帕妥珠单抗介导的心脏毒性:单中心研究。

A. Acibuca, A. Uçar, A. Sümbül, A. Sezer, Ş. Demircan, H. Müderrisoğlu, Ö. Özyi̇lkan
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引用次数: 0

摘要

帕妥珠单抗介导的心脏毒性:单中心研究。目的:最近的临床试验表明,与单抗曲妥珠单抗相比,帕妥珠单抗联合曲妥珠单抗可改善细胞对治疗的反应,并提供生存期获益。然而,它引起了人们对心脏毒性的附加风险的担忧。帕妥珠单抗引起的心脏毒性的实际数据是有限的。材料和方法:纳入2017年1月至2022年6月期间接受曲妥珠单抗联合帕妥珠单抗治疗并定期接受经胸超声心动图检查的乳腺癌患者,作为对照访视的一部分。我们采用描述性统计分析来评估患者的特征和治疗方法,这些特征和治疗方法可能会增加心脏不良事件的风险。在帕妥珠单抗治疗期间,通过二维超声心动图在基线和每三个月测量左心室射血分数(LVEF)来评估心脏毒性,并将LVEF下降定义为> 10%至低于55%。结果:118例患者符合纳入标准。人口年龄中位数为51岁(41-60岁)。帕妥珠单抗治疗的中位持续时间为15(9-57)周。两名患者因过敏反应而停止了帕妥珠单抗治疗,另外两名患者因心脏毒性而停止了治疗。两名患者的LVEF均未恢复到基线值。结论:在目前的研究中,心脏毒性的发生率(1.69%)并不高于单抗曲妥珠单抗的预期。以往研究的数据和本研究的结果支持帕妥珠单抗不会增加心脏毒性。尽管如此,仍需要大规模的临床试验来验证帕妥珠单抗在现实世界中的心脏安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pertuzumab-mediated Cardiotoxicity: A Single Center Study.
Pertuzumab-mediated Cardiotoxicity: A Single Center Study. Objective: Recent clinical trials have shown that adding pertuzumab to trastuzumab improved the cellular response to therapy and provides a survival benefit compared with trastuzumab alone. However, it has raised concerns about additive risk of cardiotoxicity. Real life data on pertuzumab-induced cardiotoxicity are limited. Materials and Methods: Patients a diagnosis of breast cancer who had been treated trastuzumab plus pertuzumab between January 2017 and June 2022 and had undergone regularly transthoracic echocardiography, as a part of control visits, in our medical center were included. We performed descriptive statistical analysis to evaluate the patients’ characteristics and therapies, which could increase the risk of cardiac adverse events. Cardiotoxicity was evaluated by serial left ventricular ejection fraction (LVEF) measuring by 2D echocardiography at baseline and every three months during pertuzumab therapy and was defined as a decrease in LVEF > 10% to below 55%. Results: There were 118 patients fulfilling the inclusion criteria. The median age of the population was 51 (41-60) years. The median duration of pertuzumab therapy was 15 (9–57) weeks. Pertuzumab therapy was discontinued in two patients because of an allergic reaction and in other two patients due to cardiotoxicity. The reduced LVEF did not recover to baseline values in either patient. Conclusion: The incidence of cardiotoxicity (1.69%) in the current study was no higher than expected for trastuzumab alone. Data from previous studies and the results of this study support that pertuzumab causes no increase in cardiotoxicity. Still, large clinical trials are needed to verify the cardiac safety of pertuzumab in a real-world setting.
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