Efficacy of mepolizumab in elderly patients with severe asthma and overlapping COPD in real-world settings: A retrospective observational study.


Journal

Respiratory investigation
ISSN: 2212-5353
Titre abrégé: Respir Investig
Pays: Netherlands
ID NLM: 101581124

Informations de publication

Date de publication:
Jul 2021
Historique:
received: 29 09 2020
revised: 14 01 2021
accepted: 16 02 2021
pubmed: 15 4 2021
medline: 27 10 2021
entrez: 14 4 2021
Statut: ppublish

Résumé

Asthma and chronic obstructive pulmonary disease (COPD) are the most common respiratory diseases, presenting overlapping prevalence with age. Mepolizumab is a humanized monoclonal antibody targeting interleukin-5. In major randomized clinical trials, this antibody reportedly reduced the circulating eosinophil count, exacerbation rate, and oral corticosteroid (OCS) dosage in patients with severe eosinophilic asthma. However, data regarding the efficacy of mepolizumab in elderly patients with asthma and overlapping COPD are limited. This was a single-center, retrospective, observational study. Elderly patients (age ≥65 years) administered mepolizumab between August 2016 and March 2019 were enrolled and the effects of mepolizumab on the eosinophil level, exacerbation numbers, OCS dosage, and lung functions were assessed. We compared treatment responses in patients with asthma and COPD overlap (ACO) with responses observed in patients with severe asthma alone. Adverse events were also evaluated. Twenty patients (10 men and 10 women), with a mean age of 77.5 ± 1.3 years, were included. Mepolizumab significantly reduced the blood eosinophil count, as well as significantly decreased clinically significant exacerbation, in both populations. The OCS dosage was significantly reduced in patients treated receiving maintenance OCS therapy. However, mepolizumab did not improve lung function in either population, and no significant difference was observed in treatment responses between patients with asthma alone and ACO. Mepolizumab may be effective in elderly patients with eosinophilic asthma and ACO.

Sections du résumé

BACKGROUND BACKGROUND
Asthma and chronic obstructive pulmonary disease (COPD) are the most common respiratory diseases, presenting overlapping prevalence with age. Mepolizumab is a humanized monoclonal antibody targeting interleukin-5. In major randomized clinical trials, this antibody reportedly reduced the circulating eosinophil count, exacerbation rate, and oral corticosteroid (OCS) dosage in patients with severe eosinophilic asthma. However, data regarding the efficacy of mepolizumab in elderly patients with asthma and overlapping COPD are limited.
METHODS METHODS
This was a single-center, retrospective, observational study. Elderly patients (age ≥65 years) administered mepolizumab between August 2016 and March 2019 were enrolled and the effects of mepolizumab on the eosinophil level, exacerbation numbers, OCS dosage, and lung functions were assessed. We compared treatment responses in patients with asthma and COPD overlap (ACO) with responses observed in patients with severe asthma alone. Adverse events were also evaluated.
RESULTS RESULTS
Twenty patients (10 men and 10 women), with a mean age of 77.5 ± 1.3 years, were included. Mepolizumab significantly reduced the blood eosinophil count, as well as significantly decreased clinically significant exacerbation, in both populations. The OCS dosage was significantly reduced in patients treated receiving maintenance OCS therapy. However, mepolizumab did not improve lung function in either population, and no significant difference was observed in treatment responses between patients with asthma alone and ACO.
CONCLUSIONS CONCLUSIONS
Mepolizumab may be effective in elderly patients with eosinophilic asthma and ACO.

Identifiants

pubmed: 33849780
pii: S2212-5345(21)00041-1
doi: 10.1016/j.resinv.2021.02.009
pii:
doi:

Substances chimiques

Anti-Asthmatic Agents 0
Antibodies, Monoclonal, Humanized 0
mepolizumab 90Z2UF0E52

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

478-486

Informations de copyright

Copyright © 2021 The Japanese Respiratory Society. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of Interest The authors have no conflicts of interest to declare.

Auteurs

Shoko Isoyama (S)

Department of Respiratory Medicine, Hiroshima Prefectural Hospital, Hiroshima, Japan; Department of Molecular and Internal Medicine, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.

Nobuhisa Ishikawa (N)

Department of Respiratory Medicine, Hiroshima Prefectural Hospital, Hiroshima, Japan. Electronic address: n-ishikawa@hph.pref.hiroshima.jp.

Kosuke Hamai (K)

Department of Respiratory Medicine, Hiroshima Prefectural Hospital, Hiroshima, Japan.

Mirai Matsumura (M)

Department of Respiratory Medicine, Hiroshima Prefectural Hospital, Hiroshima, Japan.

Hiroki Kobayashi (H)

Department of Rheumatology, Hiroshima Prefectural Hospital, Hiroshima, Japan.

Akio Nomura (A)

Department of Respiratory Medicine, Hiroshima Prefectural Hospital, Hiroshima, Japan; Department of Molecular and Internal Medicine, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.

Sayaka Ueno (S)

Department of Respiratory Medicine, Hiroshima Prefectural Hospital, Hiroshima, Japan.

Takuya Tanimoto (T)

Department of Respiratory Medicine, Hiroshima Prefectural Hospital, Hiroshima, Japan.

Hiroyuki Maeda (H)

Department of Rheumatology, Hiroshima Prefectural Hospital, Hiroshima, Japan.

Hiroshi Iwamoto (H)

Department of Molecular and Internal Medicine, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.

Noboru Hattori (N)

Department of Molecular and Internal Medicine, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.

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Classifications MeSH