Evidence map›Paper›PMID 41887530›Full record

ArticleJHEP reports : innovation in hepatology2026

Deep learning-based generation of synthetic multiphasic MRI in hepatocellular carcinoma and cirrhosis.

Sara A Abosabie, Salma A S Abosabie, Weicheng Dai, Junlin Yang, Moritz Gross, Jeffrey Weinreb, Margarita V Revzin, Gaurav Parmar, Chenyu You, MingDe Lin and 6 more

Abstract read
In one paragraph

Article in JHEP reports : innovation in hepatology, 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

16 authors.

Sara A AbosabieDepartment of Radiology and Biomedical Imaging, Yale University School of Medicine, New Haven, CT 06520, USA; Department of Radiology, Charité-Universitätsmedizin Berlin, Campus Virchow Klinikum, 13353 Berlin, Germany.
Salma A S AbosabieDepartment of Radiology and Biomedical Imaging, Yale University School of Medicine, New Haven, CT 06520, USA; Department of Radiology, Charité-Universitätsmedizin Berlin, Campus Virchow Klinikum, 13353 Berlin, Germany; Institute of Experimental Biomedicine, University Hospital Wuerzburg, 97080 Wuerzburg, Germany; Rudolf Virchow Center for Integrative and Translational Bioimaging, Julius Maximilians University of Wuerzburg, 97080 Wuerzburg, Germany.
Weicheng DaiDepartment of Radiology and Biomedical Imaging, Yale University School of Medicine, New Haven, CT 06520, USA.
Junlin YangDepartment of Radiology and Biomedical Imaging, Yale University School of Medicine, New Haven, CT 06520, USA.
Moritz GrossDepartment of Radiology and Biomedical Imaging, Yale University School of Medicine, New Haven, CT 06520, USA; Department of Radiology, Charité-Universitätsmedizin Berlin, Campus Virchow Klinikum, 13353 Berlin, Germany.
Jeffrey WeinrebDepartment of Radiology and Biomedical Imaging, Yale University School of Medicine, New Haven, CT 06520, USA.
Margarita V RevzinDepartment of Radiology and Biomedical Imaging, Yale University School of Medicine, New Haven, CT 06520, USA.
Gaurav ParmarDepartment of Radiology and Biomedical Imaging, Yale University School of Medicine, New Haven, CT 06520, USA.
Chenyu YouDepartment of Radiology and Biomedical Imaging, Yale University School of Medicine, New Haven, CT 06520, USA; Department of Applied Mathematics and Statistics, Stony Brook University, Stony Brook, NY 11794, USA.
MingDe LinDepartment of Radiology and Biomedical Imaging, Yale University School of Medicine, New Haven, CT 06520, USA; Visage Imaging, Inc., San Diego, CA 91230, USA.
Olivia GaddumDepartment of Radiology and Biomedical Imaging, Yale University School of Medicine, New Haven, CT 06520, USA; Department of Radiology, Charité-Universitätsmedizin Berlin, Campus Virchow Klinikum, 13353 Berlin, Germany.
Bernhard GebauerDepartment of Radiology, Charité-Universitätsmedizin Berlin, Campus Virchow Klinikum, 13353 Berlin, Germany.
Lynn Jeanette SavicDepartment of Radiology, Charité-Universitätsmedizin Berlin, Campus Virchow Klinikum, 13353 Berlin, Germany; Berlin Institute of Health at Charité-Universitätsmedizin Berlin, 10115 Berlin, Germany; Experimental Clinical Research Center (ECRC) at Charité-Universitätsmedizin Berlin and Max-Delbrück-Centrum für Molekulare Medizin (MDC), 13125 Berlin, Germany.
David C MadoffDepartment of Radiology and Biomedical Imaging, Yale University School of Medicine, New Haven, CT 06520, USA; Department of Medicine, Section of Medical Oncology, Yale University School of Medicine, New Haven, CT 06520, USA; Department of Surgery, Section of Surgical Oncology, Yale University School of Medicine, New Haven, CT 06520, USA.
James S DuncanDepartment of Radiology and Biomedical Imaging, Yale University School of Medicine, New Haven, CT 06520, USA; Department of Medicine, Liver Center, Section of Digestive Diseases, Yale University School of Medicine, New Haven, CT 06520, USA; Department of Biomedical Engineering, School of Engineering and Applied Sciences, New Haven, CT 06520, USA.
Julius ChapiroDepartment of Radiology and Biomedical Imaging, Yale University School of Medicine, New Haven, CT 06520, USA; Department of Medicine, Liver Center, Section of Digestive Diseases, Yale University School of Medicine, New Haven, CT 06520, USA; Department of Biomedical Engineering, School of Engineering and Applied Sciences, New Haven, CT 06520, USA. Electronic address: julius.chapiro@yale.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND &

aimsThere is growing interest in reducing contrast medium use and the lengthy scan duration in liver imaging. This proof of concept study evaluated the feasibility of deep learning-based generation of synthetic 3D liver contrast-enhanced multiphasic magnetic resonance imaging (MRI) exams, which are similar to ground-truth exams in hepatocellular carcinoma and cirrhosis.

methodsMRI exams from patients with hepatocellular carcinoma (HCC) or cirrhosis at a single academic center were retrospectively collected. A 3D cycle-consistent generative adversarial network was trained to generate synthetic 3D T1-weighted contrast-enhanced multiphasic liver MRI exams, including arterial, portal venous, delayed, and hepatobiliary phases, using two pre-contrast T1-weighted and T2-weighted input phases. Quantitative performance evaluated similarity, error, and overlap metrics between synthetic and ground-truth exams. For the qualitative multireader study, three blinded radiologists assessed the ground-truth and synthetic MRI exams using a comprehensive questionnaire. Questionnaire tasks 1-5 comprised: visual Turing test (ground-truth vs. synthetic nature), image quality, anatomic accuracy, disease diagnosability, and artifacts. Task 6 comprised Liver Imaging Reporting and Data System features.

resultsThe study included 3,198 MRI phases from 533 MRI exams from 185 patients with HCC (mean age, 62.1 years ± 9.7 [SD]; 141 men) and 182 patients with cirrhosis (54.4 years ± 10.0; 111 men). Synthetic MRI exams achieved high quantitative and qualitative similarity to ground-truth exams. Quantitative analysis demonstrated high structural similarity index (0.86 ± 0.03), overlap (0.97 ± 0.05), and low symmetric mean absolute percent error (0.63 ± 0.23%). The qualitative multireader study showed no significant difference in tasks 1-5 (p = 0.06-0.50) and high performance metrics in task 6 (accuracy: 0.76-0.86; precision: 0.96-1.00) with moderate to perfect Fleiss's Kappa inter-rater agreement (0.58-1.00, p <0.001).

conclusionsDeep learning enabled the generation of synthetic 3D liver contrast-enhanced multiphasic MRI exams from pre-contrast sequences, achieving high quantitative and qualitative similarity to ground-truth images. IMPACT AND IMPLICATIONS: This work demonstrates the early feasibility of generating high-quality, 3D contrast-enhanced multiphasic liver MRI exams from pre-contrast sequences, with synthetic exams showing strong agreement with ground-truth across quantitative metrics and key qualitative criteria, including the visual Turing test, image quality, disease diagnosability, anatomic accuracy, artifact severity, and HCC Liver Imaging Reporting and Data System features. Despite the model currently representing a proof of concept based on a moderate single-center dataset, with a need for larger multicenter studies and external validation, the results highlight the potential to transform liver MRI workflows by reducing contrast media costs and potential side effects, significantly shortening acquisition time, especially the prolonged 20-min hepatobiliary phase, and improving accessibility for patients unable to tolerate contrast-enhanced MRI because of renal impairment, contrast agent allergy, or claustrophobia.

Indexed as

Carcinoma, HepatocellularDeep LearningLiver CirrhosisLiver NeoplasmsMagnetic Resonance ImagingContrast MediaFeasibility StudiesFemaleGenerative Adversarial NetworksGenerative Artificial IntelligenceHumansImaging, Three-DimensionalLiverMaleMiddle AgedProof of Concept StudyContrast MediaCirrhosisContrast-enhanced multiphasic liver MRIDeep learningGenerative adversarial networksHepatocellular carcinomaSynthetic 3D contrast-enhanced liver MRI

Identifiers

PMID41887530
PMCPMC13251683

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.