Department of Dermatology and Venereology, All India Institute of Medical Sciences, Bhubaneswar, India.
Department of Pathology and Lab Medicine, All India Institute of Medical Sciences, Bhubaneswar, India.
J Cutan Med Surg. 2024 Sep-Oct;28(5):497-502. doi: 10.1177/12034754241266128. Epub 2024 Jul 26.
Alopecia areata totalis and universalis are disabling conditions and therapeutically challenging as they are refractory to conventional options. Tofacitinib is a Janus-kinase (JAK) inhibitor utilized to treat alopecia areata (AA) as an off-label drug. In India, FDA-approved JAK inhibitors such as baricitinib and ritlecitinib are not available. There are only a few case reports on tofacitinib in AA in the Indian population. We present the data of 9 pediatric cases of clinically and histologically proven alopecia areata totalis (AT) and alopecia universalis (AU), for whom oral tofacitinib was given after baseline investigations. The following parameters were analysed: Photographic image and severity of alopecia tool (SALT) score at baseline, 3 months and 6 months, and Children Dermatology Life Quality Index (cDLQI) at baseline and 6 months. The mean ± standard deviation ( ± SD) of the SALT score and cDLQI( ± SD) at baseline were 95 ± 5 and 17 ± 2. At weeks 4 and weeks 12, the SALT ( ± SD) score was 92.7 ± 6.1 and 34.35 ± 11.16, respectively. At weeks 24, the SALT ( ± SD) score and cDLQI ( ± SD) were 3.33 ± 5 and 6 ± 2. The final reduction in SALT score from the baseline was 100% in 6/9 cases (66.67%), 75% to 99% in 3/9 (22.23%), and 50 to 75% in 1/9 (11.12%). We also observed minimal adverse effects (one child developed herpes zoster) with tofacitinib. Our study demonstrates that oral tofacitinib represents a viable modality in managing difficult-to-treat pediatric AA, such as AT and AU, with a good safety profile.
斑秃是一种使人致残的疾病,治疗极具挑战性,因为它对常规治疗方案没有反应。托法替尼是一种用于治疗斑秃的 Janus 激酶 (JAK) 抑制剂,被作为一种超适应证药物使用。在印度,FDA 批准的 JAK 抑制剂如巴瑞替尼和瑞特替尼并不适用。只有少数关于印度人群中托法替尼治疗斑秃的病例报告。我们报告了 9 例临床和组织学确诊的全秃 (AT) 和普秃 (AU) 儿科病例的数据,这些患者在基线检查后接受了口服托法替尼治疗。分析了以下参数:基线时的照片图像和脱发严重程度工具 (SALT) 评分、3 个月和 6 个月时的评分,以及基线时和 6 个月时的儿童皮肤病生活质量指数 (cDLQI)。SALT 评分和 cDLQI( ± SD) 的平均值 ± 标准差 ( ± SD) 在基线时分别为 95 ± 5 和 17 ± 2。在第 4 周和第 12 周时,SALT( ± SD)评分分别为 92.7 ± 6.1 和 34.35 ± 11.16。在第 24 周时,SALT( ± SD)评分和 cDLQI( ± SD)分别为 3.33 ± 5 和 6 ± 2。从基线开始,SALT 评分的最终降幅为 100%的有 6/9 例(66.67%),75%至 99%的有 3/9 例(22.23%),50%至 75%的有 1/9 例(11.12%)。我们还观察到托法替尼有轻微的不良反应(1 例患儿发生带状疱疹)。我们的研究表明,口服托法替尼是治疗难治性儿童斑秃(如 AT 和 AU)的一种可行方法,具有良好的安全性。