Suppr超能文献

生物疗法治疗显微镜下结肠炎的疗效和安全性:系统评价和荟萃分析。

Efficacy and safety of biologic therapy in microscopic colitis: systematic review and meta-analysis.

机构信息

Division of Gastroenterology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston.

Division of Hospital Medicine, Cambridge Health Alliance and Harvard Medical School, Cambridge.

出版信息

Eur J Gastroenterol Hepatol. 2022 Oct 1;34(10):1000-1006. doi: 10.1097/MEG.0000000000002409. Epub 2022 Jul 19.

Abstract

BACKGROUND

This systematic review and meta-analysis sought to evaluate the effectiveness and safety of biologic therapy in the treatment of steroid-refractory microscopic colitis (MC).

METHODS

We searched MEDLINE, Embase, Web of Science, and Cochrane Central to identify articles and abstracts reporting efficacy or safety data on biologic use (infliximab, adalimumab, certolizumab, golimumab, vedolizumab, ustekinumab, and tofacitinib) for induction and maintenance of remission in MC. We assessed clinical remission and response rates and all reported adverse events (AEs).

RESULTS

A total of 376 studies were screened yielding 13 articles (including four abstracts) with a combined information on 78 patients for efficacy and safety outcomes. Most studies were case series. Vedolizumab was used in five studies, adalimumab in three, and a combination of infliximab and adalimumab in five studies. The rates of remission were 66.08% (95% CI, 36.79-95.37%; I2 , 71%) at weeks 3-6 and 54.20% (95% CI, 39.39-69.01%; I2 , 0%) at weeks 12-16. Clinical response rates were 100% (95% CI, 88.04-100%; I2 , 0%) at weeks 3-6 and 67.20% (95% CI, 47.72-86.69%; I2 , 52%) at weeks 12-16. Most frequent AE was medication discontinuation with a pooled incidence of 16.1% (95% CI, 5.9-37.5%). No deaths attributable to biologic use were reported. The overall quality of evidence was very low due to the high risk of biases.

CONCLUSION

Low-quality evidence supports the short-term efficacy of biologics in budesonide refractory MC. While our findings represent the most comprehensive evaluation of biologic therapy in severe MC, further research including randomized clinical trials is needed to better define the role of specific agents and long-term therapy.

摘要

背景

本系统评价和荟萃分析旨在评估生物疗法在治疗类固醇难治性显微镜结肠炎(MC)中的疗效和安全性。

方法

我们检索了 MEDLINE、Embase、Web of Science 和 Cochrane 中心,以查找报告生物制剂(英夫利昔单抗、阿达木单抗、certolizumab、戈利木单抗、vedolizumab、ustekinumab 和 tofacitinib)在 MC 诱导和维持缓解中疗效或安全性数据的文章和摘要。我们评估了临床缓解和反应率以及所有报告的不良事件(AE)。

结果

共筛选出 376 项研究,得出了 13 项包含 4 项摘要的研究,这些研究共纳入了 78 例患者的疗效和安全性数据。大多数研究为病例系列研究。vedolizumab 用于 5 项研究,阿达木单抗用于 3 项研究,英夫利昔单抗和阿达木单抗联合使用用于 5 项研究。第 3-6 周时的缓解率为 66.08%(95%可信区间,36.79-95.37%;I2,71%),第 12-16 周时为 54.20%(95%可信区间,39.39-69.01%;I2,0%)。第 3-6 周时的临床反应率为 100%(95%可信区间,88.04-100%;I2,0%),第 12-16 周时为 67.20%(95%可信区间,47.72-86.69%;I2,52%)。最常见的 AE 是药物停药,合并发生率为 16.1%(95%可信区间,5.9-37.5%)。未报告与生物制剂使用相关的死亡。由于存在高度偏倚风险,证据质量总体较低。

结论

低质量证据支持生物制剂在布地奈德难治性 MC 中的短期疗效。虽然我们的研究结果代表了对严重 MC 中生物治疗的最全面评估,但需要进一步的研究,包括随机临床试验,以更好地确定特定药物的作用和长期治疗。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验