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Dupilumab reduced impact of severe exacerbations on lung function in patients with moderate-to-severe type 2 asthma.
Papi, Alberto; Corren, Jonathan; Castro, Mario; Domingo, Christian; Rogers, Linda; Chapman, Kenneth R; Jackson, Daniel J; Daizadeh, Nadia; Pandit-Abid, Nami; Gall, Rebecca; Jacob-Nara, Juby A; Rowe, Paul J; Deniz, Yamo; Ortiz, Benjamin.
Afiliação
  • Papi A; Respiratory Medicine, University of Ferrara and Emergency Department, University Hospital, Ferrara, Italy.
  • Corren J; David Geffen School of Medicine at UCLA, Los Angeles, California, USA.
  • Castro M; University of Kansas School of Medicine, Kansas City, Kansas, USA.
  • Domingo C; Pulmonary Service, Corporació Sanitària Parc Taulí, Autonomous University of Barcelona, Sabadell, Barcelona, Spain.
  • Rogers L; Icahn School of Medicine at Mount Sinai, New York, New York, USA.
  • Chapman KR; University of Toronto, Toronto, Ontario, Canada.
  • Jackson DJ; University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
  • Daizadeh N; Sanofi, Cambridge, Massachusetts, USA.
  • Pandit-Abid N; Sanofi, Bridgewater Township, New Jersey, USA.
  • Gall R; Regeneron Pharmaceuticals, Inc., Tarrytown, New York, USA.
  • Jacob-Nara JA; Sanofi, Bridgewater Township, New Jersey, USA.
  • Rowe PJ; Sanofi, Bridgewater Township, New Jersey, USA.
  • Deniz Y; Regeneron Pharmaceuticals, Inc., Tarrytown, New York, USA.
  • Ortiz B; Regeneron Pharmaceuticals, Inc., Tarrytown, New York, USA.
Allergy ; 78(1): 233-243, 2023 01.
Article em En | MEDLINE | ID: mdl-35899469
BACKGROUND: Severe asthma exacerbations increase the risk of accelerated lung function decline. This analysis examined the effect of dupilumab on forced expiratory volume in 1 s (FEV1 ) in patients with moderate-to-severe asthma and elevated type 2 biomarkers from phase 3 LIBERTY ASTHMA QUEST (NCT02414854). METHODS: Changes from baseline in pre- and post-bronchodilator (BD) FEV1 and 5-item Asthma Control Questionnaire (ACQ-5) scores were assessed in patients with elevated type 2 biomarkers at baseline (type 2-150/25: eosinophils ≥150 cells/µl and/or fractional exhaled nitric oxide [FeNO] ≥25 ppb; type 2-300/25: eosinophils ≥300 cells/µl and/or FeNO ≥25 ppb), stratified as exacerbators (≥1 severe exacerbation during the study) or non-exacerbators. RESULTS: In exacerbators and non-exacerbators, dupilumab increased pre-BD FEV1 by Week 2 vs placebo; differences were maintained to Week 52 (type 2-150/25: LS mean difference (LSMD) vs placebo: 0.17 L (95% CI: 0.10-0.24) and 0.17 L (0.12-0.23); type 2-300/25: 0.22 L (0.13-0.30) and 0.21 L (0.15-0.28)), in exacerbators and non-exacerbators, respectively (p < .0001). Similar trends were seen for post-BD FEV1 . Dupilumab vs placebo also showed significantly greater improvements in post-BD FEV1 0-42 days after first severe exacerbation in type 2-150/25 (LSMD vs placebo: 0.13 L [0.06-0.20]; p = .006) and type 2-300/25 (0.14 L [0.06-0.22]; p = .001) patients. ACQ-5 improvements were greater with dupilumab vs placebo in both groups. CONCLUSION: Dupilumab treatment led to improvements in lung function independent of exacerbations and appeared to reduce the impact of exacerbations on lung function in patients who experienced a severe exacerbation during the study.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Asma Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Revista: Allergy Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Asma Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Revista: Allergy Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Itália