医学
美波利祖马布
鼻息肉
慢性鼻-鼻窦炎
突触
神经科学
内科学
嗜酸性粒细胞
哮喘
生物
作者
Claire L Hopkins,Claus Bachert,Wytske Johanna Fokkens,Martin Y. Desrosiers,Martin Wagenmann,Stella J. Lee,Ana Sousa,Steven Smith,Neil Martin,Bhabita Mayer,Robert H. Chan,Joseph K. Han
出处
期刊:The European respiratory journal
[European Respiratory Society]
日期:2020-09-07
卷期号:: 4616-4616
被引量:15
标识
DOI:10.1183/13993003.congress-2020.4616
摘要
Background: Chronic rhinosinusitis with nasal polyps (CRSwNP) is an inflammatory disease with recalcitrant symptoms. NP tissue eosinophils lead to recurrence, which often require repeat surgeries.1 Aims: To assess the efficacy and safety of 4-weekly add-on mepolizumab 100 mg SC in adults with CRSwNP. Methods: SYNAPSE (NCT03085797), a randomised, double-blind, placebo-controlled, multicentre, 52-week study, included patients with severe bilateral NP, treated with intranasal corticosteroids; with a prior NP surgery and eligible for repeat surgery. Co-primary endpoints: changes in total endoscopic NP score (Week 52) and nasal obstruction VAS score (Weeks 49–52). Secondary endpoints: time to first NP surgery (key); overall VAS symptom score, Sinonasal Outcome Test-22 score; systemic corticosteroid (SCS) use, composite and loss of smell VAS scores. Safety was assessed. Results: Total endoscopic NP score and nasal obstruction VAS score significantly improved (p<0.001) with mepolizumab (n=206) vs placebo (n=201). Median change in endoscopic NP score showed a 1-point improvement with mepolizumab (adjusted: -0.73 [95% CI:-1.11,-0.34]); median change in nasal obstruction VAS score showed a >3-point improvement (adjusted: -3.14 [-4.09,-2.18]). All secondary endpoints significant. Mepolizumab reduced NP surgery by 57% (hazard ratio 0.43 [0.25,0.76];p=0.003), improved SNOT-22, VAS (overall, composite, loss of smell) and SCS use. No new safety issues with mepolizumab. Nasopharyngitis was the most common AE (23–25%). Conclusions: Mepolizumab improved NP size and sinonasal symptoms and reduced NP surgery and SCS use in adults with severe CRSwNP and may be a treatment option in this population. Funding: GSK [GSK ID:205687]
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