Evidence map›Paper›PMID 40951530›Full record

ArticleJournal of clinical and translational hepatology2025

Hepatocellular Carcinoma Risk Stratification for Cirrhosis Patients: Integrating Radiomics and Deep Learning Computed Tomography Signatures of the Liver and Spleen into a Clinical Model.

Rong Fan, Ya-Ru Shi, Lei Chen, Chuan-Xin Wang, Yun-Song Qian, Yan-Hang Gao, Chun-Ying Wang, Xiao-Tang Fan, Xiao-Long Liu, Hong-Lian Bai and 17 more

Abstract read
In one paragraph

Article in Journal of clinical and translational hepatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

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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

27 authors.

Rong FanDepartment of Infectious Diseases, Nanfang Hospital, Southern Medical University; Guangdong Provincial Key Laboratory for Prevention and Control of Major Liver Diseases; Guangdong Provincial Clinical Research Center for Viral Hepatitis; Key Laboratory of Infectious Diseases Research in South China, Ministry of Education, Guangzhou, Guangdong, China.
Ya-Ru ShiDepartment of Infectious Diseases, Nanfang Hospital, Southern Medical University; Guangdong Provincial Key Laboratory for Prevention and Control of Major Liver Diseases; Guangdong Provincial Clinical Research Center for Viral Hepatitis; Key Laboratory of Infectious Diseases Research in South China, Ministry of Education, Guangzhou, Guangdong, China.
Lei ChenInternational Cooperation Laboratory on Signal Transduction, National Center for Liver Cancer, Eastern Hepatobiliary Surgery Institute/Hospital, Shanghai, China.
Chuan-Xin WangDepartment of Clinical Laboratory, The Second Hospital, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, China.
Yun-Song QianHepatology Department, Ningbo Hwamei Hospital, University of Chinese Academy of Sciences, Ningbo, Zhejiang, China.
Yan-Hang GaoThe First Hospital of Jilin University, Changchun, Jilin, China.
Chun-Ying WangXuzhou Infectious Diseases Hospital, Xuzhou, Jiangsu, China.
Xiao-Tang FanDepartment of Hepatology, First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang, China.
Xiao-Long LiuThe United Innovation of Mengchao Hepatobiliary Technology Key Laboratory of Fujian Province, Mengchao Hepatobiliary Hospital of Fujian Medical University, Fuzhou, Fujian, China.
Hong-Lian BaiThe Department of Infectious Disease, The First People's Hospital of Foshan, Foshan, Guangdong, China.
Dan ZhengDepartment of Gastroenterology, The Central Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Guo-Qing JiangDepartment of Hepatobiliary Surgery, Clinical Medical College, Yangzhou University, Yangzhou, Jiangsu, China.
Yan-Long YuChifeng Clinical Medical School of Inner Mongolia Medical University, Chifeng, Inner Mongolia, China.
Xie-Er LiangDepartment of Infectious Diseases, Nanfang Hospital, Southern Medical University; Guangdong Provincial Key Laboratory for Prevention and Control of Major Liver Diseases; Guangdong Provincial Clinical Research Center for Viral Hepatitis; Key Laboratory of Infectious Diseases Research in South China, Ministry of Education, Guangzhou, Guangdong, China.
Jin-Jun ChenDepartment of Infectious Diseases, Nanfang Hospital, Southern Medical University; Guangdong Provincial Key Laboratory for Prevention and Control of Major Liver Diseases; Guangdong Provincial Clinical Research Center for Viral Hepatitis; Key Laboratory of Infectious Diseases Research in South China, Ministry of Education, Guangzhou, Guangdong, China.
Wei-Fen XieDepartment of Gastroenterology, Changzheng Hospital, Naval Medical University, Shanghai, China.
Lu-Tao DuDepartment of Clinical Laboratory, The Second Hospital, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, China.
Hua-Dong YanHepatology Department, Ningbo Hwamei Hospital, University of Chinese Academy of Sciences, Ningbo, Zhejiang, China.
Yu-Jin GaoXuzhou Infectious Diseases Hospital, Xuzhou, Jiangsu, China.
Hao WenState Key Laboratory of Pathogenesis, Prevention and Treatment of High Incidence Diseases in Central Asia, First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang, China.
Jing-Feng LiuThe United Innovation of Mengchao Hepatobiliary Technology Key Laboratory of Fujian Province, Mengchao Hepatobiliary Hospital of Fujian Medical University, Fuzhou, Fujian, China.
Min-Feng LiangThe Department of Infectious Disease, The First People's Hospital of Foshan, Foshan, Guangdong, China.
Fei KongThe First Hospital of Jilin University, Changchun, Jilin, China.
Jian SunDepartment of Infectious Diseases, Nanfang Hospital, Southern Medical University; Guangdong Provincial Key Laboratory for Prevention and Control of Major Liver Diseases; Guangdong Provincial Clinical Research Center for Viral Hepatitis; Key Laboratory of Infectious Diseases Research in South China, Ministry of Education, Guangzhou, Guangdong, China.
Sheng-Hong JuNurturing Center of Jiangsu Province for State Laboratory of AI Imaging & Interventional Radiology (Southeast University); Department of Radiology, Zhongda Hospital, Medical School of Southeast University, Nanjing, Jiangsu, China.
Hong-Yang WangInternational Cooperation Laboratory on Signal Transduction, National Center for Liver Cancer, Eastern Hepatobiliary Surgery Institute/Hospital, Shanghai, China.
Jin-Lin HouDepartment of Infectious Diseases, Nanfang Hospital, Southern Medical University; Guangdong Provincial Key Laboratory for Prevention and Control of Major Liver Diseases; Guangdong Provincial Clinical Research Center for Viral Hepatitis; Key Laboratory of Infectious Diseases Research in South China, Ministry of Education, Guangzhou, Guangdong, China.ORCID https://orcid.org/0000-0001-8230-8583

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aims: Given the high burden of hepatocellular carcinoma (HCC), risk stratification in patients with cirrhosis is critical but remains inadequate. In this study, we aimed to develop and validate an HCC prediction model by integrating radiomics and deep learning features from liver and spleen computed tomography (CT) images into the established age-male-ALBI-platelet (aMAP) clinical model. Methods: Patients were enrolled between 2018 and 2023 from a Chinese multicenter, prospective, observational cirrhosis cohort, all of whom underwent 3-phase contrast-enhanced abdominal CT scans at enrollment. The aMAP clinical score was calculated, and radiomic (PyRadiomics) and deep learning (ResNet-18) features were extracted from liver and spleen regions of interest. Feature selection was performed using the least absolute shrinkage and selection operator. Results: Among 2,411 patients (median follow-up: 42.7 months [IQR: 32.9-54.1]), 118 developed HCC (three-year cumulative incidence: 3.59%). Chronic hepatitis B virus infection was the main etiology, accounting for 91.5% of cases. The aMAP-CT model, which incorporates CT signatures, significantly outperformed existing models (area under the receiver-operating characteristic curve: 0.809-0.869 in three cohorts). It stratified patients into high-risk (three-year HCC incidence: 26.3%) and low-risk (1.7%) groups. Stepwise application (aMAP → aMAP-CT) further refined stratification (three-year incidences: 1.8% [93.0% of the cohort] vs. 27.2% [7.0%]). Conclusions: The aMAP-CT model improves HCC risk prediction by integrating CT-based liver and spleen signatures, enabling precise identification of high-risk cirrhosis patients. This approach personalizes surveillance strategies, potentially facilitating earlier detection and improved outcomes.

Indexed as

Deep learningHepatocellular carcinomaLiver cirrhosisMachine learningPrediction algorithmsRadiomics

Identifiers

PMID40951530
PMCPMC12422879

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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.