Evidence map›Paper›PMID 40901605›Full record

ArticleWorld journal of hepatology2025

Biparametric magnetic resonance imaging-based radiomic and deep learning models for predicting Ki-67 risk stratification in hepatocellular carcinoma.

Xue-Yong Zuo, Hai-Feng Liu

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Article in World journal of hepatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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4 citing papers in PubMed.

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5 · Who and what money

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2 authors.

Xue-Yong ZuoDepartment of Gastroenterology, Third Affiliated Hospital of Soochow University, Changzhou 213003, Jiangsu Province, China. zuoxueyong@outlook.com.
Hai-Feng LiuDepartment of Radiology, Third Affiliated Hospital of Soochow University: Changzhou First People's Hospital, Changzhou 213003, Jiangsu Province, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHepatocellular carcinoma (HCC) is a prevalent and life-threatening cancer with increasing incidence worldwide. High Ki-67 risk stratification is closely associated with higher recurrence rates and worse outcomes following curative therapies in patients with HCC. However, the performance of radiomic and deep transfer learning (DTL) models derived from biparametric magnetic resonance imaging (bpMRI) in predicting Ki-67 risk stratification and recurrence-free survival (RFS) in patients with HCC remains limited.

aimTo develop a nomogram model integrating bpMRI-based radiomic and DTL signatures for predicting Ki-67 risk stratification and RFS in patients with HCC.

methodsThis study included 198 patients with histopathologically confirmed HCC who underwent preoperative bpMRI. Ki-67 risk stratification was categorized as high (> 20%) or low (≤ 20%) according to immunohistochemical staining. Radiomic and DTL signatures were extracted from the T2-weighted and arterial-phase images and combined through a random forest algorithm to establish radiomic and DTL models, respectively. Multivariate regression analysis identified clinical risk factors for high Ki-67 risk stratification, and a predictive nomogram model was developed.

resultsA nonsmooth margin and the absence of an enhanced capsule were independent factors for high Ki-67 risk stratification. The area under the curve (AUC) of the clinical model was 0.77, while those of the radiomic and DTL models were 0.81 and 0.87, respectively, for the prediction of high Ki-67 risk stratification, and the nomogram model achieved a better AUC of 0.92. The median RFS times for patients with high and low Ki-67 risk stratification were 33.00 months and 66.73 months, respectively (

conclusionOur developed nomogram model demonstrated good performance in predicting Ki-67 risk stratification and predicting survival outcomes in patients with HCC.

Indexed as

Deep transfer learningHepatocellular carcinomaKi-67RadiomicsRecurrence-free survival

Identifiers

PMID40901605
PMCPMC12400337

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