Papatheodoridi Alkistis, Lekakis Vasileios, Chatzigeorgiou Antonios, Papatheodoridis George
Department of Clinical Therapeutics, Medical School of National and Kapodistrian University of Athens, "Alexandra" General Hospital of Athens, 11528 Athens, Greece.
First Department of Gastroenterology, Medical School of National and Kapodistrian University of Athens, General Hospital of Athens "Laiko", 11527 Athens, Greece.
Cancers (Basel). 2025 Mar 20;17(6):1042. doi: 10.3390/cancers17061042.
Circulating cell-free DNA (cfDNA) has emerged as a compelling candidate of liquid biopsy markers for the diagnosis and prognosis of several cancers. We systematically reviewed data on the role of cfDNA markers in the diagnosis, prognosis and treatment of hepatocellular carcinoma (HCC). Early studies suggested that levels of circulating cfDNA, mitochondrial DNA and cfDNA integrity are higher in patients with HCC than chronic liver diseases. In subsequent studies, methylation changes in circulating tumor DNA (ctDNA) as well as cfDNA fragmentation patterns and circulating nucleosomes were found to offer high sensitivity (>60%) and excellent specificity (>90%) for HCC diagnosis. The predictive role of cfDNA markers and ctDNA has been assessed in a few studies including untreated patients with HCC providing promising results for prediction of survival. However, port-hepatectomy detection of cfDNA/ctDNA markers or copy number variation indicators of cfDNA seem to reflect minimum residual disease and thus a high risk for HCC recurrence. The same markers can be useful for prediction after transarterial chemoembolization, radiofrequency ablation, radiotherapy and even systemic therapies. In conclusion, cfDNA markers can be useful in HCC surveillance, improving early diagnosis rates, as well as for monitoring treatment effectiveness and minimal residual disease post-treatment.
循环游离DNA(cfDNA)已成为多种癌症诊断和预后的液体活检标志物的有力候选者。我们系统地回顾了cfDNA标志物在肝细胞癌(HCC)诊断、预后和治疗中的作用的数据。早期研究表明,HCC患者的循环cfDNA、线粒体DNA水平和cfDNA完整性高于慢性肝病患者。在随后的研究中,发现循环肿瘤DNA(ctDNA)的甲基化变化以及cfDNA片段化模式和循环核小体对HCC诊断具有高灵敏度(>60%)和出色的特异性(>90%)。cfDNA标志物和ctDNA的预测作用已在一些研究中进行了评估,包括未经治疗的HCC患者,为生存预测提供了有前景的结果。然而,肝切除术后对cfDNA/ctDNA标志物或cfDNA拷贝数变异指标的检测似乎反映了最小残留疾病,因此HCC复发风险很高。相同的标志物可用于经动脉化疗栓塞、射频消融、放疗甚至全身治疗后的预测。总之,cfDNA标志物可用于HCC监测,提高早期诊断率,以及监测治疗效果和治疗后最小残留疾病。