利来替尼治疗亚洲斑秃患者的疗效和安全性:ALLEGRO 2b/3期试验的亚组分析

IF 2.9 3区 医学 Q2 DERMATOLOGY
Xingqi Zhang, Yanting Ye, Weiling Sun, Youyu Sheng, Misaki Kinoshita-Ise, Taisuke Ito, Cheng-Che Lan, Ohsang Kwon, Gregor Schaefer, Robert Wolk, Shasha Hu, Qiankun Sun, Yimeng Shen, Masayo Sakaki-Yumoto
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引用次数: 0

摘要

这项针对ALLEGRO 2b/3期研究(NCT3732807)的亚组分析评估了多剂量利来替尼(一种口服JAK3/TEC家族激酶抑制剂)治疗亚洲斑秃(AA)患者的疗效和安全性。≥12岁AA和≥50%头皮脱发的患者每天接受一次利来替尼50或30 mg(有或没有4周200 mg负荷剂量[“200/50”或“200/30”])或10 mg或安慰剂,持续24周,随后延长24周,其中最初分配给安慰剂的患者切换到200/50或50 mg。在这个亚组分析中,亚洲患者在达到脱发严重程度工具(SALT)评分≤20分,SALT≤10分,眉毛评估(EBA)评分≥2级改善或正常评分,睫毛评估(ELA)评分≥2级改善或正常评分后,在第48周进行评估。安全受到全程监控。共有186名亚洲患者被随机分配到利来替尼200/50 mg (n = 33)、200/30 mg (n = 28)、50 mg (n = 43)、30 mg (n = 34)、10 mg (n = 17)、安慰剂至200/50 mg (n = 14)或安慰剂至50 mg (n = 17)组。接受利来替尼≥30 mg治疗的患者在第24周达到SALT评分≤20的比例为9.1%-36.4%,而10 mg组为0%,安慰剂组为3.2%。在第48周,26.5%-55.6%接受利来替尼≥30 mg治疗的患者达到了SALT≤20的应答。在第48周,接受利来替尼≥30 mg治疗的患者中,EBA缓解的比例为41.9%-71.1%,ELA缓解的比例为40.7%-57.9%。最常见的不良反应是鼻咽炎、毛囊炎、上呼吸道感染和荨麻疹。无严重或机会性感染、主要不良心血管事件、血栓栓塞事件、恶性肿瘤或死亡报告。Ritlecitinib在≥12年AA和≥50%脱发的亚洲患者中显示了48周的临床疗效和可接受的安全性。亚洲亚群的结果与ALLEGRO-2b/3研究中的总体人群一致。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Efficacy and safety of ritlecitinib in Asian patients with alopecia areata: A subgroup analysis of the ALLEGRO phase 2b/3 trial

Efficacy and safety of ritlecitinib in Asian patients with alopecia areata: A subgroup analysis of the ALLEGRO phase 2b/3 trial

This subgroup analysis of the ALLEGRO phase 2b/3 study (NCT3732807) assessed the efficacy and safety of multiple doses of ritlecitinib, an oral JAK3/TEC family kinase inhibitor, in Asian patients with alopecia areata (AA). Patients aged ≥12 years with AA and ≥50% scalp hair loss received once-daily ritlecitinib 50 or 30 mg (with or without 4-week 200-mg loading dose [“200/50” or “200/30”]) or 10 mg or placebo for 24 weeks, followed by a 24-week extension, in which patients initially assigned to placebo switched to 200/50 or 50 mg. In this subgroup analysis, Asian patients with response based on achieving a Severity of Alopecia Tool (SALT) score ≤20, SALT ≤10, ≥2-grade improvement or normal score on the eyebrow assessment (EBA) scale, and ≥2-grade improvement or normal score on the eyelash assessment (ELA) scale were evaluated through week 48. Safety was monitored throughout. In total, 186 Asian patients were randomized to ritlecitinib 200/50 mg (n = 33), 200/30 mg (n = 28), 50 mg (n = 43), 30 mg (n = 34), 10 mg (n = 17), placebo to 200/50 mg (n = 14), or placebo to 50 mg (n = 17). The proportions of patients treated with ritlecitinib ≥30 mg achieving a SALT score ≤20 response were 9.1%–36.4% at week 24 vs 0% for the 10-mg group and 3.2% for placebo. At week 48, 26.5%–55.6% of patients treated with ritlecitinib ≥30 mg achieved a SALT ≤20 response. At week 48, the proportions of patients treated with ritlecitinib ≥30 mg with EBA response were 41.9%–71.1% and with ELA response were 40.7%–57.9%. The most common adverse events were nasopharyngitis, folliculitis, upper respiratory tract infection, and urticaria. No serious or opportunistic infections, major adverse cardiovascular events, thromboembolic events, malignancies, or deaths were reported. Ritlecitinib demonstrated clinical efficacy and acceptable safety over 48 weeks in Asian patients ≥12 years with AA and ≥50% hair loss. Results for the Asian subpopulation were consistent with the overall population in the ALLEGRO-2b/3 study.

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来源期刊
Journal of Dermatology
Journal of Dermatology 医学-皮肤病学
CiteScore
4.60
自引率
9.70%
发文量
368
审稿时长
4-8 weeks
期刊介绍: The Journal of Dermatology is the official peer-reviewed publication of the Japanese Dermatological Association and the Asian Dermatological Association. The journal aims to provide a forum for the exchange of information about new and significant research in dermatology and to promote the discipline of dermatology in Japan and throughout the world. Research articles are supplemented by reviews, theoretical articles, special features, commentaries, book reviews and proceedings of workshops and conferences. Preliminary or short reports and letters to the editor of two printed pages or less will be published as soon as possible. Papers in all fields of dermatology will be considered.
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