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非那雄胺相关性阴茎弯曲/ Peyronie 病不良事件报告是否值得进一步临床研究?基于美国食品药品监督管理局(FDA)和欧洲药品管理局(EMA)药物警戒数据库的比例失调分析。

Are finasteride-related penile curvature/Peyronie's disease Adverse Event Reports worthy of further clinical investigation? Disproportionality analysis based on both the Food and Drug Administration (FDA) and the European Medicines Agency (EMA) pharmacovigilance databases.

机构信息

Università Vita-Salute San Raffaele, Milan, Italy.

Division of Experimental Oncology/Unit of Urology, URI, IRCCS Ospedale San Raffaele, Milan, Italy.

出版信息

Int J Impot Res. 2023 Aug;35(5):465-471. doi: 10.1038/s41443-022-00568-2. Epub 2022 May 5.

Abstract

A limited number of studies have described patients on finasteride showing findings which were consistent with Peyronie's disease (PD). We aimed to detect a pharmacovigilance signal of possible association between finasteride and PD-related clinical features. The Food and Drug Administration (FDA) Adverse Event Reporting System (FAERS) database was queried to identify the ten drugs which were associated the most with the adverse drug reactions (ADRs) recorded as "penile curvature" and/or "Peyronie's disease". A similar analysis, including the same drugs, was carried out for the EMA (European Medicines Agency) EudraVigilance (EV) database. Descriptive data have been analyzed, and Proportional Reporting Ratios (PRRs) have been computed against the other nine drugs of the database. Overall, 860 reports of "penile curvature" and/or "Peyronie's disease", were identified in the FAERS database, 214 of which (24.9%) were associated with finasteride. Most reports (56.9%) were submitted by healthcare professionals. Where a treatment-indication was stated, the vast majority of reports (176/210; 83.8%) were associated with androgenetic alopecia. The outcome of most ADRs was "serious" (82.2%), with 96 ADRs resulting in levels of permanent disability. For 97/214 individual cases, penile curvature/PD reports were not part of a syndromic cluster suggestive of post-finasteride syndrome (PFS). The PRR resulted 6.6 (95% CI: 5.6-7.8) and 11.8 (95% CI: 9.08-15.33), respectively, in the FAERS and in the EV databases. Notwithstanding the related limitations and biasing factors of pharmacovigilance studies based on spontaneous reporting, the PRR values here identified should be interpreted as strong signals of disproportionality. These findings, per se, are however not useful to confirm any causal association. Clinical studies are needed to investigate on the possible role for finasteride in causing PD-related clinical features, an hypothesis which remains highly speculative due to the very questionable quality of present data.

摘要

已有少量研究描述了服用非那雄胺的患者出现了符合佩罗尼氏病(PD)的表现。我们旨在检测非那雄胺与 PD 相关临床特征之间可能存在关联的药物警戒信号。我们查询了美国食品药品监督管理局(FDA)不良事件报告系统(FAERS)数据库,以确定与记录为“阴茎弯曲”和/或“佩罗尼氏病”的不良药物反应(ADR)最相关的十种药物。对包含相同药物的欧洲药品管理局(EMA)欧洲药品警戒数据库(EV)也进行了类似的分析。已经分析了描述性数据,并针对数据库中的其他九种药物计算了比例报告比值(PRR)。总体而言,在 FAERS 数据库中,共识别出 860 例“阴茎弯曲”和/或“佩罗尼氏病”报告,其中 214 例(24.9%)与非那雄胺相关。大多数报告(56.9%)由医疗保健专业人员提交。在报告治疗适应症的情况下,绝大多数报告(176/210;83.8%)与雄激素性脱发相关。大多数 ADR 的结果为“严重”(82.2%),96 例 ADR 导致永久性残疾。对于 214 例个体病例中的 97 例,阴茎弯曲/PD 报告并非提示非那雄胺综合征(PFS)的综合征性簇的一部分。PRR 分别在 FAERS 和 EV 数据库中得出 6.6(95%CI:5.6-7.8)和 11.8(95%CI:9.08-15.33)。尽管基于自发报告的药物警戒研究存在相关限制和偏倚因素,但此处确定的 PRR 值应被视为不成比例的强烈信号。这些发现本身并不能用于确认任何因果关联。需要进行临床研究来调查非那雄胺在引起 PD 相关临床特征方面的可能作用,由于现有数据的质量非常可疑,因此该假设仍然具有高度推测性。

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