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Real-life effects of benralizumab on airway oscillometry in severe eosinophilic asthma

INTRODUCTION: Eosinophil depletion with benralizumab reduces exacerbations and improves disease control and FEV(1) in patients with severe eosinophilic asthma. However, few studies have investigated the effect of biologics on small airways dysfunction (SAD) even though the latter correlates better w...

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Autores principales: Chan, Rory, Lipworth, Brian J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10201257/
https://www.ncbi.nlm.nih.gov/pubmed/37208039
http://dx.doi.org/10.1136/bmjresp-2022-001472
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author Chan, Rory
Lipworth, Brian J
author_facet Chan, Rory
Lipworth, Brian J
author_sort Chan, Rory
collection PubMed
description INTRODUCTION: Eosinophil depletion with benralizumab reduces exacerbations and improves disease control and FEV(1) in patients with severe eosinophilic asthma. However, few studies have investigated the effect of biologics on small airways dysfunction (SAD) even though the latter correlates better with poor asthma control and type 2 inflammation. METHODS: 21 GINA-defined severe asthma patients who were treated with benralizumab and who had baseline oscillometry-defined SAD were included in this study. Here, SAD was diagnosed only if patients satisfied both R5–R20≥0.10 kPa/L/s and AX≥1.0 kPa/L. The mean duration of follow-up between pre-benralizumab versus post-benralizumab clinical measurements was 8 months. RESULTS: Mean values for FEV(1)% and FVC% but not FEF(25%–75%) significantly increased following benralizumab, along with significant reductions in Asthma Control Questionnaire (ACQ). There were no significant improvements in R5–R20, X5 or AX, while the mean (SEM) PBE count fell to 23 (14) cells/µL. In a responder analysis, n=8/21 and n=12/21 patients experienced improvements exceeding biological variability of 0.04 kPa/L/s and 0.39 kPa/L in R5–R20 and AX, respectively, in severe asthma. N=10/21, n=10/21 and n=11/21 patients experienced improvements in FEV(1), FEF(25–75) and FVC exceeding biological variability of 150 mL, 0.210 L/s and 150 mL, respectively. In contrast, n=15/21 patients experienced an improvement in ACQ greater than minimal clinical important difference of 0.5 units. CONCLUSION: Eosinophil depletion with benralizumab improves spirometry and asthma control but does not improve spirometry-measured or oscillometry-measured SAD in severe asthma in a real-life setting.
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spelling pubmed-102012572023-05-23 Real-life effects of benralizumab on airway oscillometry in severe eosinophilic asthma Chan, Rory Lipworth, Brian J BMJ Open Respir Res Asthma INTRODUCTION: Eosinophil depletion with benralizumab reduces exacerbations and improves disease control and FEV(1) in patients with severe eosinophilic asthma. However, few studies have investigated the effect of biologics on small airways dysfunction (SAD) even though the latter correlates better with poor asthma control and type 2 inflammation. METHODS: 21 GINA-defined severe asthma patients who were treated with benralizumab and who had baseline oscillometry-defined SAD were included in this study. Here, SAD was diagnosed only if patients satisfied both R5–R20≥0.10 kPa/L/s and AX≥1.0 kPa/L. The mean duration of follow-up between pre-benralizumab versus post-benralizumab clinical measurements was 8 months. RESULTS: Mean values for FEV(1)% and FVC% but not FEF(25%–75%) significantly increased following benralizumab, along with significant reductions in Asthma Control Questionnaire (ACQ). There were no significant improvements in R5–R20, X5 or AX, while the mean (SEM) PBE count fell to 23 (14) cells/µL. In a responder analysis, n=8/21 and n=12/21 patients experienced improvements exceeding biological variability of 0.04 kPa/L/s and 0.39 kPa/L in R5–R20 and AX, respectively, in severe asthma. N=10/21, n=10/21 and n=11/21 patients experienced improvements in FEV(1), FEF(25–75) and FVC exceeding biological variability of 150 mL, 0.210 L/s and 150 mL, respectively. In contrast, n=15/21 patients experienced an improvement in ACQ greater than minimal clinical important difference of 0.5 units. CONCLUSION: Eosinophil depletion with benralizumab improves spirometry and asthma control but does not improve spirometry-measured or oscillometry-measured SAD in severe asthma in a real-life setting. BMJ Publishing Group 2023-05-19 /pmc/articles/PMC10201257/ /pubmed/37208039 http://dx.doi.org/10.1136/bmjresp-2022-001472 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Asthma
Chan, Rory
Lipworth, Brian J
Real-life effects of benralizumab on airway oscillometry in severe eosinophilic asthma
title Real-life effects of benralizumab on airway oscillometry in severe eosinophilic asthma
title_full Real-life effects of benralizumab on airway oscillometry in severe eosinophilic asthma
title_fullStr Real-life effects of benralizumab on airway oscillometry in severe eosinophilic asthma
title_full_unstemmed Real-life effects of benralizumab on airway oscillometry in severe eosinophilic asthma
title_short Real-life effects of benralizumab on airway oscillometry in severe eosinophilic asthma
title_sort real-life effects of benralizumab on airway oscillometry in severe eosinophilic asthma
topic Asthma
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10201257/
https://www.ncbi.nlm.nih.gov/pubmed/37208039
http://dx.doi.org/10.1136/bmjresp-2022-001472
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