Hidradenitis Suppurativa and JAK Inhibitors: A Review of the Published Literature

化脓性汗腺炎 医学 托法替尼 临床试验 系统回顾 皮肤病科 贾纳斯激酶 顶泌 随机对照试验 疾病 痤疮 梅德林 内科学 病理 类风湿性关节炎 细胞因子 政治学 法学
作者
Fabrizio Martora,Massimiliano Scalvenzi,Angelo Ruggiero,Luca Potestio,Teresa Battista,Matteo Megna
出处
期刊:Medicina-lithuania [Multidisciplinary Digital Publishing Institute]
卷期号:59 (4): 801-801 被引量:40
标识
DOI:10.3390/medicina59040801
摘要

Background: Hidradenitis suppurativa (HS), also known as acne inversa or Verneuil’s disease, is a chronic, inflammatory, recurrent, and debilitating skin disease of the hair follicles characterized by inflammatory, painful, deep-rooted lesions in the areas of the body characterized by the presence of the apocrine glands. Unfortunately, huge unmet needs still remain for its treatment. Objective: The purpose of our review was collecting all cases, case series, trials, and ongoing studies available in the literature on the use of this class of drugs for HS. Materials and Methods: The investigated manuscripts included trials, reviews, letters to the editor, real-life studies, case series, and reports. Manuscripts were identified, screened, and extracted for the relevant data following the PRISMA (preferred reporting items for systematic reviews and meta-analyses) guidelines. Results: We selected 56 articles of which 25 met the selection criteria for our review. Among the JAK inhibitors to date, there is only one published clinical trial in the literature (Janus kinase 1 inhibitor INCB054707), a real-life study with 15 patients up to week 24 in which upadacitinib was used and a case series where tofacitinib was successfully used. Conversely, there are several ongoing clinical trials. Conclusions: Results to date in the literature show promising levels of efficacy and the safety of JAK inhibitors in HS. Several clinical trials are underway from which it will be very important to compare the available data. There are still too few studies conducted with a low sample size, so it remains critical to investigate this issue further in the future with a real-life study involving a large sample of patients in order to provide safe and viable therapeutic alternatives for HS.
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