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培塞利珠单抗治疗阿达木单抗治疗失败后的重度化脓性汗腺炎:真实世界经验。

Certolizumab pegol in the treatment of severe hidradenitis suppurativa after adalimumab failure: A real-life experience.

机构信息

Department of Dermatology and Venereology, Gulhane Training and Research Hospital, University of Health Sciences, Ankara, Turkey.

出版信息

Dermatol Ther. 2022 Nov;35(11):e15782. doi: 10.1111/dth.15782. Epub 2022 Sep 4.

Abstract

There exists an unmet need to treat hidradenitis suppurativa (HS) despite several approved therapeutic agents for its treatment. We sought to investigate the role of certolizumab pegol in severe, recalcitrant HS patients unresponsive to adalimumab. This retrospective cohort includes HS patients over 18 years of age who had a history of unresponsiveness to adalimumab and whose treatments were switched to certolizumab pegol with dosing similar to psoriasis (400 mg every 2 weeks). For subjects who achieved a hidradenitis suppurativa clinical response (HiSCR) following 12 and 24 weeks of treatment, dermatological life quality index (DLQI), abscess, inflammatory nodule count (AN count), and International Hidradenitis Suppurativa Severity Score System (IHS4) were evaluated as outcome measures. Eleven severe, recalcitrant HS patients with Hurley stage III HS were enrolled for this study. All patients were male and had a history of prior adalimumab exposure. Only three (27.2%) patients also had a history of using biologic agents other than adalimumab for HS. Six of 11 patients (54.5%) achieved HiSCR at week 12. However, two among these six responders lost response at week 24 despite continued therapy (HiSCR at week 24: 33.3%). The decrease in DLQI (p: 0.017 and 0.021) and IHS4 (p: 0.008 and 0.007) scores of the patients at weeks 12 and 24 showed a significant difference compared to the baseline. Certolizumab pegol is a promising treatment option for severe, recalcitrant HS patients who are unresponsive to adalimumab.

摘要

尽管已有多种批准的治疗药物用于治疗化脓性汗腺炎,但仍存在未满足的治疗需求。我们旨在研究培塞利珠单抗在对阿达木单抗无反应的重度、难治性化脓性汗腺炎患者中的作用。该回顾性队列纳入了年龄大于 18 岁的化脓性汗腺炎患者,这些患者既往对阿达木单抗无反应,且其治疗方案已转换为培塞利珠单抗,剂量与银屑病相似(每 2 周 400mg)。对于在治疗 12 周和 24 周后达到化脓性汗腺炎临床应答(HiSCR)的患者,评估了皮肤病生活质量指数(DLQI)、脓肿、炎症性结节计数(AN 计数)和国际化脓性汗腺炎严重程度评分系统(IHS4)作为结局指标。本研究纳入了 11 例严重、难治性 III 期 Hurley 化脓性汗腺炎患者。所有患者均为男性,且均有既往阿达木单抗暴露史。仅有 3 例(27.2%)患者也有既往使用阿达木单抗以外的生物制剂治疗化脓性汗腺炎的病史。11 例患者中,有 6 例(54.5%)在 12 周时达到 HiSCR。然而,这 6 例应答者中有 2 例在 24 周时失去应答(24 周时的 HiSCR:33.3%)。与基线相比,患者在第 12 周和第 24 周时的 DLQI(p:0.017 和 0.021)和 IHS4(p:0.008 和 0.007)评分均显著降低。培塞利珠单抗是一种有前途的治疗选择,可用于对阿达木单抗无反应的重度、难治性化脓性汗腺炎患者。

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