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一项来自FAERS数据库的真实世界药物安全性监测研究,涉及单独接受帕博利珠单抗以及联合乐伐替尼治疗的肝细胞癌患者。

A real-world drug safety surveillance study from the FAERS database of hepatocellular carcinoma patients receiving pembrolizumab alone and plus lenvatinib.

作者信息

Wang Huaxiang, Li Junjun, Zhu Xiuling, Wang Ruling, Wan Yunyan

机构信息

Department of Hepatobiliary and Pancreatic Surgery, Taihe Hospital, Affiliated Hospital of Hubei University of Medicine, Shiyan, 442000, Hubei, China.

Department of Emergency Department, The Third People's Hospital of Fujian University of Traditional Chinese Medicine, Fuzhou, 350108, Fujian, China.

出版信息

Sci Rep. 2025 Jan 9;15(1):1425. doi: 10.1038/s41598-025-85831-4.

Abstract

Pembrolizumab plus Lenvatinib is regarded as a significant treatment option for advanced unresectable hepatocellular carcinoma (HCC). This study aims to meticulously monitor and identify adverse events (AEs) related to this combined therapy, enhance patient safety, and offer evidence-based recommendations for the appropriate use of these drugs. We gathered adverse drug reactions (ADRs)-related data from the FAERS database for HCC patients who received Pembrolizumab, both alone and in combination with Lenvatinib from the first quarter of 2014 to the fourth quarter of 2023. ADRs signal detection was performed using the ROR, PRR, BCPNN, MHRA, and MGPS methods. We gathered data on 459 and 358 AEs from patients with HCC treated with pembrolizumab alone and in combination with lenvatinib, respectively. Using four signal quantification techniques, we identified 50 and 38 distinct AEs, which were classified into 15 different System organ class (SOC) categories. Notably, the most common AEs associated with pembrolizumab were gastrointestinal disorders and hepatobiliary disorders. In both patient groups, the most frequently reported AEs were hepatic encephalopathy, blood bilirubin increased and diarrhea. We also observed some unexpected significant AEs, such as dehydration, skin ulcers, and intestinal perforation. The countries reporting the highest number of AEs were the United States, followed by China, France, and Japan. The median onset time for AEs related to pembrolizumab alone and its combination with lenvatinib was 80.5 days (interquartile range 20.0-217.3 days) and 77.5 days (interquartile range 19.7-212.3 days), respectively. This study offers new insights into the monitoring and management of ADRs in HCC patients receiving pembrolizumab alone or in combination with lenvatinib. It is crucial to closely monitor the safety of this treatment regimen in HCC patients to avoid serious AEs.

摘要

帕博利珠单抗联合乐伐替尼被视为晚期不可切除肝细胞癌(HCC)的一种重要治疗选择。本研究旨在细致监测并识别与这种联合治疗相关的不良事件(AE),提高患者安全性,并为这些药物的合理使用提供循证建议。我们从FAERS数据库收集了2014年第一季度至2023年第四季度接受帕博利珠单抗单药治疗以及联合乐伐替尼治疗的HCC患者的药物不良反应(ADR)相关数据。使用风险比(ROR)、比例报告比(PRR)、贝叶斯置信传播神经网络(BCPNN)、药品和保健品管理局(MHRA)以及多信号概率结构(MGPS)方法进行ADR信号检测。我们分别从接受帕博利珠单抗单药治疗和联合乐伐替尼治疗的HCC患者中收集了459例和358例AE的数据。使用四种信号量化技术,我们识别出50种和38种不同的AE,这些AE被归类为15个不同的系统器官类别(SOC)。值得注意的是,与帕博利珠单抗相关的最常见AE是胃肠道疾病和肝胆疾病。在两个患者组中,最常报告的AE是肝性脑病、血胆红素升高和腹泻。我们还观察到一些意外的严重AE,如脱水、皮肤溃疡和肠穿孔。报告AE数量最多的国家是美国,其次是中国、法国和日本。与帕博利珠单抗单药治疗及其联合乐伐替尼相关的AE的中位发生时间分别为80.5天(四分位间距20.0 - 217.3天)和77.5天(四分位间距19.7 - 212.3天)。本研究为接受帕博利珠单抗单药治疗或联合乐伐替尼治疗的HCC患者的ADR监测和管理提供了新的见解。密切监测HCC患者这种治疗方案的安全性以避免严重AE至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ea1/11718235/44973344353e/41598_2025_85831_Fig1_HTML.jpg

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