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外用地尔戈替尼治疗慢性手部湿疹。

Topical delgocitinib for the treatment of chronic hand eczema.

作者信息

Abdelhalim Asaad, Yilmaz Orhan, Elshaikh Berair Mohamed, Torres Tiago

机构信息

Allergy and Clinical Immunology Department, King Khalid Hospital, Hafar Al Batin, Saudi Arabia.

College of Medicine, University of Saskatchewan, Saskatoon, Canada.

出版信息

J Dermatolog Treat. 2025 Dec;36(1):2479126. doi: 10.1080/09546634.2025.2479126. Epub 2025 Mar 17.

Abstract

PURPOSE

Chronic hand eczema (CHE) is a prevalent dermatological condition characterized by significant morbidity and impaired quality of life. Delgocitinib, a pan-JAK inhibitor, has emerged as a promising topical treatment for CHE, targeting key cytokine-mediated inflammatory pathways involved in the disease. Delgocitinib 20 mg/g (2%) cream was approved by the European Medicines Agency (EMA) in 2024 for moderate-to-severe CHE, and its U.S. Food and Drug Administration (FDA) review is currently in progress.

MATERIALS AND METHODS

PubMed, Medline and ClinicalTrials.gov were searched up to January 21, 2025, using specific search terms related to delgocitinib and chronic hand eczema.

RESULTS AND CONCLUSIONS

Clinical trials have demonstrated its effectiveness in improving disease severity, including eczema signs and symptoms such as pain and itching, and enhancing patient-reported outcomes compared to vehicle. Topical delgocitinib has shown a favorable safety profile, with most adverse events being mild and unrelated to treatment. Serious adverse events were rare, and treatment discontinuation due to adverse events was minimal. This narrative review synthesizes current evidence on topical delgocitinib's clinical utility and safety in CHE, positioning it as a valuable therapeutic option. Further comparative studies are needed to evaluate its efficacy against oral JAK inhibitors and other topical immunosuppressants, providing insight into optimizing treatment strategies for this chronic condition.

摘要

目的

慢性手部湿疹(CHE)是一种常见的皮肤病,具有较高的发病率和生活质量受损的特点。泛JAK抑制剂地尔戈替尼已成为一种有前景的CHE局部治疗药物,靶向参与该疾病的关键细胞因子介导的炎症途径。地尔戈替尼20mg/g(2%)乳膏于2024年获得欧洲药品管理局(EMA)批准用于治疗中度至重度CHE,其美国食品药品监督管理局(FDA)的审查目前正在进行中。

材料和方法

截至2025年1月21日,使用与地尔戈替尼和慢性手部湿疹相关的特定检索词在PubMed、Medline和ClinicalTrials.gov上进行检索。

结果与结论

临床试验已证明其在改善疾病严重程度方面的有效性,包括湿疹的体征和症状,如疼痛和瘙痒,并与赋形剂相比提高了患者报告的结局。局部用地尔戈替尼已显示出良好的安全性,大多数不良事件为轻度且与治疗无关。严重不良事件罕见,因不良事件导致的治疗中断极少。本叙述性综述综合了关于局部用地尔戈替尼在CHE中的临床效用和安全性的现有证据,将其定位为一种有价值的治疗选择。需要进一步的比较研究来评估其与口服JAK抑制剂和其他局部免疫抑制剂相比的疗效,为优化这种慢性疾病的治疗策略提供见解。

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