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单中心应用度普利尤单抗治疗炎症性肠病伴特应性皮炎或银屑病样皮炎患者的经验。

A Single-Center Experience with Dupilumab for Atopic or Psoriasiform Dermatitis in Patients with Inflammatory Bowel Disease.

机构信息

Division of Pediatric Gastroenterology & Nutrition, Department of Pediatrics Mount Sinai, Icahn School of Medicine, 1 Gustave L Levy Place, Box 1656, New York, NY, 10029, USA.

出版信息

Dig Dis Sci. 2023 Apr;68(4):1121-1124. doi: 10.1007/s10620-022-07684-5. Epub 2022 Sep 5.

Abstract

INTRODUCTION

Dupilumab blocks IL4/IL13 and is used in atopic disease. There are concerns that blockade may lead to inflammatory bowel disease (IBD) inception or activity. Limited data exist on the use of this therapy in patients with IBD; we aimed to describe our experience using dupilumab in IBD to treat concomitant atopic dermatitis (AD) or anti-TNF-induced dermatitis.

METHODS

We analyzed the electronic medical records (2018-2022) in a single, tertiary care center to identify patients with IBD on dupilumab. Clinical and demographic data were gathered, including disease location/behavior, personal/family history of atopy, indication for and response to dupilumab, IBD medication history, and adverse events.

RESULTS

Seventeen patients (65% Crohn's) were identified with IBD on dupilumab for dermatitis; 9 for severe AD and 8 for a worsened dermatitis, either AD or psoriasiform dermatitis (PD), induced by anti-TNF. They were treated for a median 1.2 [IQR 0.6-2.3] years. All patients had a dermatologic response to dupilumab and remained on dupilumab at last follow-up. No adverse events were identified, including no increase in IBD activity. In those with dermatitis worsened or induced by anti-TNF, all started dupilumab in combination with another biologic: 3 with anti-TNF, 4 with ustekinumab, and 1 with vedolizumab. Seven of the eight had a response to the initial combination of biologics; however, one patient using dupilumab-anti-TNF ultimately changed to combination dupilumab-ustekinumab to achieve resolution of the dermatitis.

CONCLUSION

Dupilumab is safe and effective for dermatitis in patients with IBD, both primary atopic dermatitis and dermatitis induced or worsened by anti-TNF.

摘要

简介

度普利尤单抗可阻断 IL4/IL13 并用于特应性疾病。有观点认为,阻断可能会导致炎症性肠病(IBD)的发生或活动。目前关于该疗法在 IBD 患者中的应用数据有限;我们旨在描述我们使用度普利尤单抗治疗 IBD 合并特应性皮炎(AD)或抗 TNF 诱导性皮炎的经验。

方法

我们分析了单中心的电子病历(2018-2022 年),以确定使用度普利尤单抗治疗的 IBD 患者。收集了临床和人口统计学数据,包括疾病部位/行为、特应性的个人/家族史、度普利尤单抗的适应证和反应、IBD 药物治疗史和不良反应。

结果

共发现 17 例(65%为克罗恩病)IBD 患者因皮炎而使用度普利尤单抗;9 例为严重 AD,8 例为因抗 TNF 而恶化的皮炎,或 AD 或银屑病样皮炎(PD)。中位治疗时间为 1.2 年[IQR 0.6-2.3]。所有患者对度普利尤单抗均有皮肤反应,且在最后一次随访时仍在使用度普利尤单抗。未发现不良反应,包括 IBD 活动无增加。在因抗 TNF 而恶化或诱导的皮炎患者中,所有人均开始使用度普利尤单抗联合另一种生物制剂:3 例联合抗 TNF,4 例联合乌司奴单抗,1 例联合维得利珠单抗。8 例中有 7 例对初始生物制剂联合治疗有反应;然而,1 例使用度普利尤单抗-抗 TNF 的患者最终改为联合度普利尤单抗-乌司奴单抗以解决皮炎。

结论

度普利尤单抗治疗 IBD 患者的皮炎,无论是原发性 AD 还是抗 TNF 诱导或加重的皮炎,均安全有效。

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