Abstract

BackgroundSmoking is a major risk factor for COPD and may impact the efficacy of COPD treatments; however, a large proportion of COPD patients continue to smoke following diagnosis.MethodsThis post-hoc analysis of pooled data from the replicate 12-week, placebo-controlled GEM1 and GEM2 studies assessed the impact of smoking status on the efficacy and safety of glycopyrrolate 15.6 μg twice daily vs placebo in patients with moderate-to-severe COPD. Data from 867 patients enrolled in GEM1 and GEM2 were pooled for analysis and grouped by smoking status (57% current smokers, 43% ex-smokers). Forced expiratory volume in 1 s (FEV1) area under the curve from 0 to 12 h, trough FEV1, forced vital capacity, St George’s Respiratory Questionnaire (SGRQ) total score, COPD assessment test (CAT) score, transition dyspnea index (TDI) focal score, daily symptom scores, and rescue medication use were assessed in current smokers and ex-smokers. Incidences of adverse events (AEs) and serious AEs (SAEs) were also assessed.ResultsTreatment with glycopyrrolate resulted in significant improvements in all lung function measures, independent of smoking status. In both current and ex-smokers, changes from baseline in trough FEV1 were less marked in patients taking inhaled corticosteroids (ICS) than those not receiving ICS. Changes from baseline in SGRQ total score and rescue medication use were significantly greater with glycopyrrolate compared with placebo, regardless of smoking status. Changes in the CAT score, TDI focal score, and daily symptom scores significantly improved versus placebo, but only in current smokers. Improvements in patient-reported outcomes (PROs) with glycopyrrolate relative to placebo were numerically greater in current smokers than ex-smokers. The incidences of AEs and SAEs were similar regardless of smoking status.ConclusionsIn this post-hoc analysis of GEM1 and GEM2, glycopyrrolate use led to significant improvements in lung function, independent of baseline smoking status; improvements were less marked among patients receiving background ICS, regardless of baseline smoking status. Improvements in PROs were greater with glycopyrrolate than placebo, and the magnitude of changes was numerically greater among current smokers. The safety profile of glycopyrrolate was comparable between current smokers and ex-smokers.

Highlights

  • Smoking is a major risk factor for chronic obstructive pulmonary disease (COPD) and may impact the efficacy of COPD treatments; a large proportion of COPD patients continue to smoke following diagnosis

  • Patient demographics and baseline characteristics Data from 867 patients enrolled in GEM1 and GEM2 were pooled for analysis

  • Additional prospective studies are needed to better understand the impact of smoking status on clinical outcomes with different bronchodilators available for the treatment of patients with COPD. In this post-hoc analysis of pooled data from the GEM1 and GEM2 studies, Glycopyrrolate inhalation powder (GLY) treatment led to significant improvements in lung function, St George’s Respiratory Questionnaire (SGRQ) total score, and rescue medication use vs placebo in both smokers and exsmokers

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Summary

Introduction

Smoking is a major risk factor for COPD and may impact the efficacy of COPD treatments; a large proportion of COPD patients continue to smoke following diagnosis. 12-week Phase III studies, Glycopyrrolate Effect on syMptoms and lung function 1 and 2 (GEM1 and GEM2), demonstrated the efficacy and safety of GLY vs placebo in patients with moderate-to-severe COPD and a smoking history of ≥10 pack-years [14, 15]. Treatment with GLY resulted in significantly improved lung function, as assessed by forced expiratory volume in 1 s (FEV1) area under the curve from 0 to 12 h (AUC0–12h) and trough FEV1, as well as patient-reported outcomes (PROs) [14, 15] compared with placebo. In the primary analysis of the GEM1 and GEM2 studies, it was shown that the primary endpoint, FEV1 AUC0–12h was improved to a similar extent in both current and exsmokers [14, 15]

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