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乌司奴单抗联合静脉输注:在化脓性汗腺炎中的疗效。

Ustekinumab with Intravenous Infusion: Results in Hidradenitis Suppurativa.

机构信息

Hospital Parc Taulí, Sabadell, Spain,

Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

出版信息

Dermatology. 2020;236(1):21-24. doi: 10.1159/000501075. Epub 2019 Jul 9.

Abstract

Adalimumab is the only approved biological therapy for hidradenitis suppurativa (HS). The last published recommendations support the use of other off-label biologic therapies. We report on a multicentric retrospective review of patients with HS treated with an ustekinumab dosing schedule of intravenous infusion adjusted by weight, followed by a subcutaneous maintenance dose of 90 mg every 8 weeks, as recently approved for Crohn's disease. The minimal follow-up period required for inclusion was 16 weeks. A total of 14 patients from six hospitals were included. In 50% of the treated patients, therapeutic outcomes, measured by means of the Hidradenitis Suppurativa Clinical Response (HiSCR) and decrease of Dermatology Life Quality Index (DLQI) and visual analog scale (VAS) of pain, were reached at week 16. In 71.42% of patients DLQI and VAS of pain improved, irrespective of achievement of HiSCR. Two patients abandoned treatment due to lack of efficacy or patient preferences. No ustekinumab-related adverse effects were reported. The results are limited by the retrospective nature of the study, the short follow-up period, and the small patient number. This therapeutic regime proved to be safe and showed moderate efficacy in treating HS with failure to previous biologic therapy. Ideally, the efficacy of ustekinumab in HS should be tested in randomized and controlled clinical trials.

摘要

阿达木单抗是治疗化脓性汗腺炎(HS)的唯一获批的生物疗法。最近发表的建议支持使用其他未批准的生物疗法。我们报告了一项多中心回顾性研究,该研究纳入了 14 名接受乌司奴单抗治疗的 HS 患者,治疗方案为根据体重调整静脉输注剂量,然后每 8 周皮下给予 90mg 维持剂量,该方案最近已获批用于治疗克罗恩病。纳入研究的最小随访时间为 16 周。共有来自六家医院的 14 名患者纳入研究。在接受治疗的患者中,50%的患者在第 16 周时达到了治疗效果,通过化脓性汗腺炎临床应答(HiSCR)和皮肤病生活质量指数(DLQI)以及疼痛视觉模拟评分(VAS)来衡量。71.42%的患者无论是否达到 HiSCR,DLQI 和疼痛 VAS 均有所改善。两名患者因疗效不佳或患者意愿而放弃治疗。未报告与乌司奴单抗相关的不良反应。研究结果受到研究的回顾性、随访时间短和患者数量少的限制。该治疗方案被证明是安全的,并且对先前生物治疗失败的 HS 具有中度疗效。理想情况下,应在随机对照临床试验中测试乌司奴单抗治疗 HS 的疗效。

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