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A Competent Hepatocyte Model Examining Hepatitis B Virus Entry through Sodium Taurocholate Cotransporting Polypeptide as a Therapeutic Target
Published on: May 10, 2022
Prediction models of hepatocellular carcinoma development in chronic hepatitis B patients
1Hye Won Lee, Sang Hoon Ahn, Department of Internal Medicine, Yonsei University College of Medicine, Seoul 03722, South Korea.
Insights
Identifying hepatocellular carcinoma (HCC) risk in chronic hepatitis B (CHB) patients is crucial. This review summarizes HCC prediction models and introduces new noninvasive scoring systems for better patient management.
Area of Science:
- Hepatology and Viral Hepatitis Research
- Oncology and Cancer Risk Prediction
- Medical Diagnostics and Biomarkers
Background:
- Chronic hepatitis B virus (HBV) infection is a leading cause of liver cirrhosis and hepatocellular carcinoma (HCC).
- Universal antiviral therapy and HCC surveillance strategies for all chronic hepatitis B (CHB) patients are globally burdensome.
- Accurate risk stratification is essential for effective CHB patient management and resource allocation.
Purpose of the Study:
- To review existing and novel HCC prediction models for CHB patients.
- To identify tools for classifying HCC development risk in CHB.
- To introduce noninvasive scoring systems incorporating liver stiffness for fibrosis assessment.
Main Methods:
- Systematic review and summarization of established HCC risk scores (IPM, CU-HCC, GAG-HCC, NGM-HCC, REACH-B, Page-B).
- Introduction of new scoring systems utilizing liver stiffness measurements (LSM) from transient elastography.
- Inclusion of models like LSM-HCC and modified REACH-B (mREACH-B) for noninvasive fibrosis assessment.
Main Results:
- Existing HCC risk scores, primarily validated in treatment-naïve Asian CHB patients, demonstrate high negative predictive values (≥95%).
- Novel models incorporating liver stiffness measurements offer noninvasive alternatives for fibrosis and HCC risk assessment.
- The study highlights a range of predictive tools, from traditional risk factors to advanced elastography-based scores.
Conclusions:
- Accurate prediction of HCC risk in CHB patients is vital for personalized management.
- A variety of validated HCC prediction models exist, with ongoing development of noninvasive tools.
- New scoring systems integrating liver stiffness show promise for improved, noninvasive risk stratification in CHB.
Abstract:
Chronic hepatitis B virus (HBV) infection is a major cause of cirrhosis and hepatocellular carcinoma (HCC). Applying the same strategies for antiviral therapy and HCC surveillance to all chronic hepatitis B (CHB) patients would be a burden worldwide. To properly manage CHB patients, it is necessary to identify and classify the risk for HCC development in such patients. Several HCC risk scores based on risk factors such as cirrhosis, age, male gender, and high viral load have been used, and have negative predictive values of ≥ 95%. Most of these have been derived from, and internally validated in, treatment-naïve Asian CHB patients. Herein, we summarized various HCC prediction models, including IPM (Individual Prediction Model), CU-HCC (Chinese University-HCC), GAG-HCC (Guide with Age, Gender, HBV DNA, Core Promoter Mutations and Cirrhosis-HCC), NGM-HCC (Nomogram-HCC), REACH-B (Risk Estimation for Hepatocellular Carcinoma in Chronic Hepatitis B), and Page-B score. To develop a noninvasive test of liver fibrosis, we also introduced a new scoring system that uses liver stiffness values from transient elastography, including an LSM (Liver Stiffness Measurement)-based model, LSM-HCC, and mREACH-B (modified REACH-B).
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