@article{44f74c3f692a45d5a2042f7a58bd78b8,
title = "Dupilumab reduces systemic corticosteroid use and sinonasal surgery rate in CRSwNP",
abstract = "Background: Chronic rhinosinusitis with nasal polyps (CRSwNP) is a type 2 inflammatory disease with a high symptom burden and poor quality of life. Treatment options include recurrent surgeries and/or frequent systemic corticosteroids (SCS). Dupilumab, a fully human monoclonal antibody, blocks the shared receptor component for interleukin-4 and interleukin-13, key drivers of type 2-mediated inflammation. We report results of pooled analyses from 2 randomised, double-blind, placebo-controlled phase 3 studies (SINUS 24 [NCT02912468]; SINUS-52 [NCT02898454]) to evaluate dupilumab effect versus placebo in adults with CRSwNP with/without SCS use and sinonasal surgery. Methodology: SINUS-24 patients were randomised 1:1 to subcutaneous dupilumab 300 mg (n=143) or placebo (n=133) every 2 weeks (q2w) for 24 weeks. SINUS-52 patients were randomised 1:1:1 to 52 weeks of subcutaneous dupilumab 300 mg q2w (n=150), 24 weeks q2w followed by 28 weeks of dupilumab 300 mg every 4 weeks (n=145) or 52 weeks of placebo q2w (n=153). Results: Dupilumab reduced the number of patients undergoing sinonasal surgery (82.6%), the need for in-study SCS use (73.9%), and SCS courses (75.3%). Significant improvements were observed with dupilumab vs placebo regardless of prior sinonasal sur gery or SCS use in nasal polyp, nasal congestion, Lund-MacKay, and Sinonasal Outcome Test (22-items) scores, and the University of Pennsylvania Smell Identification Test. Conclusions: Dupilumab demonstrated significant improvements in disease signs and symptoms and reduced the need for sinonasal surgery and SCS use versus placebo in patients with severe CRSwNP, regardless of SCS use in the previous 2 years, or prior sinonasal surgery.",
keywords = "Nasal polyps, Paranasal sinus diseases, Rhinitis, Sinusitis",
author = "M. Desrosiers and Mannent, {L. P.} and N. Amin and Canonica, {G. W.} and Hellings, {P. W.} and P. Gevaert and J. Mullol and Lee, {S. E.} and S. Fujieda and Han, {J. K.} and C. Hopkins and W. Fokkens and R. Jankowski and Cho, {S. H.} and X. Mao and M. Zhang and Rice, {M. S.} and Khan, {A. H.} and S. Kamat and N. Patel and Graham, {N. M.H.} and M. Ruddy and C. Bachert",
note = "Funding Information: This research was sponsored by Sanofi and Regeneron Pharmaceuticals Inc. ClinicalTrials.gov Identifiers: NCT02912468 (SINUS-24) and NCT02898454 (SINUS-52). Funding Information: board member; Kyorin Pharmaceuticals – speaker fees. Han JK: Sanofi – advisory board member. Hopkins C: GlaxoSmithKline, Optinose, Sanofi Genzyme, Smith and Nephew – advisory board member. Fokkens W: BioInspire Technologies, GlaxoSmithKline, Meda Pharmaceuticals, Sanofi – research grants. Jankowski R: ALK, Laboratoire de la Mer, Regeneron Pharmaceuticals, Inc., Sa-nofi – advisory board member. Cho SH: Regeneron Pharmaceuticals, Inc., Sanofi – research grant. Bachert C: ALK, AstraZeneca, GlaxoSmithKline, Mylan, Novartis, Sanofi, Stallergenes Greer – advisory board member and speakers{\textquoteright}fees. Funding Information: The authors thank the patients and their families for their participation in the studies; their colleagues for their support; Nora Crikelair (Regeneron Pharmaceuticals, Inc.) and Dianne Barry and Nadia Daizadeh (Sanofi) for their contributions, and J{\'e}r{\^o}me Msihid (Sanofi) for statistical analyses. Writing/editorial support in the preparation of this manuscript was provided by Sin{\'e}ad Holland, PhD, of Excerpta Medica, funded by Sanofi Genzyme and Regeneron Pharmaceuticals, Inc. Publisher Copyright: {\textcopyright} 2021, International Rhinologic Society. All rights reserved.",
year = "2021",
doi = "10.4193/Rhin20.415",
language = "English",
volume = "59",
pages = "301--311",
journal = "Rhinology",
issn = "0300-0729",
number = "3",
}