Chronic Spontaneous Urticaria Combined Atopic Dermatitis/Other Atopic Comorbidities: Clinical Characteristics, Therapeutic Response to Omalizumab, and Drug Survival

医学 奥马佐单抗 血管性水肿 特应性皮炎 不利影响 内科学 药品 哮喘 慢性荨麻疹 回顾性队列研究 免疫球蛋白E 皮肤病科 生存分析 过敏 胃肠病学 共病 药物反应 过敏反应 药物不良反应 治疗效果 免疫病理学 总体生存率 免疫学 过敏性哮喘
作者
Ruiguo Li,Anqi Chen,Xianjie Yang,Xuewei Huang,Shifei Li,Zhikun Mu,Ran Li,Zhiqiang Song,Qiquan Chen
出处
期刊:Dermatitis [Lippincott Williams & Wilkins]
卷期号:: 17103568261455284-17103568261455284
标识
DOI:10.1177/17103568261455284
摘要

Background: Atopic comorbidities are common in chronic spontaneous urticaria (CSU), yet their impact on clinical presentation and omalizumab response remains poorly defined. Objective: To compare clinical profiles and omalizumab treatment outcomes in CSU patients with atopic dermatitis (AD) and other atopic comorbidities (OACs). Methods: This single-center retrospective study included 381 CSU patients treated with ≥3 doses of omalizumab (300 mg/4 weeks) and followed ≥6 months (January 2023–March 2025). Based on the presence or history of atopic comorbidities, patients were stratified into 3 groups: CSU with AD (CSU-AD, n = 76), CSU with OACs (CSU-OACs, n = 93), and CSU with no atopic comorbidities (CSU-NA, n = 212). Clinical features, treatment response (efficacy, speed, and adverse events), and—among 12-month completers—dose reduction/discontinuation and drug survival rates were analyzed. Results: Of all enrolled patients, 44.4% had comorbid allergic diseases. CSU-OACs patients had earlier onset ( P = 0.033) and higher angioedema prevalence ( P = 0.042); CSU-AD showed higher baseline UAS7 ( P = 0.031). Overall omalizumab response rates did not differ significantly among the 3 groups ( P = 0.115), but a significantly higher portion of faster-response speed was observed in CSU-OAC ( P = 0.019). Adverse events were significantly higher in CSU-OACs ( P = 0.004), especially injection-site reactions ( P = 0.033) and systemic effects (eg, headache and fatigue; P = 0.025). Drug survival was significantly higher in the CSU-OAC vs. CSU-NA group ( P = 0.007). Conclusion: CSU-AD differs only in higher baseline activity, otherwise resembling CSU-NA in treatment response and drug survival. CSU-OACs exhibit not only distinct features such as earlier onset, higher angioedema risk, faster response, and higher drug survival but also more adverse events, indicating that CSU-OAC requires individualized management. Larger multicenter studies are needed to further define the impact of AD and OACs in CSU.
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