Abstract

BackgroundSevere asthma is associated with a broad range of phenotypes and clinical characteristics. This analysis assessed whether select baseline patient characteristics could prognosticate mepolizumab efficacy in severe eosinophilic asthma.MethodsThis was a post hoc meta-analysis of data from the Phase III MENSA (NCT01691521/MEA115588) and MUSCA (NCT02281318/200862) studies. Patients aged ≥ 12 years with severe eosinophilic asthma and a history of exacerbations were randomised to receive placebo (MENSA/MUSCA), mepolizumab 75 mg intravenously (MENSA) or 100 mg subcutaneously (SC) (MENSA/MUSCA) every 4 weeks for 32 (MENSA) or 24 (MUSCA) weeks. The primary endpoint was the annual rate of clinically significant exacerbations; other outcomes included the proportion of patients with no exacerbations and changes from baseline in pre-bronchodilator forced expiratory volume in 1 s (FEV1), St George’s Respiratory Questionnaire (SGRQ) total score and Asthma Control Questionnaire (ACQ)-5 score. Analyses were performed by baseline age of asthma onset (< 18 years; 18–40 years; ≥ 40 years); lung function (% predicted FEV1 ≤ 60; 60–80; > 80); airway reversibility (reversible [≥ 12% change in FEV1]; non-reversible [< 12% change in FEV1]); perennial and/or seasonal allergen sensitivity (yes/no); asthma control (uncontrolled [ACQ-5 score ≥ 1.5]; partial/complete control [ACQ-5 score < 1.5]).ResultsOverall, 936 patients received mepolizumab 100 mg SC or placebo. Across age at asthma onset, lung function and airway reversibility subgroups, mepolizumab reduced the rate of clinically significant exacerbations by 49–63% versus placebo. Improvements in lung function, SGRQ total score and ACQ-5 score were also seen with mepolizumab versus placebo across most age and lung function subgroups. Clinically significant exacerbations were reduced with mepolizumab versus placebo irrespective of season or allergen sensitivity; SGRQ total and ACQ-5 scores were generally improved across seasons.ConclusionsMepolizumab efficacy was consistent for patients with varying age at asthma onset, lung function, airway reversibility and allergen sensitivities at baseline. Our results indicate that mepolizumab is likely to be beneficial for patients with severe eosinophilic asthma with a broad range of baseline clinical characteristics; large-scale real-world studies are needed to confirm the external validity of these findings.Trial registration Post hoc meta-analysis of data from MENSA (NCT01691521/MEA115588) and MUSCA (NCT02281318/200862)

Highlights

  • Severe asthma is associated with a broad range of phenotypes and clinical characteristics

  • Lemiere et al Respir Res (2021) 22:184 for patients with severe eosinophilic asthma with a broad range of baseline clinical characteristics; large-scale realworld studies are needed to confirm the external validity of these findings

  • Age of asthma onset subgroups Across all age of asthma onset subgroups, mepolizumab was associated with reductions of 49–62% in the annual rate of clinically significant exacerbations compared with placebo (Fig. 1A)

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Summary

Introduction

Severe asthma is associated with a broad range of phenotypes and clinical characteristics This analysis assessed whether select baseline patient characteristics could prognosticate mepolizumab efficacy in severe eosinophilic asthma. Mepolizumab is a targeted, humanised anti-interleukin (IL)-5 monoclonal antibody that prevents IL-5 from binding to its receptor mainly on eosinophils, and selectively inhibits eosinophilic inflammation [4]. It is currently approved for the treatment of severe eosinophilic asthma in patients ≥ 6 years of age in multiple regions worldwide and for the treatment of eosinophilic granulomatosis with polyangiitis in adults in the USA [5, 6]. Owing to the heterogenous nature of severe asthma, it is of clinical interest to investigate whether any other patient characteristics can affect the response to mepolizumab treatment; knowledge of these characteristics could assist clinicians involved in patient management

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