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Feasibility of Discontinuing Biologics in Severe Asthma: An Algorithmic Approach

In severe asthma with type 2 (T2) inflammation, biologics targeting key mediators of T2 inflammation, including interleukin (IL)-5, IL-4/IL-13, and immunoglobulin (Ig)E, remarkably improve the management of severe asthma, providing new insights into the clinical course of asthma such as disease modi...

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Autores principales: Hamada, Kazuki, Oishi, Keiji, Murata, Yoriyuki, Hirano, Tsunahiko, Matsunaga, Kazuto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8665775/
https://www.ncbi.nlm.nih.gov/pubmed/34908847
http://dx.doi.org/10.2147/JAA.S340684
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author Hamada, Kazuki
Oishi, Keiji
Murata, Yoriyuki
Hirano, Tsunahiko
Matsunaga, Kazuto
author_facet Hamada, Kazuki
Oishi, Keiji
Murata, Yoriyuki
Hirano, Tsunahiko
Matsunaga, Kazuto
author_sort Hamada, Kazuki
collection PubMed
description In severe asthma with type 2 (T2) inflammation, biologics targeting key mediators of T2 inflammation, including interleukin (IL)-5, IL-4/IL-13, and immunoglobulin (Ig)E, remarkably improve the management of severe asthma, providing new insights into the clinical course of asthma such as disease modification and broad modulation of T2 inflammation. Once severe asthma has become a “controllable” condition, the question of discontinuation of biologics arises due to cost and side effects. The studies on discontinuing biologics in asthma demonstrate that some of patients successfully discontinue biologics, indicating that it is a feasible option in a subset of patients. Incorporating the evidence of discontinuation, we propose the criteria for the discontinuation of biologics. Our proposed criteria for the discontinuation of biologics consist of an absence of asthma symptoms (asthma control questionnaire [ACQ] score < 1.5 or asthma control test [ACT] score > 19), no asthma exacerbations, no use of oral corticosteroids, normalized spirometry (forced exhaled volume in 1 second [FEV(1)] ≥ 80%), suppressed T2 inflammation (blood eosinophil counts < 300 μL and fractional exhaled nitric oxide [FeNO] < 50 ppb), and control of asthma comorbidities. Real-world evidence verified a subset of patients achieving highly well-controlled conditions after use of biologics, namely super-responders, who are candidates for the discontinuation of biologics. If super-responders meet all of the criteria, they are allowed to discontinue biological therapies. Our proposed algorithm may support physicians’ treatment decisions for patients receiving biologics.
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spelling pubmed-86657752021-12-13 Feasibility of Discontinuing Biologics in Severe Asthma: An Algorithmic Approach Hamada, Kazuki Oishi, Keiji Murata, Yoriyuki Hirano, Tsunahiko Matsunaga, Kazuto J Asthma Allergy Review In severe asthma with type 2 (T2) inflammation, biologics targeting key mediators of T2 inflammation, including interleukin (IL)-5, IL-4/IL-13, and immunoglobulin (Ig)E, remarkably improve the management of severe asthma, providing new insights into the clinical course of asthma such as disease modification and broad modulation of T2 inflammation. Once severe asthma has become a “controllable” condition, the question of discontinuation of biologics arises due to cost and side effects. The studies on discontinuing biologics in asthma demonstrate that some of patients successfully discontinue biologics, indicating that it is a feasible option in a subset of patients. Incorporating the evidence of discontinuation, we propose the criteria for the discontinuation of biologics. Our proposed criteria for the discontinuation of biologics consist of an absence of asthma symptoms (asthma control questionnaire [ACQ] score < 1.5 or asthma control test [ACT] score > 19), no asthma exacerbations, no use of oral corticosteroids, normalized spirometry (forced exhaled volume in 1 second [FEV(1)] ≥ 80%), suppressed T2 inflammation (blood eosinophil counts < 300 μL and fractional exhaled nitric oxide [FeNO] < 50 ppb), and control of asthma comorbidities. Real-world evidence verified a subset of patients achieving highly well-controlled conditions after use of biologics, namely super-responders, who are candidates for the discontinuation of biologics. If super-responders meet all of the criteria, they are allowed to discontinue biological therapies. Our proposed algorithm may support physicians’ treatment decisions for patients receiving biologics. Dove 2021-12-07 /pmc/articles/PMC8665775/ /pubmed/34908847 http://dx.doi.org/10.2147/JAA.S340684 Text en © 2021 Hamada et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Review
Hamada, Kazuki
Oishi, Keiji
Murata, Yoriyuki
Hirano, Tsunahiko
Matsunaga, Kazuto
Feasibility of Discontinuing Biologics in Severe Asthma: An Algorithmic Approach
title Feasibility of Discontinuing Biologics in Severe Asthma: An Algorithmic Approach
title_full Feasibility of Discontinuing Biologics in Severe Asthma: An Algorithmic Approach
title_fullStr Feasibility of Discontinuing Biologics in Severe Asthma: An Algorithmic Approach
title_full_unstemmed Feasibility of Discontinuing Biologics in Severe Asthma: An Algorithmic Approach
title_short Feasibility of Discontinuing Biologics in Severe Asthma: An Algorithmic Approach
title_sort feasibility of discontinuing biologics in severe asthma: an algorithmic approach
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8665775/
https://www.ncbi.nlm.nih.gov/pubmed/34908847
http://dx.doi.org/10.2147/JAA.S340684
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