Effect of Tezepelumab on Sino-Nasal Outcome Test (SNOT)-22 Domain and Symptom-Specific Scores in Patients with Severe, Uncontrolled Asthma and a History of Chronic Rhinosinusitis with Nasal Polyps
Authors:
- Joshua S. JacobsJJJoshua S. Jacobs
- Joseph K. HanJHJoseph K. Han
- Jason K. LeeJLJason K. Lee
- Tanya M. LaidlawTLTanya M. Laidlaw
- Nicole L. MartinNMNicole L. Martin
- Scott CaveneySCScott Caveney
- Christopher S. AmbroseCAChristopher S. Ambrose
- Neil MartinNMNeil Martin
- Joseph D. SpahnJSJoseph D. Spahn
- Flavia C. L. HoyteFHFlavia C. L. Hoyte
Open Access
- 8 November 2024
- journal article
- research article
- Published by Springer Nature in Advances in Therapy
- Vol. 42 (1) , 510-522
Abstract
Introduction Tezepelumab blocks the activity of thymic stromal lymphopoietin, an epithelial cytokine implicated in the pathogenesis of asthma and chronic rhinosinusitis with nasal polyps (CRSwNP). In a previous analysis, tezepelumab improved asthma and rhinosinusitis symptoms compared with placebo in patients with severe, uncontrolled asthma and a history of CRSwNP in the 2 years before randomization in the NAVIGATOR study. This post hoc analysis of patients with a CRSwNP diagnosis at any time before randomization in NAVIGATOR enabled domain and symptom-specific analyses of Sino-Nasal Outcome Test (SNOT)-22 outcomes. Methods Patients (aged 12–80 years) with severe, uncontrolled asthma were randomized to tezepelumab 210 mg or placebo subcutaneously every 4 weeks for 52 weeks. SNOT-22 total, domain, and item scores were assessed in patients with a history of CRSwNP. Annualized asthma exacerbation rate (primary efficacy outcome), pre-bronchodilator forced expiratory volume in 1 s, and Asthma Control Questionnaire-6, Asthma Quality of Life Questionnaire (standardized) for patients 12 years and older, and Asthma Symptom Diary scores were also assessed in patients with and without a history of CRSwNP. Results Of 1059 patients with severe asthma, 165 (15.6%) had a history of CRSwNP. Tezepelumab treatment resulted in sustained improvements versus placebo in SNOT-22 total score throughout the 52-week study period [least-squares mean difference (95% confidence interval) − 11.08 (− 17.80, − 4.35)]. Tezepelumab improved all five SNOT-22 domain scores (sleep, nasal, function, ear/facial, and emotion) and the five SNOT-22 item scores of most clinical interest (decreased sense of smell/taste, nasal blockage, reduced productivity, waking up tired, and cough). Tezepelumab improved asthma-related clinical outcomes in patients with and without a history of CRSwNP. Conclusion In patients with severe, uncontrolled asthma and a history of CRSwNP, tezepelumab improved rhinosinusitis symptoms across multiple domains, as well as asthma exacerbations, lung function, asthma control, and health-related quality of life. ClinicalTrials.gov Identifier NCT03347279 (https://classic.clinicaltrials.gov/ct2/show/NCT03347279).Keywords
Funding Information
- AstraZeneca
- Amgen
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