首页> 外文期刊>Lung cancer: Journal of the International Association for the Study of Lung Cancer >Identification and monitoring of somatic mutations in circulating cell-free tumor DNA in lung cancer patients
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Identification and monitoring of somatic mutations in circulating cell-free tumor DNA in lung cancer patients

机译:肺癌患者循环无细胞肿瘤DNA中体细胞突变的鉴定与监测

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Objectives: Circulating cell-free tumor DNA (ctDNA) isolated from the peripheral blood of non-small-cell lung cancer (NSCLC) patients provides biomarkers for both therapeutic target selection, particularly when direct tumor biopsy is unfeasible, and also for drug resistance monitoring. This study evaluates the reliability and feasibility of ctDNA analysis in an in-house clinical molecular diagnostic workflow.Materials and methods: Mutation profiling by both standard methods and Next-Generation sequencing (NGS) was carried out and compared on 2 independent lung cancer patient cohorts. Cohort 1 consisted of 50 EGFR-mutated NSCLC patients, established on tumour biopsy, for whom ctDNA was collected at disease progression after TKI-inhibitor treatment and could be used to monitor drug resistance. Cohort 2 consisted of 50 newly diagnosed lung cancer patients for whom tumour biopsy was not possible and only ctDNA was available, providing the possibility of biomarker identification.Results: ctDNA analysis of Cohort 1 verified the persistence of the tumour-detected EGFR activating mutation at disease progression by both standard and NGS methods, in 84% and 92% of the cases respectively. The T790M EGFR resistance mutation was identified in 71% of the ctDNA EGFR mutated samples providing vital information for their disease management. In newly diagnosed Cohort 2 patients, EGFR activating mutations were detected in 16% of the patients by both standard and NGS analysis of ctDNA in peripheral blood, providing indication to targeted-therapy otherwise unavailable for this group of patients.Conclusion: The presented study investigated lung cancer ctDNA analysis, comparing conventional methods versus NGS sequencing, and demonstrated the successful use of plasma ctDNA as a template for targeted NGS tumor gene panel in an in-house routine clinical practice. More importantly, these data underline the advantages of the clinical application of ctDNA NGS analysis for identification of therapeutic targets, real-time monitoring of therapy, and resistance mechanisms in lung cancer patients.
机译:目标:从非小细胞肺癌(NSCLC)患者的外周血中分离的循环无细胞肿瘤DNA(CTDNA)为治疗目标选择提供生物标志物,特别是当直接肿瘤活组织检查是不可行的,并且还用于耐药性监测。该研究评估了CTDNA分析在内部临床分子诊断工作流程中的可靠性和可行性。通过标准方法和下一代测序(NGS)进行突变分析,并在2名独立的肺癌患者队列中进行比较。群组1由50名EGFR-突变的NSCLC患者组成,在TKI抑制剂治疗后在疾病进展中收集CTDNA,可用于监测耐药性。队列2由50名新诊断的肺癌患者组成,该患者不可能,只有CTDNA可获得,提供生物标志物鉴定的可能性。结果:CTDNA分析群组1验证了肿瘤检测到的EGFR激活突变在疾病中持续存在标准和NGS方法的进展分别为84%和92%的病例。在71%的CTDNA EGFR突变样本中鉴定了T790M EGFR抗性突变,为其疾病管理提供重要信息。在新诊断的群组患者中,通过标准和NGS分析在外周血中的标准和NGS分析中检测到EGFR活化突变,以靶向治疗的标准和NGS分析,为本患者提供靶向治疗的指示。结论:所提出的研究肺癌CTDNA分析,比较常规方法与NGS测序,并证明了在内部常规临床实践中成功地使用血浆CTDNA作为靶向NGS肿瘤基因面板的模板。更重要的是,这些数据强调了CTDNA NGS分析鉴定治疗靶标的临床应用的优点,肺癌患者的实时监测和抗性机制。

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