Teprotumumab-Related Hearing Loss: A Large-Scale Analysis and Review of Voluntarily Reported Patient Complaints to the Food and Drug Administration (FDA).

IF 1.2 4区 医学 Q3 OPHTHALMOLOGY
Gerald McGwin, Cynthia Owsley, Matthew G Vicinanzo
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引用次数: 0

Abstract

Purpose: Accumulating case reports and series have suggested that teprotumumab may significantly increase the risk of hearing impairment that, in some cases, does not resolve. This study investigates the association between hearing impairment and teprotumumab use.

Methods: A disproportionality analysis was conducted using the United States Food and Drug Administration Adverse Event Reporting System, a publicly accessible database used for postmarketing surveillance and research. All adverse event reports containing the terms "teprotumumab" or "Tepezza" and a similar comparison group from all patients with the same indications for teprotumumab use (e.g., autoimmune thyroiditis, endocrine ophthalmopathy, and hyperthyroidism) but who had not received the drug were selected. Hearing impairment events were identified using the hearing impairment Standardized MedDRA Query.

Results: A total of 940 teprotumumab-associated adverse events were identified, including 84 hearing-related adverse events, with the first reported to the Food and Drug Administration in April 2020. A comparison group of 32,794 nonteprotumumab adverse events was identified with 127 hearing-related adverse events reported. Use of teprotumumab in patients with thyroid conditions was associated with a nearly 24-fold (proportional reporting ratio [PRR] 23.6, 95% confidence interval [CI]: 18.1-30.8) increased likelihood of any hearing disorder ( p value <0.0001). The association was specifically elevated for a variety of deafness conditions (e.g., bilateral deafness [PRR: 41.9; 95% CI: 12.8-136.9]), Eustachian tube disorders (PRR: 34.9; 95% CI: 4.9-247.4), hypoacusis (PRR: 10.1; 95% CI: 7.6-13.3), and tinnitus (PRR: 8.7; 95% CI: 6.2-12.1).

Conclusions: Patients treated with teprotumumab should receive warnings regarding the increased risk of hearing-related impairments and receive audiometry before, during, and after treatment.

与特罗单抗相关的听力损失:对自愿向美国食品药品管理局(FDA)报告的患者投诉的大规模分析和回顾。
目的:不断积累的病例报告和系列研究表明,替普鲁单抗可能会显著增加听力损伤的风险,在某些病例中,听力损伤无法缓解。本研究调查了听力损伤与使用替普鲁单抗之间的关联:方法:使用美国食品和药物管理局不良事件报告系统进行了比例失调分析,该系统是一个可公开访问的数据库,用于上市后监测和研究。我们选取了所有含有 "替普鲁单抗 "或 "Tepezza "字样的不良事件报告,并从所有具有相同替普鲁单抗适应症(如自身免疫性甲状腺炎、内分泌眼病和甲状腺功能亢进症)但未接受过该药物治疗的患者中选取了一个相似的对比组。使用听力损伤标准化 MedDRA 查询确定听力损伤事件:结果:共发现940例泰普鲁单抗相关不良事件,包括84例听力相关不良事件,其中第一例于2020年4月上报美国食品药品管理局。对比组共发现32794例非特普鲁单抗不良事件,其中报告了127例与听力相关的不良事件。甲状腺疾病患者使用替普鲁单抗会导致听力相关不良事件增加近24倍(比例报告比[PRR]23.6,95%置信区间[CI]:18.1-30.8):18.1-30.8)增加:接受替普鲁单抗治疗的患者应收到关于听力相关损伤风险增加的警告,并在治疗前、治疗期间和治疗后接受听力测定。
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来源期刊
CiteScore
2.50
自引率
10.00%
发文量
322
审稿时长
3-8 weeks
期刊介绍: Ophthalmic Plastic and Reconstructive Surgery features original articles and reviews on topics such as ptosis, eyelid reconstruction, orbital diagnosis and surgery, lacrimal problems, and eyelid malposition. Update reports on diagnostic techniques, surgical equipment and instrumentation, and medical therapies are included, as well as detailed analyses of recent research findings and their clinical applications.
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