Department of Epidemiology and Health Statistics, School of Public Health, Southeast University, Nanjing, China.
Key Laboratory of Environmental Medicine Engineering, Ministry of Education, School of Public Health, Southeast University, Nanjing, China.
Can J Gastroenterol Hepatol. 2021 Aug 2;2021:9996358. doi: 10.1155/2021/9996358. eCollection 2021.
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.
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.
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).
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.
乙型肝炎慢性(CHB)患者肝细胞癌(HCC)风险预测模型的性能不确定。本研究旨在通过系统综述和荟萃分析,批判性地评估这些预测模型透明和外部验证性能的报告。
截至 2020 年 10 月 17 日,对 Web of Science 和 PubMed 进行了系统检索,以寻找已发表的研究。使用预测个体预后或诊断的多变量模型的透明报告(TRIPOD)工具来批判性地评估六个模型(CU-HCC、GAG-HCC、PAGE-B、mPAGE-B、REACH-B 和 mREACH-B)的外部验证报告的质量。基于荟萃分析,计算受试者工作特征曲线下面积(AUC)值以估计汇总的外部验证性能。还进行了亚组分析和荟萃回归以探索异质性。
我们的荟萃分析纳入了 2011 年至 2020 年期间发表的 22 项研究。纳入研究对 TRIPOD 的依从性为 59%至 90%(中位数,74%;四分位距(IQR),70%,79%)。六个模型的 AUC 值范围为 0.715 至 0.778。在抗病毒治疗亚组中,mREACH-B、GAG-HCC 和 mPAGE-B 的 AUC 值分别为 0.785、0.760 和 0.778。在肝硬化亚组中,所有模型的区分性能均较差(AUC<0.7)。
充分报告校准和缺失值的处理情况将有助于提高 CHB 相关 HCC 风险预测的外部验证报告的质量。有必要为肝硬化患者开发特定的 HCC 风险预测模型。