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Effectiveness of Tralokinumab for Moderate-to-Severe Atopic Dermatitis Involving the Head-and-Neck Area: A Multicenter Retrospective Cohort Study

医学 头颈部 回顾性队列研究 特应性皮炎 皮肤病科 多中心研究 队列研究 儿科 外科 内科学 随机对照试验
作者
Gianluca Avallone,Luca Valtellini,Gianluca Tavoletti,Luca Mastorino,Martina Maurelli,Eugenia Veronica Di Brizzi,Elena Ippoliti,Francesca Barei,Davide Termini,Pietro Quaglino,Michela Ortoncelli,Giampiero Girolomoni,Anna Balato,Niccolò Gori,Ketty Peris,Angelo Valerio Marzano,Silvia Mariel Ferrucci,Simone Ribero
出处
期刊:Dermatitis [Lippincott Williams & Wilkins]
标识
DOI:10.1177/17103568251363249
摘要

Background: Atopic dermatitis (AD) affecting the head and neck (H&N) area poses a clinical challenge due to the unique anatomical and physiological features of this region. Despite its well-documented impact on quality of life (QoL), evidence on the effectiveness of tralokinumab in treating AD specifically in the H&N area remains limited. Objective: To assess the clinical outcomes of tralokinumab in AD patients with H&N involvement, informing clinical decision-making and improving patient care. Methods: A multicenter, retrospective cohort study across 5 Italian tertiary referral hospitals. Patients were stratified by H&N involvement, and treatment outcomes were assessed using the Eczema Area and Severity Index (EASI), EASI H&N, Investigator Global Assessment (IGA), Numerical Rating Scale (NRS) pruritus, NRS sleep, Dermatology Life Quality Index, Patient-Oriented Eczema Measure, and Atopic Dermatitis Control Tool. Results: Among 211 patients, 145 (68.7%) had H&N involvement. A significant reduction in EASI H&N scores from baseline to weeks 12-16 (38.1%) and week 24 (54.5%) was achieved. Significant improvements in IGA, NRS pruritus, and NRS sleep, and QoL measures emerged within 12-16 weeks and persisted at 24 weeks. Compared with patients without H&N involvement, those with H&N involvement exhibited a stronger atopic background and showed no evidence of reduced drug survival. Adverse events, mainly conjunctivitis, were comparable between groups. Conclusions: Tralokinumab is effective and well-tolerated in managing moderate-to-severe AD involving the H&N area, even in biologic-experienced patients. These findings support its use as a targeted therapy addressing both clinical and psychosocial burdens of H&N AD.
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