A short-course and season-oriented Stapokibart strategy for moderate-to-severe seasonal allergic rhinitis: Real-world evidence from Northern China

医学 不利影响 观察研究 生活质量(医疗保健) 随机对照试验 内科学 多中心研究 过敏 一氧化氮 鼻腔给药 临床试验 鼻塞 普通感冒 疾病 儿科 鼻子 呼出气一氧化氮
作者
Xu Li,Peize Liu,Mengwei Wu,He Geng,Chao Wang,Ling Zhou,原 廣美,H Li,Yan Sun,Na Liu,Yunqing Zhang,Na Zhang,Tingting Gao,Jingjing Wang,Peng Jin,Lili Zhi
出处
期刊:World Allergy Organization Journal [Elsevier BV]
卷期号:19 (9): 101447-101447
标识
DOI:10.1016/j.waojou.2026.101447
摘要

Background Seasonal allergic rhinitis (SAR) imposes a substantial disease burden worldwide. In Northern China, Artemisia pollen is the dominant autumn allergen, and many patients with moderate-to-severe SAR remain inadequately controlled despite intranasal corticosteroids and antihistamines. Stapokibart, an IL-4Rα–blocking monoclonal antibody, has shown efficacy in randomized trials, but real-world evidence and season-oriented treatment strategies remain limited. We evaluated the effectiveness and safety of Stapokibart and explored the feasibility of a short-course, season-oriented biologic strategy in SAR. Methods This multicenter observational case series included 37 adults with Artemisia -driven SAR uncontrolled by standard therapy between August and December 2025. Patients received Stapokibart 600 mg at baseline, followed by 300 mg at week 2. Clinical outcomes, including Total Nasal Symptom Score (TNSS), VAS-Nose, VAS-Ophthalmic, Rhinoconjunctivitis Quality of Life Questionnaire (RQLQ), and Medication Score, were assessed at baseline and weeks 1, 2, 4, 6, 12, and 16. Peripheral eosinophils, total IgE, and fractional nasal Nitric Oxide at a flow rate of 10 mL/(FnNO10) were measured at baseline, week 4, and week 16. Safety was monitored throughout follow-up. Results Stapokibart produced rapid and sustained symptom improvement. TNSS decreased from 9.22 ± 1.11 at baseline to 2.87 ± 1.32 at week 1 and 0.97 ± 0.83 at week 4, remaining low through week 16 (0.19 ± 0.40). Similar improvements were observed in VAS and RQLQ scores, accompanied by a marked reduction in medication use. FnNO10 decreased significantly by week 4 and remained suppressed at week 16, whereas total IgE showed no significant change. No serious adverse events occurred. Conclusions A two-dose, season-oriented Stapokibart regimen achieved rapid and durable symptom control with favorable safety in real-world SAR. This pragmatic strategy may represent a practical biologic approach aligned with seasonal disease dynamics.
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