Zhang Xiaobing, Shan Huiguo, Pan Hongyu, Zhong Qian, Fang Qiang, Xu Yun, Liu Yun, Qu Shuping
Department of Hepatobiliary Surgery, Eastern Surgery Hospital, Second Military Medical University, Shanghai, China.
Department of Oncology, The Affiliated Hepatobiliary Dongtai Hospital of Jiangsu Vocational College of Medicine, Jiangsu, China.
Int J Biol Markers. 2025 Mar;40(1):55-66. doi: 10.1177/03936155251315500. Epub 2025 Mar 3.
BackgroundHepatobiliary cancers present a heterogeneous group of diseases, and molecular residual disease (MRD) evaluation based on circulating tumor DNA (ctDNA) is anticipated to offer greater sensitivity in monitoring disease progression than glycoprotein-based tumor markers such as alpha-fetoprotein or carbohydrate antigen 19-9 (CA199).MethodsThe panels for MRD surveillance were customized for each patient based on their specific genetic mutation characteristics. The changes in ctDNA mean variant allele frequencies (mVAF) and single nucleotide variants (SNVs) were analyzed from baseline to post-operative and between post-operative measurements.ResultsA unique tumor-informed whole-exome sequencing (WES) assay revealed significant variations in gene mutations between individuals. Among 63 cases, a total of 1952 SNVs were detected in tumor tissue from 63 patients using WES; only 6 loci (0.3%) were shared by at least 2 patients, indicating that over 95% of the 20-40 loci screened were unique to individual patients . Only 17 gene alterations were common to at least 2 patients, suggesting that alterations vary widely between individuals. The mVAF and the number of SNVs in ctDNA at baseline was dramatically higher than in first post-operative MRD (MRD1). The mVAF clearance was observed in three patients, whose ctDNA was positive at MRD1 but subsequently became negative at the second post-operative MRD (MRD2). Patients exhibiting vascular invasion demonstrated a significant increase in mVAF levels and SNV numbers. Furthermore, we revealed that mVAF levels were significantly associated with clinicopathologic characteristics, including gender, age, tumor subtype, stage, metastasis, vascular invasion, hepatitis B, liver cirrhosis, and tumor differentiation. Importantly, we have shown that the detection of an MRD-guided medication regimen modification is crucial to achieve clinical complete remission.ConclusionsThis study provided data supporting the use of a more reliable assay for MRD analysis in hepatobiliary cancers based on a tumor-informed assay. Dynamic monitoring of post-operative MRD is important for assessing disease progression, risk of recurrence, and response to treatment.
背景
肝胆癌是一组异质性疾病,基于循环肿瘤DNA(ctDNA)的分子残留疾病(MRD)评估有望在监测疾病进展方面比基于糖蛋白的肿瘤标志物(如甲胎蛋白或糖类抗原19-9(CA199))具有更高的敏感性。
方法
根据每位患者的特定基因突变特征定制MRD监测面板。分析从基线到术后以及术后测量之间ctDNA平均变异等位基因频率(mVAF)和单核苷酸变异(SNV)的变化。
结果
一种独特的肿瘤知情全外显子组测序(WES)检测显示个体之间基因突变存在显著差异。在63例病例中,使用WES在63例患者的肿瘤组织中总共检测到1952个SNV;至少2例患者共有6个位点(0.3%),这表明所筛查的20 - 40个位点中超过95%是个体患者特有的。至少2例患者共有仅17种基因改变,这表明个体之间的改变差异很大。基线时ctDNA中的mVAF和SNV数量显著高于首次术后MRD(MRD1)。在3例患者中观察到mVAF清除,其ctDNA在MRD1时为阳性,但随后在第二次术后MRD(MRD2)时变为阴性。表现出血管侵犯的患者mVAF水平和SNV数量显著增加。此外,我们发现mVAF水平与临床病理特征显著相关,包括性别、年龄、肿瘤亚型、分期、转移、血管侵犯、乙型肝炎、肝硬化和肿瘤分化。重要的是,我们已经表明检测MRD指导的药物治疗方案调整对于实现临床完全缓解至关重要。
结论
本研究提供的数据支持在肝胆癌中基于肿瘤知情检测使用更可靠的MRD分析检测方法。术后MRD的动态监测对于评估疾病进展、复发风险和治疗反应很重要。