗治疗的人群中,超过60%的患者1-左心室射血分数显著降低。2-不同的指南显示不同的心脏毒性风险,需要持续的心脏肿瘤监测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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