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基于FAERS的多发性骨髓瘤蛋白酶体抑制剂不良事件信号挖掘

Signal mining of adverse events of proteasome inhibitors in multiple myeloma based on FAERS.

作者信息

Peng Yuan, Zhou Yuying, Shu Kaisen, Jia Xu, Zhong Yan

机构信息

Department of Pharmacy, Affiliated Hospital of North Sichuan Medical College, Nanchong, Sichuan, China.

School of Pharmacy, North Sichuan Medical College, Nanchong, Sichuan, China.

出版信息

Front Pharmacol. 2024 Sep 3;15:1396378. doi: 10.3389/fphar.2024.1396378. eCollection 2024.

Abstract

OBJECTIVE

To mine and analyze adverse events (AEs) related to proteasome inhibitors in multiple myeloma based on the FDA Adverse Event Reporting System (FAERS), providing references for rational clinical medication.

METHODS

AE data related to multiple myeloma proteasome inhibitors were collected from the FAERS from the first quarter of 2010 to the first quarter of 2024. Signal mining of AEs was conducted using the reporting odds ratio method and Bayesian confidence propagation neural network method.

RESULTS

A total of 8,805 reports for bortezomib, 5,264 for carfilzomib, and 8,771 for ixazomib were collected, with corresponding AE signals of 474, 279, and 287, respectively, involving 23, 21, and 22 System Organ Classes (SOCs). The report information for the three drugs tended to be consistent: more cases were reported in males than in females; the majority of patients were 65 years and over; AEs mostly occurred within 6 months of medication; the outcomes primarily consisted of hospitalization, prolonged hospital stay, and other serious adverse events; the primary reporting country was the United States. The most affected SOCs were infections and infestations, general disorders and administration site conditions, and blood and lymphatic system disorders.

CONCLUSION

The overall distribution of AEs for the three multiple myeloma proteasome inhibitors was consistent, but there were certain differences in specific AE signal characteristics, which should be noted in clinical applications.

摘要

目的

基于美国食品药品监督管理局不良事件报告系统(FAERS)挖掘和分析与多发性骨髓瘤蛋白酶体抑制剂相关的不良事件(AE),为临床合理用药提供参考。

方法

收集2010年第一季度至2024年第一季度FAERS中与多发性骨髓瘤蛋白酶体抑制剂相关的AE数据。采用报告比值比法和贝叶斯置信传播神经网络法对AE进行信号挖掘。

结果

共收集到硼替佐米报告8805份、卡非佐米报告5264份、伊沙佐米报告8771份,相应的AE信号分别为474个、279个和287个,涉及23个、21个和22个系统器官类别(SOC)。三种药物的报告信息趋于一致:男性报告的病例多于女性;大多数患者年龄在65岁及以上;AE大多发生在用药后6个月内;结局主要包括住院、住院时间延长及其他严重不良事件;主要报告国家为美国。受影响最严重的SOC为感染和寄生虫感染、全身疾病和给药部位状况以及血液和淋巴系统疾病。

结论

三种多发性骨髓瘤蛋白酶体抑制剂AE的总体分布一致,但具体AE信号特征存在一定差异,临床应用中应予以注意。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/795f/11405236/f78abce2ded4/fphar-15-1396378-g001.jpg

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