Evidence map›Paper›PMID 41894123›Full record

ArticleJapanese journal of radiology2026

Conventional MRI/CT for differentiation of IDH-mutant adult-type diffuse gliomas: revisited with a new imaging feature "scFLAIR-D".

Yuji Ohizumi, Ryo Kurokawa, Yusuke Watanabe, Mariko Kurokawa, Yosuke Kitagawa, Masashi Nomura, Hirokazu Takami, Nobuhito Saito, Osamu Abe

Abstract read
In one paragraph

Article in Japanese journal of radiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Review
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.

Yuji OhizumiDepartment of Radiology, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan.
Ryo KurokawaDepartment of Radiology, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan. kuroro63@gmail.com.ORCID http://orcid.org/0000-0002-1186-8900
Yusuke WatanabeDepartment of Radiology, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan.
Mariko KurokawaDepartment of Radiology, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan.
Yosuke KitagawaDepartment of Neurosurgery, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan.
Masashi NomuraDepartment of Neurosurgery, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan.
Hirokazu TakamiDepartment of Neurosurgery, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan.
Nobuhito SaitoDepartment of Neurosurgery, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan.
Osamu AbeDepartment of Radiology, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo test whether a refined definition of the T2-FLAIR mismatch sign (redefined T2FM) and a newly defined subcortical FLAIR signal drop (scFLAIR-D) on conventional MRI improve presurgical discrimination between astrocytoma, IDH-mutant (AST) and oligodendroglioma, IDH-mutant and 1p/19q-codeleted (ODG). MATERIALS AND

methodsIn this single-center retrospective study (January 2021-July 2025), adults with IDH-mutant adult-type diffuse glioma and preoperative T2-weighted and FLAIR MRI were included. Two blinded readers (with senior adjudication) scored five features: redefined T2FM (includes partial but excludes subcortical-only mismatch), scFLAIR-D (focal FLAIR hypointensity confined to subcortical white matter within T2-hyperintensity), multiple necrotic/cystic foci (≥ 2 cavities), cortical predominance (> 50% cortical volume), and calcification (CT).

resultsForty-one patients were included (median age 42 years; 24 men; 16 AST, 25 ODG). AST significantly more often showed redefined T2FM (AST: 87.5% [14/16] vs. ODG: 20.0% [5/25]; p < 0.001) than ODG. ODG significantly more often showed scFLAIR-D (AST: 6.3% [1/16] vs. ODG: 44.0% [11/25]; p = 0.013), multiple necrotic/cystic foci (12.5% [2/16] vs. 56.0% [14/25]; p = 0.008), and calcification (0% [0/16] vs. 50.0% [12/24 patients with preoperative CT]; p < 0.001); cortical predominance trended higher (31.3% [5/16] vs. 64.0% [16/25]; p = 0.058). For predicting AST, redefined T2FM achieved 87.5% sensitivity and 80.0% specificity. For predicting ODG, scFLAIR-D achieved 44.0% sensitivity and 93.8% specificity. Two or more ODG-favored features (scFLAIR-D, multiple necrotic/cystic foci, calcification) identified ODG with 100% specificity, whereas redefined T2FM without ODG-favored features identified AST with 96.0% specificity.

conclusionA refined T2FM definition improves sensitivity for AST while preserving high specificity. scFLAIR-D serves as a simple, specific marker of ODG; in combination, these routine features yield high rule-in specificity to support presurgical planning and early therapeutic counseling. Refining T2FM to include partial but exclude subcortical-only mismatch increased sensitivity for astrocytoma, IDH-mutant (87.5%) while preserving specificity (80.0%). Newly defined scFLAIR-D was highly specific for oligodendroglioma, IDH-mutant and 1p/19q-codeleted (93.8%). Combining these qualitative MRI/CT features yielded high rule-in specificities for lineage discrimination.

Indexed as

Brain NeoplasmsGliomaIsocitrate DehydrogenaseMagnetic Resonance ImagingTomography, X-Ray ComputedAdultAgedDiagnosis, DifferentialFemaleHumansMaleMiddle AgedMutationOligodendrogliomaRetrospective StudiesIsocitrate DehydrogenaseAstrocytomaComputed tomographyMagnetic resonance imagingOligodendrogliomaT2-FLAIR mismatchWorld Health Organization

Identifiers

PMID41894123
PMCPMC13315118

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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.