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Dupilumab Efficacy in Patients with GINA-Defined Type 2 Asthma: TRAVERSE
( William W. Busse ),( Eric D. Bateman ),( Ian D. Pavord ),( Nadia Daizadeh ),( Yamo Deniz ),( Paul J. Rowe ),( Juby A. Jacob-nara ),( Rebecca Gall ),( Nami Pandit-abid ),( Benjamin Ortiz ) 대한결핵 및 호흡기학회 2021 대한결핵 및 호흡기학회 추계학술대회 초록집 Vol.129 No.-
Background The Global Initiative for Asthma (GINA) 2020 report recommends add-on biologics for patients with type 2 asthma (≥150 blood eosinophils/μL or FeNO ≥20ppb, largely allergen-driven disease). Dupilumab, a fully human monoclonal antibody, blocks the shared receptor component for interleukin (IL)-4/13, key and central drivers of type 2 inflammation. In QUEST (NCT02414854), add-on dupilumab 200/300mg every 2 weeks vs placebo reduced exacerbations and improved forced expiratory volume in 1 second (FEV1) in patients with uncontrolled, moderate-to-severe asthma. TRAVERSE, a single-arm, open-label extension study (NCT02134028), evaluated the long-term safety and efficacy of dupilumab in patients from QUEST. The objective was to assess the long-term efficacy of dupilumab in patients according to baseline type 2 biomarkers and allergic status as suggested by GINA. Methods Patients who received dupilumab or placebo in QUEST received dupilumab 300mg in TRAVERSE for up to 96 weeks. We evaluated annualized severe exacerbation rate (AER) and pre-BD FEV1 in type 2 patients with/without evidence of allergic asthma phenotype (serum total IgE ≥30 IU/mL and ≥1 perennial aeroallergen-specific IgE ≥0.35kU/L at parent study baseline). Results Dupilumab reduced AERs and improved pre-BD FEV1 in patients with elevated eosinophils or FeNO. These effects were sustained throughout TRAVERSE (Table). Allergic phenotype did not influence the efficacy of dupilumab. Conclusions Dupilumab reduced severe exacerbations and improved FEV1 for up to 96 weeks in patients with type 2 inflammatory asthma as specified in recent GINA recommendations, irrespective of allergic phenotype.