Wang Bingqing, Zhao Kaidi, Xian Ningyi, Ren Landong, Liu Jiashu, Tu Chen, Zhang Dewu
Department of Dermatology, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Department of Dermatology, Xi'an Children's Hospital, Xi'an, China.
Front Pharmacol. 2025 May 16;16:1497708. doi: 10.3389/fphar.2025.1497708. eCollection 2025.
Vismodegib, an inhibitor of the Hedgehog signaling pathway, has been widely used in the treatment of advanced basal cell carcinoma. Given its critical role in managing advanced basal cell carcinoma and the relatively high rate of treatment discontinuation, it is crucial to comprehensively understand its safety profile in real-world settings.
This study analyzed all adverse event reports that identified vismodegib as the primary suspected drug since 2012 in the FDA Adverse Event Reporting System database. Disproportionality analysis was conducted using four algorithms: Reporting odds ratio, proportional reporting ratio, multi-item gamma Poisson shrinker, and Bayesian confidence propagation neural network to assess the safety profile of vismodegib in clinical practice. Additionally, this study employed the Weibull distribution to model the risk of adverse events over time.
A total of 7,733 adverse event reports associated with vismodegib were identified from the FDA Adverse Event Reporting System database. Data mining identified positive signals for on-label adverse events, such as muscle spasms, taste alterations, alopecia, fatigue, and weight decreased. Notably, potential off-label adverse events including squamous cell carcinoma, dehydration and dysphagia were also detected. The median time to onset for these adverse events was 69 days post-drug administration, highlighting the importance of close monitoring, particularly within the initial 2 months of treatment.
This study provides valuable insights into the real-world safety profile of vismodegib. It not only confirms the known adverse events on the label, but also suggests several potential novel adverse events, thereby supporting a more informed and rational use of vismodegib in clinical practice.
维莫德吉是一种Hedgehog信号通路抑制剂,已广泛用于治疗晚期基底细胞癌。鉴于其在治疗晚期基底细胞癌中的关键作用以及相对较高的治疗中断率,全面了解其在实际临床环境中的安全性至关重要。
本研究分析了自2012年以来美国食品药品监督管理局不良事件报告系统数据库中所有将维莫德吉确定为主要可疑药物的不良事件报告。使用四种算法进行不成比例分析:报告比值比、比例报告比、多项目伽马泊松收缩器和贝叶斯置信传播神经网络,以评估维莫德吉在临床实践中的安全性。此外,本研究采用威布尔分布对不良事件随时间的风险进行建模。
从美国食品药品监督管理局不良事件报告系统数据库中识别出总共7733份与维莫德吉相关的不良事件报告。数据挖掘确定了标签上不良事件的阳性信号,如肌肉痉挛、味觉改变、脱发、疲劳和体重减轻。值得注意的是,还检测到潜在的标签外不良事件,包括鳞状细胞癌、脱水和吞咽困难。这些不良事件的中位发病时间为给药后69天,突出了密切监测的重要性,尤其是在治疗的最初2个月内。
本研究为维莫德吉的实际安全性提供了有价值的见解。它不仅证实了标签上已知的不良事件,还提示了几种潜在的新不良事件,从而支持在临床实践中更明智、合理地使用维莫德吉。