Prospective, Single-Arm, Longitudinal Study of Biomarkers in Real-World Patients with Severe Asthma

被引:19
作者
Buhl, Roland [1 ]
Korn, Stephanie [1 ]
Menzies-Gow, Andrew [2 ]
Aubier, Michel [3 ]
Chapman, Kenneth R. [4 ,5 ]
Canonica, Giorgio W. [6 ]
Picado, Cesar [7 ]
Donica, Margarita [8 ]
Kuhlbusch, Klaus [9 ]
Korom, Stephan [10 ]
Hanania, Nicola A. [11 ]
机构
[1] Johannes Gutenberg Univ Mainz, Mainz, Germany
[2] Royal Brompton Hosp, Lung Div, London, England
[3] Univ Paris Diderot, Dept Pneumol, Fac Med, Paris, France
[4] Univ Hlth Network, Asthma & Airway Ctr, Toronto, ON, Canada
[5] Univ Toronto, Toronto, ON, Canada
[6] Humanitas Univ & Res Hosp, Ist Ricovero & Cura Carattere Sci IRCCS, Milan, Italy
[7] Univ Barcelona, Dept Pulmonol & Resp Allergy, Inst Invest Biomed August Pi i Sunyer IDIBAPS, Hosp Clin Barcelona,Invest Biomed Red Enfermedade, Barcelona, Spain
[8] F Hoffmann La Roche Ltd, Pharma Dev Biostat Oncol, Basel, Switzerland
[9] F Hoffmann La Roche Ltd, Global Prod Dev Med Affairs Resp, Basel, Switzerland
[10] F Hoffmann La Roche Ltd, Global Prod Dev, Med Affairs Immunol Infect Dis & Ophthalmol, Basel, Switzerland
[11] Baylor Coll Med, Airways Clin Res Ctr, Houston, TX 77030 USA
关键词
Periostin; biomarker; blood eosinophil; exacerbation; severe asthma; AIRWAY INFLAMMATION; LEBRIKIZUMAB; MEPOLIZUMAB;
D O I
10.1016/j.jaip.2020.03.038
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
BACKGROUND: ARIETTA was a prospective, single-arm, noninterventional, multicenter study in patients with severe asthma. OBJECTIVE: To examine the predictive and prognostic abilities of type 2 biomarkers for severe asthma outcomes. METHODS: Adult patients with severe asthma receiving daily inhaled corticosteroids (fluticasone propionate >= 500 mg or equivalent) and >= 1 second controller medication were enrolled. Biomarker, clinical, and safety data were collected over 52 weeks. The primary endpoint was the asthma exacerbation rate over 52 weeks in serum periostin-high (>= 50 ng/mL at baseline) versus periostin-low subgroups (<50 ng/mL). Correlations between biomarker levels (periostin, blood eosinophils, IgE, and fractional exhaled nitric oxide [FeNO]) and between central and local laboratory measurements (blood eosinophils and IgE) were assessed. The study was terminated before planned enrollment was completed. RESULTS: Of 465 patients, 66.5% were female, 13.3% were receiving oral corticosteroids, 42.4% had >= 1 exacerbation in the previous year, 52.0% were periostin-high, and 87.5% had type 2 inflammation (blood eosinophils >= 150 cells/mL and/or FeNO >= 25 ppb and/or positive skin allergen test). Biomarker levels correlated poorly with each other. Central and local laboratory blood eosinophil and IgE measurements generally agreed. No difference was observed in exacerbation rates over 52 weeks between periostin-high and periostin-low patients (rate ratio, 0.93; 95% confidence interval, 0.67-1.28; P = .642). Results suggested higher exacerbation rates in patients with blood eosinophils >= 300 cells/mu L and FeNO >= 25 ppb. CONCLUSIONS: No prognostic value for serum periostin related to exacerbations was detected. Higher blood eosinophils combined with increased FeNO were potentially associated with increased exacerbation rates. (C) 2020 The Authors. Published by Elsevier Inc. on behalf of the American Academy of Allergy, Asthma & Immunology
引用
收藏
页码:2630 / +
页数:16
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