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Authordc.contributor.authorPanettieri, Reynold A. 
Authordc.contributor.authorWelte, Tobias 
Authordc.contributor.authorShenoy, Kartik V. 
Authordc.contributor.authorKorn, Stephanie 
Authordc.contributor.authorJandl, Margret 
Authordc.contributor.authorKerwin, Edward M. 
Authordc.contributor.authorFeijoo Seoane, Rosa 
Authordc.contributor.authorBarker, Peter 
Authordc.contributor.authorOlsson, Richard F. 
Authordc.contributor.authorMartin, Ubaldo J. 
Admission datedc.date.accessioned2020-05-08T14:18:39Z
Available datedc.date.available2020-05-08T14:18:39Z
Publication datedc.date.issued2020
Cita de ítemdc.identifier.citationJournal of Asthma and Allergy 2020:13 115–126es_ES
Identifierdc.identifier.other10.2147/JAA.S240044
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/174581
Abstractdc.description.abstractObjective: In the SOLANA trial, we sought to physiologically characterize benralizumab's onset of effect and maintenance of that effect for patients with severe eosinophilic asthma. Methods: SOLANA (NCT02869438) was a multicenter, randomized, double-blind, parallel-group, placebo-controlled, Phase IIIb study conducted at 49 centers in six countries (Chile, Germany, Hungary, the Philippines, South Korea, and the United States). Eligible patients with baseline blood eosinophil counts >= 300 cells/mu L were randomized to subcutaneous benralizumab (30 mg) or placebo administered at Days 0, 28, and 56. The primary endpoint was the average change from baseline in prebronchodilator forced expiratory volume in 1 s (pre-BD FEV1) during the Day 28.Day 84 period for benralizumab vs placebo. Secondary endpoints included patient-reported outcomes (PROs). A subset of patients participated in a whole-body plethysmography substudy. Safety was also assessed. Results: In total, 233 patients were randomized to benralizumab (n=118) or placebo (n=115). Improvement from baseline in pre-BD FEV1 with benralizumab 30 mg was not statistically significant compared with placebo (least-squares mean change difference [95% confidence interval] 57 mL [-22 to 135]; p=0.16). Compared with placebo, benralizumab demonstrated early (Day 7) nonstatistically significant improvements in whole-body plethysmography assessments of hyperinflation and clinically meaningful improvements in PRO measures (Asthma Control Questionnaire 6 at Day 14 and St. George's Respiratory Questionnaire at Day 28), which were maintained over the treatment period. Benralizumab's safety profile was commensurate with previously reported studies. Conclusion: The observed early changes in lung volume despite relatively small improvements in airflow obstruction suggest that the anti-inflammatory effect of benralizumab may be manifested as deflation over time for patients with hyperinflation, who potentially have a greater degree of airway remodeling. This early effect could partially explain the rapid PRO improvements observed for certain patients.es_ES
Patrocinadordc.description.sponsorshipAstraZenecaes_ES
Lenguagedc.language.isoenes_ES
Publisherdc.publisherDove Medical Presses_ES
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
Sourcedc.sourceJournal of Asthma and Allergyes_ES
Keywordsdc.subjectAnti–IL-5Rαes_ES
Keywordsdc.subjectBenralizumabes_ES
Keywordsdc.subjectInterleukin-5es_ES
Keywordsdc.subjectRandomized controlled triales_ES
Keywordsdc.subjectEosinophilices_ES
Keywordsdc.subjectSevere asthmaes_ES
Títulodc.titleOnset of effect, changes in airflow obstruction and lung volume, and health-related quality of life Improvements with benralizumab for patients with Severe Eosinophilic Asthma: Phase IIIb Randomized, Controlled Trial (SOLANA)es_ES
Document typedc.typeArtículo de revistaes_ES
dcterms.accessRightsdcterms.accessRightsAcceso Abierto
Catalogueruchile.catalogadorctces_ES
Indexationuchile.indexArtículo de publicación ISI
Indexationuchile.indexArtículo de publicación SCOPUS


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile