Real-World Effectiveness of Mepolizumab in Patients With Chronic Rhinosinusitis With Nasal Polyps: Findings From the European CRS Outcome Registry (CHRINOSOR)
Status PubMed-not-MEDLINE Jazyk angličtina Země Anglie, Velká Británie Médium print
Typ dokumentu časopisecké články
Grantová podpora
GlaxoSmithKline
PubMed
41620390
PubMed Central
PMC12860572
DOI
10.1002/clt2.70153
Knihovny.cz E-zdroje
- Klíčová slova
- CRSwNP, asthma, biologic, mepolizumab, real world evidence, registry,
- Publikační typ
- časopisecké články MeSH
BACKGROUND: The SYNAPSE phase 3 study demonstrated that mepolizumab significantly improves nasal polyp score (NPS), quality of life and symptom severity in patients with chronic rhinosinusitis with nasal polyps (CRSwNP). OBJECTIVE: We aimed to evaluate mepolizumab effectiveness in a real-world cohort from 12 tertiary centers in 6 European countries. METHODOLOGY: A retrospective analysis was conducted in 110 CRSwNP patients (comorbid asthma: 86.4%). CRS-related outcomes were analyzed at baseline, 24 and 52 weeks of mepolizumab. Treatment response was evaluated based on EUFOREA 2021 criteria. RESULTS: Significant improvements in NPS, Sinonasal Outcome Test-22 (SNOT-22), and visual analog scale (VAS) symptom scores were observed at 24 and 52 weeks compared to baseline. Further improvement between weeks 24 and 52 was observed for NPS and SNOT-22. Asthma Control Test (ACT) also improved significantly by week 24 (ACT score ≥ 20: 64.5%). At least one response criterion (change in SNOT-22 ≥ 8.9, NPS ≥ 1, VAS total sinus symptoms ≥ 20, VAS nasal blockage ≥ 20, VAS loss of smell ≥ 20) was met by 85.6% and 78.7% of patients at 24 and 52 weeks, respectively. A more stringent composite response (SNOT-22 < 30, NPS < 4, VAS total sinus symptoms < 50, and VAS nasal blockage < 50) was achieved in 18.3% and 44.6% of patients at 24 and 52 weeks, respectively. CONCLUSION: Mepolizumab demonstrated clinically meaningful benefits in a real-world CRSwNP population, with nearly half of patients achieving a beneficial composite treatment response by week 52. Notably, progressive improvements between weeks 24 and 52 underscore the value of prolonged therapy and the importance of evaluating treatment response at one year.
Allergology Department Hospital Universitario de Terrassa Barcelona Spain
Clinic for ENT diseases and Head and Neck Surgery University Clinic Münster Münster Germany
Department of General ORL Head and Neck Surgery Medical University of Graz Graz Austria
Department of Life Sciences Health and Health Professions Link Campus University Rome Italy
Department of Oral and Maxillofacial Sciences Sapienza University Rome Italy
Department of Otorhinolaryngology Head and Neck Surgery UZ Leuven Leuven Belgium
Department of Otorhinolaryngology Ordensklinikum Linz Linz Austria
Department of Otorhinolaryngology Universitätsklinikum Düsseldorf Dusseldorf Germany
Galenus Health Tielrode Belgium
Otorhinolaryngology Department Hospital Universitari Germans Trias i Pujol Barcelona Spain
Service d'Otorhinolaryngologie Cliniques Universitaires Saint Luc Brussels Belgium
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