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Effectiveness of benralizumab in severe eosinophilic asthma: Distinct sub‐phenotypes of response identified by cluster analysis

BACKGROUND: Benralizumab is effective in severe eosinophilic asthma (SEA), but suboptimal responses are observed in some patients. Although several factors have been associated with benralizumab response, no cluster analysis has yet been undertaken to identify different responsiveness sub‐phenotypes...

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Autores principales: Di Bona, Danilo, Crimi, Claudia, D’Uggento, Angela Maria, Benfante, Alida, Caiaffa, Maria Filomena, Calabrese, Cecilia, Campisi, Raffaele, Carpagnano, Giovanna Elisiana, Ciotta, Domenico, D'Amato, Maria, Pelaia, Corrado, Pelaia, Girolamo, Pellegrino, Simona, Scichilone, Nicola, Scioscia, Giulia, Ribecco, Nunziata, Spadaro, Giuseppe, Valenti, Giuseppe, Vatrella, Alessandro, Crimi, Nunzio, Macchia, Luigi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9293293/
https://www.ncbi.nlm.nih.gov/pubmed/34608696
http://dx.doi.org/10.1111/cea.14026
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author Di Bona, Danilo
Crimi, Claudia
D’Uggento, Angela Maria
Benfante, Alida
Caiaffa, Maria Filomena
Calabrese, Cecilia
Campisi, Raffaele
Carpagnano, Giovanna Elisiana
Ciotta, Domenico
D'Amato, Maria
Pelaia, Corrado
Pelaia, Girolamo
Pellegrino, Simona
Scichilone, Nicola
Scioscia, Giulia
Ribecco, Nunziata
Spadaro, Giuseppe
Valenti, Giuseppe
Vatrella, Alessandro
Crimi, Nunzio
Macchia, Luigi
author_facet Di Bona, Danilo
Crimi, Claudia
D’Uggento, Angela Maria
Benfante, Alida
Caiaffa, Maria Filomena
Calabrese, Cecilia
Campisi, Raffaele
Carpagnano, Giovanna Elisiana
Ciotta, Domenico
D'Amato, Maria
Pelaia, Corrado
Pelaia, Girolamo
Pellegrino, Simona
Scichilone, Nicola
Scioscia, Giulia
Ribecco, Nunziata
Spadaro, Giuseppe
Valenti, Giuseppe
Vatrella, Alessandro
Crimi, Nunzio
Macchia, Luigi
author_sort Di Bona, Danilo
collection PubMed
description BACKGROUND: Benralizumab is effective in severe eosinophilic asthma (SEA), but suboptimal responses are observed in some patients. Although several factors have been associated with benralizumab response, no cluster analysis has yet been undertaken to identify different responsiveness sub‐phenotypes. OBJECTIVE: To identify SEA sub‐phenotypes with differential responsiveness to benralizumab. METHODS: One hundred and five patients diagnosed with SEA who had completed 6 months of benralizumab treatment were included in a hierarchical cluster analysis based on a set of clinical variables that can be easily collected in routine practice (age, age at disease onset, disease length, allergen sensitization status, blood eosinophil count, IgE levels, FEV(1)% predicted, nasal polyposis, bronchiectasis). RESULTS: Four clusters were identified: Clusters 2 and 3 included patients with high levels of both IgE and eosinophils (type‐2 biomarkers high), whereas Clusters 1 and 4 included patients with only one type‐2 biomarker at a high level: IgE in Cluster 1 and eosinophils in Cluster 4. Clusters 2 and 3 (both type‐2 biomarkers high) showed the highest response rate to benralizumab in terms of elimination of exacerbations (79% and 80% respectively) compared to Clusters 1 and 4 (52% and 60% respectively). When super‐response (the absence of exacerbation without oral corticosteroid use) was assessed, Cluster 2, including patients with more preserved lung function than the other clusters, but comparable exacerbation rate, oral corticosteroid use and symptom severity, was the most responsive cluster (87.5% of patients). CONCLUSIONS: Our cluster analysis identified benralizumab differential response sub‐phenotypes in SEA, with the potential of improving disease treatment and precision management.
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spelling pubmed-92932932022-07-20 Effectiveness of benralizumab in severe eosinophilic asthma: Distinct sub‐phenotypes of response identified by cluster analysis Di Bona, Danilo Crimi, Claudia D’Uggento, Angela Maria Benfante, Alida Caiaffa, Maria Filomena Calabrese, Cecilia Campisi, Raffaele Carpagnano, Giovanna Elisiana Ciotta, Domenico D'Amato, Maria Pelaia, Corrado Pelaia, Girolamo Pellegrino, Simona Scichilone, Nicola Scioscia, Giulia Ribecco, Nunziata Spadaro, Giuseppe Valenti, Giuseppe Vatrella, Alessandro Crimi, Nunzio Macchia, Luigi Clin Exp Allergy Original Articles BACKGROUND: Benralizumab is effective in severe eosinophilic asthma (SEA), but suboptimal responses are observed in some patients. Although several factors have been associated with benralizumab response, no cluster analysis has yet been undertaken to identify different responsiveness sub‐phenotypes. OBJECTIVE: To identify SEA sub‐phenotypes with differential responsiveness to benralizumab. METHODS: One hundred and five patients diagnosed with SEA who had completed 6 months of benralizumab treatment were included in a hierarchical cluster analysis based on a set of clinical variables that can be easily collected in routine practice (age, age at disease onset, disease length, allergen sensitization status, blood eosinophil count, IgE levels, FEV(1)% predicted, nasal polyposis, bronchiectasis). RESULTS: Four clusters were identified: Clusters 2 and 3 included patients with high levels of both IgE and eosinophils (type‐2 biomarkers high), whereas Clusters 1 and 4 included patients with only one type‐2 biomarker at a high level: IgE in Cluster 1 and eosinophils in Cluster 4. Clusters 2 and 3 (both type‐2 biomarkers high) showed the highest response rate to benralizumab in terms of elimination of exacerbations (79% and 80% respectively) compared to Clusters 1 and 4 (52% and 60% respectively). When super‐response (the absence of exacerbation without oral corticosteroid use) was assessed, Cluster 2, including patients with more preserved lung function than the other clusters, but comparable exacerbation rate, oral corticosteroid use and symptom severity, was the most responsive cluster (87.5% of patients). CONCLUSIONS: Our cluster analysis identified benralizumab differential response sub‐phenotypes in SEA, with the potential of improving disease treatment and precision management. John Wiley and Sons Inc. 2021-10-16 2022-02 /pmc/articles/PMC9293293/ /pubmed/34608696 http://dx.doi.org/10.1111/cea.14026 Text en © 2021 The Authors. Clinical & Experimental Allergy published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Di Bona, Danilo
Crimi, Claudia
D’Uggento, Angela Maria
Benfante, Alida
Caiaffa, Maria Filomena
Calabrese, Cecilia
Campisi, Raffaele
Carpagnano, Giovanna Elisiana
Ciotta, Domenico
D'Amato, Maria
Pelaia, Corrado
Pelaia, Girolamo
Pellegrino, Simona
Scichilone, Nicola
Scioscia, Giulia
Ribecco, Nunziata
Spadaro, Giuseppe
Valenti, Giuseppe
Vatrella, Alessandro
Crimi, Nunzio
Macchia, Luigi
Effectiveness of benralizumab in severe eosinophilic asthma: Distinct sub‐phenotypes of response identified by cluster analysis
title Effectiveness of benralizumab in severe eosinophilic asthma: Distinct sub‐phenotypes of response identified by cluster analysis
title_full Effectiveness of benralizumab in severe eosinophilic asthma: Distinct sub‐phenotypes of response identified by cluster analysis
title_fullStr Effectiveness of benralizumab in severe eosinophilic asthma: Distinct sub‐phenotypes of response identified by cluster analysis
title_full_unstemmed Effectiveness of benralizumab in severe eosinophilic asthma: Distinct sub‐phenotypes of response identified by cluster analysis
title_short Effectiveness of benralizumab in severe eosinophilic asthma: Distinct sub‐phenotypes of response identified by cluster analysis
title_sort effectiveness of benralizumab in severe eosinophilic asthma: distinct sub‐phenotypes of response identified by cluster analysis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9293293/
https://www.ncbi.nlm.nih.gov/pubmed/34608696
http://dx.doi.org/10.1111/cea.14026
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