Department of Medicine, Faculty of Medicine, Kuwait University, Farwaniya, Kuwait,
Department of Dermatology, Farwaniya Hospital, Farwaniya, Kuwait.
Dermatology. 2019;235(2):130-136. doi: 10.1159/000494613. Epub 2018 Dec 19.
Alopecia areata (AA) is a common autoimmune disorder characterized by patchy hair loss. There are many treatments available for AA. However, treatments of severe forms of AA are not satisfactory. Recently, oral Janus kinase (JAK) inhibitors were found to be effective for the treatment of severe AA variants.
The aim of this work was to evaluate and compare the efficacy, side effects, and durability of two oral JAK inhibitor medications (ruxolitinib and tofacitinib) in the treatment of severe AA.
This study included 75 patients with AA with more than 30% scalp hair loss, alopecia totalis, and alopecia universalis randomized into 2 groups. The first group (n = 38) received ruxolitinib 20 mg twice daily, and the second group (n = 37) received oral tofacitinib 5 mg twice daily. The treatment continued for 6 months followed by 3 months of follow-up off therapy. Efficacy of treatment was assessed by monitoring the change in the Severity of Alopecia Tool (SALT) score.
Both tofacitinib and ruxolitinib induced remarkable hair regrowth, with a mean change in SALT score of 93.8 ± 3.25 in the ruxolitinib group and 95.2 ± 2.69 in the tofacitinib group. However, the ruxolitinib group showed a shorter duration for initial hair regrowth. There was no statistically significant difference between the groups regarding hair regrowth at the end of the 6-month treatment and relapse rate at the end of the 3-month follow-up. Around two thirds of cases experienced relapse. Both drugs were well tolerated, with no reported serious adverse effects.
Both ruxolitinib and tofacitinib could be considered effective and well-tolerated treatments for extensive AA.
斑秃(AA)是一种常见的自身免疫性疾病,表现为斑片状脱发。目前有许多治疗方法可用于 AA。然而,严重形式的 AA 的治疗效果并不理想。最近,发现口服 Janus 激酶(JAK)抑制剂对治疗严重 AA 变异型有效。
本研究旨在评估和比较两种口服 JAK 抑制剂(鲁索替尼和托法替尼)治疗严重 AA 的疗效、副作用和持久性。
这项研究纳入了 75 例头皮毛发丢失超过 30%、全秃和普秃的 AA 患者,将其随机分为 2 组。第 1 组(n = 38)接受鲁索替尼 20 mg,每日 2 次;第 2 组(n = 37)接受口服托法替尼 5 mg,每日 2 次。治疗持续 6 个月,然后停药 3 个月进行随访。通过监测严重度脱发评分(SALT)评分的变化来评估治疗效果。
托法替尼和鲁索替尼均能显著促进毛发生长,鲁索替尼组的 SALT 评分平均变化为 93.8 ± 3.25,托法替尼组为 95.2 ± 2.69。然而,鲁索替尼组初始毛发生长的持续时间较短。两组在 6 个月治疗结束时的毛发再生率和 3 个月随访结束时的复发率方面无统计学差异。约有三分之二的病例出现复发。两种药物均耐受良好,未报告严重不良事件。
鲁索替尼和托法替尼均可考虑作为广泛 AA 的有效且耐受良好的治疗方法。