Benralizumab Effectiveness in Severe Asthma Is Independent of Previous Biologic Use

被引:41
作者
Jackson, David J. [1 ,2 ]
Burhan, Hassan [3 ]
Menzies-Gow, Andrew [4 ]
Pfeffer, Paul [5 ]
Nanzer, Alexandra [1 ]
Gil, Esther Garcia [6 ]
Morris, Tamsin [7 ]
Tran, Trung N. [8 ]
Hirsch, Ian [9 ]
Dube, Sabada [7 ]
机构
[1] Guys & St Thomas NHS Trust, Guys Severe Asthma Ctr, London SE1 9RT, England
[2] Sci Kings Coll London, Asthma UK Ctr, Sch Immunol & Microbial Sci, London, England
[3] Royal Liverpool & Broadgreen Univ Hosp NHS Trust, Liverpool, Merseyside, England
[4] Royal Brompton Hosp, London, England
[5] Barts Hlth NHS Trust, London, England
[6] AstraZeneca, BioPharmaceut Med, Global Med Resp, Barcelona, Spain
[7] AstraZeneca, UK Med & Sci Affairs, Luton, Beds, England
[8] AstraZeneca, Gaithersburg, MD USA
[9] AstraZeneca, BioPharmaceut R&D, Cambridge, England
关键词
Atopy; Benralizumab; Biologic; Fractional exhaled nitric oxide; Oral corticosteroids; Patient-reported outcomes; Real-world study; Severe eosinophilic asthma; DOUBLE-BLIND; EFFICACY; MULTICENTER; MEPOLIZUMAB; LIFE;
D O I
10.1016/j.jaip.2022.02.014
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
BACKGROUND: Benralizumab is an IL-5 receptor alpha-directed cytolytic mAb that depletes eosinophils, reducing exacerbations and oral corticosteroid (OCS) use, and improves asthma control for patients with severe eosinophilic asthma (SEA). Data on response in patients previously treated with other biologic therapies are limited. OBJECTIVE: To describe real-world clinical outcomes with benralizumab for patients with and without prior biologic use for uncontrolled SEA. METHODS: This retrospective study compared clinical outcomes before and after benralizumab initiation in adults with uncontrolled SEA with 3 or more asthma exacerbations in the previous 12 months or on maintenance OCS treatment. Outcomes included exacerbations, OCS use, patient-reported outcomes, and health care resource utilization, including emergency department visits and hospitalizations. RESULTS: In all, 208 patients were enrolled, including 90 (43.3%) with previous experience with an alternate biologic for SEA. Benralizumab led to an 81% reduction in exacerbation rate, with 48% of patients with previous exacerbations experiencing none after 48 weeks. Overall, 67% of patients requiring baseline maintenance OCS achieved greater than or equal to 50% reduction in daily OCS dosage, and 53% eliminated maintenance OCS. Clinically meaningful improvements in patient-reported outcomes were seen, with response at 4 weeks predicting longer-term benefits. Health care resource utilization also decreased. Improvements were observed irrespective of previous biologic experience, fractional exhaled nitric oxide concentrations, atopic status, or other baseline characteristics. CONCLUSIONS: In a multicenter real-world setting, patients with uncontrolled SEA achieved substantial improvements in all clinical outcome measures with benralizumab irrespective of previous biologic use, atopic status, or baseline fractional exhaled nitric oxide concentration. (C) 2022 The Authors. Published by Elsevier Inc. on behalf of the American Academy of Allergy, Asthma & Immunology.
引用
收藏
页码:1534 / +
页数:15
相关论文
共 27 条
[1]   Mepolizumab reduces exacerbations in patients with severe eosinophilic asthma, irrespective of body weight/body mass index: meta-analysis of MENSA and MUSCA [J].
Albers, Frank C. ;
Papi, Alberto ;
Taille, Camille ;
Bratton, Daniel J. ;
Bradford, Eric S. ;
Yancey, Steven W. ;
Kwon, Namhee .
RESPIRATORY RESEARCH, 2019, 20 (1)
[2]   Baseline patient factors impact on the clinical efficacy of benralizumab for severe asthma [J].
Bleecker, Eugene R. ;
Wechsler, Michael E. ;
FitzGerald, J. Mark ;
Menzies-Gow, Andrew ;
Wu, Yanping ;
Hirsch, Ian ;
Goldman, Mitchell ;
Newbold, Paul ;
Zangrilli, James G. .
EUROPEAN RESPIRATORY JOURNAL, 2018, 52 (04)
[3]   Efficacy and safety of benralizumab for patients with severe asthma uncontrolled with high-dosage inhaled corticosteroids and long-acting β2-agonists (SIROCCO): a randomised, multicentre, placebo-controlled phase 3 trial [J].
Bleecker, Eugene R. ;
FitzGerald, J. Mark ;
Chanez, Pascal ;
Papi, Alberto ;
Weinstein, Steven F. ;
Barker, Peter ;
Sproule, Stephanie ;
Gilmartin, Geoffrey ;
Aurivillius, Magnus ;
Werkstrom, Viktoria ;
Goldman, Mitchell .
LANCET, 2016, 388 (10056) :2115-2127
[4]   Efficacy of mepolizumab add-on therapy on health-related quality of life and markers of asthma control in severe eosinophilic asthma (MUSCA): a randomised, double-blind, placebo-controlled, parallel-group, multicentre, phase 3b trial [J].
Chupp, Geoffrey L. ;
Bradford, Eric S. ;
Albers, Frank C. ;
Bratton, Daniel J. ;
Wang-Jairaj, Jie ;
Nelsen, Linda M. ;
Trevor, Jennifer L. ;
Magnan, Antoine ;
ten Brinke, Anneke .
LANCET RESPIRATORY MEDICINE, 2017, 5 (05) :390-400
[5]  
FitzGerald JM, 2016, LANCET, V388, P2128, DOI [10.1016/s0140-6736(16)31322-8, 10.1016/S0140-6736(16)31322-8]
[6]   Onset of effect and impact on health-related quality of life, exacerbation rate, lung function, and nasal polyposis symptoms for patients with severe eosinophilic asthma treated with benralizumab (ANDHI): a randomised, controlled, phase 3b trial (vol 9 pg 260, 2021) [J].
Harrison, Tim W. ;
Chanez, Pascal ;
Menzella, Francesco ;
Canonica, Giorgio Walter ;
Louis, Renaud ;
Cosio, Borja G. ;
Lugogo, Njira L. ;
Mohan, Arjun ;
Burden, Annie ;
McDermott, Lawrence ;
Garcia Gil, Esther ;
Zangrilli, James G. .
LANCET RESPIRATORY MEDICINE, 2021, 9 (03) :E29-E29
[7]   Eosinophilic and Noneosinophilic Asthma An Expert Consensus Framework to Characterize Phenotypes in a Global Real-Life Severe Asthma Cohort [J].
Heaney, Liam G. ;
de Llano, Luis Perez ;
Al-Ahmad, Mona ;
Backer, Vibeke ;
Busby, John ;
Canonica, Giorgio Walter ;
Christoff, George C. ;
Cosio, Borja G. ;
FitzGerald, J. Mark ;
Heffler, Enrico ;
Iwanaga, Takashi ;
Jackson, David J. ;
Menzies-Gow, Andrew N. ;
Papadopoulos, Nikolaos G. ;
Papaioannou, Andriana, I ;
Pfeffer, Paul E. ;
Popov, Todor A. ;
Porsbjerg, Celeste M. ;
Rhee, Chin Kook ;
Sadatsafavi, Mohsen ;
Tohda, Yuji ;
Wang, Eileen ;
Wechsler, Michael E. ;
Alacqua, Marianna ;
Altraja, Alan ;
Bjermer, Leif ;
Bjornsdottir, Unnur S. ;
Bourdin, Arnaud ;
Brusselle, Guy G. ;
Buhl, Roland ;
Costello, Richard W. ;
Hew, Mark ;
Koh, Mariko Siyue ;
Lehmann, Sverre ;
Lehtimaki, Lauri ;
Peters, Matthew ;
Taille, Camille ;
Taube, Christian ;
Tran, Trung N. ;
Zangrilli, James ;
Bulathsinhala, Lakmini ;
Carter, Victoria A. ;
Chaudhry, Isha ;
Eleangovan, Neva ;
Hosseini, Naeimeh ;
Kerkhof, Marjan ;
Murray, Ruth B. ;
Price, Chris A. ;
Price, David B. .
CHEST, 2021, 160 (03) :814-830
[8]   Composite type-2 biomarker strategy versus a symptom-risk-based algorithm to adjust corticosteroid dose in patients with severe asthma: a multicentre, single-blind, parallel group, randomised controlled trial [J].
Heaney, Liam G. ;
Busby, John ;
Hanratty, Catherine E. ;
Djukanovic, Ratko ;
Woodcock, Ashley ;
Walker, Samantha M. ;
Hardman, Timothy C. ;
Arron, Joseph R. ;
Choy, David F. ;
Bradding, Peter ;
Brightling, Christopher E. ;
Chaudhuri, Rekha ;
Cowan, Douglas C. ;
Mansur, Adel H. ;
Fowler, Stephen J. ;
Niven, Robert M. ;
Howarth, Peter H. ;
Lordan, James L. ;
Menzies-Gow, Andrew ;
Harrison, Tim W. ;
Robinson, Douglas S. ;
Holweg, Cecile T. J. ;
Matthews, John G. ;
Pavord, Ian D. .
LANCET RESPIRATORY MEDICINE, 2021, 9 (01) :57-68
[9]   The relationship between FENO and effectiveness of mepolizumab and benralizumab in severe eosinophilic asthma [J].
Hearn, Andrew P. ;
Kavanagh, Joanne ;
d'Ancona, Grainne ;
Roxas, Cris ;
Green, Linda ;
Thomson, Louise ;
Fernandes, Marianna ;
Kent, Brian D. ;
Dhariwal, Jaideep ;
Nanzer, Alexanda M. ;
Jackson, David J. .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE, 2021, 9 (05) :2093-+
[10]   The prevalence of severe refractory asthma [J].
Hekking, Pieter-Paul W. ;
Wener, Reinier R. ;
Amelink, Marijke ;
Zwinderman, Aelko H. ;
Bouvy, Marcel L. ;
Bel, Elisabeth H. .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2015, 135 (04) :896-902