Evidence map›Paper›PMID 40384997›Full record

ArticleAmerican journal of translational research2025

Associations between dynamic-contrast enhanced MRI with histopathological features in atypical HCC using spatial co-registration with biopsy.

Hans-Jonas Meyer, Johann Potratz, Dörthe Jechorek, Kai Ina Schramm, Jan Borggrefe, Alexey Surov

Abstract read
In one paragraph

Article in American journal of translational research, 2025. 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. Article
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.

Hans-Jonas MeyerDepartment of Diagnostic and Interventional Radiology, University of Leipzig Leipzig, Germany.
Johann PotratzDepartment of Pathology, Otto von Guericke University Magdeburg, Germany.
Dörthe JechorekDepartment of Pathology, Otto von Guericke University Magdeburg, Germany.
Kai Ina SchrammDepartment of Radiology and Nuclear Medicine, Otto von Guericke University Magdeburg, Germany.
Jan BorggrefeDepartment of Radiology, Mühlenkreiskliniken Minden, Ruhr-University Bochum Bochum, Germany.
Alexey SurovDepartment of Radiology, Mühlenkreiskliniken Minden, Ruhr-University Bochum Bochum, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe relationships between histopathology and imaging remain elusive and investigating the underlying causes of tumor microstructure that result in an imaging phenotype is of clinical importance. In the present study, cross-sectional guided biopsy specimens were used to correlate prebioptic magnetic resonance imaging (MRI) with immunohistochemical staining of histopathologic specimens using precise spatial biopsy localization.

methodsOverall, 52 patients with atypical hepatocellular carcinoma (HCC) were included in the present analysis. All patients were imaged with a 1.5 T clinical scanner at least one month prior to biopsy. The contrast-enhanced dynamic sequences were analyzed with quantified signal intensities. The bioptic specimens were obtained by cross-sectional guided biopsy and was further analyzed for cell density, proliferation index (Ki 67), tumor-infiltrating lymphocytes, tumor-stroma ratio.

resultsPer high power field, the mean values of the histologic parameters were as follows: the tumor-stroma ratio was 17.1 ± 20, the cell count was 147.0 ± 60.3, the CD45 count was 7.3 ± 8.0 and the Ki 67-index was 16.9 ± 16.5%. There were no statistically significant correlations between the MRI signal intensities and cell count, tumor-stroma ratio and CD45 count. There was a moderate inverse correlation that was identified between arterial phase signal intensities and Ki 67 max (r=-0.41, P=0.002) and Ki 67 mean (r=-0.37, P=0.005). The signal intensities of the hepatobiliary phase were statistically significantly different between high and low proliferating HCC using thresholds of 20% and 10% (P=0.01 and P=0.02, respectively). The resulting AUC for the 10% threshold was 0.73 and 0.67 for the 20% threshold.

conclusionDCE-MRI is associated with Ki 67 index in atypical HCC. The hepatobiliary phase could discriminate HCCs according to their Ki 67 index. Quantitative MRI could be used as an imaging-based surrogate for proliferative HCC. Further studies are needed to validate the present results.

Indexed as

HCCMRIproliferation potential

Identifiers

PMID40384997
PMCPMC12082541

What OpenQuestion holds

Textmetadata
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.