Cardiotoxicity of the adjuvant trastuzumab in a Saudi population: clinical experience of a single institution

Q4 Medicine Forum of Clinical Oncology Pub Date : 2016-06-01 DOI:10.1515/fco-2016-0007
R. Hamed, K. Salim, A. Alzahrani, S. Elsamany
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引用次数: 3

Abstract

Abstract Purpose Adjuvant trastuzumab is currently an internationally standard for the treatment of localised breast cancer that over express HER2 with the most adverse effect being cardiotoxicity. We conducted this study to evaluate the cardiac safety of trastuzumab in clinical practice. Methods This study is a retrospective observational single institutional study conducted in the Oncology Center of King Abdulla Medical City (KAMC), Makkah, Saudi Arabia, from June 2011 to January 2014. We evaluated the incidence of cardio toxicity and associated risk factors during adjuvant trastuzumab treatment. Results Of 57 patients, 20 patients (35%) exhibited cardiotoxicity. About 14% of patients had drop of left ventricular ejection fraction (LVEF) below 50%, whilst 10% and 15% drop of LVEF below their baseline levels were found in 30% and 5% of patients, respectively. About 98.3% of our patients have completed treatment, of whom 21% had a provisional interruption because of a fall in LVEF. A definitive trastuzumab discontinuation has been made in 1.75% of cases because of a nonregressive reduction in LVEF. Analysis of risk factors related to trastuzumab cardio toxicity found that patients older than 40 years were more likely to develop cardio toxicity compared to those younger than 40 years. This difference was statistically significant (p = 0.042). Conclusion In our study, the cardiac safety seems comparable with the literature data. Trastuzumab-related cardiotoxicity is manifested by an asymptomatic decrease in the LVEF and less commonly by clinical heart failure. Most instances are transient, asymptomatic and reversible.
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辅助曲妥珠单抗在沙特人群中的心脏毒性:单一机构的临床经验
目的辅助曲妥珠单抗是目前治疗HER2过表达的局部乳腺癌的国际标准,其最大的不良反应是心脏毒性。我们开展这项研究是为了在临床实践中评估曲妥珠单抗的心脏安全性。方法本研究是2011年6月至2014年1月在沙特阿拉伯麦加阿卜杜拉国王医疗城(KAMC)肿瘤中心进行的回顾性观察性单机构研究。我们评估了辅助曲妥珠单抗治疗期间心脏毒性和相关危险因素的发生率。结果57例患者中,20例(35%)出现心脏毒性。约14%的患者左室射血分数(LVEF)低于50%,而30%和5%的患者LVEF分别低于基线水平10%和15%。约98.3%的患者完成了治疗,其中21%的患者因LVEF下降而暂时中断治疗。由于LVEF的非退行性降低,1.75%的病例最终停用曲妥珠单抗。对曲妥珠单抗心脏毒性相关危险因素的分析发现,与40岁以下的患者相比,40岁以上的患者更容易发生心脏毒性。差异有统计学意义(p = 0.042)。结论在我们的研究中,心脏安全性似乎与文献数据相当。曲妥珠单抗相关的心脏毒性表现为LVEF的无症状降低,临床心力衰竭较少。大多数病例是短暂的、无症状的和可逆的。
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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来源期刊
Forum of Clinical Oncology
Forum of Clinical Oncology Medicine-Oncology
CiteScore
0.50
自引率
0.00%
发文量
3
审稿时长
6 weeks
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