JAK抑制剂治疗特应性皮炎患者的有效性和安全性:一项多中心真实世界回顾性研究

IF 3.4 4区 医学 Q1 DERMATOLOGY
Filip Rob, Jan Hugo, Jiří Horažďovský, Yvetta Vantuchová, Jarmila Čelakovská, Lucie Jarešová, Marie Policarová, Jan Šternberský, Martina Kojanová, Petra Cetkovská, Terézia Thomová, Kristýna Sokolová, Jan Finsterle, Hana Janatová, Lenka Tomaško, Lenka Čáková, Martin Tichý, Martin Cetkovský, Michaela Nováková
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引用次数: 0

摘要

简介:Janus激酶(JAK)抑制剂是治疗特应性皮炎(AD)的新疗法;然而,只有有限的数据存在于他们的有效性在病人之前的生物治疗失败。方法:完成至少16周JAK抑制剂治疗的中重度AD患者根据先前的dupilumab暴露情况分为亚组:先前没有暴露的患者和因缺乏疗效而停止治疗的患者(dupilumab无应答者[DNR])。在第16周和第24周(如有)评估湿疹面积和严重程度指数(EASI)、DLQI和瘙痒数值评定量表(瘙痒NRS)与基线的变化。记录随访期间的不良事件。结果:共纳入241例患者;148人接受upadacitinib (99 dupilumab-naïve, 49例dupilumab失败),47人接受baricitinib (32 dupilumab-naïve, 15例dupilumab失败),46人接受abrocitinib (35 dupilumab-naïve, 11例dupilumab失败)。在第16周,upadacitinib组86% naïve对82% DNR患者达到EASI-75缓解,abrocitinib组91% naïve对73% DNR患者达到缓解,baricitinib组81% naïve对67% DNR患者达到缓解。82% naïve对upadacitinib的DNR患者,76%对abrocitinib的DNR患者,83% naïve对91%,72% naïve对baricitinib的DNR患者,40%达到瘙痒NRS降低≥4点。结论:总之,我们的回顾性分析表明,既往dupilumab失败并未显著影响JAK抑制剂治疗AD的短期有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Effectiveness and Safety of JAK Inhibitors in Patients With Atopic Dermatitis Unresponsive Versus Naïve to Dupilumab: A Multicentric Real-World Retrospective Study

Effectiveness and Safety of JAK Inhibitors in Patients With Atopic Dermatitis Unresponsive Versus Naïve to Dupilumab: A Multicentric Real-World Retrospective Study

Introduction: Janus kinase (JAK) inhibitors are novel therapies for atopic dermatitis (AD); however, only limited data exist on their effectiveness in patients with previous failures in biological treatment.

Methods: Patients with moderate-to-severe AD and having completed a minimum of 16 weeks of JAK inhibitor therapy were divided into subgroups based on prior dupilumab exposure: those without prior exposure and those whose treatment was discontinued due to lack of efficacy (dupilumab nonresponders [DNR]). Eczema Area and Severity Index (EASI), DLQI, and Itch Numeric Rating Scale (Itch NRS) changes from baseline were assessed in Weeks 16 and 24 (when available). Adverse events during the follow-up were recorded.

Results: In total, 241 patients were included; 148 received upadacitinib (99 dupilumab-naïve, 49 post-dupilumab failure), 47 were with baricitinib (32 dupilumab-naïve, 15 post-dupilumab failure), and 46 received abrocitinib (35 dupilumab-naïve, 11 post-dupilumab failure). At Week 16, an EASI-75 response in the upadacitinib group was achieved in 86% naïve versus 82% DNR patients, 91% naïve versus 73% DNR patients in the abrocitinib group, and 81% naïve versus 67% DNR in the baricitinib group. Itch NRS ≥ 4-point reduction was achieved in 82% naïve versus 76% DNR patients on upadacitinib, 83% naïve versus 91% DNR patients on abrocitinib, and 72% naïve versus 40% DNR patients on baricitinib.

Conclusion: In conclusion, our retrospective analysis suggests that previous dupilumab failure did not significantly affect the short-term effectiveness of JAK inhibitor therapy for AD.

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来源期刊
Dermatologic Therapy
Dermatologic Therapy 医学-皮肤病学
CiteScore
7.00
自引率
8.30%
发文量
711
审稿时长
3 months
期刊介绍: Dermatologic Therapy has been created to fill an important void in the dermatologic literature: the lack of a readily available source of up-to-date information on the treatment of specific cutaneous diseases and the practical application of specific treatment modalities. Each issue of the journal consists of a series of scholarly review articles written by leaders in dermatology in which they describe, in very specific terms, how they treat particular cutaneous diseases and how they use specific therapeutic agents. The information contained in each issue is so practical and detailed that the reader should be able to directly apply various treatment approaches to daily clinical situations. Because of the specific and practical nature of this publication, Dermatologic Therapy not only serves as a readily available resource for the day-to-day treatment of patients, but also as an evolving therapeutic textbook for the treatment of dermatologic diseases.
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