Evidence map›Paper›PMID 42269821›Full record

ArticleJournal of vascular and interventional radiology : JVIR2026

CT Radiomics to Predict Regenerative Biomarker Expression after Liver Venous Embolization: Proof-of-Concept in a Porcine Model.

Jana Nguyenová, Junlin Yang, Xuchen Zhang, Annabella Shewarega, Jonathan Tefera, Tom N Kuhn, Bernhard Gebauer, Lynn J Savic, Julius Chapiro, David C Madoff

Abstract read
In one paragraph

Article in Journal of vascular and interventional radiology : JVIR, 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

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

10 authors.

Jana NguyenováDepartment of Radiology, Charité-Universitaetsmedizin Berlin, Berlin, Germany.
Junlin YangDepartment of Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, Connecticut.
Xuchen ZhangDepartment of Pathology, Section of Gastrointestinal and Liver Pathology, Yale School of Medicine, New Haven, Connecticut.
Annabella ShewaregaDepartment of Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, Connecticut.
Jonathan TeferaDepartment of Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, Connecticut.
Tom N KuhnDepartment of Neurology, Universitaetsmedizin Mannheim, Mannheim, Germany.
Bernhard GebauerDepartment of Radiology, Charité-Universitaetsmedizin Berlin, Berlin, Germany.
Lynn J SavicDepartment of Radiology, Charité-Universitaetsmedizin Berlin, Berlin, Germany.
Julius ChapiroDepartment of Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, Connecticut; Department of Medicine, Section of Digestive Diseases, Yale School of Medicine, New Haven, Connecticut; Department of Biomedical Engineering, Yale School of Engineering and Applied Sciences, New Haven, Connecticut.
David C MadoffDepartment of Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, Connecticut; Department of Medicine, Section of Medical Oncology, Yale School of Medicine, New Haven, Connecticut; Department of Surgery, Section of Surgical Oncology, Yale School of Medicine, New Haven, Connecticut. Electronic address: david.madoff@yale.edu.

Funding

Quantitative Multimodal Imaging Biomarkers for Combined Locoregional and Immunotherapy of Liver CancerR01CA206180 · NCI · YALE UNIVERSITY · PI CHAPIRO, JULIUS, DUNCAN, JAMES S · 2016 to 2025
$6.1M
NCI NIH HHS R01 CA206180
6 · The paper itself

Abstract

purposeTo evaluate regeneration after liver venous embolization in healthy and cirrhotic swine and to assess computed tomography (CT) radiomics for predicting these markers. MATERIALS AND

methodsTwenty-two pigs with healthy (n = 11) or cirrhotic (n = 11) livers underwent portal vein embolization (PVE) with microspheres and coils, n-butyl cyanoacrylate, combined PVE and hepatic vein embolization (PVE + HVE), or sham control. Four weeks after intervention, future liver remnant (FLR) tissue was analyzed for angiogenesis, proliferation, and epithelial integrity using vascular endothelial growth factor (VEGF), angiopoietin-1, Ki-67, and cytokeratin 8/18/19 immunofluorescence and for apoptosis in the embolized lobe using caspase 3. Spearman correlations were computed between biomarker expression and relative FLR hypertrophy. Biomarkers were dichotomized into high versus low groups based on group-specific means. Logistic regression (LR) and random forest (RF) models were trained on baseline CT radiomics using repeated fivefold cross-validation (100 iterations) to predict biomarker expression. Model performance was assessed by mean area under the curve (AUC), with 95% CIs estimated from the 2.5th and 97.5th percentiles across runs.

resultsAll animals completed the study. PVE + HVE resulted in significantly higher expression of VEGF, Ki-67, angiopoietin-1, and caspase 3 than sham controls in both liver conditions (all P < .05). Angiogenesis was greater after PVE + HVE than after PVE in healthy (P < .01) and cirrhotic (P < .001) livers. Ki-67 showed the highest predictive performance (RF AUC, 0.84; LR AUC, 0.81).

conclusionsLiver venous embolization induces distinct regenerative responses in healthy and cirrhotic swine. Baseline CT radiomics demonstrated moderate discriminative performance for predicting regenerative biomarkers.

Indexed as

Embolization, TherapeuticHepatic VeinsLiverLiver CirrhosisLiver RegenerationPortal VeinRadiomicsTomography, X-Ray ComputedAngiogenic ProteinsAnimalsApoptosisBiomarkersCell ProliferationDisease Models, AnimalEnbucrilateFemaleAngiogenic ProteinsBiomarkersEnbucrilate

Identifiers

PMID42269821
PMCPMC13621344

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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.