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Age of asthma onset does not impact the response to omalizumab

Different ages of asthma onset can lead to similar clinical symptoms but have different underlying mechanisms that may influence treatment response. This post-hoc analysis assessed response to omalizumab in relation to the age of asthma onset. Using pooled data from two phase III studies (patients 1...

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Autores principales: Rogers, Linda, Holweg, Cecile TJ, Pazwash, Hooman, Ko, Jinnie, Louie, Samuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10071096/
https://www.ncbi.nlm.nih.gov/pubmed/36852748
http://dx.doi.org/10.1177/14799731231159673
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author Rogers, Linda
Holweg, Cecile TJ
Pazwash, Hooman
Ko, Jinnie
Louie, Samuel
author_facet Rogers, Linda
Holweg, Cecile TJ
Pazwash, Hooman
Ko, Jinnie
Louie, Samuel
author_sort Rogers, Linda
collection PubMed
description Different ages of asthma onset can lead to similar clinical symptoms but have different underlying mechanisms that may influence treatment response. This post-hoc analysis assessed response to omalizumab in relation to the age of asthma onset. Using pooled data from two phase III studies (patients 12–75 years), changes in exacerbation rates, forced expiratory volume in 1 second (FEV(1)) and inhaled corticosteroids (ICS) were assessed by age of asthma onset (<18 [n = 574], 18–40 [n = 360], >40 years [n = 136]). Exacerbations (week 16) were reduced with omalizumab versus placebo in all subgroups (relative rate reduction [95% confidence interval]: <18, −53.1% [–73.6,–16.6]; 18–40, −68.3% [–85.5,–31.0]; >40, −38.4% [–77.3,67.4]). FEV(1) increased with omalizumab in all subgroups; increases were sustained in <18 and 18–40 years subgroups, but not in >40 years subgroup. ICS dose reductions (week 28) were greater with omalizumab versus placebo, regardless of age of asthma onset, as were percentages of patients with ICS doses reduced by at least 50% and 100%. In conclusion, omalizumab-treated patients had lower exacerbation rates and were more frequently able to reduce/discontinue ICS versus placebo, regardless of age of asthma onset, therefore omalizumab may be beneficial to all eligible patients with allergic asthma. TRIAL REGISTRATION: These studies were conducted before clinical trial registration was required; therefore, clinical trial registration numbers are not available.
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spelling pubmed-100710962023-04-05 Age of asthma onset does not impact the response to omalizumab Rogers, Linda Holweg, Cecile TJ Pazwash, Hooman Ko, Jinnie Louie, Samuel Chron Respir Dis Research Letter Different ages of asthma onset can lead to similar clinical symptoms but have different underlying mechanisms that may influence treatment response. This post-hoc analysis assessed response to omalizumab in relation to the age of asthma onset. Using pooled data from two phase III studies (patients 12–75 years), changes in exacerbation rates, forced expiratory volume in 1 second (FEV(1)) and inhaled corticosteroids (ICS) were assessed by age of asthma onset (<18 [n = 574], 18–40 [n = 360], >40 years [n = 136]). Exacerbations (week 16) were reduced with omalizumab versus placebo in all subgroups (relative rate reduction [95% confidence interval]: <18, −53.1% [–73.6,–16.6]; 18–40, −68.3% [–85.5,–31.0]; >40, −38.4% [–77.3,67.4]). FEV(1) increased with omalizumab in all subgroups; increases were sustained in <18 and 18–40 years subgroups, but not in >40 years subgroup. ICS dose reductions (week 28) were greater with omalizumab versus placebo, regardless of age of asthma onset, as were percentages of patients with ICS doses reduced by at least 50% and 100%. In conclusion, omalizumab-treated patients had lower exacerbation rates and were more frequently able to reduce/discontinue ICS versus placebo, regardless of age of asthma onset, therefore omalizumab may be beneficial to all eligible patients with allergic asthma. TRIAL REGISTRATION: These studies were conducted before clinical trial registration was required; therefore, clinical trial registration numbers are not available. SAGE Publications 2023-02-28 /pmc/articles/PMC10071096/ /pubmed/36852748 http://dx.doi.org/10.1177/14799731231159673 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Research Letter
Rogers, Linda
Holweg, Cecile TJ
Pazwash, Hooman
Ko, Jinnie
Louie, Samuel
Age of asthma onset does not impact the response to omalizumab
title Age of asthma onset does not impact the response to omalizumab
title_full Age of asthma onset does not impact the response to omalizumab
title_fullStr Age of asthma onset does not impact the response to omalizumab
title_full_unstemmed Age of asthma onset does not impact the response to omalizumab
title_short Age of asthma onset does not impact the response to omalizumab
title_sort age of asthma onset does not impact the response to omalizumab
topic Research Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10071096/
https://www.ncbi.nlm.nih.gov/pubmed/36852748
http://dx.doi.org/10.1177/14799731231159673
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