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他卡西醇治疗儿童全秃和普秃:来自印度的回顾性分析。

Tofacitinib in Pediatric Alopecia Areata Totalis and Alopecia Universalis: A Retrospective Analysis From India.

机构信息

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.

出版信息

J Cutan Med Surg. 2024 Sep-Oct;28(5):497-502. doi: 10.1177/12034754241266128. Epub 2024 Jul 26.

Abstract

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.

摘要

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。

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