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Impact of Dupilumab on Sinonasal Symptoms and Outcomes in Severe Chronic Rhinosinusitis With Nasal Polyps.

Authors :
Hopkins, Claire
Mullol, Joaquim
Khan, Asif H.
Lee, Stella E.
Wagenmann, Martin
Hellings, Peter
Fokkens, Wytske
Msihid, Jérôme
Nair, Radhika
Kamat, Siddhesh
Nash, Scott
Radwan, Amr
Jacob‐Nara, Juby A.
Deniz, Yamo
Rowe, Paul J.
Source :
Otolaryngology-Head & Neck Surgery; Apr2024, Vol. 170 Issue 4, p1173-1182, 10p
Publication Year :
2024

Abstract

Objectives: To assess the severity of the top 5 22‐item Sino‐Nasal Outcome Test (SNOT‐22) items ranked most important by patients with chronic rhinosinusitis with nasal polyps (CRSwNP), the effect of dupilumab on these items, and their association with objective disease measures. Study Design: Post hoc analysis of the SINUS‐24 (NCT02912468) and SINUS‐52 (NCT02898454) clinical trials. Setting: Multinational, multicenter, randomized, double‐blind, placebo‐controlled, parallel‐group studies. Methods: Patients ranked the SNOT‐22 items most affecting their health at baseline. Item symptom severity (0‐5 scale) was assessed at baseline, Week 24 (W24), and Week 52 (W52). Changes in nasal polyps score (NPS) and Lund–Mackay (LMK) scores were assessed in patients with/without SNOT‐22 items improvements of at least 1 severity group point at W24 and W52. Results: The SNOT‐22 items ranked most important at baseline were "decreased sense of smell/taste" (87% of patients), followed by "nasal blockage" (82%), "postnasal discharge" (40%), "thick nasal discharge" (37%), and "wake up at night" (26%); 82%, 61%, 32%, 40%, and 26% of patients reported severe symptoms (score 4 or 5) for these items, respectively. Dupilumab improved score severity for all top 5 items versus placebo at W24 and W52. Improvements in NPS and LMK scores were numerically greater in patients with improvements in the SNOT‐22 top 5 items. Conclusion: Loss of smell/taste was ranked as the most important symptom by patients with CRSwNP. Dupilumab reduced the severity of the top 5 most important SNOT‐22 items versus placebo, in parallel with improvements in objective disease measures. Clinical Trial Registration: SINUS‐24 and SINUS‐52 clinical trials were registered with ClinicalTrials.gov, identifiers NCT02912468 and NCT02898454, respectively. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01945998
Volume :
170
Issue :
4
Database :
Complementary Index
Journal :
Otolaryngology-Head & Neck Surgery
Publication Type :
Academic Journal
Accession number :
176212248
Full Text :
https://doi.org/10.1002/ohn.627