• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

在中度至重度特应性皮炎患者中,早期使用伊伐替尼缓解瘙痒可改善生活质量、工作效率和睡眠质量:一项III期试验的事后分析

Early itch relief with ivarmacitinib improves quality of life, working productivity, and sleep quality in patients with moderate-to-severe atopic dermatitis: a post hoc analysis of a phase III trial.

作者信息

Zhu Chengyao, Feng Bo, Pan Jiayao, Ma Jun, Hu Binbin, Liu Lunfei

机构信息

Department of Dermatology, The Fourth Affiliated Hospital of School of Medicine, and International School of Medicine, International Institutes of Medicine, Zhejiang University, Yiwu, China.

出版信息

J Dermatolog Treat. 2025 Dec;36(1):2558995. doi: 10.1080/09546634.2025.2558995. Epub 2025 Sep 10.

DOI:10.1080/09546634.2025.2558995
PMID:40931395
Abstract

BACKGROUND

Ivarmacitinib (SHR0302), a selective Janus kinase-1 inhibitor, is a novel treatment for moderate-to-severe atopic dermatitis (AD).

OBJECTIVES

This post hoc analysis evaluated the impact of early itch relief with ivarmacitinib on quality of life (QoL), working productivity, and sleep quality in affected patients.

METHODS

Data from ivarmacitinib treatment groups in a phase III trial (NCT04875169) were analyzed. Patients were classified as early itch responders (EIR; ≥4-point reduction in Worst Itch Numeric Rating Scale at week 4) or non-early itch responders (non-EIR). Outcomes included the Dermatology Life Quality Index (DLQI) total score, DLQI 0/1 response rate, DLQI work/study item, and the Patient-Oriented Eczema Measure (POEM) sleep item.

RESULTS

Of 225 patients, 90 were EIR and 135 were non-EIR. The EIR group showed significantly greater improvements in DLQI total score, DLQI 0/1 response rate, and work productivity from week 4 through week 52 compared to the non-EIR group. Sleep disturbance due to itch was also significantly improved in the EIR group from week 4 to week 40, though the difference at week 52 was not statistically significant.

CONCLUSIONS

Early itch relief with ivarmacitinib showed significant improvements in QoL, sleep, and work productivity in patients with moderate-to-severe AD.

摘要

背景

吡弗替尼(SHR0302)是一种选择性 Janus 激酶-1 抑制剂,是治疗中重度特应性皮炎(AD)的新型药物。

目的

本事后分析评估了吡弗替尼早期缓解瘙痒对受累患者生活质量(QoL)、工作效率和睡眠质量的影响。

方法

分析了一项 III 期试验(NCT04875169)中吡弗替尼治疗组的数据。患者被分为早期瘙痒缓解者(EIR;第 4 周时最差瘙痒数字评定量表评分降低≥4 分)或非早期瘙痒缓解者(非 EIR)。结局指标包括皮肤病生活质量指数(DLQI)总分、DLQI 0/1 缓解率、DLQI 工作/学习项目以及患者导向性湿疹量表(POEM)睡眠项目。

结果

225 例患者中,90 例为 EIR,135 例为非 EIR。与非 EIR 组相比,EIR 组从第 4 周直至第 52 周在 DLQI 总分、DLQI 0/1 缓解率和工作效率方面改善更为显著。从第 4 周直至第 40 周,EIR 组因瘙痒导致的睡眠障碍也显著改善,尽管在第 52 周时差异无统计学意义。

结论

吡弗替尼早期缓解瘙痒在中重度 AD 患者的生活质量、睡眠和工作效率方面显示出显著改善。

相似文献

1
Early itch relief with ivarmacitinib improves quality of life, working productivity, and sleep quality in patients with moderate-to-severe atopic dermatitis: a post hoc analysis of a phase III trial.在中度至重度特应性皮炎患者中,早期使用伊伐替尼缓解瘙痒可改善生活质量、工作效率和睡眠质量:一项III期试验的事后分析
J Dermatolog Treat. 2025 Dec;36(1):2558995. doi: 10.1080/09546634.2025.2558995. Epub 2025 Sep 10.
2
Ruxolitinib Cream Monotherapy Improved Symptoms and Quality of Life in Adults and Adolescents with Mild-to-Moderate Atopic Dermatitis: Patient-Reported Outcomes from Two Phase III Studies.芦可替尼乳膏单药治疗改善了轻至中度特应性皮炎成人和青少年的症状及生活质量:两项III期研究的患者报告结果
Am J Clin Dermatol. 2025 Jan;26(1):121-137. doi: 10.1007/s40257-024-00901-z. Epub 2024 Nov 15.
3
Ivarmacitinib for Moderate to Severe Atopic Dermatitis in Adults and Adolescents: A Phase 3 Randomized Clinical Trial.伊伐替尼用于成人和青少年中重度特应性皮炎:一项3期随机临床试验。
JAMA Dermatol. 2025 Apr 30. doi: 10.1001/jamadermatol.2025.0982.
4
Long-Term Disease Control and Minimal Disease Activity of Head and Neck Atopic Dermatitis in Patients Treated with Tralokinumab up to 4 Years.使用曲罗芦单抗治疗长达4年的头颈部特应性皮炎患者的长期疾病控制和最小疾病活动度
Am J Clin Dermatol. 2025 Mar 14. doi: 10.1007/s40257-025-00931-1.
5
Efficacy and safety of rilzabrutinib in patients with moderate-to-severe atopic dermatitis: 16-week results from a proof-of-concept phase II clinical trial.瑞扎布替尼治疗中重度特应性皮炎患者的疗效和安全性:一项概念验证性II期临床试验的16周结果
Br J Dermatol. 2025 Aug 18;193(3):424-433. doi: 10.1093/bjd/ljaf156.
6
Patient-Reported Outcomes in Adults with Moderate-to-Severe Atopic Dermatitis Treated with Stapokibart over 52 weeks: A Post Hoc Analysis of a Phase 3 Trial.使用Stapokibart治疗52周的中度至重度特应性皮炎成人患者的患者报告结局:一项3期试验的事后分析
Adv Ther. 2025 Jul 12. doi: 10.1007/s12325-025-03284-7.
7
Long-term management of moderate-to-severe atopic dermatitis with lebrikizumab and concomitant topical corticosteroids: a 68-week randomized double-blind placebo-controlled phase III trial in Japan (ADhere-J).使用乐必妥单抗和外用糖皮质激素联合治疗中重度特应性皮炎的长期管理:在日本进行的一项为期68周的随机双盲安慰剂对照III期试验(ADhere-J)
Br J Dermatol. 2025 Mar 18;192(4):597-610. doi: 10.1093/bjd/ljae394.
8
Clinically Meaningful Improvements in Adolescents with Moderate-to-Severe Atopic Dermatitis Treated with Tralokinumab who did not Achieve Clear or Almost Clear Skin at Week 16.在第16周时皮肤未达到清除或几乎清除状态的中度至重度特应性皮炎青少年患者中,使用曲罗替尼单抗治疗后的临床意义改善情况。
Dermatol Ther (Heidelb). 2025 Jul 28. doi: 10.1007/s13555-025-01484-1.
9
Improved quality of life in patients treated with lebrikizumab monotherapy is mediated by improvements in itch and sleep: results from two phase III trials in patients with moderate-to-severe atopic dermatitis.接受乌帕替尼单药治疗的患者生活质量改善是由瘙痒和睡眠改善介导的:两项中度至重度特应性皮炎患者III期试验的结果
Clin Exp Dermatol. 2025 May 23;50(6):1188-1192. doi: 10.1093/ced/llae541.
10
Rapid Itch Improvement and Skin Clearance with Upadacitinib Versus Placebo (Measure Up 1 and Measure Up 2) and Versus Dupilumab (Heads Up): Results from Three Phase 3 Clinical Trials in Patients with Moderate-to-Severe Atopic Dermatitis.与安慰剂(“Measure Up 1”和“Measure Up 2”研究)及度普利尤单抗(“Heads Up”研究)相比,乌帕替尼可快速改善瘙痒并清除皮肤症状:三项针对中度至重度特应性皮炎患者的3期临床试验结果
Dermatol Ther (Heidelb). 2025 Jun 2. doi: 10.1007/s13555-025-01443-w.