Evidence map›Paper›PMID 19264686›Full record

Trial reportThe New England journal of medicine2009

Mepolizumab and exacerbations of refractory eosinophilic asthma.

Pranabashis Haldar, Christopher E Brightling, Beverley Hargadon, Sumit Gupta, William Monteiro, Ana Sousa, Richard P Marshall, Peter Bradding, Ruth H Green, Andrew J Wardlaw and 1 more

Erratum issued 3 registry-linked trialsOpen access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The New England journal of medicine, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to 3 registered trials, which are not on this map. Cited by 652 papers, 8 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
652citing papers in PubMed, 8 pooled it
75.4field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01471327 phase1completednot on this mapstarted 2011, after this paper: background citation

A Single Blind, Placebo Controlled, Parallel Group, Single Ascending Intravenous Dose Study to Assess Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of SB-240563 (Mepolizumab) in Healthy Japanese Male Subjects.

TypeinterventionalSponsorGlaxoSmithKlineRan2011 to 2012Enrolled35ConditionsAsthmaArmsSB-240563, Placebo
NCT01520051 phase3unknown statusnot on this mapstarted 2012, after this paper: background citation

The Efficacy of Mepolizumab Treatment on Rhinovirus Induced Asthma Exacerbations

TypeinterventionalSponsorAcademisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)Ran2012 to 2014Enrolled48ConditionsAsthma, Viral InfectionArmsMepolizumab, Placebo
NCT02559791 phase2 / phase3completednot on this mapstarted 2015, after this paper: background citation

Route of Administration of Anti-IL5 Monoclonal Antibody in Prednisone-dependent Eosinophilic Asthma

TypeinterventionalSponsorMcMaster UniversityRan2015 to 2017Enrolled10ConditionsSevere Persistent Asthma, Eosinophilic BronchitisArmsReslizumab, Placebo
3 · Its place in the literature

Who cites it

652 citing papers in PubMed, 8 syntheses or guidelines pooled it, 1,867 citations in OpenAlex.

  1. Pooled it
  2. Biologic agents licensed for severe asthma: a systematic review and meta-analysis of randomised controlled trials.European respiratory review : an official journal of the European Respiratory Society · 2024
    Pooled it
  3. Pooled it
  4. Pooled it
  5. Anti-IL-5 therapies for asthma.The Cochrane database of systematic reviews · 2022
    Pooled it
  6. Pooled it
  7. Pooled it
  8. Pooled it
  9. Trial
  10. Trial
  11. Trial
  12. Trial
  13. Trial
  14. StoppingThe European respiratory journal · 2022
    Trial
  15. Pulmonary Innate Lymphoid Cell Responses during Rhinovirus-induced Asthma ExacerbationsAmerican journal of respiratory and critical care medicine · 2021
    Trial
  16. Trial
  17. Single-Session Bronchial Thermoplasty Guided byAmerican journal of respiratory and critical care medicine · 2020
    Trial
  18. Article
  19. Review
  20. Article

592 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 2 countries.

Pranabashis HaldarInstitute for Lung Health, Glenfield Hospital, University Hospitals of Leicester National Health Service Trust, Leicester, United Kingdom.
Christopher E Brightling
Beverley Hargadon
Sumit Gupta
William Monteiro
Ana Sousa
Richard P Marshall
Peter Bradding
Ruth H Green
Andrew J Wardlaw
Ian D Pavord
Glenfield Hospital · GBNational Health Service · GBGlaxoSmithKline (Brazil) · BR

Funding

Wellcome Trust 082265
6 · The paper itself

Abstract

backgroundExacerbations of asthma are associated with substantial morbidity and mortality and with considerable use of health care resources. Preventing exacerbations remains an important goal of therapy. There is evidence that eosinophilic inflammation of the airway is associated with the risk of exacerbations.

methodsWe conducted a randomized, double-blind, placebo-controlled, parallel-group study of 61 subjects who had refractory eosinophilic asthma and a history of recurrent severe exacerbations. Subjects received infusions of either mepolizumab, an anti-interleukin-5 monoclonal antibody (29 subjects), or placebo (32) at monthly intervals for 1 year. The primary outcome measure was the number of severe exacerbations per subject during the 50-week treatment phase. Secondary outcomes included a change in asthma symptoms, scores on the Asthma Quality of Life Questionnaire (AQLQ, in which scores range from 1 to 7, with lower values indicating more severe impairment and a change of 0.5 unit considered to be clinically important), forced expiratory volume in 1 second (FEV(1)) after use of a bronchodilator, airway hyperresponsiveness, and eosinophil counts in the blood and sputum.

resultsMepolizumab was associated with significantly fewer severe exacerbations than placebo over the course of 50 weeks (2.0 vs. 3.4 mean exacerbations per subject; relative risk, 0.57; 95% confidence interval [CI], 0.32 to 0.92; P=0.02) and with a significant improvement in the score on the AQLQ (mean increase from baseline, 0.55 vs. 0.19; mean difference between groups, 0.35; 95% CI, 0.08 to 0.62; P=0.02). Mepolizumab significantly lowered eosinophil counts in the blood (P<0.001) and sputum (P=0.002). There were no significant differences between the groups with respect to symptoms, FEV(1) after bronchodilator use, or airway hyperresponsiveness. The only serious adverse events reported were hospitalizations for acute severe asthma.

conclusionsMepolizumab therapy reduces exacerbations and improves AQLQ scores in patients with refractory eosinophilic asthma. The results of our study suggest that eosinophils have a role as important effector cells in the pathogenesis of severe exacerbations of asthma in this patient population. (Current Controlled Trials number, ISRCTN75169762.)

Indexed as

AdultAgedAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAsthmaBiomarkersDouble-Blind MethodDrug Therapy, CombinationEosinophiliaEosinophilsFemaleForced Expiratory VolumeHospitalizationHumansInterleukin-5Leukocyte CountAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedBiomarkersInterleukin-5mepolizumabPrednisolone

Identifiers

PMID19264686
PMCPMC3992367
OpenAlexW1988758075

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.