Evidence map›Paper›PMID 34210787›Full record

ArticleThe European respiratory journal2022

Glucocorticoid toxicity reduction with mepolizumab using the Glucocorticoid Toxicity Index.

P Jane McDowell, John H Stone, Yuqing Zhang, Kirsty Honeyford, Louise Dunn, R Jayne Logan, Lorcan P A McGarvey, Claire A Butler, Liam G Heaney

Open access · hybridAbstract read
In one paragraph

Article in The European respiratory journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

9 citing papers in PubMed, 24 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

9 authors at 3 institutions in 2 countries.

P Jane McDowellWellcome-Wolfson Centre for Experimental Medicine, School of Medicine, Dentistry, and Biological Sciences, Queen's University Belfast, Belfast, UK.ORCID 0000-0003-2063-7992
John H StoneDivision of Rheumatology, Allergy, and Clinical Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Yuqing ZhangDivision of Rheumatology, Allergy, and Clinical Immunology, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Kirsty HoneyfordDept of Respiratory Medicine, Belfast City Hospital, Belfast Health and Social Care Trust, Belfast, UK.
Louise DunnDept of Respiratory Medicine, Belfast City Hospital, Belfast Health and Social Care Trust, Belfast, UK.
R Jayne LoganDept of Respiratory Medicine, Belfast City Hospital, Belfast Health and Social Care Trust, Belfast, UK.
Lorcan P A McGarveyWellcome-Wolfson Centre for Experimental Medicine, School of Medicine, Dentistry, and Biological Sciences, Queen's University Belfast, Belfast, UK.
Claire A ButlerDept of Respiratory Medicine, Belfast City Hospital, Belfast Health and Social Care Trust, Belfast, UK.
Liam G HeaneyWellcome-Wolfson Centre for Experimental Medicine, School of Medicine, Dentistry, and Biological Sciences, Queen's University Belfast, Belfast, UK l.heaney@qub.ac.uk.
Belfast Health and Social Care Trust · GBQueen's University Belfast · GBHarvard University · US

Funding

Medical Research Council MR/M016579/1
6 · The paper itself

Abstract

backgroundReduction in glucocorticoid exposure is the primary benefit of new biologic treatments in severe asthma, but there is currently no evidence that reduction in glucocorticoid exposure corresponds to a proportionate reduction in associated toxicity.

objectivesTo use the validated Glucocorticoid Toxicity Index (GTI) to assess change in glucocorticoid toxicity after 12 months treatment with mepolizumab, and compare toxicity change to glucocorticoid reduction and change in patient-reported outcome measures (PROMs).

methodsA longitudinal, real-world prospective cohort of 101 consecutive patients with severe asthma commenced on mepolizumab in a specialist UK regional severe asthma clinic. GTI toxicity assessment, cumulative glucocorticoid exposure and PROMs were recorded on commencing mepolizumab (V1), and after 12 months treatment (V2).

resultsThere was significant reduction in oral glucocorticoid exposure (V1 median 4280 mg prednisolone per year (interquartile range 3083-5475 mg)

conclusionMepolizumab resulted in substantial oral glucocorticoid reduction, but this did not correlate with reduction in oral glucocorticoid toxicity, which varies widely at the individual patient level. Oral glucocorticoid reduction is not a comprehensive measure of response to mepolizumab.

Indexed as

Anti-Asthmatic AgentsGlucocorticoidsAntibodies, Monoclonal, HumanizedHumansProspective StudiesAnti-Asthmatic AgentsAntibodies, Monoclonal, HumanizedGlucocorticoidsmepolizumab

Identifiers

PMID34210787
PMCPMC8770919
OpenAlexW3177087646

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Registered trials

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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.