Tezepelumab can Restore Normal Lung Function in Patients with Severe, Uncontrolled Asthma: Pooled Results from the PATHWAY and NAVIGATOR Studies

被引:0
作者
Pavord, Ian D. [1 ]
Brightling, Christopher E. [2 ]
Korn, Stephanie [3 ,4 ]
Martin, Nicole L. [5 ]
Ponnarambil, Sandhia S. [6 ]
Molfino, Nestor A. [7 ]
Parnes, Jane R. [8 ]
Ambrose, Christopher S. [9 ]
机构
[1] Univ Oxford, Natl Inst Hlth & Care Res, Oxford Biomed Res Ctr, Nuffield Dept Med,Resp Med, Oxford, Oxon, England
[2] Univ Leicester, Inst Lung Hlth, Natl Inst Hlth & Care Res, Leicester Biomed Res Ctr, Leicester, Leics, England
[3] IKF Pneumol Mainz, Mainz, Germany
[4] Thoraxklin Heidelberg, Heidelberg, Germany
[5] Cytel Inc, Late Stage Dev Resp & Immunol, BioPharmaceut R&D, Biometr,AstraZeneca, Waltham, MA USA
[6] AstraZeneca, Late Stage Dev Resp & Immunol, BioPharmaceut R&D, Cambridge, England
[7] Amgen Inc, Global Dev, Thousand Oaks, CA USA
[8] Amgen Inc, Amgen Early Dev, Thousand Oaks, CA USA
[9] AstraZeneca, Resp & Immunol, BioPharmaceut Med, Gaithersburg, MD USA
关键词
Biologic; Lung function; Pre-bronchodilator percent predicted normal; Randomized placebo-controlled trial; Severe asthma; Tezepelumab; ADULTS;
D O I
10.1007/s41030-025-00294-2
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Introduction: This post hoc analysis assessed the ability of tezepelumab treatment to restore normal lung function in patients with severe, uncontrolled asthma with abnormal lung function at baseline pooled from the PATHWAY and NAVIGATOR studies. Methods: PATHWAY and NAVIGATOR were multicentre, randomized, double-blind, placebo-controlled studies. Patients (12-80 years old) included in this analysis received tezepelumab 210 mg subcutaneously every 4 weeks or matched placebo for 52 weeks. Patients had a percent predicted pre-bronchodilator (BD) forced expiratory volume in 1 s (FEV1) of < 80% (< 90% for adolescents in NAVIGATOR) at screening. The change from baseline to week 52 in pre-BD FEV1 was assessed by baseline percent predicted pre-BD FEV1 subgroup [abnormal (< 80%) and normal (>= 80%)]. The proportion of patients with abnormal lung function at baseline who achieved normal lung function at week 52 was assessed overall and by biomarker level and disease duration subgroups. Results: Of the 665 and 669 patients who received tezepelumab or placebo, respectively, 564 and 569 had abnormal lung function at baseline. Tezepelumab improved the pre-BD FEV1 from baseline to week 52 versus placebo by 0.14 L [95% confidence interval (CI) 0.09-0.19] and 0.13 L (95% CI 0.01-0.24) in patients with abnormal and normal lung function at baseline, respectively. A higher proportion of tezepelumab than placebo recipients with abnormal lung function at baseline achieved normal lung function at week 52 (17.2% vs. 9.9%, respectively). Among tezepelumab recipients, those with higher levels of type 2 inflammatory biomarkers and a shorter duration of disease at baseline were more likely to achieve normal lung function at week 52. Conclusion: In patients with severe, uncontrolled asthma, a greater proportion of tezepelumab than placebo recipients with abnormal lung function at baseline achieved normal lung function at week 52.
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页码:315 / 325
页数:11
相关论文
共 12 条
[2]   Severe exacerbations predict excess lung function decline in asthma [J].
Bai, T. R. ;
Vonk, J. M. ;
Postma, D. S. ;
Boezen, H. M. .
EUROPEAN RESPIRATORY JOURNAL, 2007, 30 (03) :452-456
[3]   Efficacy of Tezepelumab in Severe, Uncontrolled Asthma: Pooled Analysis of the PATHWAY and NAVIGATOR Clinical Trials [J].
Corren, Jonathan ;
Menzies-Gow, Andrew ;
Chupp, Geoffrey ;
Israel, Elliot ;
Korn, Stephanie ;
Cook, Bill ;
Ambrose, Christopher S. ;
Hellqvist, Asa ;
Roseti, Stephanie L. ;
Molfino, Nestor A. ;
Llanos, Jean-Pierre ;
Martin, Neil ;
Bowen, Karin ;
Griffiths, Janet M. ;
Parnes, Jane R. ;
Colice, Gene .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2023, 208 (01) :13-24
[4]   Thymic stromal lymphopoietin: its role and potential as a therapeutic target in asthma [J].
Gauvreau, Gail M. ;
Sehmi, Roma ;
Ambrose, Christopher S. ;
Griffiths, Janet M. .
EXPERT OPINION ON THERAPEUTIC TARGETS, 2020, 24 (08) :777-792
[5]   Efficacy of tezepelumab in patients with severe asthma and persistent airflow obstruction [J].
Israel, Elliot ;
Castro, Mario ;
Ambrose, Christopher S. ;
Llanos, Jean-Pierre ;
Molfino, Nestor A. ;
Martin, Nicole L. ;
Ponnarambil, Sandhia S. ;
Martin, Neil .
ERJ OPEN RESEARCH, 2024, 10 (06)
[6]   Association of forced expiratory volume with disease duration and sputum neutrophils in chronic asthma [J].
Little, SA ;
MacLeod, KJ ;
Chalmers, GW ;
Love, JG ;
McSharry, C ;
Thomson, NC .
AMERICAN JOURNAL OF MEDICINE, 2002, 112 (06) :446-452
[7]   Tezepelumab in Adults and Adolescents with Severe, Uncontrolled Asthma [J].
Menzies-Gow, Andrew ;
Corren, Jonathan ;
Bourdin, Arnaud ;
Chupp, Geoffrey ;
Israel, Elliot ;
Wechsler, Michael E. ;
Brightling, Christopher E. ;
Griffiths, Janet M. ;
Hellqvist, Asa ;
Bowen, Karin ;
Kaur, Primal ;
Almqvist, Gun ;
Ponnarambil, Sandhia ;
Colice, Gene .
NEW ENGLAND JOURNAL OF MEDICINE, 2021, 384 (19) :1800-1809
[8]  
Nordenmark LH, 2023, NEJM EVID, V2, DOI 10.1056/EVIDoa2300135
[9]   Airway remodeling contributes to the progressive loss of lung function in asthma: An overview [J].
Pascual, RM ;
Peters, SP .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2005, 116 (03) :477-486
[10]   Persistence of both reversible airway obstruction and higher blood eosinophils may predict lung function decline in severe asthma [J].
Sposato, Bruno ;
Scalese, Marco ;
Ricci, Alberto ;
Rogliani, Paola ;
Paggiaro, Pierluigi .
CLINICAL RESPIRATORY JOURNAL, 2021, 15 (02) :237-243