Evidence map›Paper›PMID 39792964›Full record

ArticlePloS one2025

Cerebral blood flow and histological analysis for the accurate differentiation of infiltrating tumor and vasogenic edema in glioblastoma.

Hideki Kuroda, Yoshiko Okita, Atsuko Arisawa, Reina Utsugi, Koki Murakami, Ryuichi Hirayama, Noriyuki Kijima, Hideyuki Arita, Manabu Kinoshita, Yasunori Fujimoto and 4 more

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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

14 authors.

Hideki KurodaDepartment of Neurosurgery, Osaka University Graduate School of Medicine, Osaka, Japan.
Yoshiko OkitaDepartment of Neurosurgery, Osaka University Graduate School of Medicine, Osaka, Japan.ORCID 0000-0002-2943-238X
Atsuko ArisawaDepartment of Diagnostic Radiology, Osaka University Graduate School of Medicine, Osaka, Japan.
Reina UtsugiDepartment of Neurosurgery, Osaka University Graduate School of Medicine, Osaka, Japan.
Koki MurakamiDepartment of Neurosurgery, Osaka University Graduate School of Medicine, Osaka, Japan.
Ryuichi HirayamaDepartment of Neurosurgery, Osaka University Graduate School of Medicine, Osaka, Japan.
Noriyuki KijimaDepartment of Neurosurgery, Osaka University Graduate School of Medicine, Osaka, Japan.
Hideyuki AritaDepartment of Neurosurgery, Osaka University Graduate School of Medicine, Osaka, Japan.
Manabu KinoshitaDepartment of Neurosurgery, Osaka University Graduate School of Medicine, Osaka, Japan.ORCID 0000-0001-7923-6902
Yasunori FujimotoDepartment of Neurosurgery, Osaka University Graduate School of Medicine, Osaka, Japan.
Hajime NakamuraDepartment of Neurosurgery, Osaka University Graduate School of Medicine, Osaka, Japan.
Naoki KagawaDepartment of Neurosurgery, Osaka University Graduate School of Medicine, Osaka, Japan.ORCID 0000-0002-0674-2342
Noriyuki TomiyamaDepartment of Diagnostic Radiology, Osaka University Graduate School of Medicine, Osaka, Japan.
Haruhiko KishimaDepartment of Neurosurgery, Osaka University Graduate School of Medicine, Osaka, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGlioblastoma is characterized by neovascularization and diffuse infiltration into the adjacent tissue. T2*-based dynamic susceptibility contrast (DSC) MR perfusion images provide useful measurements of the biomarkers associated with tumor perfusion. This study aimed to distinguish infiltrating tumors from vasogenic edema in glioblastomas using DSC-MR perfusion images.

methodsData were retrospectively collected from 48 patients with primary IDH-wild-type glioblastoma and 24 patients with meningiomas (Edemas-M). First, we attempted histological verification of cell density, Ki-67 index, and microvessel areas to distinguish between non-contrast-enhancing tumors (NETs) and edema (Edemas) which were obtained from stereotactically fused T2-weighted and perfusion images. This was performed for evaluating enhancing tumors (ETs), NETs, and Edemas. Second, we also performed radiological verification to distinguish NETs from Edemas. Two neurosurgeons manually assigned the regions of interests (ROIs) to ETs, NETs, and Edemas. The DSC-MR perfusion imaging-derived parameters calculated for each ROI included the cerebral blood volume (CBV), cerebral blood flow (CBF), and mean transit time (MTT).

resultsCell density and microvessel area were significantly higher in NETs than those in Edemas (p<0.01 and p<0.05, respectively). Regarding radiological analysis, the mean CBF ratio for Edemas was significantly lower than that for NETs (p<0.01). The mean MTT ratio for Edemas was significantly higher than that for NETs. The receiver operating characteristic (ROC) analysis showed that CBF (area under the curve [AUC] = 0.890) could effectively distinguish between NETs and Edemas. The ROC analysis also showed that MTT (AUC = 0.946) could effectively distinguish between NETs and Edemas.

conclusionsDSC-MR perfusion images may prove useful in differentiating NETs from Edemas in non-contrast T2 hyperintensity regions of glioblastoma.

Indexed as

Brain EdemaBrain NeoplasmsCerebrovascular CirculationGlioblastomaAdultAgedDiagnosis, DifferentialFemaleHumansMagnetic Resonance ImagingMaleMeningiomaMiddle AgedRetrospective StudiesROC Curve

Identifiers

PMID39792964
PMCPMC11723604

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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.