InforMing the PAthway of COPD Treatment (IMPACT Trial) Single-Inhaler Triple Therapy (Fluticasone Furoate/Umeclidinium/Vilanterol) Versus Fluticasone Furoate/Vilanterol and Umeclidinium/Vilanterol in Patients With COPD: Analysis of the Western Europe and North America Regions.

Abstract

BACKGROUND:

The InforMing the Pathway of COPD Treatment (IMPACT) trial demonstrated lower moderate/severe exacerbation rates with fluticasone furoate/umeclidinium/vilanterol (FF/UMEC/VI) versus FF/VI or UMEC/VI in patients with chronic obstructive pulmonary disease (COPD) and a history of exacerbations. Since IMPACT was a global study, post-hoc analyses were conducted by geographic region to investigate potential differences in overall findings.

METHODS:

IMPACT was a 52-week, randomized, double-blind trial. Patients with symptomatic COPD and ≥1 moderate/severe exacerbation in the prior year were randomized 2:2:1 to once-daily FF/UMEC/VI 100/62.5/25µg, FF/VI 100/25µg, or UMEC/VI 62.5/25µg. Endpoints assessed in the overall, Western Europe and North America populations included on-treatment moderate/severe exacerbation (rates and time-to-first), trough forced expiratory volume in 1 second and St George's Respiratory Questionnaire (SGRQ) total score. Safety was assessed.

RESULTS:

Overall, 10,355 patients were enrolled, 3164 from Western Europe, 2639 from North America. FF/UMEC/VI significantly reduced on-treatment moderate/severe exacerbation rates versus FF/VI and UMEC/VI in Western Europe (rate ratios 0.82 [95%CI 0.74-0.91], P<.001 and 0.76 [0.67-0.87], P<.001) and in North America (0.87 [0.77-0.97], P=.014 and 0.69 [0.60-0.80], P<.001). FF/UMEC/VI reduced time-to-first moderate/severe exacerbation and improved lung function versus FF/VI and UMEC/VI in both regions, and improved SGRQ total score in Western Europe, but not North America. Safety profiles were generally similar between treatment groups/regions; the inhaled corticosteroid class effect of increased pneumonia incidence was seen in North America but not Western Europe.

CONCLUSION:

Consistent with intent-to-treat results, FF/UMEC/VI reduced moderate/severe exacerbation rate and risk and improved lung function in Western Europe and North America; however, between-regions differences were seen for SGRQ total score and pneumonia incidence.

CLINICAL TRIAL REGISTRATION:

NCT02164513.

• Authors: Arnaud Bourdin, Gerard Criner, Gilles Devouassoux, Mark Dransfield, David M G Halpin, MeiLan K Han, C Elaine Jones, Ravi Kalhan, Peter Lange, Sally Lettis, David A Lipson, David A Lomas, José M Echave-Sustaeta María-Tomé, Neil Martin, Fernando J Martinez, Holly Quasny, Lynda Sail, Thomas M Siler, Dave Singh, Byron Thomashow, Henrik Watz, Robert Wise, Nicola A Hanania
• Journal: Chronic obstructive pulmonary diseases (Miami, Fla.) (Chronic Obstr Pulm Dis) Vol. 8 Issue 1 (Jan 2021) ISSN: 2372-952X [Print] United States
• PMID: 33156982 (Publication Type: Journal Article)
• Copyright: JCOPDF © 2021.