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Published on: April 6, 2017
INTREPID: single- versus multiple-inhaler triple therapy for COPD in usual clinical practice
David M G Halpin1, Sally Worsley2, Afisi S Ismaila3,4
1University of Exeter Medical School, College of Medicine and Health, University of Exeter, Exeter, UK.
Single-inhaler triple therapy with fluticasone furoate/umeclidinium/vilanterol (FF/UMEC/VI) improved COPD patient outcomes more than multiple-inhaler triple therapy (MITT). This real-world study found FF/UMEC/VI led to greater health status and lung function improvements.
Area of Science:
- Pulmonary Medicine
- Pharmacology
Background:
- Real-world data comparing single-inhaler triple therapy (MITT) with multiple-inhaler triple therapy (MITT) in COPD patients are limited.
- The effectiveness of once-daily single-inhaler fluticasone furoate (FF)/umeclidinium (UMEC)/vilanterol (VI) versus MITT was assessed in a usual clinical care setting.
Purpose of the Study:
- To compare the effectiveness of once-daily FF/UMEC/VI with clinician-chosen MITT in COPD patients.
- To evaluate health status improvement, lung function changes, and inhalation technique errors.
Main Methods:
- A multicentre, randomised, open-label, phase IV effectiveness study (INTREPID) was conducted in five European countries.
- 3092 COPD patients were randomized to receive either FF/UMEC/VI via the ELLIPTA inhaler or a non-ELLIPTA MITT.
- The primary endpoint was the proportion of COPD Assessment Test (CAT) responders at week 24.
Main Results:
- Significantly more patients were CAT responders with FF/UMEC/VI compared to non-ELLIPTA MITT (OR 1.31, p<0.001).
- Mean change from baseline in FEV1 was significantly greater with FF/UMEC/VI (50 mL difference, p<0.001).
- Critical inhalation technique errors were low in both groups (6% for FF/UMEC/VI, 3% for MITT).
Conclusions:
- Once-daily single-inhaler FF/UMEC/VI demonstrated superior effectiveness compared to non-ELLIPTA MITT in a real-world COPD setting.
- FF/UMEC/VI led to significantly greater improvements in patient health status and lung function.
- The safety profiles were similar between the two treatment groups.
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