Evidence map›Paper›PMID 40486501›Full record

ArticleFrontiers in allergy2025

Steroid-sparing benefits of biologic use in hypereosinophilic syndrome and substantial disease burden across subtypes.

Jeremiah Hwee, Lynn Huynh, Wilson da Costa, Marc E Rothenberg, Mei Sheng Duh, Rafael Alfonso-Cristancho

Abstract read
In one paragraph

Article in Frontiers in allergy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Jeremiah HweeEpidemiology, GSK, Mississauga, ON, Canada.
Lynn HuynhAnalysis Group, Inc., Boston, MA, United States.
Wilson da CostaAnalysis Group, Inc., Boston, MA, United States.
Marc E RothenbergDivision of Allergy and Immunology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati School of Medicine, Cincinnati, OH, United States.
Mei Sheng DuhAnalysis Group, Inc., Boston, MA, United States.
Rafael Alfonso-CristanchoGlobal Real-World Evidence & Health Outcomes Research, GSK, Collegeville, PA, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Limited data exist on the burden of myeloproliferative, lymphocytic and idiopathic subtypes of hypereosinophilic syndrome (M-HES, L-HES and I-HES) and the characteristics of patients with HES receiving biologic therapies. This analysis aimed to further characterize these subtypes and explore the impact of biologics in a real-world European setting. Methods: This was a Results: The analysis included 280 patients with I-HES ( Conclusions: All HES subtypes had a substantial disease burden and were commonly associated with fatigue, skin itch and pain. I-HES appeared to be more responsive to treatment than L-HES and M-HES. Biologic use for HES led to more patients experiencing clinical responses and was OCS-sparing.

Indexed as

biologicsburden of diseasecorticosteroidhypereosinophilic syndromemepolizumabretrospective study

Identifiers

PMID40486501
PMCPMC12143263

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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.