Science and Research

Dupilumab Efficacy in Uncontrolled, Moderate-to-Severe Asthma with Self-Reported Chronic Rhinosinusitis

BACKGROUND: Dupilumab, a fully human monoclonal antibody, blocks the shared receptor component for IL-4 and IL-13 signaling, key drivers of type 2 inflammation. In the phase 3 study (NCT02414854), add-on dupilumab 200 mg/300 mg every 2 weeks, versus placebo, significantly reduced severe asthma exacerbations and improved pre-bronchodilator forced expiratory volume in 1 second (FEV1) and quality-of-life measures in patients with uncontrolled, moderate-to-severe asthma, with greater efficacy observed in those with a high baseline type 2 phenotype. OBJECTIVE: To assess the efficacy and safety of dupilumab in patients with uncontrolled, moderate-to-severe asthma with or without self-reported comorbid chronic rhinosinusitis (CRS or non-CRS). METHODS: Comorbid CRS was self-reported by patients using an e-diary. Annualized severe exacerbation rates, changes from baseline in pre- and post-bronchodilator FEV1, patient-reported outcomes, type 2 biomarkers, and safety were assessed. RESULTS: CRS was self-reported by 382 of 1902 (20.1%) patients. Dupilumab 200 mg/300 mg reduced annualized severe exacerbation rates by 63%/61%, respectively, in patients with CRS, and by 42%/40% in patients without CRS (all P < .001 vs placebo). Dupilumab also improved lung function and patient-reported asthma control and quality of life, and suppressed type 2 biomarkers versus placebo in both subgroups. Clinical responses were rapid, with near-maximal responses observed at the earliest measured time points and sustained at week 52. Improvements observed in the CRS subgroup were similar to or numerically greater than those in the non-CRS subgroup. CONCLUSION: Dupilumab showed efficacy and was generally well tolerated in patients with uncontrolled, moderate-to-severe asthma with or without CRS.
  • Maspero, J. F.
  • Katelaris, C. H.
  • Busse, W. W.
  • Castro, M.
  • Corren, J.
  • Chipps, B. E.
  • Peters, A. T.
  • Pavord, I. D.
  • Ford, L. B.
  • Sher, L.
  • Rabe, K. F.
  • Rice, M. S.
  • Rowe, P.
  • Lu, Y.
  • Harel, S.
  • Jagerschmidt, A.
  • Khan, A. H.
  • Kamat, S.
  • Pirozzi, G.
  • Amin, N.
  • Ruddy, M.
  • Graham, N. M. H.
  • Mannent, L. P.
  • Teper, A.

Keywords

  • *Anti-IL-13
  • *Anti-IL-4
  • *Asthma
  • *Chronic rhinosinusitis
  • *Dupilumab
  • *Efficacy
  • *Safety
Publication details
DOI: 10.1016/j.jaip.2019.07.016
Journal: J Allergy Clin Immunol Pract
Pages: 527-539 e9 
Number: 2
Work Type: Original
Location: ARCN
Disease Area: AA
Partner / Member: CAU, Ghd
Access-Number: 31351189
See publication on PubMed

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