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在中国和日本年龄≥2 岁的轻中度特应性皮炎患者中,他克莫司软膏的疗效和安全性。

Efficacy and safety of crisaborole ointment in Chinese and Japanese patients aged ≥2 years with mild-to-moderate atopic dermatitis.

机构信息

Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.

Tianjin Academy of Traditional Chinese Medicine Affiliated Hospital, Tianjin, China.

出版信息

J Dermatol. 2023 Jul;50(7):847-855. doi: 10.1111/1346-8138.16792. Epub 2023 May 8.

Abstract

Atopic dermatitis is a chronic inflammatory skin disease with a significant impact on the overall wellbeing of patients and their families. Crisaborole ointment, 2%, is a nonsteroidal phosphodiesterase 4 inhibitor approved for the treatment of mild-to-moderate atopic dermatitis in multiple countries. However, in the key pivotal trials, a low proportion of the overall patient population was Asian, therefore the safety and efficacy of crisaborole in the Asian population with atopic dermatitis remains unclear. CrisADe CLEAR was a multicenter, randomized, double-blind, vehicle-controlled, phase 3 study (NCT04360187) to assess the efficacy and safety of crisaborole ointment in Chinese and Japanese patients aged ≥2 years with mild-to-moderate atopic dermatitis involving ≥5% treatable body surface area. Patients were randomly assigned 2:1 to receive crisaborole or vehicle twice daily for 28 days. The primary endpoint was percentage change from baseline in the Eczema Area and Severity Index total score at day 29. Additional endpoints were improvement and success per Investigator's Static Global Assessment score at day 29 and change from baseline on the Peak Pruritus Numerical Rating Scale at week 4. Safety was assessed using rates of treatment emergent adverse events, serious adverse events, and clinically significant changes in vital signs and clinical laboratory parameters. Crisaborole-treated patients showed a significantly greater reduction versus vehicle in percentage change from baseline in Eczema Area and Severity Index total score at day 29 (P = 0.0002). Response rates for achievement of Investigator's Static Global Assessment improvement and success at day 29 were significantly higher for patients treated with crisaborole versus vehicle (P = 0.0124 and P = 0.0078, respectively). Crisaborole-treated patients showed a significantly greater reduction versus vehicle in change from baseline on the Peak Pruritus Numerical Rating Scale at week 4 (P = 0.0009). No new safety signals were identified. Treatment with crisaborole was effective and well tolerated in Chinese and Japanese patients with mild-to-moderate atopic dermatitis.

摘要

特应性皮炎是一种慢性炎症性皮肤病,对患者及其家属的整体健康有重大影响。2%的克立硼罗软膏是一种非甾体磷酸二酯酶 4 抑制剂,已在多个国家获得批准用于治疗轻至中度特应性皮炎。然而,在关键的关键性试验中,总体患者人群中亚洲人的比例较低,因此克立硼罗在患有特应性皮炎的亚洲人群中的安全性和疗效仍不清楚。CrisADe CLEAR 是一项多中心、随机、双盲、安慰剂对照的 3 期研究(NCT04360187),旨在评估克立硼罗软膏在中国和日本 2 岁及以上、受累体表面积≥5%的轻至中度特应性皮炎患者中的疗效和安全性。患者按 2:1 的比例随机分配接受克立硼罗或安慰剂,每天两次,共 28 天。主要终点是第 29 天 Eczema Area and Severity Index 总评分自基线的变化百分比。次要终点是第 29 天研究者静态整体评估评分的改善和成功比例以及第 4 周 Peak Pruritus Numerical Rating Scale 自基线的变化。使用治疗出现的不良事件、严重不良事件以及生命体征和临床实验室参数的临床意义变化的发生率评估安全性。与安慰剂相比,克立硼罗治疗的患者在第 29 天 Eczema Area and Severity Index 总评分自基线的变化百分比显著更大(P=0.0002)。与安慰剂相比,第 29 天达到研究者静态整体评估改善和成功的患者比例显著更高(P=0.0124 和 P=0.0078)。与安慰剂相比,第 4 周 Peak Pruritus Numerical Rating Scale 自基线的变化,克立硼罗治疗的患者显著更大(P=0.0009)。未发现新的安全性信号。克立硼罗在中国和日本轻至中度特应性皮炎患者中是有效且耐受良好的。

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