局部JAK抑制剂Delgocitinib乳膏治疗额部纤维化性脱发的随机对照试验。

IF 5.7
Aubrey Martin, Neda Shokrian, Kristen J Kelley, Joel Correa da Rosa, Ester Del-Duca, Robert Bissonnette, Ole E Sørensen, Anders Bacher Nielsen, Emma Guttman-Yassky, Maryanne Makredes Senna
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引用次数: 0

摘要

背景:额部纤维化性脱发(FFA)是一种瘢痕性脱发,如果不治疗通常预后较差,并且没有批准的治疗方案。目的:探讨德尔古替尼乳膏对FFA病变分子特征的影响。安全性,耐受性和有效性也进行了调查。方法:这是一项2a期、随机、双盲、探索性试验,在FFA患者中使用delgocitinib霜剂20mg /g(2%)与霜剂对照。结果:共有30名患有FFA的成年女性被随机分配到德戈西替尼乳膏(n=15)或乳膏体(n=15)。12周后,T辅助1相关生物标志物CXCL9的表达显著下调(-3.10);局限性:该试验的局限性包括样本量小,生物标志物分析仅进行到第12周,以及疗效终点的探索性。结论:Delgocitinib乳膏可改善病变的转录组谱,可能有潜力作为FFA的局部治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Randomized Controlled Trial of the Topical JAK Inhibitor Delgocitinib Cream in Patients with Frontal Fibrosing Alopecia.

Background: Frontal fibrosing alopecia (FFA) is a cicatricial alopecia with generally poor prognosis if untreated, and no approved treatment options.

Objective: To evaluate changes in the molecular signature of FFA lesions after application of delgocitinib cream. Safety, tolerability and efficacy were also investigated.

Methods: This was a phase 2a, randomized, double-blind, exploratory trial of delgocitinib cream 20 mg/g (2%) versus cream vehicle in patients with FFA.

Results: A total of 30 adult females with FFA were randomized to delgocitinib cream (n=15) or cream vehicle (n=15). After 12 weeks, expression of the T helper 1-related biomarker CXCL9 was significantly downregulated (-3.10; p<0.05) while there were non-significant reductions in CXCL10 (-2.60; p<0.1), and interferon-γ (-1.49; p=0.22) in lesions treated with delgocitinib cream but not cream vehicle. Delgocitinib-treated lesions had a small but significant mean improvement in transcriptomic profile (4%; p<0.001) whereas lesions treated with cream vehicle worsened (33%). Delgocitinib cream was well tolerated and associated with improvements in exploratory clinical severity endpoints.

Limitations: Limitations of the trial include small sample size, biomarker analyses only being conducted to week 12, and the exploratory nature of efficacy endpoints.

Conclusion: Delgocitinib cream resulted in an improvement in the transcriptomic profile of lesions and may have potential as a topical treatment for FFA.

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