中华皮肤科杂志 ›› 2025, e20230772.doi: 10.35541/cjd.20230772

• 研究报道 • 上一篇    下一篇

乌帕替尼治疗6例掌跖脓疱病的临床疗效与安全性分析

张笑旭    罗素菊   

  1. 天津医科大学总医院皮肤科,天津  300052
  • 收稿日期:2023-12-28 修回日期:2025-02-28 发布日期:2025-05-12
  • 通讯作者: 罗素菊 E-mail:luosuju2005@163.com
  • 基金资助:
    国家自然科学基金(81773319)

Efficacy and safety of upadacitinib in the treatment of six cases of palmoplantar pustulosis

Zhang Xiaoxu, Luo Suju   

  1. Department of Dermatology, Tianjin Medical University General Hospital, Tianjin 300052, China
  • Received:2023-12-28 Revised:2025-02-28 Published:2025-05-12
  • Contact: Luo Suju E-mail:luosuju2005@163.com
  • Supported by:
    National Natural Science Foundation of China(81773319)

摘要: 【摘要】 目的 探讨乌帕替尼对传统治疗和/或生物制剂治疗无效或控制不佳的掌跖脓疱病的疗效和安全性。方法 收集2023年1月至2023年12月于天津医科大学总医院门诊接受乌帕替尼治疗的6例掌跖脓疱病患者,对其资料进行回顾性分析,评价掌跖脓疱病患者治疗前后皮损面积和严重程度指数(PPPASI)评分、临床医师整体评估(PPPGA)评分,记录治疗期间不良事件发生情况。结果 6例掌跖脓疱病患者,男1例,女5例,年龄(47.22 ± 8.85)岁。口服乌帕替尼15 mg/d或30 mg/d,治疗并随访12周,患者PPPASI评分由基线(17.77 ± 10.34)分降至(2.20 ± 1.73)分,达到PPPASI50、75、90、100的患者分别为6、6、2、1例,4例达到PPPGA0/1,未发生严重不良反应。结论 乌帕替尼可作为难治性掌跖脓疱病的一种新选择,其疗效和安全性仍需开展更大样本的研究评估。

关键词: 银屑病, 银屑病关节炎, Janus激酶抑制剂, 乌帕替尼, 治疗, 药物相关性副作用和不良反应

Abstract: 【Abstract】 Objective To investigate the clinical efficacy and safety of upadacitinib in the treatment of palmoplantar pustulosis that is refractory to or poorly controlled by conventional therapy and/or biological agents. Methods Clinical data were collected from 6 patients with palmoplantar pustulosis who were treated with upadacitinib at the outpatient department of Tianjin Medical University General Hospital from January 2023 to December 2023, and were retrospectively analyzed. Efficacy was evaluated by comparing the palmoplantar pustulosis area and severity index (PPPASI) scores and physician global assessment (PGA) scores in patients with palmoplantar pustulosis before and after the treatment. Adverse events were recorded during the treatment. Results Among the 6 patients with palmoplantar pustulosis, there was 1 male and 5 females, aged 47.22 ± 8.85 years. The patients were treated with oral upadacitinib at a dose of 15 mg/d or 30 mg/d. After 12 weeks of treatment and follow-up, the PPPASI scores decreased from 17.77 ± 10.34 points at baseline to 2.20 ± 1.73 points; the number of patients achieving PPPASI50, 75, 90 and 100 were 6, 6, 2 and 1, respectively, and 4 achieved PPPGA0/1. No severe adverse reactions occurred during the follow-up. Conclusion Upadacitinib may be a new option for refractory palmoplantar pustulosis, but its efficacy and safety still need to be evaluated in larger-sample studies.

Key words: Psoriasis, Arthritis, psoriatic, Janus kinase inhibitors, Upadacitinib, Therapy, Drug-related side effects and adverse reactions

引用本文

张笑旭 罗素菊. 乌帕替尼治疗6例掌跖脓疱病的临床疗效与安全性分析[J]. 中华皮肤科杂志, 2025,e20230772. doi:10.35541/cjd.20230772

Zhang Xiaoxu, Luo Suju. Efficacy and safety of upadacitinib in the treatment of six cases of palmoplantar pustulosis[J]. Chinese Journal of Dermatology,2025,e20230772. doi:10.35541/cjd.20230772