Suppr超能文献

比美吉珠单抗及其他生物制剂治疗中度至重度斑块状银屑病的疗效:系统文献综述与网状Meta分析

Efficacy of Bimekizumab and Other Biologics in Moderate to Severe Plaque Psoriasis: A Systematic Literature Review and a Network Meta-Analysis.

作者信息

Armstrong April, Fahrbach Kyle, Leonardi Craig, Augustin Matthias, Neupane Binod, Kazmierska Paulina, Betts Marissa, Freitag Andreas, Kiri Sandeep, Taieb Vanessa, Slim Mahmoud, Gomez Natalie Nunez, Warren Richard B

机构信息

Keck School of Medicine of USC, Dermatology, Los Angeles, CA, USA.

Evidera, Inc, 140 Kendrick St, 3rd Floor, Needham, MA, 02494, USA.

出版信息

Dermatol Ther (Heidelb). 2022 Aug;12(8):1777-1792. doi: 10.1007/s13555-022-00760-8. Epub 2022 Jul 7.

Abstract

INTRODUCTION

Biologic treatments are increasingly being used in the management of moderate to severe plaque psoriasis (PSO). Bimekizumab is a selective inhibitor of both interleukin (IL)-17A and IL-17F approved for the treatment of moderate to severe PSO. Although bimekizumab trials provide comparisons to secukinumab, adalimumab and ustekinumab, there are no further head-to-head comparisons of bimekizumab to other biologics. This network meta-analysis (NMA) aimed to compare the short-term efficacy of bimekizumab versus other biologic systemic therapies for moderate to severe PSO.

METHODS

A systematic literature review was conducted to identify randomised controlled trials (RCTs) in patients with moderate to severe PSO. MEDLINE, Embase, the Cochrane Central Register of Controlled Trials and the Database of Systematic Reviews and PsycINFO were searched on July 1, 2020. An enhanced multinomial Bayesian NMA model was used to evaluate the comparative efficacy in 50%, 75%, 90% and 100% improvement from baseline Psoriasis Area and Severity Index (PASI 50/75/90/100) at 10-16 weeks. The model was also adjusted for baseline risk, given the variable placebo responses across the trials.

RESULTS

Eighty-six RCTs (including 34,476 patients) were included in the NMA. IL-17 and IL-23 inhibitors were the most effective treatments across all PASI levels. At 10-16 weeks, bimekizumab had the highest probability of achieving PASI 75 (92.3%), PASI 90 (84.0%) and PASI 100 (57.8%). Bimekizumab demonstrated statistical superiority over all biologics in achieving PASI 90 and PASI 100 thresholds. For PASI 75, the benefit of bimekizumab was statistically significant compared to all other treatments except risankizumab and ixekizumab.

CONCLUSION

This analysis demonstrated that IL-17 and IL-23 inhibitors were highly effective in achieving short-term improvement among patients with moderate to severe PSO. Patients receiving bimekizumab were significantly more likely to achieve PASI 90 or PASI 100 within 10-16 weeks of the first injection than all other biologics.

摘要

引言

生物制剂在中度至重度斑块状银屑病(PSO)的治疗中应用越来越广泛。比美吉珠单抗是一种白细胞介素(IL)-17A和IL-17F的选择性抑制剂,已被批准用于治疗中度至重度PSO。尽管比美吉珠单抗试验提供了与司库奇尤单抗、阿达木单抗和优特克单抗的比较,但没有比美吉珠单抗与其他生物制剂的进一步直接对比。这项网络荟萃分析(NMA)旨在比较比美吉珠单抗与其他生物系统疗法治疗中度至重度PSO的短期疗效。

方法

进行了一项系统的文献综述,以确定中度至重度PSO患者的随机对照试验(RCT)。于2020年7月1日检索了MEDLINE、Embase、Cochrane对照试验中央注册库以及系统评价数据库和PsycINFO。使用增强的多项贝叶斯NMA模型来评估在第10 - 16周时,银屑病面积和严重程度指数(PASI 50/75/90/100)相对于基线改善50%、75%、90%和100%时的比较疗效。鉴于各试验中安慰剂反应不同,该模型还针对基线风险进行了调整。

结果

NMA纳入了86项RCT(包括34476名患者)。IL-17和IL-23抑制剂在所有PASI水平上都是最有效的治疗方法。在第10 - 16周时,比美吉珠单抗达到PASI 75(92.3%)、PASI 90(84.0%)和PASI 100(57.8%)的概率最高。在达到PASI 90和PASI 100阈值方面,比美吉珠单抗显示出优于所有生物制剂的统计学优势。对于PASI 75,与除司库奇尤单抗和依奇珠单抗之外的所有其他治疗相比,比美吉珠单抗的疗效具有统计学意义。

结论

该分析表明,IL-17和IL-23抑制剂在中度至重度PSO患者中实现短期改善方面非常有效。与所有其他生物制剂相比,接受比美吉珠单抗治疗的患者在首次注射后的10 - 16周内更有可能达到PASI 90或PASI 100。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2258/9357587/ab29bd6da031/13555_2022_760_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验