Chen Kun, Wang Junxiao, Jiang Liping, Zhao Fei, Zhang Ruochan, Wu Zhiyuan, Wang Dongmei, Jiao Yuchen, Xie Hui, Qu Chunfeng
State Key Lab of Molecular Oncology, Department of Immunology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Senior Department of Oncology, Fifth Medical Center of Chinese PLA General Hospital, Beijing, China.
J Clin Transl Hepatol. 2024 Jun 28;12(6):551-561. doi: 10.14218/JCTH.2023.00559. Epub 2024 May 20.
Hepatocellular carcinoma (HCC) cases with small nodules are commonly treated with radiofrequency ablation (RFA), but the recurrence rate remains high. This study aimed to establish a blood signature for identifying HCC with metastatic traits pre-RFA.
Data from HCC patients treated between 2010 and 2017 were retrospectively collected. A blood signature for metastatic HCC was established based on blood levels of alpha-fetoprotein and des-γ-carboxy-prothrombin, cell-free DNA (cfDNA) mutations, and methylation changes in target genes in frozen-stored plasma samples that were collected before RFA performance. The HCC blood signature was validated in patients prospectively enrolled in 2021.
Of 251 HCC patients in the retrospective study, 33.9% experienced recurrence within 1 year post-RFA. The HCC blood signature identified from these patients included des-γ-carboxy-prothrombin ≥40 mAU/mL with cfDNA mutation score, where cfDNA mutations occurred in the genes of and promoter. This signature effectively predicted 1-year post-RFA recurrence of HCC with 92% specificity and 91% sensitivity in the retrospective dataset, and with 87% specificity and 76% sensitivity in the prospective dataset (n=32 patients). Among 14 cases in the prospective study with biopsy tissues available, positivity for the HCC blood signature was associated with a higher HCC tissue score and shorter distance between HCC cells and microvasculature.
This study established an HCC blood signature in pre-RFA blood that potentially reflects HCC with metastatic traits and may be valuable for predicting the disease's early recurrence post-RFA.
小肝癌结节病例通常采用射频消融(RFA)治疗,但复发率仍然很高。本研究旨在建立一种血液标志物,用于在RFA术前识别具有转移特征的肝癌。
回顾性收集2010年至2017年接受治疗的肝癌患者的数据。基于甲胎蛋白和脱γ-羧基凝血酶原的血液水平、游离DNA(cfDNA)突变以及RFA术前采集的冷冻保存血浆样本中靶基因的甲基化变化,建立转移性肝癌的血液标志物。2021年对前瞻性纳入的患者进行了肝癌血液标志物验证。
在回顾性研究的251例肝癌患者中,33.9%在RFA术后1年内复发。从这些患者中识别出的肝癌血液标志物包括脱γ-羧基凝血酶原≥40 mAU/mL以及cfDNA突变评分,其中cfDNA突变发生在 和 启动子基因中。该标志物在回顾性数据集中有效预测了肝癌RFA术后1年复发情况,特异性为92%,敏感性为91%;在前瞻性数据集中(n = 32例患者),特异性为87%,敏感性为76%。在前瞻性研究中有活检组织的14例病例中,肝癌血液标志物阳性与较高的肝癌组织评分以及肝癌细胞与微血管之间较短的距离相关。
本研究在RFA术前血液中建立了一种肝癌血液标志物,其可能反映具有转移特征的肝癌,对预测RFA术后疾病早期复发可能具有重要价值。