Evidence map›Paper›PMID 41883547›Full record

ArticleDigital health

Radiomics-based differentiation of hepatocellular carcinoma and dysplastic nodules using noncontrast abbreviated MRI.

Jun Young Park, Yoonseok Lee, Young Jae Kim, Seung Kak Shin, Kwang Gi Kim

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

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Jun Young ParkDepartment of Translational-Clinical Medicine, Gachon University, Incheon, Republic of Korea.
Yoonseok LeeDepartment of Internal Medicine, Gachon University Gil Medical Center, Gachon University College of Medicine, Incheon, Republic of Korea.
Young Jae KimGachon Biomedical & Convergence Institute, Gachon University Gil Medical Center, Incheon, Republic of Korea.
Seung Kak ShinDepartment of Internal Medicine, Gachon University Gil Medical Center, Gachon University College of Medicine, Incheon, Republic of Korea.
Kwang Gi KimMedical Devices R&D Center, Gachon University Gil Medical Center, Incheon, Republic of Korea.ORCID https://orcid.org/0000-0001-9714-6038

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Noncontrast abbreviated magnetic resonance imaging (NC-AMRI) has emerged as a cost-effective alternative to ultrasound for hepatocellular carcinoma (HCC) surveillance; however, its diagnostic performance for differentiating dysplastic nodules (DNs) from HCC remains limited in the absence of contrast enhancement. This study investigated whether machine learning (ML)-based radiomics using noncontrast AMRI can improve discrimination between DNs and HCC. Methods: This retrospective study included 189 patients with histopathologically confirmed hepatic nodules (41 DNs and 148 HCC). NC-AMRI, defined in this study as a contrast-free abbreviated protocol excluding dynamic contrast-enhanced phases, was performed using 3.0 T MRI systems and included a limited set of four noncontrast imaging sequences: in-phase, opposed-phase, T2-weighted imaging (T2WI), and diffusion-weighted imaging (DWI). Model performance in differentiating HCC and DNs was assessed using 5-fold stratified cross-validation on the full dataset. Radiomic features were extracted from manually segmented regions of interest using an Image Biomarker Standardization Initiative (ISBI) compliant PyRadiomics pipeline feature selection was performed using recursive feature elimination after multicollinearity filtering. Logistic regression, support vector machine, random forest, and extreme gradient boosting models were trained. Results: In terms of diagnostic performance, the machine learning-based models for differentiating HCC from DNs showed AUC values of 0.798 for logistic regression, 0.790 for support vector machine, 0.781 for random forest, and 0.758 for extreme gradient boosting, with corresponding sensitivities of 0.712, 0.669, 0.698, and 0.741 and specificities of 0.756, 0.805, 0.756, and 0.610, respectively. Notably, the machine learning-based models also demonstrated good performance in distinguishing high-grade DNs from HCC, achieving AUC values of 0.783 for logistic regression, 0.751 for support vector machine, 0.800 for random forest, and 0.742 for extreme gradient boosting, with corresponding sensitivities of 0.799, 0.835, 0.727, and 0.799 and specificities of 0.700, 0.500, 0.700, and 0.600, respectively. Conclusions: Radiomics-based machine learning enhances the diagnostic performance of NC-AMRI for differentiating HCC from DNs, complementing conventional imaging and addressing key limitations of AMRI surveillance.

Indexed as

dysplastic nodulesHepatocellular carcinomamachine learningradiomics

Identifiers

PMID41883547
PMCPMC13009901

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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.