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Real-World Effectiveness of Mepolizumab in Patients With Chronic Rhinosinusitis With Nasal Polyps: Findings From the European CRS Outcome Registry (CHRINOSOR)

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00064190%3A_____%2F25%3A10001477" target="_blank" >RIV/00064190:_____/25:10001477 - isvavai.cz</a>

  • Result on the web

    <a href="https://doi.org/10.1002/clt2.70153" target="_blank" >https://doi.org/10.1002/clt2.70153</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/clt2.70153" target="_blank" >10.1002/clt2.70153</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Real-World Effectiveness of Mepolizumab in Patients With Chronic Rhinosinusitis With Nasal Polyps: Findings From the European CRS Outcome Registry (CHRINOSOR)

  • Original language description

    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 GREATER-THAN OR EQUAL TO 20: 64.5%). At least one response criterion (change in SNOT-22 GREATER-THAN OR EQUAL TO 8.9, NPS GREATER-THAN OR EQUAL TO 1, VAS total sinus symptoms GREATER-THAN OR EQUAL TO 20, VAS nasal blockage GREATER-THAN OR EQUAL TO 20, VAS loss of smell GREATER-THAN OR EQUAL TO 20) was met by 85.6% and 78.7% of patients at 24 and 52 weeks, respectively. A more stringent composite response (SNOT-22 &lt; 30, NPS &lt; 4, VAS total sinus symptoms &lt; 50, and VAS nasal blockage &lt; 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. (C) 2026 The Author(s). Clinical and Translational Allergy published by John Wiley &amp; Sons Ltd on behalf of European Academy of Allergy and Clinical Immunology.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30203 - Respiratory systems

Result continuities

  • Project

  • Continuities

    V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Others

  • Publication year

    2025

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Clinical and Translational Allergy

  • ISSN

    2045-7022

  • e-ISSN

  • Volume of the periodical

    16

  • Issue of the periodical within the volume

    2

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    11

  • Pages from-to

    nestránkováno

  • UT code for WoS article

    001704500300001

  • EID of the result in the Scopus database

    2-s2.0-105029882392