Suppr超能文献

儿童银屑病的生物制剂治疗:系统评价和荟萃分析。

Biologics for pediatric psoriasis: A systematic review and meta-analysis.

机构信息

Faculty of Medicine and Health, University of New South Wales, Randwick, New South Wales, Australia.

Department of Dermatology, Liverpool Hospital, Liverpool, New South Wales, Australia.

出版信息

Pediatr Dermatol. 2022 Jan;39(1):42-48. doi: 10.1111/pde.14870. Epub 2021 Dec 9.

Abstract

BACKGROUND

Biologics represent a promising treatment for children with moderate-to-severe psoriasis. Randomized control trials (RCTs) have been published evaluating different biologics in children with psoriasis, but no summative review exists.

OBJECTIVE

To summarize data from existing RCTs to assess the efficacy and safety of biologics in the management of pediatric psoriasis.

METHODS

A systematic review and meta-analysis of RCTs was performed from Medline, Embase, PubMed, the Cochrane Central Register of Controlled Trials, and the American College of Physicians Journal Club from inception to November 2020. Random-effects models were used to estimate the pooled effect size.

RESULTS

Five RCTs assessing adalimumab, etanercept, ixekizumab, secukinumab, and ustekinumab were included (768 patients). The odds ratio of achieving a 75% improvement in Psoriasis Area and Severity index score was 12.37 (95% CI: 6.23-24.55) at initial follow-up, defined as 12-16 weeks of treatment. The odds ratio of any adverse event was 0.95 (95% CI: 0.51-1.80) at initial follow-up, in patients treated with biologics when compared to placebo or a non-biologic agent. Limitations of this study include heterogeneity in both the study design and the biologics investigated between the RCTs included in the meta-analysis.

CONCLUSION

Biologic therapy for pediatric patients with moderate-to-severe psoriasis has high efficacy and a favorable side effect profile.

摘要

背景

生物制剂是治疗中重度银屑病儿童的一种有前途的治疗方法。已经发表了随机对照试验(RCT)来评估不同生物制剂在银屑病儿童中的疗效,但目前尚无综合评价。

目的

总结现有 RCT 的数据,评估生物制剂在儿童银屑病治疗中的疗效和安全性。

方法

从 Medline、Embase、PubMed、Cochrane 中央对照试验注册库和美国医师学会杂志俱乐部系统检索从建库至 2020 年 11 月的 RCT,采用随机效应模型汇总评估数据。

结果

纳入了 5 项 RCT 评估阿达木单抗、依那西普、依奇珠单抗、司库奇尤单抗和乌司奴单抗(768 例患者)。在初始随访(定义为治疗 12-16 周时),达到银屑病面积和严重程度指数评分改善 75%的优势比为 12.37(95%CI:6.23-24.55)。与安慰剂或非生物制剂相比,在接受生物制剂治疗的患者中,任何不良事件的优势比为 0.95(95%CI:0.51-1.80)。本研究的局限性包括纳入的 RCT 之间在研究设计和生物制剂方面存在异质性。

结论

生物疗法治疗中重度儿童银屑病具有较高的疗效和良好的副作用谱。

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