特应性皮炎中抗il -13抗体曲洛单抗早期和晚期应答者的鉴定:一项真实世界的日本研究

IF 3.2
Teppei Hagino, Hidehisa Saeki, Eita Fujimoto, Naoko Kanda
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引用次数: 0

摘要

背景:Tralokinumab是一种抗il -13抗体,是治疗特应性皮炎(AD)患者的有效药物。然而,在现实世界的实践中,曲洛单抗应答的预测因素仍不清楚。目的:本研究旨在确定曲洛单抗治疗早期和晚期反应的预测因素。早期应答者被定义为在第12周达到研究者总体评估(IGA) 0/1的患者,而晚期应答者被定义为在第12周没有IGA 0/1,但在第24周达到IGA 0/1的患者。方法:在2023年10月至2024年8月期间,对108名日本AD患者进行了一项前瞻性研究。患者的背景因素和基线临床或实验室指标在反应者和不良反应者之间进行比较。结果:与不良应答者相比,早期和晚期应答者有更高比例的全身治疗初始患者。早期应答者的女性比例较高,年龄较小,病程较短,体重指数较低,单核细胞/淋巴细胞比率较低,而晚期应答者的免疫球蛋白E、胸腺和活化调节趋化因子、血小板/淋巴细胞比率和c反应蛋白较低。结论:该研究为优化阿尔茨海默病的治疗策略提供了有价值的见解,选择可能在早期或晚期对曲仑单抗有反应的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of Early and Late Responders to Anti-IL-13 Antibody Tralokinumab in Atopic Dermatitis: A Real-World Japanese Study.

Background: Tralokinumab, an anti-IL-13 antibody, is an effective treatment for patients with atopic dermatitis (AD). However, predictive factors for responders to tralokinumab remain unclear in real-world practice. Objective: This study aimed to identify predictive factors for early and late responders to tralokinumab treatment. Early responders were defined as patients achieving investigator's global assessment (IGA) 0/1 at week 12, whereas late responders were defined as those without IGA 0/1 at week 12 but achieving IGA 0/1 at week 24. Methods: A prospective study was conducted with 108 Japanese AD patients treated with tralokinumab between October 2023 and August 2024. Patients' background factors and baseline clinical or laboratory indexes were compared between responders and poor responders. Results: Both early and late responders had a higher proportion of systemic therapy-naive patients compared with poor responders. Early responders had higher proportion of females, younger age, shorter disease duration, lower body mass index, and monocyte-to-lymphocyte ratio, whereas late responders had lower immunoglobulin E, thymus and activation-regulated chemokine, platelet-to-lymphocyte ratio, and C-reactive protein compared with poor responders. Conclusions: This study provides valuable insights for optimizing treatment strategies in AD, in selecting patients who may respond to tralokinumab at early or late phases.

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