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BackgroundRemission is proposed as a multicomponent outcome for patients with severe asthma.ObjectiveThis post hoc analysis of QUEST (NCT02414854) and TRAVERSE (NCT02134028) evaluated whether dupilumab treatment leads to clinical asthma remission (≥12 months with no severe exacerbations, zero oral corticosteroid use, stabilized or improved lung function, patient-reported asthma control <1.5) and assessed its durability in patients with uncontrolled, moderate to severe type 2 asthma (blood eosinophils ≥150 cells/μL or fractional exhaled nitric oxide ≥20 ppb at parent-study baseline) who are not receiving maintenance oral corticosteroids.MethodsIn QUEST, patients (aged ≥12 years) were randomized to dupilumab 200/300 mg or placebo every 2 weeks for 52 weeks. In TRAVERSE, all patients received dupilumab 300 mg every 2 weeks for up to 96 weeks. We assessed the proportion of patients meeting criteria for on-treatment clinical remission up to 48 weeks of TRAVERSE.ResultsAt QUEST baseline, 1,040 patients receiving dupilumab and 544 taking placebo had type 2 asthma; of those, 842 (dupilumab/dupilumab) and 437 (placebo/dupilumab) enrolled in TRAVERSE. At QUEST week 52 (year 1), 37.2% of patients receiving dupilumab met clinical remission criteria, compared with 22.2% taking placebo (all P < .001). At week 48 of TRAVERSE (year 2 overall), 42.8% (dupilumab/dupilumab) and 33.4% (placebo/dupilumab) of patients met clinical remission criteria. Overall, 29.5% of patients in the dupilumab/dupilumab group met the criteria at both years 1 and 2.ConclusionsDupilumab treatment enabled approximately one third of patients with type 2 asthma to meet the multicomponent end point for on-treatment clinical asthma remission for up to 2 years.

More information Original publication

DOI

10.1016/j.jaip.2024.10.009

Type

Journal article

Publication Date

2025-01-01T00:00:00+00:00

Volume

13

Pages

132 - 142

Total pages

10

Addresses

N, I, H, R, , O, x, f, o, r, d, , R, e, s, p, i, r, a, t, o, r, y, , B, i, o, m, e, d, i, c, a, l, , R, e, s, e, a, r, c, h, , C, e, n, t, r, e, ,, , N, u, f, f, i, e, l, d, , D, e, p, a, r, t, m, e, n, t, , o, f, , M, e, d, i, c, i, n, e, ,, , U, n, i, v, e, r, s, i, t, y, , o, f, , O, x, f, o, r, d, ,, , O, x, f, o, r, d, ,, , U, n, i, t, e, d, , K, i, n, g, d, o, m, ., , E, l, e, c, t, r, o, n, i, c, , a, d, d, r, e, s, s, :, , i, a, n, ., p, a, v, o, r, d, @, n, d, m, ., o, x, ., a, c, ., u, k, .

Keywords

Humans, Asthma, Anti-Asthmatic Agents, Treatment Outcome, Remission Induction, Double-Blind Method, Adolescent, Adult, Middle Aged, Female, Male, Randomized Controlled Trials as Topic, Clinical Trials, Phase III as Topic, Young Adult, Antibodies, Monoclonal, Humanized