Five-Year Durability of Zephyr Valves in Patients with Severe Emphysema Five-Year Durability of Zephyr Valves in Patients with Severe Emphysema

<bold>Background:</bold> Benefits of BLVR with Zephyr valves (EBV) vs a control group with severe emphysema have been shown out to 12 months. Prospective, long-term data beyond 1 year are lacking. <bold>Objective:</bold> Assess long-term durability and safety of EBV in patients treated in the LIBERATE Study (NCT 01796392). <bold>Methods:</bold> EBV treated patients evaluated annually for 5 years to assess FEV1 change from Baseline to subsequent years plus all adverse events. <bold>Results:</bold> Improvement from Baseline in FEV1 was maintained out to 5 years with change from Baseline: Mean±SD(n) of 109±201mL(115), 91±203mL(90), 53±212mL(74), 121±452mL(44), 79±275mL(40) at Year1, Year 2, Year 3, Year 4, and Year 5, respectively. Corresponding responder rates (FEV1 improvement ≥15%) were 49.6%, 48.9%, 35.1%, 36.4%, and 30.0%, respectively. The incidence of respiratory AEs and SAEs during post-procedure Years 2 through 5 are generally similar or lower than those observed during post-procedure Year 1. Most common SAEs beyond Year 1 were COPD exacerbations (range: 13.5 to 23.1%), pneumonia (3.8 to 9.6%), respiratory failure (1.8 to 11.5%), and pneumothorax (1.3 to 3.6%). There were no new types of respiratory SAEs and no increase in the frequency of respiratory SAEs compared to prior years. There were 39 deaths after Year 1 to Year 5. <bold>Conclusion:</bold> EBV treatment resulted in durable improvements in lung function out to at least 5 years with an acceptable safety profile. Even in the absence of a control group beyond year 1, the continued improvement over baseline would be considered an advantage over maximal medical treatment alone given the known decline in lung function over time.

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Published
2024-09-14
DOI
https://doi.org/10.1183/13993003.congress-2024.pa2091
Primary Topic
Chronic Obstructive Pulmonary Disease (COPD) Research
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article
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article

Five-Year Durability of Zephyr Valves in Patients with Severe Emphysema Five-Year Durability of Zephyr Valves in Patients with Severe Emphysema

Richard Sue, Gerard J. Criner, Narinder S. Shargill, Dirk‐Jan Slebos et al.
Chronic Obstructive Pulmonary Disease (COPD) Research
article

Five-Year Durability of Zephyr Valves in Patients with Severe Emphysema Five-Year Durability of Zephyr Valves in Patients with Severe Emphysema

Richard Sue, Gerard J. Criner, Narinder S. Shargill, Dirk‐Jan Slebos, Karin Klooster, Mark Vollenweider, Pallav Shah, Momen M. Wahidi, Hugo De Oliveira
article en

Abstract

<bold>Background:</bold> Benefits of BLVR with Zephyr valves (EBV) vs a control group with severe emphysema have been shown out to 12 months. Prospective, long-term data beyond 1 year are lacking. <bold>Objective:</bold> Assess long-term durability and safety of EBV in patients treated in the LIBERATE Study (NCT 01796392). <bold>Methods:</bold> EBV treated patients evaluated annually for 5 years to assess FEV1 change from Baseline to subsequent years plus all adverse events. <bold>Results:</bold> Improvement from Baseline in FEV1 was maintained out to 5 years with change from Baseline: Mean±SD(n) of 109±201mL(115), 91±203mL(90), 53±212mL(74), 121±452mL(44), 79±275mL(40) at Year1, Year 2, Year 3, Year 4, and Year 5, respectively. Corresponding responder rates (FEV1 improvement ≥15%) were 49.6%, 48.9%, 35.1%, 36.4%, and 30.0%, respectively. The incidence of respiratory AEs and SAEs during post-procedure Years 2 through 5 are generally similar or lower than those observed during post-procedure Year 1. Most common SAEs beyond Year 1 were COPD exacerbations (range: 13.5 to 23.1%), pneumonia (3.8 to 9.6%), respiratory failure (1.8 to 11.5%), and pneumothorax (1.3 to 3.6%). There were no new types of respiratory SAEs and no increase in the frequency of respiratory SAEs compared to prior years. There were 39 deaths after Year 1 to Year 5. <bold>Conclusion:</bold> EBV treatment resulted in durable improvements in lung function out to at least 5 years with an acceptable safety profile. Even in the absence of a control group beyond year 1, the continued improvement over baseline would be considered an advantage over maximal medical treatment alone given the known decline in lung function over time.

Midwestern University (US), University Medical Center Groningen (NL), Orlando Health (US), Royal Brompton & Harefield NHS Foundation Trust (GB), Royal Brompton Hospital (GB), Hospital de Clínicas de Porto Alegre (BR), Temple Lung Center (US), Arizona Pain Specialists (US), Pulmonx (United States) (US), Temple University (US)
Openalex Percentile: Top 64%
Chronic Obstructive Pulmonary Disease (COPD) Research
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