Newer Biological Agents in the Treatment of Severe Asthma: Real-World Results from a Tertiary Referral Center.


Journal

Lung
ISSN: 1432-1750
Titre abrégé: Lung
Pays: United States
ID NLM: 7701875

Informations de publication

Date de publication:
08 2020
Historique:
received: 13 02 2020
accepted: 13 06 2020
pubmed: 26 6 2020
medline: 2 9 2021
entrez: 26 6 2020
Statut: ppublish

Résumé

To determine the efficacy of IL-5 inhibitory therapy in severe, refractory asthma in a real-world clinical setting from a tertiary referral center. A retrospective chart review of patients with severe asthma treated with IL-5 biologic therapy for ≥ 6 months at Mayo Clinic in Rochester, Minnesota between January 1, 2013 and August 31, 2019. Over the study period, we identified 63 patients with a mean age of 54 who received an IL-5 inhibitor for ≥ 6 months. A total of 55 patients received mepolizumab, 2 received benralizumab, and 9 patients received both. Patients were followed up for a mean of 25 months. The mean number of months of oral prednisone use prior to biologic initiation was 64. There was a significant reduction in the median dose of prednisone in the 24 months after drug initiation (15 mg vs. 0 mg; p = < 0.0001). Similarly; there was a significant decline in the median number of asthma exacerbations in the 24 months before and after drug initiation (7 vs. 2; p = < 0.0001). The mean number of emergency room (ER) visits and hospitalizations decreased from 5.1 and 2.0 to 1.6 and 0.4 in the 24 months before and after therapy initiation (p < 0.0001 and p = 0.007, respectively) CONCLUSIONS: IL-5 inhibitory therapy is associated with significant and long-term sustained reductions in asthma exacerbation frequency, ER visits, hospitalizations, as well as oral steroid usage in a patient population with refractory steroid-dependent asthma referred to a tertiary referral center.

Identifiants

pubmed: 32583059
doi: 10.1007/s00408-020-00369-8
pii: 10.1007/s00408-020-00369-8
doi:

Substances chimiques

Adrenergic beta-Agonists 0
Anti-Asthmatic Agents 0
Antibodies, Monoclonal, Humanized 0
Biological Products 0
Glucocorticoids 0
Interleukin-5 0
Muscarinic Antagonists 0
Receptors, Interleukin-5 0
benralizumab 71492GE1FX
mepolizumab 90Z2UF0E52
Prednisone VB0R961HZT

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

653-659

Auteurs

Dayne Voelker (D)

Mayo Clinic School of Graduate Medical Education, Mayo Clinic-Rochester, 200 First Street SW, Rochester, MN, 55905, USA. voelker.dayne@mayo.edu.

Yahya Almodallal (Y)

Department of Pediatrics, Mayo Clinic-Rochester, Rochester, MN, USA.

Megan Dulohery Scrodin (MD)

Division of Pulmonary and Critical Care Medicine, Mayo Clinic-Rochester, Rochester, MN, USA.

Kaiser Lim (K)

Division of Pulmonary and Critical Care Medicine, Mayo Clinic-Rochester, Rochester, MN, USA.

Karina Keogh (K)

Division of Pulmonary and Critical Care Medicine, Mayo Clinic-Rochester, Rochester, MN, USA.

Ashokkumar Patel (A)

Division of Pulmonary and Critical Care Medicine, Mayo Clinic-Rochester, Rochester, MN, USA.

Vivek Iyer (V)

Division of Pulmonary and Critical Care Medicine, Mayo Clinic-Rochester, Rochester, MN, USA.

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Classifications MeSH