Evidence map›Paper›PMID 36740144›Full record

Trial reportThe Journal of allergy and clinical immunology2023

Comparative effectiveness of omalizumab, mepolizumab, and dupilumab in asthma: A target trial emulation.

Ayobami T Akenroye, Jodi B Segal, Guohai Zhou, Dinah Foer, Lily Li, G Caleb Alexander, Corinne A Keet, John W Jackson

Open access · hybridAbstract readClinical Trial
In one paragraph

Trial report in The Journal of allergy and clinical immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
8.9field-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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 52 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Ayobami T AkenroyeDivision of Allergy and Clinical Immunology, Brigham and Women's Hospital, Boston, Mass; Channing Division of Network Medicine, Brigham and Women's Hospital, Boston, Mass; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Md. Electronic address: aakenroye@bwh.harvard.edu.
Jodi B SegalDepartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Md; Division of General Internal Medicine, Johns Hopkins University School of Medicine, Baltimore, Md; Center for Drug Safety and Effectiveness, Johns Hopkins Bloomberg School of Public Health, Baltimore, Md.
Guohai ZhouDepartment of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Mass.
Dinah FoerDivision of Allergy and Clinical Immunology, Brigham and Women's Hospital, Boston, Mass; Division of General Internal Medicine, Brigham and Women's Hospital, Boston, Mass.
Lily LiDivision of Allergy and Clinical Immunology, Brigham and Women's Hospital, Boston, Mass.
G Caleb AlexanderDepartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Md; Division of General Internal Medicine, Johns Hopkins University School of Medicine, Baltimore, Md; Center for Drug Safety and Effectiveness, Johns Hopkins Bloomberg School of Public Health, Baltimore, Md.
Corinne A KeetDivision of Pediatric Allergy and Immunology, University of North Carolina, Chapel Hill, NC.
John W JacksonDepartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Md; Center for Drug Safety and Effectiveness, Johns Hopkins Bloomberg School of Public Health, Baltimore, Md; Department of Mental Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, Md; Department of Biostatistics, Johns Hopkins Bloomberg School of Public Health, Baltimore, Md.
Brigham and Women's Hospital · USJohns Hopkins University · USUniversity of North Carolina at Chapel Hill · US

Funding

Towards Understanding the Patient Experience of Overuse of Medical ResourcesK24AG049036 · NIA · JOHNS HOPKINS UNIVERSITY · PI SEGAL, JODI B. · 2015 to 2024
$1.6M
Effects of GLP-1 Receptor Agonists on Airway Inflammation and Platelet Activation in AsthmaK23HL161332 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI Dinah Foer · 2022 to 2026
$975k
Clinical Impact and Epidemiology of Nonsteroidal Anti-inflammatory Drug AllergiesK23AI163371 · NIAID · UNIVERSITY OF WASHINGTON · PI LI, LILY · 2021 to 2025
$921k
Systems Science for Translational Health Disparities ResearchK01HL145320 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI JACKSON, JOHN WILLIAM · 2019 to 2023
$832k
Synthesizing Trial and Real-world Data on the Use of Biologics in Patients with Severe AsthmaR00MD015767 · NIMHD · BRIGHAM AND WOMEN'S HOSPITAL · PI AKENROYE, AYOBAMI T · 2023 to 2025
$677k
Synthesizing Trial and Real-world Data on the Use of Biologics in Patients with Severe AsthmaK99MD015767 · NIMHD · JOHNS HOPKINS UNIVERSITY · PI AKENROYE, AYOBAMI T · 2021 to 2022
$196k
NHLBI NIH HHS K01 HL145320NHLBI NIH HHS K23 HL161332NHLBI NIH HHS L30 HL165481NIAID NIH HHS K23 AI163371NIA NIH HHS K24 AG049036NIMHD NIH HHS K99 MD015767NIMHD NIH HHS R00 MD015767
6 · The paper itself

Abstract

backgroundMultiple mAbs are currently approved for the treatment of asthma. However, there is limited evidence on their comparative effectiveness.

objectiveOur aim was to compare the effectiveness of omalizumab, mepolizumab, and dupilumab in individuals with moderate-to-severe asthma.

methodsWe emulated a hypothetical randomized trial using electronic health records from a large US-based academic health care system. Participants aged 18 years or older with baseline IgE levels between 30 and 700 IU/mL and peripheral eosinophil counts of at least 150 cells/μL were eligible for study inclusion. The study period extended from March 2016 to August 2021. Outcomes included the incidence of asthma-related exacerbations and change in baseline FEV

resultsIn all, 68 individuals receiving dupilumab, 68 receiving omalizumab, and 65 receiving mepolizumab met the inclusion criteria. Over 12 months of follow-up, 31 exacerbations occurred over 68 person years (0.46 exacerbations per person year) in the dupilumab group, 63 over 68 person years (0.93 per person year) in the omalizumab group, and 86 over 65 person years (1.32 per person year) in the mepolizumab group (adjusted incidence rate ratios: dupilumab vs mepolizumab, 0.28 [95% CI = 0.09-0.84]; dupilumab vs omalizumab, 0.36 [95% CI = 0.12-1.09]; and omalizumab vs mepolizumab, 0.78 [95% CI = 0.32-1.91]). The differences in the change in FEV

conclusionsAmong patients with asthma and eosinophil counts of at least 150 cells/μL and IgE levels of 30 to 700 kU/L, dupilumab was associated with greater improvements in exacerbation and FEV

Indexed as

Anti-Asthmatic AgentsAsthmaAntibodies, Monoclonal, HumanizedComparative Effectiveness ResearchHumansImmunoglobulin EOmalizumabAnti-Asthmatic AgentsAntibodies, Monoclonal, HumanizeddupilumabImmunoglobulin EmepolizumabOmalizumaballergicAsthmacomparative effectivenessdupilumabeosinophilicmAbsmepolizumabomalizumabtarget trial emulation

Identifiers

PMID36740144
PMCPMC10164684
OpenAlexW4319075002

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.