Wang Dong, Xu Yaping, Goldstein Jennifer B, Ye Ke, Hu Xi, Xiao Liang, Li Lifeng, Chang Lianpeng, Guan Yanfang, Long Guo, He Qiongzhi, Yi Xin, Zhang Jianjun, Wang Zhiming, Xia Xuefeng, Zhou Ledu
Department of General Surgery, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Geneplus-Beijing Institute, Beijing, China.
Liver Int. 2020 Aug;40(8):1997-2007. doi: 10.1111/liv.14463. Epub 2020 May 23.
BACKGROUND & AIMS: Microvascular invasion (MVI) is a critical prognostic factor for operable hepatocellular carcinoma (HCC). This study aimed to explore the performance of circulating tumour DNA (ctDNA) in evaluating MVI status preoperatively.
Seventy-three HCC patients were enrolled and randomly divided into a training cohort and a validation cohort in a 2:1 ratio, and preoperative blood and surgical tissue samples were obtained. Genomic alterations were analysed using targeted deep sequencing with a 1021-gene panel.
In training cohort, 260 somatic mutations were identified in 40 blood samples (81.6%). CtDNA mutation was verified in paired tissue sample in 39 patients (97.5%). In univariate analysis, ctDNA allele frequency (AF) and largest tumour diameter were associated with the presence of MVI, but ctDNA AF was the only independent risk factor in multivariate analysis. With the cut-off value of 0.83%, ctDNA AF determined the presence of MVI with the sensitivity of 89.7% and specificity of 80.0% in the training cohort, and the sensitivity of 78.6% and the specificity of 81.8% in the validation cohort. In preoperative evaluation, ctDNA AF, AFP level and BCLC staging were associated with recurrence-free survival in both univariate and multivariate analysis.
CtDNA can serve as an independent risk factor of MVI for operable HCC and help determining precise treatment strategies. The integration of ctDNA in the management of operable HCC may achieve better clinical outcomes.
微血管侵犯(MVI)是可手术切除肝细胞癌(HCC)的关键预后因素。本研究旨在探讨循环肿瘤DNA(ctDNA)在术前评估MVI状态中的表现。
纳入73例HCC患者,并按2:1的比例随机分为训练队列和验证队列,获取术前血液和手术组织样本。使用包含1021个基因的靶向深度测序分析基因组改变。
在训练队列中,40份血液样本(81.6%)中鉴定出260个体细胞突变。39例患者(97.5%)的配对组织样本中验证了ctDNA突变。单因素分析中,ctDNA等位基因频率(AF)和最大肿瘤直径与MVI的存在相关,但多因素分析中ctDNA AF是唯一的独立危险因素。以0.83%为临界值,ctDNA AF在训练队列中确定MVI存在的敏感性为89.7%,特异性为80.0%,在验证队列中敏感性为78.6%,特异性为81.8%。在术前评估中,单因素和多因素分析均显示ctDNA AF、甲胎蛋白(AFP)水平和BCLC分期与无复发生存相关。
CtDNA可作为可手术切除HCC中MVI的独立危险因素,并有助于确定精确的治疗策略。将ctDNA纳入可手术切除HCC的管理中可能会取得更好的临床结果。