Predictive Factors for Poor Responders to Tralokinumab in Moderate-to-Severe Atopic Dermatitis: A Real-World Analysis.

IF 3.2 Dermatitis : contact, atopic, occupational, drug Pub Date : 2025-11-01 Epub Date: 2025-02-05 DOI:10.1089/derm.2024.0515
Teppei Hagino, Hidehisa Saeki, Eita Fujimoto, Naoko Kanda
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Abstract

Abstracts: Background: Some patients with moderate-to-severe atopic dermatitis (AD) show insufficient response to treatment with tralokinumab, an anti-interleukin-13 antibody. Identifying predictive factors for poor responders to tralokinumab can help optimize treatment strategies for AD patients. Objective: To identify predictive factors for poor responders to tralokinumab, defined as an investigator's global assessment >2 at week 12 or 24. Methods: A prospective study was conducted from October 2023 to August 2024, including 109 Japanese patients with moderate-to-severe AD. Baseline features were compared between poor responders versus responders at week 12 or 24. Results: Poor responders at week 12 showed higher baseline eczema area and severity index (EASI), lactate dehydrogenase (LDH), and eosinophil-to-lymphocyte ratio (ELR) compared with responders. Poor responders at week 24 had older age, longer disease duration, and higher proportions of previous systemic therapies, previous dupilumab, or previous 15 mg upadacitinib treatment, compared with responders. Conclusions: Higher baseline EASI, LDH, and ELR may predict poor response to tralokinumab at week 12. Older age, longer disease duration, and previous usage of systemic therapy, dupilumab, or 15 mg upadacitinib may predict poor response to tralokinumab at week 24. AD patients with the above features may as well avoid tralokinumab treatment.

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中重度特应性皮炎患者对曲洛单抗不良反应的预测因素:真实世界分析
摘要:背景:一些中重度特应性皮炎(AD)患者对抗白细胞介素-13抗体曲洛单抗(tralokinumab)治疗反应不足。确定曲仑单抗不良反应的预测因素有助于优化AD患者的治疗策略。目的:确定曲洛单抗不良反应的预测因素,定义为研究者在第12周或第24周的整体评估bbb2。方法:一项前瞻性研究于2023年10月至2024年8月进行,包括109名日本中重度AD患者。在第12周或第24周比较不良应答者和应答者的基线特征。结果:与应答者相比,不良应答者在第12周表现出更高的基线湿疹面积和严重程度指数(EASI)、乳酸脱氢酶(LDH)和嗜酸性粒细胞与淋巴细胞比率(ELR)。与应答者相比,第24周不良应答者的年龄更大,病程更长,既往全身治疗、既往杜匹单抗或既往15mg upadacitinib治疗的比例更高。结论:较高的基线EASI、LDH和ELR可能预示在第12周曲洛单抗的不良反应。年龄较大、病程较长、既往使用全身治疗、杜匹单抗或15mg upadacitinib可能预测在第24周时对曲罗单抗的不良反应。具有上述特征的AD患者也可避免曲罗单抗治疗。
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