Evidence map›Paper›PMID 42265152›Full record

ArticleScientific reports2026

Developing a fully automated imaging biomarker for HCC risk assessment via MRI-based tumor segmentation and EPM.

Awj Twam, Shane A Smith, Mohamed Eltaher, Zaina Boriek, Adrian Celaya, Dontrey Bourgeois, David Martinus, Tiffany L Calderone, Laura Beretta, Jessica I Sanchez and 6 more

Abstract read
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Awj Twam *Department of Imaging Physics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. atwam@mdanderson.org.
Shane A Smith *Department of Imaging Physics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. sasmith6@mdanderson.org.
Mohamed EltaherDepartment of Imaging Physics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Zaina BoriekDepartment of Imaging Physics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Adrian CelayaDepartment of Imaging Physics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Dontrey BourgeoisDepartment of Radiation Oncology Research, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
David MartinusDepartment of GI Radiation Oncology-Research, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Tiffany L CalderoneDepartment of Molecular & Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Laura BerettaDepartment of Molecular & Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Jessica I SanchezDepartment of Molecular & Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
David W VictorDepartment of Gastroenterology, Houston Methodist Hospital, Houston, TX, USA.
Nakul GuptaDepartment of Radiology, Houston Methodist Hospital, Houston, TX, USA.
Manal HasanDepartment of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Jalal K PrasunDepartment of Hepatology, Baylor College of Medicine, Houston, TX, USA.
Eugene J KoayDepartment of GI Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
David T FuentesDepartment of Imaging Physics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Funding

Early Detection of Hepatocellular CarcinomaR01CA195524 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LAURA BERETTA, David Fuentes · 2016 to 2026
$6.5M
Delivery optimization of a transarterial ablative therapyR01CA301555 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI ERIK N CRESSMAN, David Fuentes · 2025 to 2026
$1.1M
NCI NIH HHS R01 CA195524NCI NIH HHS R01 CA301555
6 · The paper itself

Abstract

This study investigates the feasibility of using automated tumor segmentation as the region of interest for early detection of hepatocellular carcinoma (HCC) using magnetic resonance imaging (MRI). Enhancement Pattern Mapping (EPM) is used as a voxel-wise imaging biomarker within the region of interest once segmentations are generated. We implement PocketNet, a lightweight convolutional neural network, to segment liver tumors and evaluate performance. To contextualize model accuracy, we estimate the theoretical upper bound of segmentation performance through inter-observer comparisons of manual annotations. Imaging-derived features from automated segmentations are analyzed using XGBoost to assess their predictive value. Results show that automated segmentation approaches upper-bound performance for larger tumors but underperforms on smaller lesions. However, EPM features derived from automated masks demonstrate comparable predictive power to those from manual segmentations, indicating that the EPM features are stable with respect to segmentation inaccuracies. Results demonstrate that a fully automated imaging biomarker may be developed as a clinical utility for HCC risk assessment.

Indexed as

Carcinoma, HepatocellularImage Interpretation, Computer-AssistedLiver NeoplasmsMagnetic Resonance ImagingBiomarkers, TumorConvolutional Neural NetworksHumansImage Processing, Computer-AssistedRisk AssessmentBiomarkers, Tumor

Identifiers

PMID42265152
PMCPMC13493971

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.