Stratification value of nasal brushing arachidonate 15-lipoxygenase in stapokibart (CM310) treatment for patients with seasonal allergic rhinitis: Results from MERAK
Zeyi Jin, Bing Yan, Ying Li, Yang Wang, Jing Wang, Yuan Zhang, Luo Zhang, Chengshuo WangBackground:
In the MERAK study, stapokibart (an anti-IL-4Rα mAb) as an add-on treatment did not demonstrate statistical significance in improving the primary endpoint in the overall population of patients with moderate-to-severe uncontrolled seasonal allergic rhinitis (SAR).
Objective:
This study aimed to investigate biomarkers that can identify patients who may experience enhanced benefit from the add-on use of stapokibart.
Methods:
Patients were randomized 1:1:1 to stapokibart 600–300 mg once weekly, stapokibart 600–300 mg every 2 weeks, or placebo once weekly for a 4-week treatment period. The primary endpoint was the mean change from baseline in the daily reflective total nasal symptom score during 2-week treatment. Levels of prespecified biomarkers involved in the pathogenesis of SAR were determined in nasal brushings, nasal secretions, and peripheral blood samples of participants. This post hoc analysis assessed the efficacy and safety of stapokibart based on biomarker-defined subgroups. Biomarker subgroups in which patients demonstrated statistically significant improvements in the primary efficacy endpoint after treatment with stapokibart (both dose regimens compared with placebo) were considered to be of stratification value.
Results:
Among the biomarkers we screened, baseline nasal brushing arachidonate 15-lipoxygenase (
Conclusion:
In patients with moderate-to-severe uncontrolled SAR, those with higher nasal brushing