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阿达木单抗剂量强化治疗难治性化脓性汗腺炎/反向痤疮。

Adalimumab Dose Intensification in Recalcitrant Hidradenitis Suppurativa/Acne Inversa.

机构信息

Departments of Dermatology, Venereology, Allergology and Immunology, Dessau Medical Center, Brandenburg Medical School Theodor Fontane, Dessau, Germany,

European Hidradenitis Suppurativa Foundation e.V., Dessau, Germany,

出版信息

Dermatology. 2020;236(1):25-30. doi: 10.1159/000503606. Epub 2019 Oct 18.

Abstract

BACKGROUND

Adalimumab is the only approved compound for the treatment of adult patients with moderate-to-severe hidradenitis suppurativa (HS) who did not respond to a systemic classical treatment. Despite its significant short- and long-term efficacy, a percentage of patients do not respond sufficiently. Moreover, some primary responders experience a response loss with time.

OBJECTIVE

To analyse the effectiveness of adalimumab dose intensification in HS patients.

METHODS

A case series of adalimumab 80 mg/week subcutaneously (s.c.) compassionate use in patients with HS, who did not respond sufficiently or in primary responders with progressive response loss to the registered adalimumab dose of 40 mg/week s.c. Patients were collected and evaluated retrospectively. Patients' data were extracted from medical records.

RESULTS

The 14 patients collected were Caucasian with HS of Hurley stage II-III and moderate or severe International HS Severity Score System (IHS4) stage. Adalimumab dose intensification significantly improved IHS4 score, Pain Index, HS-Physician Global Assessment, pain, and Cardiff Dermatology Life Quality Index. Two young female patients with HS and Crohn's disease developed psoriatic lesions during the treatment with adalimumab 80 mg/week s.c.

CONCLUSION

An enhanced level of effectiveness was assessed in the majority of the HS patients treated with adalimumab dose intensification (80 mg/week s.c.). Larger studies are required to evaluate this observation.

摘要

背景

阿达木单抗是唯一被批准用于治疗对全身性经典治疗无反应的中重度化脓性汗腺炎(HS)成年患者的化合物。尽管阿达木单抗具有显著的短期和长期疗效,但仍有一定比例的患者反应不足。此外,一些原发性应答者随着时间的推移会出现应答丧失。

目的

分析阿达木单抗剂量强化治疗 HS 患者的疗效。

方法

采用阿达木单抗 80 mg/周皮下注射(SC)同情用药的病例系列研究,纳入对注册剂量 40 mg/周 SC 阿达木单抗治疗反应不足或原发性应答者应答逐渐丧失的 HS 患者。对患者进行回顾性收集和评估。从病历中提取患者数据。

结果

共收集了 14 例白种人 HS 患者,Hurley 分期为 II-III 期,国际 HS 严重程度评分系统(IHS4)分期为中重度。阿达木单抗剂量强化显著改善了 IHS4 评分、疼痛指数、HS-医生整体评估、疼痛和卡迪夫皮肤病生活质量指数。2 例患有 HS 和克罗恩病的年轻女性在接受阿达木单抗 80 mg/周 SC 治疗期间出现了银屑病样病变。

结论

大多数接受阿达木单抗剂量强化治疗(80 mg/周 SC)的 HS 患者的疗效得到了增强。需要更大规模的研究来评估这一观察结果。

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