Dupilumab Efficacy in Patients with Uncontrolled Moderate-to-Severe Type 2 Asthma Regardless of Perennial Aeroallergen Sensitization

被引:3
|
作者
Corren, Jonathan [1 ]
Jackson, David J. [2 ,3 ]
Casale, Thomas B. [4 ]
Borish, Larry [5 ,6 ]
Rabe, Klaus F. [7 ,8 ]
Busse, William W. [9 ]
Maspero, Jorge F. [10 ]
Jackson, Daniel J. [11 ]
Daizadeh, Nadia [12 ]
Altincatal, Arman [12 ]
Radwan, Amr [13 ]
Khodzhayev, Angela [13 ]
Djandji, Michel [12 ]
Jacob-Nara, Juby A. [12 ,14 ]
Rowe, Paul J. [14 ]
Deniz, Yamo [13 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, 10780 Santa Mon Blvd,Suite 280, Los Angeles, CA 90095 USA
[2] Kings Coll London, London, England
[3] Guys & St Thomas NHS Fdn Trust, London, England
[4] Univ S Florida, Div Allergy & Immunol, Tampa, FL 33620 USA
[5] Univ Virginia Hlth Syst, Asthma & Allerg Dis Ctr, Charlottesville, VA USA
[6] Univ Virginia Hlth Syst, Carter Immunol Ctr, Charlottesville, VA USA
[7] Airway Res Ctr North ARCN, LungenClin Grosshansdorf, German Ctr Lung Res DZL, Grosshansdorf, Germany
[8] Univ Kiel, Airway Res Ctr North ARCN, German Ctr Lung Res DZL, Kiel, Germany
[9] Univ Wisconsin, Sch Med & Publ Hlth, UW Allergy Pulm & Crit Care Med, Madison, WI USA
[10] Fdn CIDEA, Buenos Aires, DF, Argentina
[11] Univ Wisconsin, Sch Med & Publ Hlth, Madison, WI USA
[12] Sanofi, Cambridge, MA USA
[13] Regeneron Pharmaceut Inc, 777 Old Saw Mill River Rd, Tarrytown, NY 10591 USA
[14] Sanofi, Bridgewater, MA USA
来源
关键词
dupilumab; allergic asthma; type; 2; asthma; perennial aeroallergen; HUMANIZATION;
D O I
10.2147/JAA.S385645
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Purpose: Dupilumab, a fully human monoclonal antibody, blocks the shared receptor component for interleukins-4/-13, key and central drivers of type 2 (T2) inflammation in multiple diseases. In phase 3 QUEST (NCT02414854), dupilumab vs placebo significantly reduced asthma exacerbation rates (AER) and improved pre-bronchodilator forced expiratory volume in 1 second (FEV1) in patients with uncontrolled, moderate-to-severe asthma, with greater effects in patients with elevated T2 biomarkers (2150 eosinophils/mu L or fractional exhaled nitric oxide [FeNO] 225 parts per billion). Overall safety was consistent with the known dupilumab safety profile. This post hoc analysis assessed dupilumab efficacy in QUEST patients with T2 asthma with evidence of an allergic phenotype (baseline serum IgE 230 IU/mL and aeroallergen-specific IgE 20.35 IU/mL) by number of aeroallergen sensitizations: 1, 2, 3, or 24. Non-sensitized patients (serum total IgE <30 IU/mL without evidence of allergic phenotype) were also assessed.Patients and Methods: Endpoints were annualized AER, change from baseline in pre-bronchodilator FEV1 and asthma control (5-item Asthma Control Questionnaire [ACQ-5]), and FeNO and serum total IgE levels over the 52-week treatment period.Results: In all subgroups by number of allergens sensitized, dupilumab vs placebo reduced AER by 35-67% and improved both pre-bronchodilator FEV1 at Week 12 (least squares mean differences: 0.10-0.26 L across subgroups) and ACQ-5 score at Week 52 (-0.26 to -0.43). Dupilumab significantly reduced FeNO and total IgE levels at Week 52 compared with placebo. Similar results were observed in non-sensitized patients.Conclusion: Dupilumab improved clinical outcomes and reduced biomarker levels in patients with uncontrolled, moderate-to-severe T2 asthma irrespective of allergen sensitization status or number. Clinical Trial Registration:ClinicalTrials.gov Identifier: NCT02414854.
引用
收藏
页码:249 / 260
页数:12
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