Fluoxetine, fluvoxamine, and hearing loss or tinnitus after cisplatin treatment: A retrospective cohort study.

IF 2.5 4区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Journal of Investigative Medicine Pub Date : 2024-08-01 Epub Date: 2024-04-30 DOI:10.1177/10815589241247796
Joseph Magagnoli, Tammy H Cummings, James W Hardin, S Scott Sutton, Jayakrishna Ambati
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引用次数: 0

Abstract

Cisplatin use is often limited by its ototoxic side effects, which can lead to irreversible hearing loss. Preventing cisplatin-induced ototoxicity is crucial to improve patient outcomes. Fluoxetine and fluvoxamine, both selective serotonin reuptake inhibitors antidepressants, inhibit the NLR pyrin domain-containing protein 3 inflammasome, a potential therapeutic target for preventing ototoxicity. However, human studies have not evaluated if these antidepressants may protect against cisplatin-induced ototoxicity. The object of this study is to assess the association between fluoxetine or fluvoxamine use and incidence of hearing loss or tinnitus in a large cohort of patients receiving cisplatin chemotherapy. We use a retrospective cohort study within the U.S. Department of Veterans Affairs healthcare system. Adult patients with cancer who received cisplatin chemotherapy between 2000 and 2023 are included. Incidence of ototoxicity, defined by international classification of diseases revision 9-CM or international classification of diseases revision 10-CM diagnoses of hearing loss or tinnitus is compared between concurrent use of fluoxetine or fluvoxamine and cisplatin alone. A total of 20,552 patients were included. Of those, 489 received cisplatin and fluoxetine or fluvoxamine. After propensity score adjustment, the hazard of ototoxicity was lower in the group receiving fluoxetine or fluvoxamine compared to the group receiving cisplatin alone (HR = 0.62, 95% CI = (0.41-0.94)). Fluoxetine or fluvoxamine use may be associated with a reduced risk of cisplatin-induced ototoxicity. Randomized clinical trials are needed to confirm these findings and establish the efficacy of the medications in ototoxicity prevention. Further research is also warranted to investigate the potential mechanisms underlying this protective effect.

氟西汀、氟伏沙明与顺铂治疗后的听力损失或耳鸣:一项回顾性队列研究。
顺铂的耳毒性副作用可导致不可逆的听力损失,这往往限制了顺铂的使用。预防顺铂引起的耳毒性对改善患者预后至关重要。氟西汀和氟伏沙明均为选择性 5-羟色胺再摄取抑制剂类抗抑郁药,可抑制 NLR 含吡咯啉结构域蛋白 3 炎性体,这是预防耳毒性的潜在治疗靶点。然而,人类研究尚未评估这些抗抑郁药是否能防止顺铂诱发的耳毒性。本研究的目的是评估一大批接受顺铂化疗的患者中使用氟西汀或氟伏沙明与听力损失或耳鸣发生率之间的关系。我们采用的是美国退伍军人事务部医疗系统内的一项回顾性队列研究。研究对象包括 2000 年至 2023 年期间接受顺铂化疗的成年癌症患者。比较了同时使用氟西汀或氟伏沙明与单独使用顺铂之间的耳毒性发生率,耳毒性的定义是国际疾病分类修订版 9-CM 或国际疾病分类修订版 10-CM 诊断为听力损失或耳鸣。共纳入了 20,552 名患者。其中,489 人接受了顺铂和氟西汀或氟伏沙明治疗。经过倾向评分调整后,接受氟西汀或氟伏沙明治疗组的耳毒性风险低于单独接受顺铂治疗组(HR = 0.62,95% CI = (0.41-0.94))。使用氟西汀或氟伏沙明可能会降低顺铂诱发耳毒性的风险。需要进行随机临床试验来证实这些发现,并确定药物在预防耳毒性方面的疗效。此外,还需要进一步研究这种保护作用的潜在机制。
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
Journal of Investigative Medicine
Journal of Investigative Medicine 医学-医学:内科
CiteScore
4.90
自引率
0.00%
发文量
111
审稿时长
24 months
期刊介绍: Journal of Investigative Medicine (JIM) is the official publication of the American Federation for Medical Research. The journal is peer-reviewed and publishes high-quality original articles and reviews in the areas of basic, clinical, and translational medical research. JIM publishes on all topics and specialty areas that are critical to the conduct of the entire spectrum of biomedical research: from the translation of clinical observations at the bedside, to basic and animal research to clinical research and the implementation of innovative medical care.
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