Jaber Fouad, El-Serag Hashem B
Department of Internal Medicine, Section of Gastroenterology and Hepatology, Baylor College of Medicine, Houston, Texas, USA.
Hepat Oncol. 2025 Dec;12(1):2494446. doi: 10.1080/20450923.2025.2494446. Epub 2025 Apr 30.
This was a narrative review of select studies published through September of 2024. We review the shift toward multi-dimensional scores such as HCC early detection screening (HES), GALAD, ASAP, and mt-HBT represents a significant advancement in biomarker research for hepatocellular carcinoma (HCC) detection. Unlike single biomarker approaches, these scores integrate various clinical and biochemical factors to enhance predictive accuracy by reflecting different complementary aspects of disease progression and HCC oncogenesis. Proper testing and validation of biomarker scores in phase 3 biomarker studies is essential before wide use can be recommended. We also review the comparative performance of biomarker scores in phase 3 studies. The new version of HES (HES V2.0) which includes AFP, AFP L3, DCP, and changes in their levels the past one year, if available, in addition to age, platelets, albumin, ALT and underlying liver disease etiology outperforms GALAD in detecting early-stage HCC with overall 6.7% higher sensitivity, and ASAP with 13.4%-18.0% higher sensitivity, both at fixed 90% specificity. HES V2.0 is a leading candidate biomarker score for prospective testing in clinical studies of early HCC detection.
这是一篇对截至2024年9月发表的部分研究的叙述性综述。我们回顾了向多维评分的转变,如肝癌早期检测筛查(HES)、GALAD、ASAP和线粒体乙肝病毒检测(mt-HBT),这代表了肝细胞癌(HCC)检测生物标志物研究的重大进展。与单一生物标志物方法不同,这些评分整合了各种临床和生化因素,通过反映疾病进展和HCC肿瘤发生的不同互补方面来提高预测准确性。在推荐广泛使用之前,在3期生物标志物研究中对生物标志物评分进行适当的测试和验证至关重要。我们还回顾了3期研究中生物标志物评分的比较性能。新版HES(HES V2.0)除了纳入年龄、血小板、白蛋白、谷丙转氨酶(ALT)和潜在肝病病因外,还包括甲胎蛋白(AFP)、甲胎蛋白异质体L3(AFP L3)、异常凝血酶原(DCP)及其过去一年水平的变化(如果可用),在检测早期HCC方面优于GALAD,总体灵敏度高6.7%,优于ASAP,灵敏度高13.4%-18.0%,两者特异性均固定为90%。HES V2.0是早期HCC检测临床研究中进行前瞻性测试的领先候选生物标志物评分。