Evaluating the predictive value of clinical models for HBV-related hepatocellular carcinoma: A meta-analysis.

IF 3.1 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Frontiers in Medicine Pub Date : 2025-02-21 eCollection Date: 2025-01-01 DOI:10.3389/fmed.2025.1529201
Long Huang, Luhuai Feng, Yang Lu, Bobin Hu, Hongqian Liang, Aoli Ren, Hang Wang, Wenming He, Caifang Deng, Minghua Su, Jianning Jiang
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Abstract

Objectives: Chronic viral hepatitis B (CHB) is a prevalent liver disease with primary hepatic carcinoma (HCC) as a severe complication. Clinical prediction models have gained attention for predicting HBV-related HCC (HBV-HCC). This study aimed to evaluate the predictive value of existing models for HBV-HCC through meta-analysis.

Design: Meta-analysis.

Data sources: Embase, PubMed, the Chinese Biomedical Literature Service System, and the Cochrane database were used for searches between 1970 and 2022.

Methods: A meta-analysis was conducted to assess original studies on HBV-HCC prediction models. The REACH-B, GAGHCC, and CUHCC models were externally validated in a Guangxi cohort. The C-index and calibration curve evaluated 5 years predictive performance, with subgroup analysis by region and risk bias.

Results: After screening, 27 research articles were included, covering the GAGHCC, REACH-B, PAGE-B, CU-HCC, CAMD, and mPAGE-B models. The meta-analysis indicated that these models had moderate discrimination in predicting HCC risk in HBV-infected patients, with C-index values from 0.75 to 0.82. The mPAGE-B (0.79, 95% CI: 0.79-0.80), GAG-HCC (0.80, 95% CI: 0.78-0.82), and CAMD (0.80, 95% CI: 0.78-0.81) models demonstrated better discrimination than others (P < 0.05), but most studies did not report model calibration. Subgroup analysis suggested that ethnicity and research bias might contribute to differences in model discrimination. Sensitivity analysis indicated stable meta-analysis results. The REACH-B, GAGHCC, CUHCC, PAGE-B, and mPAGE-B models had average predictive performance in Guangxi, with medium to low 3 and 5 years HCC risk prediction discrimination.

Conclusion: Existing models have predictive value for HBV-infected patients but show geographical limitations and reduced effectiveness in Guangxi.

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评估hbv相关肝细胞癌临床模型的预测价值:一项荟萃分析
目的:慢性乙型病毒性肝炎(CHB)是一种常见的肝脏疾病,原发性肝癌(HCC)是一种严重的并发症。临床预测模型在预测hbv相关性HCC (HBV-HCC)方面得到了广泛关注。本研究旨在通过荟萃分析评估现有模型对HBV-HCC的预测价值。设计:荟萃分析。数据来源:Embase、PubMed、中国生物医学文献服务系统和Cochrane数据库用于1970 - 2022年间的检索。方法:对HBV-HCC预测模型的原始研究进行荟萃分析。REACH-B、GAGHCC和CUHCC模型在广西队列中进行了外部验证。c指数和校准曲线评估了5年的预测性能,并按地区和风险偏差进行了亚组分析。结果:经筛选,共纳入研究文献27篇,涵盖了GAGHCC、REACH-B、PAGE-B、CU-HCC、CAMD和PAGE-B模型。荟萃分析表明,这些模型在预测hbv感染患者的HCC风险方面有中等程度的区别,c -指数值在0.75到0.82之间。mPAGE-B (0.79, 95% CI: 0.79-0.80)、GAG-HCC (0.80, 95% CI: 0.78-0.82)和CAMD (0.80, 95% CI: 0.78-0.81)模型的鉴别效果优于其他模型(P < 0.05),但大多数研究没有报告模型校准。亚组分析表明,种族和研究偏差可能导致模型歧视的差异。敏感性分析显示meta分析结果稳定。REACH-B、GAGHCC、CUHCC、PAGE-B和PAGE-B模型在广西的预测效果一般,3年和5年HCC风险预测判别中至低。结论:现有模型对乙型肝炎患者有一定的预测价值,但存在地域局限性,在广西的有效性较低。
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来源期刊
Frontiers in Medicine
Frontiers in Medicine Medicine-General Medicine
CiteScore
5.10
自引率
5.10%
发文量
3710
审稿时长
12 weeks
期刊介绍: Frontiers in Medicine publishes rigorously peer-reviewed research linking basic research to clinical practice and patient care, as well as translating scientific advances into new therapies and diagnostic tools. Led by an outstanding Editorial Board of international experts, this multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. In addition to papers that provide a link between basic research and clinical practice, a particular emphasis is given to studies that are directly relevant to patient care. In this spirit, the journal publishes the latest research results and medical knowledge that facilitate the translation of scientific advances into new therapies or diagnostic tools. The full listing of the Specialty Sections represented by Frontiers in Medicine is as listed below. As well as the established medical disciplines, Frontiers in Medicine is launching new sections that together will facilitate - the use of patient-reported outcomes under real world conditions - the exploitation of big data and the use of novel information and communication tools in the assessment of new medicines - the scientific bases for guidelines and decisions from regulatory authorities - access to medicinal products and medical devices worldwide - addressing the grand health challenges around the world
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