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Differences in the genomic profiles of cell‐free DNA between plasma sputum urine and tumor tissue in advanced NSCLC

机译:晚期NSCLC患者血浆痰液尿液和肿瘤组织之间无细胞DNA的基因组谱差异

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摘要

Liquid biopsy has provided an efficient way for detection of gene alterations in advanced non‐small‐cell lung cancer (NSCLC). However, the correlation between systematic determination of somatic genomic alterations in liquid biopsy and tumor biopsy still remained unclear, and the concordance rate between cell‐free DNA (cfDNA) and matched tumor tissue DNA needs to be increased. A prospective study was performed to detect differences in genetic profiles of cfDNA in sputum, plasma, urine, and tumor tissue from 50 advanced NSCLC patients in parallel by the same next‐generation sequencing (NGS) platform. Driver genes alterations were identified in cfDNA sample and matched tumor sample, with an overall concordance rate of 86% in plasma cfDNA, 74% in sputum cfDNA, 70% in urine cfDNA, and 90% in cfDNA of combination of plasma, sputum, and urine. And the concordant rate of cfDNA in sputum in patients with smoking history was higher than that in patients without history of smoking (89% vs. 66%, P = 0.033) and equal to that in plasma cfDNA of the smoking patients (89% vs. 89%). In conclusion, sputum cfDNA can be considered as an alternative medium to liquid biopsy, while the complementarity of genomic profiles in cfDNA among plasma, sputum, and urine was beneficial to detect more diver genes alterations and improve the utility of liquid biopsy in advanced NSCLC (Liquid Biopsy for Detection of Driver Mutation in NSCLC; ).
机译:液体活检为检测晚期非小细胞肺癌(NSCLC)基因改变提供了一种有效的方法。然而,液体活检中的体细胞基因组改变的系统确定与肿瘤活检之间的相关性仍不清楚,并且无细胞DNA(cfDNA)与匹配的肿瘤组织DNA之间的一致性比率需要提高。进行了一项前瞻性研究,以通过相同的下一代测序(NGS)平台并行检测50例晚期NSCLC患者的痰,血浆,尿液和肿瘤组织中cfDNA的遗传谱差异。在cfDNA样本和匹配的肿瘤样本中鉴定出驱动基因的改变,血浆cfDNA的总一致性率为86%,痰cfDNA的总体一致性为74%,尿cfDNA的总体一致性为70%,cfDNA的总一致性率为90%。尿。有吸烟史的患者痰中cfDNA的一致率高于无吸烟史的患者(89%vs.66%,P = 0.033),与吸烟患者的血浆cfDNA一致(89%vs. 89%)。总之,痰cfDNA可被视为液体活检的替代培养基,而血浆,痰和尿液中cfDNA中的基因组图谱的互补性有助于检测更多的潜水员基因改变并提高液体活检在晚期NSCLC中的效用(液体活检以检测NSCLC中的驱动程序突变;)。

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