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阿达木单抗治疗化脓性汗腺炎 7 年的真实临床经验。

Seven years-experience of adalimumab therapy for Hidradenitis Suppurativa in a real-life dermatologic setting.

机构信息

Department of Medical Sciences, Section of Dermatology and Infectious Diseases, University of Ferrara, Ferrara, Italy.

出版信息

J Dermatolog Treat. 2022 Jun;33(4):2063-2067. doi: 10.1080/09546634.2021.1914309. Epub 2021 Oct 21.

Abstract

INTRODUCTION

Hidradenitis Suppurativa (HS) often causes severe impairment of the quality of life of patients affected, as it is characterized by recurrent relapses of inflammation and predisposes to retractive scars, with severe alteration of anatomy of the affected regions. Adalimumab is currently the only approved long-term biological therapy for this disease.

MATERIAL AND METHOD

We retrospectively review the data of HS patients treated with Adalimumab at the 'Hidradenitis Suppurativa Clinic', University of Ferrara, Italy since the drug was first available to October 2020. The aim is to describe our real-life experience in a clinical outpatient service. We assessed the main demographic features, therapy duration, reasons of suspension and efficacy (evaluated by HiSCR - Hidradenitis Score) in relation to surgical procedures, hospitalization, number of areas involved by the disease and BMI > 30. We also assessed the aspects related to the use of adalimumab's biosimilar.

RESULTS

Data on 76 patients, with a mean age of 38.26 ± 14.74 years and mean BMI 28.10 ± 5.92 were collected. Most of the treated patients had Hurley stage III (58/76); mean Sartorius score was 115.5 ± 55.86, mean IHS4 was 76.1 ± 44.3. A statistically significant correlation between hospitalization and cessation of adalimumab, the loss of the achievement of the HiSCR, and surgery was found. No need to do surgery was a protective factor against the failure of adalimumab treatment, meaning that the most severe cases are more likely to fail the biological therapy.

CONCLUSION

New scenarios are opening up in clinical practice: the arrival of biosimilars allow greater sustainability of expenditure, while the anti-IL17 allow the patient who has failed therapy with adalimumab a valid and safe therapeutic option to be undertaken. A comprehensive care including hospitalization, a specific antibiotic therapy and surgical treatment is often mandatory to achieve a satisfactory control of the disease.

摘要

简介

化脓性汗腺炎(HS)常导致受影响患者的生活质量严重受损,因为其特征是炎症反复发作,并易形成收缩性瘢痕,受影响区域的解剖结构严重改变。阿达木单抗是目前唯一批准用于该疾病的长期生物疗法。

材料和方法

我们回顾了自阿达木单抗首次上市以来,意大利费拉拉大学“化脓性汗腺炎诊所”治疗 HS 患者的数据,截至 2020 年 10 月。目的是描述我们在临床门诊服务中的实际经验。我们评估了主要的人口统计学特征、治疗持续时间、停药原因和疗效(通过 HiSCR-化脓性汗腺炎评分评估)与手术、住院、疾病受累区域数量和 BMI>30 之间的关系。我们还评估了阿达木单抗生物类似物使用相关的方面。

结果

共收集了 76 名患者的数据,平均年龄为 38.26±14.74 岁,平均 BMI 为 28.10±5.92。大多数接受治疗的患者处于 Hurley 分期 III 期(58/76);Sartorius 评分平均为 115.5±55.86,IHS4 平均为 76.1±44.3。住院、停止阿达木单抗治疗、失去 HiSCR 疗效和手术之间存在统计学显著相关性。无需手术是阿达木单抗治疗失败的保护因素,这意味着最严重的病例更有可能无法接受生物治疗。

结论

临床实践中出现了新的情况:生物类似物的出现允许更大的支出可持续性,而抗 IL17 则为接受阿达木单抗治疗失败的患者提供了一种有效且安全的治疗选择。全面的治疗方案包括住院、特定的抗生素治疗和手术治疗,通常是实现疾病控制的必要条件。

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