Melo Amelia, Carrascosa Jose Manuel, Torres Tiago
Instituto de Ciências Biomédicas Abel Salazar, University of Porto, Porto, Portugal.
Department of Dermatology, Germans Trias i Pujol University Hospital (HUGTP), Autonomous University of Barcelona (UAB), Badalona, Spain.
J Dermatolog Treat. 2022 Aug;33(5):2404-2413. doi: 10.1080/09546634.2021.1967268. Epub 2021 Aug 23.
Atopic dermatitis is a common, chronic and recurrent inflammatory skin disease, which often appears in childhood but can last into adulthood. It negatively impacts patients, their families and society in general. There is a therapeutic unmet need, with patients requiring new drugs that are safe and effective. The increasing knowledge of the pathophysiology of AD and the role of the Janus kinase (JAK) and signal transducer and activator of transcription (STAT) pathway in the development and maintenance of AD, has led to the development of agents blocking this intracellular signaling pathway, the JAK inhibitors. Baricitinib shows high selectivity for JAK1 and JAK2, making it appealing for the treatment of this condition. Phase II and phase III trials evaluated the efficacy and safety of baricitinib in the treatment of AD, and the results have been encouraging, showing a good efficacy and a favorable safety and tolerability profile. At the end of 2020, EMA approved baricitinib for the treatment of adult patients with moderate-to-severe atopic dermatitis who are candidates for systemic therapy, increasing the therapeutic option for this debilitating disease.
特应性皮炎是一种常见的慢性复发性炎症性皮肤病,通常在儿童期出现,但可持续至成年期。它对患者及其家庭以及整个社会都有负面影响。存在治疗需求未满足的情况,患者需要安全有效的新药。随着对特应性皮炎病理生理学以及 Janus 激酶(JAK)和信号转导及转录激活因子(STAT)通路在特应性皮炎发生和维持中的作用的认识不断增加,已导致开发出阻断这种细胞内信号通路的药物,即 JAK 抑制剂。巴瑞替尼对 JAK1 和 JAK2 具有高度选择性,使其成为治疗这种疾病的有吸引力的药物。II 期和 III 期试验评估了巴瑞替尼治疗特应性皮炎的疗效和安全性,结果令人鼓舞,显示出良好的疗效以及良好的安全性和耐受性。2020 年底,欧洲药品管理局批准巴瑞替尼用于治疗适合全身治疗的中度至重度特应性皮炎成年患者,增加了针对这种使人衰弱疾病的治疗选择。