# Real-World Effectiveness of Fluticasone Furoate/Umeclidinium/Vilanterol Initiation in Japanese Patients with Asthma Previously on Inhaled Corticosteroid/Long-Acting β2-Agonist Therapy: A Retrospective Cohort Study

**Authors:** Toru Oga, Yasuhiro Gon, Masashi Takano, Risako Ito, Chifuku Mita, Isao Mukai, Stephen G. Noorduyn, Gema Requena, Masao Yarita

PMC · DOI: 10.3390/jcm14082566 · 2025-04-09

## TL;DR

This study shows that adding a specific medication combination improves asthma control and reduces steroid use in Japanese patients.

## Contribution

The study evaluates the real-world effectiveness of a triple therapy in asthma patients previously on ICS/LABA.

## Key findings

- Asthma exacerbation rates decreased by 20% after initiating FF/UMEC/VI therapy.
- Use of oral corticosteroids and short-acting β2-agonists significantly reduced following treatment initiation.

## Abstract

Background: Japanese guidelines recommend the addition of a long-acting muscarinic antagonist for patients with asthma uncontrolled on inhaled corticosteroid/long-acting β2-agonist (ICS/LABA) therapy, the effectiveness of which is evaluated here. Methods: Retrospective, observational, single-arm cohort study in patients with asthma initiating fluticasone furoate/umeclidinium/vilanterol (FF/UMEC/VI) following ICS/LABA, using independently analyzed data from Japanese claims databases: JMDC and Medical Data Vision (MDV). The index date was that of the first FF/UMEC/VI prescription. Outcomes were assessed during a 12-month follow-up versus a 12-month pre-index period (baseline) and included asthma exacerbations, oral corticosteroid (OCS) use, and short-acting β2-agonist (SABA) use. P-values associated with rate ratios (RRs) were estimated using Conditional Poisson regression. Results: Overall, 3229 patients in the JMDC database and 1135 in the MDV database were included. Following FF/UMEC/VI initiation, the total annualized moderate–severe asthma exacerbation rate in the JMDC database reduced from 0.50 to 0.40 per-person-per-year (PPPY) (RR [95% confidence interval]: 0.78 [0.73, 0.84]; p < 0.001), with similar reductions in the MDV database: 0.53 to 0.42 PPPY (0.79 [0.70, 0.89]; p < 0.001). In both databases, there was a 20% reduction (JMDC: 0.80 [0.73, 0.88]; p < 0.001; MDV: 0.80 [0.68, 0.94]; p = 0.005) in patients with ≥1 OCS prescription after FF/UMEC/VI initiation. The proportion of patients with ≥1 SABA canister prescription dropped by 31% 0.69 [0.57, 0.84]; p < 0.001) in the JMDC database and 23% (0.77 [0.66, 0.90]; p < 0.001) in the MDV database. Conclusions: This suggests FF/UMEC/VI is effective in improving asthma exacerbations and reducing OCS and SABA use in Japanese patients previously using ICS/LABA in real-world clinical practice.

## Linked entities

- **Chemicals:** fluticasone furoate (PubChem CID 9854489), umeclidinium (PubChem CID 11519070), vilanterol (PubChem CID 10184665)
- **Diseases:** asthma (MONDO:0004979)

## Full-text entities

- **Diseases:** Asthma (MESH:D001249)
- **Chemicals:** Vilanterol (MESH:C550468), Inhaled Corticosteroid (-), Fluticasone Furoate (MESH:C523187), Umeclidinium (MESH:C573971)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12028120/full.md

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Source: https://tomesphere.com/paper/PMC12028120