静脉注射英夫利昔单抗与皮下注射英夫利昔单抗在炎症性肠病患者缓解率、安全性、成本和患者偏好方面的比较:一项系统综述和荟萃分析

Alejandro Nieto Dominguez , Abhishek Bhurwal , Hemant Mutneja , Sarah E. Eichinger , Bhanu Pinnam , Daniel Guifarro Rivera , Chun-Wei Pan
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引用次数: 0

摘要

背景和目的英夫利昔单抗被广泛用作炎症性肠病(IBD)的主要治疗药物,传统上是静脉给药。皮下(SC)制剂似乎提供了更方便的给药途径。这是一项系统综述和荟萃分析,比较了静脉(IV)和SC给药途径英夫利昔单抗的结果。方法分析1997年1月1日至2023年9月9日期间,所有观察性研究和随机对照试验,比较IV和SC英夫利昔单抗治疗成年IBD患者的疗效、有效性、安全性、成本和患者偏好。主要结果是比较SC和IV英夫利昔单抗在IBD患者中的缓解率。次要结果是定性和定量地分析IV英夫利昔单抗与SC英夫利昔单抗的不同安全性和不良事件,比较两组之间的成本,并评估我们系统评价中发现的不同研究中的患者偏好。结果定性综合纳入研究20篇,定量综合纳入研究9篇,共960例患者。IV组和SC组在8周、6个月和1年的临床缓解率无显著差异。改用SC英夫利昔单抗总体上是安全的。使用SC英夫利昔单抗的患者满意度更高,并具有额外的成本节约效益。结论系统评价和荟萃分析显示,SC英夫利昔单抗可能是一种安全、经济、耐受性良好的替代方案,可实现IBD患者的疾病缓解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Comparison of Intravenous Infliximab Versus Subcutaneous Infliximab on Remission Rates, Safety, Costs, Patient Preferences in Patients With Inflammatory Bowel Disease: A Systematic Review and Meta-Analysis

Background and Aims

Infliximab, widely used as a mainstay treatment of inflammatory bowel disease (IBD), is traditionally administered intravenously. The subcutaneous (SC) formulation appears to offer a more convenient route of administration. This is a systematic review and meta-analysis comparing the outcomes of intravenous (IV) and SC routes of administration of Infliximab.

Methods

All observational studies and randomized controlled trials comparing efficacy, effectiveness, safety, costs, and patient preferences between IV vs SC infliximab in adult human patients with IBD between January 1, 1997, and September 9, 2023, were analyzed. The primary outcome was comparison of the remission rates between SC and IV infliximab in IBD patients. Secondary outcomes were analyzing the different safety profiles and adverse events of IV infliximab vs SC infliximab qualitatively and quantitatively, comparing costs between both groups and evaluating patient preferences among the different studies found on our systematic review.

Results

Twenty studies were included in the qualitative synthesis and 9 were included in the quantitative synthesis, with a total of 960 patients. There was no significant difference in clinical remission rates between the IV and SC infliximab groups at 8 weeks, 6 months, and 1 year. Switching to SC infliximab was overall safe. Patient satisfaction was higher in patients using SC infliximab, with additional cost-saving benefits.

Conclusion

The systematic review and meta-analysis reveal that SC infliximab could be a safe, cost-effective, well tolerated alternative for achieving disease remission in patients with IBD.
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来源期刊
Gastro hep advances
Gastro hep advances Gastroenterology
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