首页> 美国卫生研究院文献>Balkan Journal of Medical Genetics : BJMG >Results of Liquid Biopsy Studies by Next Generation Sequencing in Patients with Advanced Stage Non-small Cell Lung Cancer: Single Center Experience from Turkey
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Results of Liquid Biopsy Studies by Next Generation Sequencing in Patients with Advanced Stage Non-small Cell Lung Cancer: Single Center Experience from Turkey

机译:晚期非小细胞肺癌患者通过下一代测序进行液体活检研究的结果:来自土耳其的单中心经验

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摘要

Several studies demonstrated the utility of plasma-based cell-free circulating tumor DNA (ccfDNA) in determination of mutations in non-small cell lung cancer (NSCLC). We aimed to report our results of next generation sequencing (NGS) using liquid biopsy in patients with NSCLC. Patients with advanced stage NSCLC were enrolled and their genomic profiling results were recorded. Next generation sequencing targeted panel includes 19 hot-spot genes. The plasma was separated from the peripheral blood sample and ccfDNAs were isolated for NGS. We performed genomic profiling in 100 patients (20 females and 80 males) with a median age of 59.3 (range 26-79). A second liquid biopsy was performed in eight patients who developed progressive disease after the first treatment. The study population had adenocarcinoma (AC) ( = 73), squamous cell carcinoma (SCC) ( = 14), or NSCLC-NOS (not otherwise specified) ( = 13). In the SCC group, three of 14 patients had variants on and genes. In the AC and NSCLC-NOS groups, 39 out of 86 patients (45.3%) had variants. The most common one was in the gene ( = 27, 31.4%) including seven mutations related to drug resistance and two were polymorphisms. Three patients had both driver and resistance mutations ( T790M, = 2; exon 2 G12S and exon 14 E1012K, = 1). Fifteen patients (17.4%) had an activating mutation and eight patients (9.3%) had variants in the gene. We reported our results regarding genomic profiling related to treatment using liquid biopsy in patients with NSCLC. Advantages of this method are the non invasiveness and reproducibility.
机译:几项研究证明了基于血浆的无细胞循环肿瘤DNA(ccfDNA)在确定非小细胞肺癌(NSCLC)突变中的效用。我们旨在报告我们使用液体活检对NSCLC患者进行下一代测序(NGS)的结果。晚期NSCLC患者入组并记录其基因组分析结果。下一代测序靶向专家组包括19个热点基因。从外周血样品中分离血浆,并分离出用于cfgDNA的NGS。我们对100位患者(20位女性和80位男性)进行了基因组分析,中位年龄为59.3(范围26-79)。在第一次治疗后发生进展性疾病的八名患者中进行了第二次液体活检。研究人群患有腺癌(AC)(= 73),鳞状细胞癌(SCC)(= 14)或NSCLC-NOS(未另作说明)(= 13)。在SCC组中,每14例患者中有3例具有on和基因变异。在AC和NSCLC-NOS组中,有86名患者中有39名(45.3%)有变异。最常见的是该基因(= 27,占31.4%),包括与耐药性有关的七个突变,两个是多态性。三名患者同时具有驱动程序和抵抗力突变(T790M,= 2;外显子2 G12S和外显子14 E1012K,= 1)。 15名患者(17.4%)具有激活突变,而8名患者(9.3%)具有基因变异。我们报告了有关使用液体活检治疗NSCLC患者相关基因组分析的结果。这种方法的优点是无创性和可重复性。

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