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The efficacy and safety of JAK inhibitors for alopecia areata: A systematic review and meta-analysis of prospective studies

Background: Due to the lack of comprehensive evidence based on prospective studies, the efficacy and safety of Janus Kinase (JAK) inhibitors (including tofacitinib, ruxolitinib, baricitinib, ritlecitinib and brepocitinib) for alopecia areata (AA) are yet to be proved. Methods: The systematic review...

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Autores principales: Yan, Diqin, Fan, Huaying, Chen, Min, Xia, Lin, Wang, Simin, Dong, Wenliang, Wang, Qian, Niu, Suping, Rao, Huiying, Chen, Liming, Nie, Xiaoyan, Fang, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9449963/
https://www.ncbi.nlm.nih.gov/pubmed/36091777
http://dx.doi.org/10.3389/fphar.2022.950450
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author Yan, Diqin
Fan, Huaying
Chen, Min
Xia, Lin
Wang, Simin
Dong, Wenliang
Wang, Qian
Niu, Suping
Rao, Huiying
Chen, Liming
Nie, Xiaoyan
Fang, Yi
author_facet Yan, Diqin
Fan, Huaying
Chen, Min
Xia, Lin
Wang, Simin
Dong, Wenliang
Wang, Qian
Niu, Suping
Rao, Huiying
Chen, Liming
Nie, Xiaoyan
Fang, Yi
author_sort Yan, Diqin
collection PubMed
description Background: Due to the lack of comprehensive evidence based on prospective studies, the efficacy and safety of Janus Kinase (JAK) inhibitors (including tofacitinib, ruxolitinib, baricitinib, ritlecitinib and brepocitinib) for alopecia areata (AA) are yet to be proved. Methods: The systematic review and meta-analysis was performed pursuant to the Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) guideline and registered on PROSPERO (CRD42022303007). Results: Fourteen prospective studies (5 RCTs and 9 non-RCTs), enrolling a total of 1845 patients with AA, were included for quantitative analysis. In RCTs, oral JAK inhibitors resulted in higher good response rate compared with control (RR: 6.86, 95% CI: 2.91–16.16); topical JAK inhibitors did not show any difference compared with control (RR: 1.00, 95% CI: 0.31–3.18). In non-RCTs, the pooled rate of good response to oral, topical and sublingual JAK inhibitors were 63% (95% CI: 44%–80%), 28% (95% CI: 1%–72%) and 11% (95% CI: 1%–29%), respectively. The pooled recurrence rate in patients treated with JAK inhibitors was 54% (95% CI: 39%–69%), mainly due to the withdrawal of JAK inhibitors. In RCTs, no difference was found in the risk of experiencing most kind of adverse events; in non-RCTs, the reported adverse events with high incidence rate were mostly mild and manageable. Conclusion: JAK inhibitors are efficacious and generally well-tolerated in treating AA with oral administration, whereas topical or sublingual administration lacks efficacy. Subgroup analyses indicate that baricitinib, ritlecitinib and brepocitinib seem to have equal efficacy for AA in RCTs; ruxolitinib (vs. tofacitinib) and AA (vs. AT/AU) are associated with better efficacy outcomes in non-RCT. Due to the high recurrence rate after withdrawal of JAK inhibitors, continuous treatment should be considered to maintain efficacy. Systematic Review Registration: PROSPERO: CRD 42022303007
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spelling pubmed-94499632022-09-08 The efficacy and safety of JAK inhibitors for alopecia areata: A systematic review and meta-analysis of prospective studies Yan, Diqin Fan, Huaying Chen, Min Xia, Lin Wang, Simin Dong, Wenliang Wang, Qian Niu, Suping Rao, Huiying Chen, Liming Nie, Xiaoyan Fang, Yi Front Pharmacol Pharmacology Background: Due to the lack of comprehensive evidence based on prospective studies, the efficacy and safety of Janus Kinase (JAK) inhibitors (including tofacitinib, ruxolitinib, baricitinib, ritlecitinib and brepocitinib) for alopecia areata (AA) are yet to be proved. Methods: The systematic review and meta-analysis was performed pursuant to the Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) guideline and registered on PROSPERO (CRD42022303007). Results: Fourteen prospective studies (5 RCTs and 9 non-RCTs), enrolling a total of 1845 patients with AA, were included for quantitative analysis. In RCTs, oral JAK inhibitors resulted in higher good response rate compared with control (RR: 6.86, 95% CI: 2.91–16.16); topical JAK inhibitors did not show any difference compared with control (RR: 1.00, 95% CI: 0.31–3.18). In non-RCTs, the pooled rate of good response to oral, topical and sublingual JAK inhibitors were 63% (95% CI: 44%–80%), 28% (95% CI: 1%–72%) and 11% (95% CI: 1%–29%), respectively. The pooled recurrence rate in patients treated with JAK inhibitors was 54% (95% CI: 39%–69%), mainly due to the withdrawal of JAK inhibitors. In RCTs, no difference was found in the risk of experiencing most kind of adverse events; in non-RCTs, the reported adverse events with high incidence rate were mostly mild and manageable. Conclusion: JAK inhibitors are efficacious and generally well-tolerated in treating AA with oral administration, whereas topical or sublingual administration lacks efficacy. Subgroup analyses indicate that baricitinib, ritlecitinib and brepocitinib seem to have equal efficacy for AA in RCTs; ruxolitinib (vs. tofacitinib) and AA (vs. AT/AU) are associated with better efficacy outcomes in non-RCT. Due to the high recurrence rate after withdrawal of JAK inhibitors, continuous treatment should be considered to maintain efficacy. Systematic Review Registration: PROSPERO: CRD 42022303007 Frontiers Media S.A. 2022-08-24 /pmc/articles/PMC9449963/ /pubmed/36091777 http://dx.doi.org/10.3389/fphar.2022.950450 Text en Copyright © 2022 Yan, Fan, Chen, Xia, Wang, Dong, Wang, Niu, Rao, Chen, Nie and Fang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Yan, Diqin
Fan, Huaying
Chen, Min
Xia, Lin
Wang, Simin
Dong, Wenliang
Wang, Qian
Niu, Suping
Rao, Huiying
Chen, Liming
Nie, Xiaoyan
Fang, Yi
The efficacy and safety of JAK inhibitors for alopecia areata: A systematic review and meta-analysis of prospective studies
title The efficacy and safety of JAK inhibitors for alopecia areata: A systematic review and meta-analysis of prospective studies
title_full The efficacy and safety of JAK inhibitors for alopecia areata: A systematic review and meta-analysis of prospective studies
title_fullStr The efficacy and safety of JAK inhibitors for alopecia areata: A systematic review and meta-analysis of prospective studies
title_full_unstemmed The efficacy and safety of JAK inhibitors for alopecia areata: A systematic review and meta-analysis of prospective studies
title_short The efficacy and safety of JAK inhibitors for alopecia areata: A systematic review and meta-analysis of prospective studies
title_sort efficacy and safety of jak inhibitors for alopecia areata: a systematic review and meta-analysis of prospective studies
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9449963/
https://www.ncbi.nlm.nih.gov/pubmed/36091777
http://dx.doi.org/10.3389/fphar.2022.950450
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