Gastroenterology Unit, National Institute of Gastroenterology-IRCCS "Saverio de Bellis", Castellana Grotte, 70013 Bari, Italy.
National Institute of Gastroenterology-IRCCS "Saverio de Bellis", Castellana Grotte, 70013 Bari, Italy.
Int J Mol Sci. 2023 Feb 21;24(5):4286. doi: 10.3390/ijms24054286.
The most common primary liver cancer is hepatocellular carcinoma (HCC), and its mortality rate is increasing globally. The overall 5-year survival of patients with liver cancer is currently 10-20%. Moreover, because early diagnosis can significantly improve prognosis, which is highly correlated with tumor stage, early detection of HCC is critical. International guidelines advise using α-FP biomarker with/without ultrasonography for HCC surveillance in patients with advanced liver disease. However, traditional biomarkers are sub-optimal for risk stratification of HCC development in high-risk populations, early diagnosis, prognostication, and treatment response prediction. Since about 20% of HCCs do not produce α-FP due to its biological diversity, combining α-FP with novel biomarkers can enhance HCC detection sensitivity. There is a chance to offer promising cancer management methods in high-risk populations by utilizing HCC screening strategies derived from new tumor biomarkers and prognostic scores created by combining biomarkers with distinct clinical parameters. Despite numerous efforts to identify molecules as potential biomarkers, there is no single ideal marker in HCC. When combined with other clinical parameters, the detection of some biomarkers has higher sensitivity and specificity in comparison with a single biomarker. Therefore, newer biomarkers and models, such as the Lens culinaris agglutinin-reactive fraction of Alpha-fetoprotein (α-FP), α-FP-L3, Des-γ-carboxy-prothrombin (DCP or PIVKA-II), and the GALAD score, are being used more frequently in the diagnosis and prognosis of HCC. Notably, the GALAD algorithm was effective in HCC prevention, particularly for cirrhotic patients, regardless of the cause of their liver disease. Although the role of these biomarkers in surveillance is still being researched, they may provide a more practical alternative to traditional imaging-based surveillance. Finally, looking for new diagnostic/surveillance tools may help improve patients' survival. This review discusses the current roles of the most used biomarkers and prognostic scores that may aid in the clinical management of HCC patients.
最常见的原发性肝癌是肝细胞癌(HCC),其全球死亡率正在上升。目前,肝癌患者的总体 5 年生存率为 10-20%。此外,由于早期诊断可以显著改善预后,而预后与肿瘤分期高度相关,因此早期发现 HCC 至关重要。国际指南建议在晚期肝病患者中使用 α-FP 生物标志物联合/不联合超声进行 HCC 监测。然而,传统生物标志物在高危人群中 HCC 发展的风险分层、早期诊断、预后和治疗反应预测方面并不理想。由于 HCC 的生物多样性,约 20%的 HCC 不产生 α-FP,因此结合 α-FP 与新型生物标志物可以提高 HCC 的检测灵敏度。通过利用源自新型肿瘤生物标志物的 HCC 筛查策略和结合具有不同临床参数的生物标志物创建的预后评分,为高危人群提供有前景的癌症管理方法是有机会的。尽管已经做出了许多努力来鉴定潜在的生物标志物分子,但在 HCC 中没有单一的理想标志物。与单一生物标志物相比,一些生物标志物的联合检测在诊断中的灵敏度和特异性更高。因此,新型生物标志物和模型,如 Lens culinaris agglutinin-reactive fraction of Alpha-fetoprotein (α-FP)、α-FP-L3、Des-γ-carboxy-prothrombin (DCP 或 PIVKA-II) 和 GALAD 评分,在 HCC 的诊断和预后中得到了更频繁的应用。值得注意的是,GALAD 算法在 HCC 预防中非常有效,特别是对于肝硬化患者,无论其肝病的病因如何。尽管这些生物标志物在监测中的作用仍在研究中,但它们可能为基于传统成像的监测提供更实用的替代方法。最后,寻找新的诊断/监测工具可能有助于改善患者的生存率。本文讨论了目前使用最广泛的生物标志物和预后评分的作用,这些标志物和评分可能有助于 HCC 患者的临床管理。