Department of Pharmacology, West China School of Basic Sciences & Forensic Medicine, Animal Research Institute, Sichuan University, Chengdu, China.
Department of Dermatology, West China Hospital, Sichuan University, Chengdu, China.
J Eur Acad Dermatol Venereol. 2020 Jan;34(1):192-201. doi: 10.1111/jdv.15937. Epub 2019 Oct 10.
Recent insights showed the possibility of using JAK inhibitors for the treatment of alopecia areata (AA). Most of the previous articles evaluated the overall efficacy of existing JAK inhibitors rather than evaluating one of them alone. Currently, the benefit and risk profile of tofacitinib for the treatment of AA is still not clear.
To estimate the safety and efficacy of tofacitinib in patients with AA based on summarizing the clinical outcomes.
The systematic review and meta-analysis was performed according to PRISMA guidelines. ROBINS-I (Risk of Bias in Non-randomized Studies-of Interventions) was used for quality assessment.
We enrolled 14 studies including six clinical trials and eight observational studies with 275 patients. The result of meta-analysis showed that tofacitinib has reasonable effectiveness in patients with AA. The pooled good/complete hair regrowth rate of tofacitinib treating patient with AA was 54.0% (95% CI: 46.3%-61.5%), and the pooled rate of partial response in patients with AA taking tofacitinib was 26.1% (20.7-32.2%). Approximately a quarter of patients had experience of relapse, most of which was reported due to discontinuation of tofacitinib. In terms of toxicity, reported adverse effects included only mild symptoms. Upper respiratory infection, headache and acne were the most common adverse events.
Tofacitinib seems to be a promising drug for the treatment of AA with only mild adverse effects. More thorough larger sized randomized clinical trials are required to further assess the safety and clinical efficacy of tofacitinib for the treatment of AA.
最近的研究结果表明,JAK 抑制剂可能用于治疗斑秃(AA)。之前的大多数文章评估了现有的 JAK 抑制剂的总体疗效,而不是单独评估其中一种。目前,托法替尼治疗 AA 的获益与风险状况尚不清楚。
通过总结临床结局,评估托法替尼治疗 AA 患者的安全性和疗效。
根据 PRISMA 指南进行系统评价和荟萃分析。采用 ROBINS-I(干预非随机研究的偏倚风险)评估质量。
我们纳入了 14 项研究,包括 6 项临床试验和 8 项观察性研究,共 275 例患者。荟萃分析结果表明,托法替尼治疗 AA 患者具有合理的疗效。托法替尼治疗 AA 患者的完全/良好毛发生长率为 54.0%(95%CI:46.3%-61.5%),托法替尼治疗 AA 患者的部分缓解率为 26.1%(20.7%-32.2%)。约四分之一的患者出现复发,多数是由于停止使用托法替尼。关于毒性,报告的不良反应仅包括轻度症状。上呼吸道感染、头痛和痤疮是最常见的不良事件。
托法替尼似乎是治疗 AA 的一种有前途的药物,只有轻度不良反应。需要更彻底的更大规模的随机临床试验来进一步评估托法替尼治疗 AA 的安全性和临床疗效。