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Response to Mepolizumab Treatment in Patients with Severe Eosinophilic Asthma and Atopic Phenotypes.
Prazma, Charlene M; Idzko, Marco; Douglass, Jo Anne; Bourdin, Arnaud; Mallett, Stephen; Albers, Frank C; Yancey, Steven W.
Afiliação
  • Prazma CM; Respiratory Therapeutic Area, GSK, Research Triangle Park, NC, USA.
  • Idzko M; Division of Pneumology, Medical University of Vienna, Vienna, Austria.
  • Douglass JA; Department of Pneumology, University Hospital Freiburg, Freiburg, Germany.
  • Bourdin A; The Royal Melbourne Hospital and University of Melbourne, Melbourne, VIC, Australia.
  • Mallett S; Departement de Pneumologie et Addictologie, Hôpital Arnaud de Villeneuve, CHU Montpellier, Montpellier, France.
  • Albers FC; PhyMedExp, University of Montpellier, Montpellier, France.
  • Yancey SW; Clinical Statistics, GSK, Uxbridge, Middlesex, UK.
J Asthma Allergy ; 14: 675-683, 2021.
Article em En | MEDLINE | ID: mdl-34163180
ABSTRACT

PURPOSE:

Improved understanding of characteristics that may influence treatment response across phenotypes may help guide treatment decisions. PATIENTS AND

METHODS:

This was a post hoc analysis of MENSA, a multicenter, randomized, double-blind, placebo-controlled trial (NCT01691521). Patients aged ≥12 years with severe eosinophilic asthma received mepolizumab (75 mg intravenously or 100 mg subcutaneously) or placebo, plus standard of care, every 4 weeks for 32 weeks. Outcomes assessed were the annualized rate of clinically significant exacerbations and change from baseline in Asthma Control Questionnaire (ACQ)-5 score. Subgroup analyses were performed by baseline blood eosinophil count (<150, ≥150-300, ≥300 cells/µL) within atopic subgroups (non-atopic [specific immunoglobulin E <0.35 kU/L], atopic [≥0.35-17.5 kU/L], strongly atopic [>17.5 kU/L]), and by house dust mite (HDM) sensitivity.

RESULTS:

Of 576 patients analyzed, 272 were non-atopic, 181 were atopic and 94 were strongly atopic; 29 had missing atopy data. In patients with blood eosinophil counts ≥300 cells/µL, mepolizumab versus placebo reduced clinically significant exacerbations by 74%, 43% and 25% in the non-atopic, atopic and strongly atopic subgroups. Similar reductions were observed in all atopic subgroups in other blood eosinophil count categories where there were sufficient patient numbers for analysis, except for non-atopic patients with baseline blood eosinophil counts of <150 cells/µL. Improvements in ACQ-5 scores of -0.75, -0.73 and -0.78 with mepolizumab versus placebo were observed in non-atopic, atopic and strongly atopic patients with blood eosinophil counts ≥300 cells/µL; consistent improvements in ACQ-5 were not observed in patients with blood eosinophil counts <150 or ≥150-300 cells/µL. Reductions in clinically significant exacerbations with mepolizumab versus placebo were also observed irrespective of sensitivity to HDMs.

CONCLUSION:

Mepolizumab was associated with a trend for reductions in clinically significant exacerbations and improved asthma control versus placebo in patients with severe eosinophilic asthma, irrespective of atopic status or HDM sensitivity.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Prognostic_studies / Qualitative_research Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Clinical_trials / Prognostic_studies / Qualitative_research Idioma: En Ano de publicação: 2021 Tipo de documento: Article