Geographic Differences in Dupilumab Treatment Outcomes for Atopic Dermatitis: A Systematic Review and Meta‐Regression Analysis

地理变异 医学 湿疹面积及严重程度指数 荟萃分析 杜皮鲁玛 心理干预 人口学 不利影响 临床试验 析因分析 入射(几何) 特应性皮炎 内科学 位置 梅德林 年轻人 流行病学 系统回顾 事后 随机对照试验 子群分析 基线(sea)
作者
Shauni De Vriese,Hafsa Belasri,Fariza Mishaal Saiema Badloe,Lize Dimitri,Jan Gutermuth,Inge Kortekaas Krohn
出处
期刊:Allergy [Wiley]
卷期号:81 (2): 358-372 被引量:2
标识
DOI:10.1111/all.70144
摘要

Dupilumab, a monoclonal antibody targeting interleukins (IL)-4/IL-13 signaling, demonstrated efficacy in clinical trials for atopic dermatitis. However, real-world variability remains underexplored. A systematic review with meta-regression was conducted to primarily assess geographic influences on dupilumab efficacy measured by percentage eczema area severity index (EASI) reduction and secondly, the presence of adverse events (AEs). Searches were conducted in PubMed, Web of Science, Embase, and Cochrane CENTRAL (PROSPERO:CRD42024579722). Risk of bias was assessed using the Cochrane risk-of-bias tool for nonrandomized studies of interventions (ROBINS-1). Prior to model fitting, articles were subdivided by geographic region. Subsequently, meta-regression analysis was adjusted for geographic region, baseline EASI score, and proportion of female participants. To identify geographic differences, post hoc analysis was performed. Twenty-eight articles were included, covering 509 East Asians, 1604 Northern/Central Europeans, and 4429 Southern Europeans. Baseline EASI scores were highest in East Asians. However, meta-regression revealed that Southern Europeans experienced a 15.33% greater EASI reduction compared with East Asians (95% CI: 6.8%-23.9%, p = 0.0012) and a 10.2% higher reduction compared with Northern/Central Europeans (95% CI: 0.6%-19.8%, p = 0.0434). Additionally, AEs were most frequent in Northern/Central Europeans (95% CI: 0.610-7.633) compared to East Asians (95% CI: 0.145-1.267) and Southern Europeans (95% CI: 0.113-0.484), with geographic variation in AE types. Geographic factors appear to influence dupilumab's clinical outcomes, though the underlying mechanism remains unknown. Trial Registration: PROSPERO: CRD42024579722.
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