Scientific publications
Triple Therapy and Clinical Control in B+ COPD Patients: A Pragmatic, Prospective, Randomized Trial. Scientific Publication
Alvar Agusti 1 , José Luis Lopez-Campos 2 , Marc Miravitlles 3 , Juan Jose Soler-Cataluña 4 , Jose Maria Marin 5 , Borja G Cosio 6 , Bernardino Alcázar-Navarrete 7 , Jose Maria Echave-Sustaeta 8 , Ciro Casanova 9 , German Peces-Barba 10 , Juan Pablo de-Torres 11 , Alberto Fernandez-Villar 12 , Julio Ancochea 13 , Felipe Villar-Alvarez 14 , Miguel Roman-Rodriguez 15 , Jesus Molina 16 , Juan Luis Garcia-Rivero 17 , Cruz Gonzalez 18 , Patricia Sobradillo 19 , Rosa Faner 20 , Carolina Peña 21 , Raj Sharma 22 , Bartolome R Celli 23
Introduction: Treatment with LABA/LAMA is recommended in GOLD B patients. We hypothesized that triple therapy (LABA/LAMA/ICS) will be superior to LABA/LAMA in achieving and maintaining clinical control (CC), a composite outcome that considers both impact and disease stability in a subgroup of GOLD B patients (here termed GOLD B+ patients) characterized by: (1) remaining symptomatic (CAT≥10) despite regular LABA/LAMA therapy; (2) having suffered one moderate exacerbation in the previous year; and (3) having blood eosinophil counts (BEC) ≥150cells/μL.
Methods: The ANTES B+ study is a prospective, multicenter, open label, randomized, pragmatic, controlled trial designed to test this hypothesis. It will randomize 1028 B+ patients to continue with their usual LABA/LAMA combination prescribed by their attending physician or to begin fluticasone furoate (FF) 92μg/umeclidinium (UMEC) 55μg/vilanterol (VI) 22μg in a single inhaler q.d. for 12 months. The primary efficacy outcome will be the level of CC achieved. Secondary outcomes include the clinical important deterioration index (CID), annual rate of exacerbations, and FEV1. Exploratory objectives include the interaction of BEC and smoking status, all-cause mortality and proportion of patients on LABA/LAMA arm that switch therapy arms. Safety analysis include adverse events and incidence of pneumonia.
Results: The first patient was recruited on February 29, 2024; results are expected in the first quarter of 2026.
Conclusions: The ANTES B+ study is the first to: (1) explore the efficacy and safety of triple therapy in a population of B+ COPD patients and (2) use a composite index (CC) as the primary result of a COPD trial.
CITATION Arch Bronconeumol. 2024 Apr 25:S0300-2896(24)00116-9. doi: 10.1016/j.arbres.2024.04.008
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