Department of Dermatology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Department of Dermatology and Allergology, University Medical Center Utrecht, Utrecht, The Netherlands.
J Dermatol. 2019 Aug;46(8):680-685. doi: 10.1111/1346-8138.14982. Epub 2019 Jun 12.
Systemic treatment options for chronic hand eczema are limited. Dupilumab is used in atopic dermatitis (AD) but is not licensed for (isolated) hand eczema. In this observational prospective study we aimed to determine the response of hand eczema to dupilumab in patients with AD. Adult patients with hand eczema and AD received dupilumab s.c. at a 600 mg loading dose, followed by 300 mg every 2 weeks. Primary outcome was a minimum improvement of 75% on the Hand Eczema Severity Index after 16 weeks (HECSI-75). Secondary outcomes were severity, measured using the Photographic guide; quality of life improvement as patient-reported outcome, measured using the Dermatology Life Quality Index (DLQI); and AD severity, measured using the Eczema Area and Severity Index (EASI). Forty-seven patients were included (32 males; mean age, 45 years). HECSI-75 was achieved by 28 (60%). Mean HECSI score reduction was 49.2 points (range, 0-164; 95% within-subject confidence interval, 46.4-52.0), which was already significantly decreased after 4 weeks (P < 0.001). DLQI score mean improvement was 8.8 points (standard deviation [SD], 6.0) or 70.0% decrease (SD, 26.4) (P < 0.001). Eighteen patients (38%) were classified as responders on the Photographic guide. There was no difference in response between chronic fissured and recurrent vesicular clinical subtypes. Similar percentages of patients achieving EASI-75 and HECSI-75 were seen after 16 weeks. In conclusion, this study shows a favorable response of hand eczema to dupilumab in patients with AD. This raises the question whether a response will also be seen in isolated hand eczema.
慢性手部湿疹的全身性治疗选择有限。度普利尤单抗用于特应性皮炎(AD),但未获得(孤立性)手部湿疹的适应证。在这项观察性前瞻性研究中,我们旨在确定 AD 患者手部湿疹对度普利尤单抗的反应。患有手部湿疹和 AD 的成年患者接受度普利尤单抗皮下注射,起始剂量为 600mg,随后每 2 周 300mg。主要结局是在 16 周后手部湿疹严重指数(HECSI)改善≥75%(HECSI-75)。次要结局是使用照片指南评估的严重程度改善;使用皮肤病生活质量指数(DLQI)评估的患者报告结局的生活质量改善;以及使用湿疹面积和严重度指数(EASI)评估的 AD 严重程度。共纳入 47 例患者(32 例男性;平均年龄 45 岁)。28 例(60%)患者达到 HECSI-75。平均 HECSI 评分降低 49.2 分(范围,0-164;95%个体内置信区间,46.4-52.0),在 4 周时已经明显降低(P<0.001)。DLQI 评分平均改善 8.8 分(标准差 [SD],6.0)或 70.0%降低(SD,26.4)(P<0.001)。18 例(38%)患者根据照片指南被归类为有反应者。慢性裂隙和复发性水疱性临床亚型的反应无差异。在 16 周后,达到 EASI-75 和 HECSI-75 的患者百分比相似。总之,这项研究表明 AD 患者手部湿疹对度普利尤单抗有良好的反应。这提出了一个问题,即在孤立性手部湿疹中是否也会看到反应。