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探索用于斑秃的 Janus 激酶抑制剂:全面综述。

Exploring Janus kinase inhibitors for alopecia areata: a comprehensive review.

机构信息

Faculty of Life Sciences and Education, University of South Wales, Pontypridd, UK.

Faculty of Life Sciences and Education, University of South Wales, Pontypridd, UK -

出版信息

Ital J Dermatol Venerol. 2024 Aug;159(4):380-389. doi: 10.23736/S2784-8671.24.07894-0. Epub 2024 May 23.

DOI:10.23736/S2784-8671.24.07894-0
PMID:38780910
Abstract

INTRODUCTION

Alopecia areata poses a significant challenge due to its chronic autoimmune nature, leading to psychosocial impacts. Recent strides in understanding the disease have spotlighted Janus kinase (JAK) inhibitors as potential therapies. This comprehensive review aims to assess Baricitinib's efficacy and safety in treating scalp, eyebrow, and eyelash alopecia areata, and compare the effectiveness of Ritlecitinib and Brepocitinib.

EVIDENCE ACQUISITION

Conducting a thorough electronic literature search, we focused on clinical studies of JAK inhibitors for moderate to severe alopecia areata from 2015 onward. Key databases, including MEDLINE, PubMed, Cochrane Library, EMBASE, Google Scholar, and Medscape, were utilized. Primary outcomes included changes in the Severity of Alopecia Tool (SALT) score, with safety data evaluating adverse events and serious adverse events. The risk of bias was assessed using the Cochrane Risk of Bias Tool.

EVIDENCE SYNTHESIS

Among the twelve studies identified, Baricitinib demonstrated superior efficacy over placebo at 24 weeks, with both 2mg and 4mg dosages significantly reducing SALT scores. Comparative efficacy at 24 weeks for Baricitinib, Brepocitinib, and Ritlecitinib showed similar effectiveness compared to placebo, with a marginal superiority observed for Baricitinib 4mg. All JAK inhibitors were well-tolerated, with reported adverse events primarily being mild and manageable.

CONCLUSIONS

Collectively, the reviewed studies affirm JAK inhibitors, particularly Baricitinib, as promising treatments for moderate to severe alopecia areata. These inhibitors exhibit superior efficacy, as indicated by notable reductions in SALT scores, and are well-tolerated, with predominantly mild and manageable adverse events.

摘要

简介

斑秃由于其慢性自身免疫性质,导致心理社会影响,因此具有很大的挑战性。最近在疾病认识方面的进展强调了 Janus 激酶(JAK)抑制剂作为潜在治疗方法的潜力。本综述旨在评估巴瑞替尼治疗头皮、眉毛和睫毛斑秃的疗效和安全性,并比较里夫西替尼和布罗替尼的疗效。

证据获取

我们进行了全面的电子文献检索,重点关注 2015 年以来 JAK 抑制剂治疗中重度斑秃的临床研究。使用了关键数据库,包括 MEDLINE、PubMed、Cochrane 图书馆、EMBASE、Google Scholar 和 Medscape。主要结局包括严重程度脱发工具(SALT)评分的变化,安全性数据评估不良事件和严重不良事件。使用 Cochrane 偏倚风险工具评估偏倚风险。

证据综合

在确定的 12 项研究中,巴瑞替尼在 24 周时优于安慰剂,2mg 和 4mg 剂量均显著降低 SALT 评分。巴瑞替尼、布罗替尼和里夫西替尼在 24 周时的疗效比较显示,与安慰剂相比,疗效相似,但巴瑞替尼 4mg 有轻微优势。所有 JAK 抑制剂均具有良好的耐受性,报告的不良事件主要为轻度和可管理的。

结论

综上所述,综述研究证实 JAK 抑制剂,特别是巴瑞替尼,是中重度斑秃有前途的治疗方法。这些抑制剂表现出优异的疗效,SALT 评分显著降低,且耐受性良好,不良事件主要为轻度且可管理。

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