Bronchial Thermoplasty in Patients With Severe Asthma at 5 Years: The Post-FDA Approval Clinical Trial Evaluating Bronchial Thermoplasty in Severe Persistent Asthma Study.


Journal

Chest
ISSN: 1931-3543
Titre abrégé: Chest
Pays: United States
ID NLM: 0231335

Informations de publication

Date de publication:
03 2022
Historique:
received: 23 06 2021
revised: 07 10 2021
accepted: 12 10 2021
pubmed: 15 11 2021
medline: 19 4 2022
entrez: 14 11 2021
Statut: ppublish

Résumé

Bronchial thermoplasty is a device-based treatment for subjects ≥ 18 years of age with severe asthma poorly controlled with inhaled corticosteroids and long-acting beta-agonists. The Post-FDA Approval Clinical Trial Evaluating Bronchial Thermoplasty in Severe Persistent Asthma (PAS2) study collected data on patients with severe asthma undergoing this procedure. What are the 5-year efficacy and safety results in patients with severe asthma who have undergone bronchial thermoplasty? This was a prospective, open-label, observational, multicenter study conducted in the United States and Canada. Subjects 18 to 65 years of age who were taking inhaled corticosteroids ≥ 1,000 μg/d (beclomethasone or equivalent) and long-acting beta-agonists ≥ 80 μg/d (salmeterol or equivalent) were included. Severe exacerbations, hospitalization, ED visits, and medication usage were evaluated for the 12 months prior to and at years 1 through 5 posttreatment. Spirometry was evaluated at baseline and at years 1 through 5 posttreatment. A total of 284 subjects were enrolled at 27 centers; 227 subjects (80%) completed 5 years of follow-up. By year 5 posttreatment, the proportion of subjects with severe exacerbations, ED visits, and hospitalizations was 42.7%, 7.9%, and 4.8%, respectively, compared with 77.8%, 29.4%, and 16.1% in the 12 months prior to treatment. The proportion of subjects on maintenance oral corticosteroids decreased from 19.4% at baseline to 9.7% at 5 years. Analyses of subgroups based on baseline clinical and biomarker characteristics revealed a statistically significant clinical improvement among all subgroups. Five years after treatment, subjects experienced decreases in severe exacerbations, hospitalizations, ED visits, and corticosteroid exposure. All subgroups demonstrated clinically significant improvement, suggesting that bronchial thermoplasty improves asthma control in different asthma phenotypes. ClinicalTrials.gov; No.: NCT01350336; URL: www. gov.

Sections du résumé

BACKGROUND
Bronchial thermoplasty is a device-based treatment for subjects ≥ 18 years of age with severe asthma poorly controlled with inhaled corticosteroids and long-acting beta-agonists. The Post-FDA Approval Clinical Trial Evaluating Bronchial Thermoplasty in Severe Persistent Asthma (PAS2) study collected data on patients with severe asthma undergoing this procedure.
RESEARCH QUESTION
What are the 5-year efficacy and safety results in patients with severe asthma who have undergone bronchial thermoplasty?
STUDY DESIGN AND METHODS
This was a prospective, open-label, observational, multicenter study conducted in the United States and Canada. Subjects 18 to 65 years of age who were taking inhaled corticosteroids ≥ 1,000 μg/d (beclomethasone or equivalent) and long-acting beta-agonists ≥ 80 μg/d (salmeterol or equivalent) were included. Severe exacerbations, hospitalization, ED visits, and medication usage were evaluated for the 12 months prior to and at years 1 through 5 posttreatment. Spirometry was evaluated at baseline and at years 1 through 5 posttreatment.
RESULTS
A total of 284 subjects were enrolled at 27 centers; 227 subjects (80%) completed 5 years of follow-up. By year 5 posttreatment, the proportion of subjects with severe exacerbations, ED visits, and hospitalizations was 42.7%, 7.9%, and 4.8%, respectively, compared with 77.8%, 29.4%, and 16.1% in the 12 months prior to treatment. The proportion of subjects on maintenance oral corticosteroids decreased from 19.4% at baseline to 9.7% at 5 years. Analyses of subgroups based on baseline clinical and biomarker characteristics revealed a statistically significant clinical improvement among all subgroups.
INTERPRETATION
Five years after treatment, subjects experienced decreases in severe exacerbations, hospitalizations, ED visits, and corticosteroid exposure. All subgroups demonstrated clinically significant improvement, suggesting that bronchial thermoplasty improves asthma control in different asthma phenotypes.
CLINICAL TRIAL REGISTRATION
ClinicalTrials.gov; No.: NCT01350336; URL: www.
CLINICALTRIALS
gov.

Identifiants

pubmed: 34774528
pii: S0012-3692(21)04274-4
doi: 10.1016/j.chest.2021.10.044
pii:
doi:

Substances chimiques

Adrenal Cortex Hormones 0

Banques de données

ClinicalTrials.gov
['NCT01350336']

Types de publication

Journal Article Multicenter Study Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

614-628

Informations de copyright

Copyright © 2021 American College of Chest Physicians. Published by Elsevier Inc. All rights reserved.

Auteurs

Geoffrey Chupp (G)

Yale University, New Haven, CT. Electronic address: geoffrey.chupp@yale.edu.

Joel N Kline (JN)

University of Iowa Hospitals and Clinics, Iowa City, IA.

Sumita B Khatri (SB)

Cleveland Clinic Respiratory Institute Cleveland, OH.

Charlene McEvoy (C)

HealthPartners Institute, St Paul, MN.

Gerard A Silvestri (GA)

Medical University of South Carolina, Charleston, SC.

Adrian Shifren (A)

Washington University School of Medicine, St Louis, MO.

Mario Castro (M)

University of Kansas School of Medicine, Kansas City, KS.

Sundeep Bansal (S)

Penn Highlands Healthcare, DuBois, PA.

Marc McClelland (M)

Spectrum Health Hospitals, Grand Rapids, MI.

Mark Dransfield (M)

University of Alabama at Birmingham, Birmingham, AL.

Jennifer Trevor (J)

University of Alabama at Birmingham, Birmingham, AL.

Nick Kahlstrom (N)

St Joseph Medical Center, Tacoma, WA.

Michael Simoff (M)

Henry Ford Hospital, Detroit, MI.

Momen M Wahidi (MM)

Duke University School of Medicine, Durham, NC.

Carla R Lamb (CR)

Lahey Hospital and Medical Center, Burlington, MA.

J Scott Ferguson (JS)

University of Wisconsin Madison, Madison, WI.

Andrew Haas (A)

University of Pennsylvania, Philadelphia, PA.

D Kyle Hogarth (DK)

University of Chicago, Chicago, IL.

Richard Tejedor (R)

LSU Health Science Center, New Orleans, LA.

Jennifer Toth (J)

Penn State University, Hershey, PA.

Jamie Hey (J)

Pulmonary Associates of Richmond, Richmond, VA.

Adnan Majid (A)

Beth Israel Deaconess Medical Center, Boston, MA.

Peter LaCamera (P)

St Elizabeth's Medical Center of Boston, Inc, Boston, MA.

J Mark Fitzgerald (JM)

University of British Columbia, Vancouver, BC, Canada.

Kyle Enfield (K)

University of Virginia Health System, Charlottesville, VA.

G Mark Grubb (GM)

Boston Scientific, Marlborough, MA.

Edmund A McMullen (EA)

Boston Scientific, Marlborough, MA.

Jennifer L Olson (JL)

Boston Scientific, Marlborough, MA.

Michel Laviolette (M)

Laval University, Québec, QC, Canada.

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Classifications MeSH