Dupilumab Induces Long-Term On-Treatment Clinical Remission in Patients With Type 2 Asthma

被引:5
作者
Pavord, Ian D. [1 ]
Rabe, Klaus F. [2 ,3 ]
Israel, Elliot [4 ,5 ]
Szefler, Stanley J. [6 ]
Brusselle, Guy [7 ]
Pandit-Abid, Nami [8 ]
Altincatal, Arman [9 ]
Chen, Zhen [10 ]
Amin, Nikhil [10 ,13 ]
Khan, Asif H. [11 ]
Lederer, David J. [10 ]
Zhang, Yi [10 ]
Rowe, Paul J. [8 ]
Deniz, Yamo [10 ]
Radwan, Amr [10 ]
Jacob-Nara, Juby A. [8 ]
Busse, William W. [12 ]
机构
[1] Univ Oxford, NIHR Oxford Resp Biomed Res Ctr, Nuffield Dept Med, Oxford, England
[2] Lungen Clin Grosshansdorf, Grosshansdorf, Germany
[3] Christian Albrechts Univ Kiel, Airway Res Ctr North, German Ctr Lung Res, Grosshansdorf, Germany
[4] Harvard Med Sch, Dept Pediat, Boston, MA USA
[5] Brigham & Womens Hosp, Pulm & Crit Care Div, Boston, MA USA
[6] Univ Colorado, Sch Med, Dept Surg, Aurora, CO USA
[7] Ghent Univ Hosp, Dept Resp Med, Ghent, Belgium
[8] Sano fi, Bridgewater, NJ USA
[9] Sanofi, Cambridge, MA USA
[10] Regeneron Pharmaceut Inc, Tarrytown, NY USA
[11] Sanofi, Chilly Mazarin, France
[12] Univ Wisconsin, Sch Med & Publ Hlth, Dept Med, Madison, WI USA
[13] Regeneron Pharmaceut Inc, Tarrytown, NY USA
关键词
Asthma; Type; 2; inflammation; Dupilumab; Remission; Exacerbations; HUMANIZATION; TRAVERSE;
D O I
10.1016/j.jaip.2024.10.009
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background Remission is proposed as a multicomponent outcome for patients with severe asthma. Objective This 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/mu L or fractional exhaled nitric oxide >= 20 ppb at parent-study baseline) who are not receiving maintenance oral corticosteroids. Methods In 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. Results At 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. Conclusions Dupilumab 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. (c) 2024 The Authors. Published by Elsevier Inc. on behalf of the American Academy of Allergy, Asthma & Immunology. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/bync-nd/4.0/).
引用
收藏
页码:132 / 142
页数:11
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