基于肿瘤信息检测的分子残留病评估可预测肝胆癌的疾病进展和术后复发:初步研究。

IF 2.3 4区 医学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Xiaobing Zhang, Huiguo Shan, Hongyu Pan, Qian Zhong, Qiang Fang, Yun Xu, Yun Liu, Shuping Qu
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引用次数: 0

摘要

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)评估预计在监测疾病进展方面比基于糖蛋白的肿瘤标志物(如甲胎蛋白或碳水化合物抗原19-9 (CA199))提供更高的敏感性。方法:MRD监测面板是根据每个患者特定的基因突变特征定制的。分析ctDNA平均变异等位基因频率(mVAF)和单核苷酸变异(snv)的变化,从基线到术后以及术后测量之间。结果:一种独特的肿瘤信息全外显子组测序(WES)分析揭示了个体之间基因突变的显著差异。在63例患者中,WES共检测到63例肿瘤组织中存在1952个snv;只有6个基因座(0.3%)被至少2名患者共享,这表明在筛选的20-40个基因座中,95%以上是个体患者独有的。只有17个基因改变在至少2名患者中是共同的,这表明个体之间的改变差异很大。基线时ctDNA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,他们的ctDNA在MRD1中呈阳性,但随后在第二次术后MRD (MRD2)中变为阴性。出现血管侵犯的患者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指导的药物方案修改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基于肿瘤信息分析的更可靠的肝癌MRD分析方法的使用。动态监测术后MRD对于评估疾病进展、复发风险和治疗反应非常重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular residual disease assessment based on tumor-informed assay predict disease progression and postoperative recurrence of hepatobiliary cancer: A preliminary study.

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.

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来源期刊
International Journal of Biological Markers
International Journal of Biological Markers 医学-生物工程与应用微生物
CiteScore
4.10
自引率
0.00%
发文量
43
期刊介绍: IJBM is an international, online only, peer-reviewed Journal, which publishes original research and critical reviews primarily focused on cancer biomarkers. IJBM targets advanced topics regarding the application of biomarkers in oncology and is dedicated to solid tumors in adult subjects. The clinical scenarios of interests are screening and early diagnosis of cancer, prognostic assessment, prediction of the response to and monitoring of treatment.
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