Real-World Experience of Tofacitinib and Baricitinib Use in Alopecia Areata in Greek Population: A Retrospective Analysis With Focus on Safety.

IF 2.5 4区 医学 Q2 DERMATOLOGY Dermatology practical & conceptual Pub Date : 2024-04-01 DOI:10.5826/dpc.1402a73
Zoe Apalla, Efterpi Zafiriou, Effimia Zagkliverinou, Angeliki-Viktoria Roussaki-Schulze, Polyxeni Gidarokosta, Niki Ntavari, Stella Sakellaropoulou, Maria Boziou, Anastasia Emvalomati, Eirini Kyrmanidou, Elizabeth Lazaridou
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Abstract

Introduction: The introduction of Janus Kinase inhibitors (JAKi) seems to revolutionize the field of alopecia areata (AA) therapeutics. However, real-world data are still missing.

Objectives: To provide evidence about effectiveness and safety of tofacitinib and baricitinib in AA in real-world settings and describe baseline disease characteristics and patients profiles that are considered good candidates for JAKi in the daily practice. Furthermore, we intended to investigate potential correlations between baseline characteristics and treatment outcomes.

Methods: We retrospectively reviewed the databases of two tertiary Hospitals in Greece, to identify individuals of any age currently being treated with systemic JAKi for severe AA.

Results: We identified 42 individuals, including 3 adolescents. In our cohort, 52.3% (22/42) were under tofacitinib and 47.6% (20/42) under baricitinib treatment. Efficacy analysis was performed on the subgroup of 30 patients that had completed at least a 3-month follow-up on treatment. In the latter group, mean time on treatment was 10 months. Mean Severity of Alopecia Tool and mean Dermatology Life Quality Index scores decreased from 84.46% and 12.86 at baseline, to 43.26% and 6.63, respectively. Complete response (CR) was recorded in 4 (13.33%), partial in 12 (40%) and no response in 14 patients (46.66%), correspondingly. Seventeen out of 42 (40.5%) individuals in total, reported at least 1 adverse event. No patient required hospitalization. Among 15 patients (35.7%) who got COVID-19, one suffered from serious infection. The 3 adolescents achieved CR with no significant adverse events.

Conclusions: Real-world data suggest efficacy and safety of JAKi in severe forms of AA. Tolerability is optimal in younger individuals.

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在希腊人群中使用托法替尼和巴利昔尼治疗斑秃的真实世界经验:以安全性为重点的回顾性分析。
导言:Janus 激酶抑制剂(JAKi)的问世似乎将彻底改变斑秃(AA)治疗领域。然而,真实世界的数据仍然缺失:目的:提供托法替尼和巴利昔尼在现实世界中治疗斑秃的有效性和安全性的证据,并描述基线疾病特征和在日常实践中被认为是JAKi良好候选者的患者情况。此外,我们还打算研究基线特征与治疗结果之间的潜在相关性:我们回顾性地查看了希腊两家三级医院的数据库,以确定目前正在接受全身性 JAKi 治疗的任何年龄的重症 AA 患者:结果:我们发现了42名患者,其中包括3名青少年。在我们的队列中,52.3%(22/42)的患者接受了托法替尼治疗,47.6%(20/42)的患者接受了巴利昔尼治疗。疗效分析针对至少完成了 3 个月随访的 30 例患者分组进行。后一组患者的平均治疗时间为 10 个月。脱发严重程度工具(Severity of Alopecia Tool)和皮肤科生活质量指数(Dermatology Life Quality Index)的平均得分分别从基线时的84.46%和12.86分降至43.26%和6.63分。4 名患者(13.33%)完全应答,12 名患者(40%)部分应答,14 名患者(46.66%)无应答。42名患者中有17名(40.5%)报告了至少一次不良反应。没有患者需要住院治疗。在接受 COVID-19 治疗的 15 名患者(35.7%)中,有一人出现严重感染。3名青少年达到了CR,且无明显不良反应:真实世界的数据表明,JAKi对重症AA具有疗效和安全性。结论:真实世界的数据表明,JAKi对重症AA具有疗效和安全性,对年轻人的耐受性最佳。
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217
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