{"title":"Predictors for the Efficacy of 4-Week Dupilumab Treatment in Atopic Dermatitis Patients.","authors":"Ling Yu, Cheng Lian, Linfeng Li, JianGuo Li, Shoumin Zhang","doi":"10.2147/JAA.S508697","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Atopic dermatitis (AD) is a common inflammatory disease with heterogeneous clinical features. Certain meaningful phenotypes and clinical features may help better classify AD patients for personalized medicine. To our knowledge, no ideal predictors have been found so far. We aim to investigate clinical predictors for the 4-week efficacy of dupilumab treatment in AD patients in the real world.</p><p><strong>Methods: </strong>Two hundred and thirty-three AD patients treated with dupilumab were enrolled between June 2020 and December 2023. Patients' information, characteristics, and medical history were collected. They were evaluated at the baseline and 4 weeks after dupilumab treatment and divided into groups according to the Investigator's Global Assessment (IGA) and peak pruritus numerical rating scale (PP-NRS) score. Statistical analyses were used to evaluate potential predictors.</p><p><strong>Results: </strong>Age increase, late-onset, erythroderma type, and elevation of total serum IgE level were risk factors for poor response after 4-week treatment. Female, atopic personal or family history, and allergic rhinitis were factors for better response. Multivariate logistic regression analysis showed extrinsic AD had a poor reaction than intrinsic AD (OR=4.792,95% CI 1.460-15.732, <i>p</i>=0.010), so did chronic eczema to acute-subacute eczema (OR=2.386,95% CI 1.247-4.566, <i>p</i>=0.009). Trends to decrease the risk were found for allergic rhinitis (OR=0.315,95% CI 0.202-0.967, <i>p</i>=0.001), and atopic family history (OR=0.442,95% CI 0.159-0.622, <i>p</i>=0.041).</p><p><strong>Conclusion: </strong>Extrinsic AD and chronic lichenoid eczema are risk factors for poor response to 4-week dupilumab treatment, which suggests that AD patients with extrinsic and chronic lichenoid eczema may need more patience for long-term treatment or make other options.</p>","PeriodicalId":15079,"journal":{"name":"Journal of Asthma and Allergy","volume":"18 ","pages":"331-337"},"PeriodicalIF":3.7000,"publicationDate":"2025-03-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11890359/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Asthma and Allergy","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2147/JAA.S508697","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"ALLERGY","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Atopic dermatitis (AD) is a common inflammatory disease with heterogeneous clinical features. Certain meaningful phenotypes and clinical features may help better classify AD patients for personalized medicine. To our knowledge, no ideal predictors have been found so far. We aim to investigate clinical predictors for the 4-week efficacy of dupilumab treatment in AD patients in the real world.
Methods: Two hundred and thirty-three AD patients treated with dupilumab were enrolled between June 2020 and December 2023. Patients' information, characteristics, and medical history were collected. They were evaluated at the baseline and 4 weeks after dupilumab treatment and divided into groups according to the Investigator's Global Assessment (IGA) and peak pruritus numerical rating scale (PP-NRS) score. Statistical analyses were used to evaluate potential predictors.
Results: Age increase, late-onset, erythroderma type, and elevation of total serum IgE level were risk factors for poor response after 4-week treatment. Female, atopic personal or family history, and allergic rhinitis were factors for better response. Multivariate logistic regression analysis showed extrinsic AD had a poor reaction than intrinsic AD (OR=4.792,95% CI 1.460-15.732, p=0.010), so did chronic eczema to acute-subacute eczema (OR=2.386,95% CI 1.247-4.566, p=0.009). Trends to decrease the risk were found for allergic rhinitis (OR=0.315,95% CI 0.202-0.967, p=0.001), and atopic family history (OR=0.442,95% CI 0.159-0.622, p=0.041).
Conclusion: Extrinsic AD and chronic lichenoid eczema are risk factors for poor response to 4-week dupilumab treatment, which suggests that AD patients with extrinsic and chronic lichenoid eczema may need more patience for long-term treatment or make other options.
背景:特应性皮炎(AD)是一种常见的炎症性疾病,具有不同的临床特征。某些有意义的表型和临床特征可能有助于更好地对特应性皮炎患者进行分类,从而实现个性化医疗。据我们所知,迄今为止尚未发现理想的预测指标。我们的目的是在现实世界中研究杜必鲁单抗治疗AD患者4周疗效的临床预测因素:2020年6月至2023年12月期间,233名接受杜比单抗治疗的AD患者被纳入研究。收集了患者的信息、特征和病史。根据研究者全球评估(IGA)和瘙痒峰值数字评分量表(PP-NRS)评分将患者分为不同组别,并在基线和杜比鲁单抗治疗4周后对其进行评估。统计分析用于评估潜在的预测因素:结果:年龄增长、晚发、红斑类型和血清总 IgE 水平升高是 4 周治疗后反应不佳的风险因素。而女性、特应性个人或家族病史以及过敏性鼻炎则是较好反应的因素。多变量逻辑回归分析显示,外源性 AD 的反应比内源性 AD 差(OR=4.792,95% CI 1.460-15.732,p=0.010),慢性湿疹比急性-亚急性湿疹的反应也差(OR=2.386,95% CI 1.247-4.566,p=0.009)。过敏性鼻炎(OR=0.315,95% CI 0.202-0.967,p=0.001)和特应性家族史(OR=0.442,95% CI 0.159-0.622,p=0.041)的风险呈下降趋势:外源性AD和慢性苔藓样湿疹是4周dupilumab治疗反应不佳的危险因素,这表明患有外源性和慢性苔藓样湿疹的AD患者可能需要更多耐心接受长期治疗或做出其他选择。
期刊介绍:
An international, peer-reviewed journal publishing original research, reports, editorials and commentaries on the following topics: Asthma; Pulmonary physiology; Asthma related clinical health; Clinical immunology and the immunological basis of disease; Pharmacological interventions and new therapies.
Although the main focus of the journal will be to publish research and clinical results in humans, preclinical, animal and in vitro studies will be published where they shed light on disease processes and potential new therapies.