Airway Scaffolds for Emphysema-related Hyperinflation: Six-Month Results from the BREATHE Trial

<b>Rationale:</b> Despite advancements in emphysema treatment, high morbidity and mortality rates highlight the need for innovative therapies. A novel self-expanding nitinol airway scaffold was designed to alleviate lung hyperinflation by connecting emphysematous parenchyma with central bronchi, releasing trapped air. <b>Objectives:</b> To assess the feasibility, safety, and initial outcomes of airway scaffolds in treating emphysema-related hyperinflation. <b>Methods:</b> We conducted a pooled analysis of two first-in-human studies (NCT05949645, NCT05854550) involving patients with heterogeneous or homogeneous emphysema treated bronchoscopically with up to three permanent airway scaffolds per lung. <b>Measurements and Main Results:</b> The primary outcome was safety, measured by procedure- and/or device-related serious adverse events over 6 months. Secondary outcomes were technical feasibility, pulmonary function, quality of life, symptoms, exercise capacity at 3 and 6 months, and airway patency assessment by high-resolution computed tomography. Sixty severe emphysema patients (33 female, 27 male; mean age, 66 ± 8 yr; mean residual volume percent predicted, 255 ± 47%) were included. Ninety-eight procedures were performed, and 328 airway scaffolds were successfully placed. A proportion of 21.7% of patients experienced at least one related serious adverse event within 6 months, including pneumonia (10.0%) and chronic obstructive pulmonary disease exacerbation (5.0%), but no pneumothoraxes occurred. Residual volume improved (decreased) from baseline by a mean [95% confidence interval] of 866 [626, 1,106] ml at 3 months and 753 [512, 994] ml at 6 months. Clinically meaningful improvements were further observed in spirometry, quality of life, symptoms, and exercise capacity. <b>Conclusions:</b> This study provides the first clinical evidence of the feasibility, safety, and initial outcomes after treatment with airway scaffolds in patients with emphysema-related hyperinflation.

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Publication Details

Journal
American Journal of Respiratory and Critical Care Medicine
Published
2025-06-13
DOI
https://doi.org/10.1164/rccm.202502-0378oc
Citations
4
Primary Topic
Chronic Obstructive Pulmonary Disease (COPD) Research
Type
article
Field-Weighted Citation Impact
6.07
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article

Airway Scaffolds for Emphysema-related Hyperinflation: Six-Month Results from the BREATHE Trial

Arschang Valipour, Christopher Michael Orton, Marlies van Dijk, Martin L Mayse et al.
4 citations
American Journal of Respiratory and Critical Care Medicine
Chronic Obstructive Pulmonary Disease (COPD) Research
6.07
article

Airway Scaffolds for Emphysema-related Hyperinflation: Six-Month Results from the BREATHE Trial

Arschang Valipour, Christopher Michael Orton, Marlies van Dijk, Martin L Mayse, Jemma J. Christie, T. David Koster, Justin Garner, Jonathan Williamson, Alvin Ing, Dirk‐Jan Slebos, Daniel Steinfort, Anand Tana, Karin Klooster, Pallav L. Shah, K Welz, Theresa Klemm
article en
4 citations

Abstract

<b>Rationale:</b> Despite advancements in emphysema treatment, high morbidity and mortality rates highlight the need for innovative therapies. A novel self-expanding nitinol airway scaffold was designed to alleviate lung hyperinflation by connecting emphysematous parenchyma with central bronchi, releasing trapped air. <b>Objectives:</b> To assess the feasibility, safety, and initial outcomes of airway scaffolds in treating emphysema-related hyperinflation. <b>Methods:</b> We conducted a pooled analysis of two first-in-human studies (NCT05949645, NCT05854550) involving patients with heterogeneous or homogeneous emphysema treated bronchoscopically with up to three permanent airway scaffolds per lung. <b>Measurements and Main Results:</b> The primary outcome was safety, measured by procedure- and/or device-related serious adverse events over 6 months. Secondary outcomes were technical feasibility, pulmonary function, quality of life, symptoms, exercise capacity at 3 and 6 months, and airway patency assessment by high-resolution computed tomography. Sixty severe emphysema patients (33 female, 27 male; mean age, 66 ± 8 yr; mean residual volume percent predicted, 255 ± 47%) were included. Ninety-eight procedures were performed, and 328 airway scaffolds were successfully placed. A proportion of 21.7% of patients experienced at least one related serious adverse event within 6 months, including pneumonia (10.0%) and chronic obstructive pulmonary disease exacerbation (5.0%), but no pneumothoraxes occurred. Residual volume improved (decreased) from baseline by a mean [95% confidence interval] of 866 [626, 1,106] ml at 3 months and 753 [512, 994] ml at 6 months. Clinically meaningful improvements were further observed in spirometry, quality of life, symptoms, and exercise capacity. <b>Conclusions:</b> This study provides the first clinical evidence of the feasibility, safety, and initial outcomes after treatment with airway scaffolds in patients with emphysema-related hyperinflation.

American Journal of Respiratory and Critical Care MedicineVol. 211(7)
The Royal Melbourne Hospital (AU), University Medical Center Groningen (NL), The University of Melbourne (AU), University of Groningen (NL), Royal Brompton & Harefield NHS Foundation Trust (GB), Royal Brompton Hospital (GB), Meta (United States) (US), Karl Landsteiner Society (AT), Imperial College London (GB), Macquarie University (AU)
Openalex Percentile: Top 4%
Chronic Obstructive Pulmonary Disease (COPD) Research
6.07
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