Olfactory Outcomes With Dupilumab in Chronic Rhinosinusitis With Nasal Polyps
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, randomizované kontrolované studie
PubMed
34628065
DOI
10.1016/j.jaip.2021.09.037
PII: S2213-2198(21)01104-1
Knihovny.cz E-zdroje
- Klíčová slova
- Anosmia, Chronic rhinosinusitis with nasal polyps, Dupilumab, Sense of smell, Type 2 inflammation,
- MeSH
- chronická nemoc MeSH
- čich MeSH
- dospělí MeSH
- humanizované monoklonální protilátky MeSH
- kvalita života MeSH
- lidé MeSH
- nosní polypy * komplikace farmakoterapie chirurgie MeSH
- rýma * farmakoterapie MeSH
- sinusitida * farmakoterapie MeSH
- výsledek terapie MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- randomizované kontrolované studie MeSH
- Názvy látek
- dupilumab MeSH Prohlížeč
- humanizované monoklonální protilátky MeSH
BACKGROUND: Loss of smell (LoS) is one of the most troublesome and difficult-to-treat symptoms of severe chronic rhinosinusitis with nasal polyps (CRSwNP). OBJECTIVE: To assess the impact of dupilumab on sense of smell in severe CRSwNP. METHODS: In the randomized SINUS-24 and SINUS-52 studies, adults with severe CRSwNP received dupilumab 300 mg subcutaneously or matching placebo every 2 weeks for 24 or 52 weeks, respectively. Smell was assessed using daily patient-reported LoS score (0-3) and University of Pennsylvania Smell Identification Test (UPSIT; 0-40). Data from the 2 studies were pooled through week 24. Relationships between patient phenotypes and smell outcomes were also assessed. RESULTS: We randomized 724 patients (286 placebo, 438 dupilumab); mean CRSwNP duration was 11 years; 63% had prior sinonasal surgery. Mean baseline LoS was 2.74. Dupilumab produced rapid improvement in LoS, evident by day 3, which improved progressively throughout the study periods (least squares mean difference vs placebo -0.07 [95% CI -0.12 to -0.02]; nominal P < .05 at day 3, and -1.04 [-1.17 to -0.91]; P < .0001 at week 24). Dupilumab improved mean UPSIT by 10.54 (least squares mean difference vs placebo 10.57 [9.40-11.74]; P < .0001) at week 24 from baseline (score 13.90). Improvements were unaffected by CRSwNP duration, prior sinonasal surgery, or comorbid asthma and/or nonsteroidal anti-inflammatory drug-exacerbated respiratory disease. Baseline olfaction scores correlated with all measured local and systemic type 2 inflammatory markers except serum total immunoglobulin E. CONCLUSIONS: Dupilumab produced rapid and sustained improvement in sense of smell, alleviating a cardinal symptom of severe CRSwNP.
Centre de recherche du Centre hospitalier de l'Université de Montreal Montreal Quebec Canada
Eastern Virginia Medical School Norfolk Va
Faculty of Health Studies University of Pardubice Pardubice Czech Republic
Ghent University Ghent Belgium
Ghent University Ghent Belgium; Karolinska Institutet Stockholm Sweden
Hospital Clínic IDIBAPS Universitat de Barcelona CIBERES Barcelona Catalonia Spain
Regeneron Pharmaceuticals Inc Tarrytown NY
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