Abstract

Background The performance of risk prediction models for hepatocellular carcinoma (HCC) in patients with chronic hepatitis B (CHB) was uncertain. The aim of the study was to critically evaluate the reports of transparent and external validation performances of these prediction models based on system review and meta-analysis. Methods A systematic search of the Web of Science and PubMed was performed for studies published until October 17, 2020. The transparent reporting of a multivariable prediction model for the individual prognosis or diagnosis (TRIPOD) tool was used to critically evaluate the quality of external validation reports for six models (CU-HCC, GAG-HCC, PAGE-B, mPAGE-B, REACH-B, and mREACH-B). The area under the receiver operator characteristic curve (AUC) values was to estimate the pooled external validating performance based on meta-analysis. Subgroup analysis and metaregression were also performed to explore heterogeneity. Results Our meta-analysis included 22 studies published between 2011 and 2020. The compliance of the included studies to TRIPOD ranged from 59% to 90% (median, 74%; interquartile range (IQR), 70%, 79%). The AUC values of the six models ranged from 0.715 to 0.778. In the antiviral therapy subgroups, the AUC values of mREACH-B, GAG-HCC, and mPAGE-B were 0.785, 0.760, and 0.778, respectively. In the cirrhosis subgroup, all models had poor discrimination performance (AUC < 0.7). Conclusions A full report of calibration and handling of missing values would contribute to a greater improvement in the quality of external validation reports for CHB-related HCC risk prediction. It was necessary to develop a specific HCC risk prediction model for patients with cirrhosis.

Highlights

  • Hepatitis B virus (HBV) was one of the crucial causes of hepatocellular carcinoma (HCC), accounting for approximately 50% of all cases of HCC [1, 2]

  • Most of them received antiviral therapy during the follow-up period, including nucleotides, interferon, and lamivudine. e setting of all included studies was limited to hospitals. e median sample size was 1000 (interquartile range (IQR): 557, 1505)

  • Using the TRIPOD tool, we found that the compliance of these studies to items of TRIPOD was at a medium level

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Summary

Introduction

Hepatitis B virus (HBV) was one of the crucial causes of hepatocellular carcinoma (HCC), accounting for approximately 50% of all cases of HCC [1, 2]. It was noteworthy that the incidence of CHB-related HCC was increasing, especially in Western countries [5]. If HCC can be diagnosed earlier in the monitoring process, the diversity of treatment options and the probability of cure would be higher and the long-term prognosis would certainly be improved. Risk prediction models had a long history in being used for predicting the incidence of HCC in patients with CHB. E highly popular and recognized models were as follows: CU-HCC, GAG-HCC, PAGE-B, mPAGE-B, REACH-B, and mREACH-B [6, 7]. Existing models have been developed in different settings, such as untreated patients, receiving antiviral therapy patients, and mixed patients. Published guidelines seldom provided standard methods to assess HCC risk prediction in patients with CHB [8,9,10].

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