Kunimasa Kei, Kamada Risa, Oka Toru, Oboshi Makiko, Kimura Madoka, Inoue Takako, Tamiya Motohiro, Nishikawa Tatsuya, Yasui Taku, Shioyama Wataru, Nishino Kazumi, Imamura Fumio, Kumagai Toru, Fujita Masashi
Department of Thoracic Oncology, Osaka International Cancer Institute, Osaka, Japan.
Department of Onco-Cardiology, Osaka International Cancer Institute, Osaka, Japan.
JACC CardioOncol. 2020 Mar 17;2(1):1-10. doi: 10.1016/j.jaccao.2020.02.003. eCollection 2020 Mar.
The purpose of this study was to assess osimertinib-associated cardiac adverse events (AEs) in a real-world setting, using a retrospective single-center cohort study in Japan.
Cases of osimertinib-associated cardiac AEs have been reported but remain poorly understood.
A total of 123 cases of advanced non-small cell lung cancer (NSCLC) with confirmed mutations who received osimertinib monotherapy from 2014 to 2019 at the Osaka International Cancer Institute (Osaka, Japan) were evaluated. Cardiac AEs were defined according to Common Terminology Criteria for Adverse Events (CTCAE) version 5.0. Changes in left ventricular ejection fraction (LVEF) and rates of cancer therapeutics-related cardiac dysfunction (CTRCD), defined as a ≥10 % absolute decline in LVEF from baseline to a value of <53%, were further assessed in 36 patients in whom serial measurements of LVEF were obtained before and during osimertinib treatment.
Severe cardiac AEs (CTCAE grade 3 or higher) occurred in 6 patients (4.9%) after osimertinib administration. These AEs included acute myocardial infarction (n = 1), heart failure with reduced LVEF (n = 3), and valvular heart disease (n = 2). Five of the 6 patients had a history of cardiovascular risk factors or disease. Myocardial biopsies in 2 of the patients showed cardiomyocyte hypertrophy and lipofuscin deposition. In 36 patients assessed with serial LVEF, LVEF declined from 69.4 ± 4.2% to 63.4 ± 10.5% with osimertinib therapy (p < 0.001). CTRCD occurred in 4 patients with a nadir LVEF of 40.3 ± 9.1% with osimertinib.
In this retrospective cohort analysis, the incidence of cardiac AEs in patients treated with osimertinib was 4.9%. Additional prospective data collected from patients with NSCLC treated with osimertinib will be important in understanding the incidence, pathophysiology, and management of cardiac AEs with osimertinib.
本研究旨在通过日本一项回顾性单中心队列研究,评估在真实世界环境中奥希替尼相关的心脏不良事件(AE)。
已有奥希替尼相关心脏AE的病例报道,但仍了解不足。
对2014年至2019年在大阪国际癌症研究所(日本大阪)接受奥希替尼单药治疗的123例确诊有特定突变的晚期非小细胞肺癌(NSCLC)患者进行评估。心脏AE根据不良事件通用术语标准(CTCAE)第5.0版进行定义。在36例于奥希替尼治疗前和治疗期间进行了左心室射血分数(LVEF)系列测量的患者中,进一步评估LVEF的变化以及癌症治疗相关心脏功能障碍(CTRCD)的发生率,CTRCD定义为LVEF从基线绝对下降≥10%至<53%。
奥希替尼给药后,6例患者(4.9%)发生严重心脏AE(CTCAE 3级或更高)。这些AE包括急性心肌梗死(n = 1)、LVEF降低的心力衰竭(n = 3)和心脏瓣膜病(n = 2)。6例患者中有5例有心血管危险因素或疾病史。2例患者的心肌活检显示心肌细胞肥大和脂褐素沉积。在36例接受LVEF系列评估的患者中,奥希替尼治疗使LVEF从69.4±4.2%降至63.4±10.5%(p < 0.001)。奥希替尼治疗期间,4例患者发生CTRCD,LVEF最低点为40.3±9.1%。
在这项回顾性队列分析中,接受奥希替尼治疗的患者心脏AE的发生率为4.9%。从接受奥希替尼治疗的NSCLC患者中收集的更多前瞻性数据,对于了解奥希替尼相关心脏AE的发生率、病理生理学和管理至关重要。