Evidence map›Paper›PMID 40042093›Full record

ArticleCancer medicine2025

HBX Multi-Mutations Combined With Traditional Screening Indicators to Establish a Nomogram Contributes to Precisely Stratify the High-Risk Population of Hepatocellular Carcinoma.

Chao-Jun Zhang, Xiao-Mei Chen, Chang Yan, Rui-Bo Lv, Sanchun An, Yun-Xin Gao, Tian-Ren Huang, Wei Deng

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Article in Cancer medicine, 2025. 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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5 · Who and what money

Authors and funding

8 authors.

Chao-Jun ZhangDepartment of Experimental Research, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, China.
Xiao-Mei ChenDepartment of Experimental Research, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, China.
Chang YanDepartment of Radiation Oncology, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, People's Republic of China.
Rui-Bo LvDepartment of Experimental Research, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, China.
Sanchun AnDepartment of Experimental Research, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, China.
Yun-Xin GaoGuangdong Forevergen Medical Technology Co Ltd, Foshan, Guangdong, China.
Tian-Ren HuangDepartment of Experimental Research, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, China.
Wei DengDepartment of Experimental Research, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, China.ORCID https://orcid.org/0000-0003-0946-5579

Funding

1. National Natural Science Foundation of China 821606382. The Guangxi Natural Science Foundation 2021GXNSFAA2200943. The Guangxi Natural Science Foundation 2019GXNSFDA2450014. 2018 Guangxi One Thousand Young and Middle-aged College and University Backbone Teachers Cultivation Program (To Wei Deng) and Advanced Innovation Teams and Xinghu Scholars Program of Guangxi Medical University
6 · The paper itself

Abstract

backgroundHepatocellular carcinoma (HCC) is one of the most prevalent malignant tumors, often diagnosed at an advanced stage with limited treatment options and a poor prognosis. The present study aimed to identify the risk factors (RFs) for HCC and develop a nomogram incorporating dominant HBX mutations to predict the risk of HCC occurrence in high-risk (HR) populations.

methodsWe collected early HCC screening and monitoring factors from cohorts of HCC patients and HR populations, including gender, age, AFP, ALT, as well as hepatitis B virus (HBV) infection and mutation indicators such as hepatitis B surface antigen (HBsAg), HBV DNA replication level, HBV genotype, and high-frequency mutations in HBX. Independent predictive factors for HCC onset were determined through both univariate and multivariate logistic regression analyses. Two nomograms with and without HBX mutation data were established to predict the risk of HCC incidence in HR populations, and their performance was evaluated using calibration curves, receiver operating characteristic (ROC) curves, as well as decision curve analysis (DCA).

resultsA total of 312 participants were included. Independent RFs for HCC onset were identified as A1762T+G1764A multi-mutations, T1753C/G/A+A1762T+G1764A multi-mutations, and ALT > 40 U/L. The area under the curve (AUC) of the diagnostic nomogram with HBX mutation data was 0.835 in the training set and 0.869 in the testing set for the nomogram. Besides, the AUC of the diagnostic nomogram without HBX mutation data in the training set was 0.798 and 0.818 in the testing set. The calibration curve together with DCA indicated that the nomogram containing HBX mutation data had better predictive performance.

conclusionsThe established nomograms predicted the risk of HCC occurrence in HR populations with good accuracy, providing a valuable reference for precise stratification of HR populations and HCC screening.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsMutationNomogramsTrans-ActivatorsViral Regulatory and Accessory ProteinsAdultAgedEarly Detection of CancerFemaleHepatitis B virusHumansMaleMiddle AgedPrognosisRisk Assessmenthepatitis B virus X proteinTrans-ActivatorsViral Regulatory and Accessory ProteinsdiagnosticHBV mutationhepatocellular carcinomanomogrampredictive model

Identifiers

PMID40042093
PMCPMC11880911

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