利用日本药物警戒数据库对老年患者中奥希替尼相关不良事件进行比例分析

Takashi Omoto, Junichi Asaka, Kenzo Kudo
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摘要

背景/目的:对于表皮生长因子受体突变阳性的晚期非小细胞肺癌老年患者来说,奥希替尼是一种耐受性良好的一线或二线治疗选择。然而,奥希替尼在老年患者中的安全性还需要进一步研究。在此,我们利用日本药物不良事件报告(JADER)数据库,通过比例失调分析确定了老年患者各种奥希替尼相关不良事件(AEs)的安全性信号:2004年4月至2023年3月的JADER数据库数据来自药品和医疗器械管理局网站。老年患者(≥70岁)中奥西替尼相关AE的安全信号检测采用相对老年报告几率比(ROR)确定。对于奥希替尼相关的AEs,我们提取了92个首选术语(PTs)和9个标准化MedDRA查询(SMQs):结果:在老年患者中发现了 "心肌病(PT)"和 "心肌病(SMQ)"的安全信号。最常与 "心肌病(SMQ)"相关的症状包括 "射血分数下降(PT)"、"心肌病(PT)"和 "应激性心肌病(PT)"。值得注意的是,这些结果中有 53.7% 为 "恢复 "或 "缓解"。老年患者出现 "心肌病(SMQ)"的中位时间为 85 天(范围=2-537 天):我们证明,与奥希替尼相关的心肌病患者相比,≥70 岁的患者有可能患上更多的奥希替尼相关心肌病。
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Disproportionality Analysis of Osimertinib-related Adverse Events in Elderly Patients Using the Japanese Pharmacovigilance Database.

Background/aim: Osimertinib is a well-tolerated first- or second-line treatment option for elderly patients with epidermal growth factor receptor mutation-positive advanced non-small cell lung cancer. However, the safety of osimertinib in elderly patients requires further investigation. Herein, we identified safety signals for various osimertinib-related adverse events (AEs) in elderly patients by disproportionality analysis using the Japanese Adverse Drug Event Report (JADER) database.

Patients and methods: Data from the JADER database from April 2004 to March 2023 were obtained from the Pharmaceuticals and Medical Devices Agency website. Safety signal detection for osimertinib-related AEs in elderly patients (≥70 years old) was determined using the relative elderly reporting odds ratio (ROR). For osimertinib-related AEs, we extracted 92 preferred terms (PTs) and nine standardized MedDRA queries (SMQs).

Results: Safety signals in elderly patients were detected for "Cardiomyopathy (PT)" and "Cardiomyopathy (SMQ)". The symptoms most frequently associated with "Cardiomyopathy (SMQ)" included "Ejection fraction decreased (PT)", "Cardiomyopathy (PT)", and "Stress cardiomyopathy (PT)". Notably, 53.7% of these outcomes were "Recovery" or "Remission". The median time to the onset of "Cardiomyopathy (SMQ)" in elderly patients was 85 days (range=2-537 days).

Conclusion: We demonstrated that patients ≥70 years potentially have increased osimertinib-related cardiomyopathy compared with patients <70 years. In the future, it is necessary to conduct research focusing on cardiomyopathy in elderly patients.

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