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局部外用鲁索替尼治疗类脂质渐进性坏死:一项前瞻性、开放性研究。

Topical Ruxolitinib in the Treatment of Necrobiosis Lipoidica: A Prospective, Open-Label Study.

机构信息

Department of Dermatology, Mayo Clinic, Scottsdale, Arizona, USA.

Division of Biomedical Statistics and Informatics, Department of Health Sciences Research, Mayo Clinic, Rochester, Minnesota, USA.

出版信息

J Invest Dermatol. 2024 Sep;144(9):1994-2001.e4. doi: 10.1016/j.jid.2023.11.027. Epub 2024 Feb 27.

Abstract

Necrobiosis lipoidica (NL) is a rare granulomatous disease. There are few effective treatments for NL. We sought to investigate the efficacy and safety of the Jak1/2 inhibitor, ruxolitnib, in the treatment of NL and identify the biomarkers associated with the disease and treatment response. We conducted an open-label, phase 2 study of ruxolitinib in 12 patients with NL. We performed transcriptomic analysis of tissue samples before and after treatment. At week 12, the mean NL lesion score decreased by 58.2% (SD = 28.7%, P = .003). Transcriptomic analysis demonstrated enrichment of type I and type II IFN pathways in baseline disease. Weighted gene coexpression network analysis demonstrated post-treatment changes in IFN pathways with key hub genes IFNG and signal transducer and activator of transcription 1 gene STAT1. Limitations include small sample size and a study group limited to patients with <10% body surface area. In conclusion, ruxolitinib is an effective treatment for NL and targets the key pathogenic mediators of the disease.

摘要

硬斑病(NL)是一种罕见的肉芽肿性疾病。目前针对 NL 并没有特别有效的治疗方法。我们旨在研究 Jak1/2 抑制剂芦可替尼治疗 NL 的疗效和安全性,并确定与疾病和治疗反应相关的生物标志物。我们进行了一项开放标签、2 期芦可替尼治疗 NL 的临床试验,共纳入 12 名 NL 患者。我们对治疗前后的组织样本进行了转录组分析。治疗 12 周后,NL 病变评分平均下降了 58.2%(标准差 28.7%,P=.003)。转录组分析显示,基线疾病中存在 I 型和 II 型 IFN 途径的富集。加权基因共表达网络分析显示,治疗后 IFN 途径发生变化,关键枢纽基因 IFNG 和信号转导和转录激活因子 1 基因 STAT1。局限性包括样本量小且研究组仅限于体表面积<10%的患者。总之,芦可替尼是治疗 NL 的一种有效方法,针对疾病的关键致病介质。

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