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Dupilumab improves outcomes in patients with chronic rhinosinusitis with nasal polyps irrespective of gender: results from the SINUS-52 trial.
Fokkens, Wytske J; Bachert, Claus; Hopkins, Claire; Marglani, Osama; Praestgaard, Amy; Nash, Scott; Deniz, Yamo; Rowe, Paul J; Sacks, Harry; Jacob-Nara, Juby A.
Afiliação
  • Fokkens WJ; Department of Otorhinolaryngology Amsterdam University Medical Centres Amsterdam The Netherlands.
  • Bachert C; Department of Otorhinolaryngology - Head and Neck Surgery University Hospital of Münster Münster Germany.
  • Hopkins C; International Airway Research Center First Affiliated Hospital, Sun Yat-sen University Guangzhou China.
  • Marglani O; Department of Otorhinolaryngology King's College London London UK.
  • Praestgaard A; Department of Ophthalmology and Otolaryngology - Head and Neck Surgery Umm Al-Qura University Makkah Saudi Arabia.
  • Nash S; King Faisal Specialist Hospital and Research Center Jeddah Saudi Arabia.
  • Deniz Y; Department of Biostatistics Sanofi Cambridge MA USA.
  • Rowe PJ; Medical Affairs Regeneron Pharmaceuticals Inc. Tarrytown NY USA.
  • Sacks H; Medical Affairs Regeneron Pharmaceuticals Inc. Tarrytown NY USA.
  • Jacob-Nara JA; Global Medical Affairs Sanofi Bridgewater NJ USA.
Clin Transl Immunology ; 13(6): e1511, 2024.
Article em En | MEDLINE | ID: mdl-38854740
ABSTRACT

Objectives:

This post hoc analysis assessed disease characteristics and response to dupilumab treatment in male and female patients with severe chronic rhinosinusitis with nasal polyps (CRSwNP) (SINUS-52 study; NCT02898454).

Methods:

Patients received dupilumab 300 mg or placebo every 2 weeks for 52 weeks on background intranasal corticosteroids. Efficacy was assessed through Week 52 using nasal polyp score (NPS), nasal congestion/obstruction score, loss of smell score and University of Pennsylvania Smell Identification Test score. Disease-specific health-related quality of life (HRQoL) was assessed using the 22-item Sino-Nasal Outcome Test (SNOT-22).

Results:

The analysis included 192 male and 111 female patients. Female patients had higher mean SNOT-22 total score (56.6 vs. 49.1, P < 0.01) and more coexisting asthma (78.4% vs. 46.4%, P < 0.0001) and non-steroidal anti-inflammatory drug-exacerbated respiratory disease (NSAID-ERD) (38.7% vs. 18.8%, P = 0.0001) than male patients, but other baseline characteristics were similar. Dupilumab significantly improved CRSwNP outcomes vs. placebo at Week 52, regardless of gender least squares mean differences (95% confidence interval) for NPS were -2.33 (-2.80, -1.86) in male and -2.54 (-3.18, -1.90) in female patients (both P < 0.0001 vs. placebo), and for SNOT-22 were -19.2 (-24.1, -14.2) in male and -24.4 (-31.5, -17.3) in female patients (both P < 0.0001 vs. placebo). There were no significant efficacy-by-gender interactions.

Conclusion:

Female patients had greater asthma, NSAID-ERD and HRQoL burden at baseline than male patients. Dupilumab treatment significantly improved objective and subjective outcomes compared with placebo, irrespective of gender.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Clin Transl Immunology Ano de publicação: 2024 Tipo de documento: Article País de publicação: Austrália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Clin Transl Immunology Ano de publicação: 2024 Tipo de documento: Article País de publicação: Austrália