首页|基于真实世界的派安普利单抗临床应用及安全性分析

基于真实世界的派安普利单抗临床应用及安全性分析

扫码查看
目的 探讨基于真实世界派安普利单抗的临床应用及安全性.方法 收集某肿瘤专科医院 2022 年 4 月至 12 月使用派安普利单抗的患者 13 例,回顾性分析其基本信息、临床诊断、用药信息等临床应用情况及安全性.结果 13 例患者中,男女性别比为 1∶1.6,年龄(61.1±14.5)岁,53.85%的患者合并慢性疾病.派安普利单抗在临床使用中存在超适应证(100.00%)、联用其他抗肿瘤药物(76.92%)等超药品说明书用药情况;药品不良反应(ADR)发生率为23.08%,其中,3级ADR 2例,分别为腹泻和肝功能损伤.结论 派安普利单抗发生的ADR与药品说明书中的ADR类似,应进一步扩大样本量,把握使用指征,确保安全、合理用药.
Clinical Application and Safety of Penpulimab Based on Real-World Study
Objective To investigate the clinical application and safety of penpulimab in the real world.Methods Thirteen patients treated with penpulimab from April to December 2022 in a cancer hospital were selected,and the patients' basic information,clinical diagnosis,medication information,and other clinical application and safety were retrospectively analyzed.Results Among the 13 patients,the gender ratio of male to female was 1∶1.6,the age was(61.1±14.5)years old,and 53.85%of the patients had chronic diseases.Off-label use of pembrolizumab occurred in clinical use,such as unapproved indications(100.00%)and combinations with other antineoplastic agents(76.92%).The incidence of adverse drug reactions(ADRs)was 23.08%,with two cases of grade Ⅲ ADRs,including diarrhea and liver function damage.Conclusion The ADRs of penpulimab are similar to the ADRs mentioned in the drug package insert,and the sample size should be further expanded to grasp the indications for use and ensure safe and rational medication.

penpulimabreal-world studysafety

朱文靖、戴钰洁、姚媛、秦越、王君萍

展开 >

中国科学院合肥肿瘤医院,安徽 合肥 230031

派安普利单抗 真实世界研究 安全性

中国科学院合肥物质科学研究院院长基金

YZJ2023QN48

2024

中国药业
重庆市食品药品监督管理局

中国药业

CSTPCD
影响因子:1.369
ISSN:1006-4931
年,卷(期):2024.33(1)
  • 5