Mayer Stefanie, Schmidtke-Schrezenmeier Gerlinde, Buske Christian, Rücker Frank G, Barth Thomas F E, Möller Peter, Marienfeld Ralf
Institute of Pathology, University Medical Center Ulm, 89070 Ulm, Germany.
Department of Internal Medicine II, University Medical Center Ulm, 89070 Ulm, Germany.
Cancers (Basel). 2020 Jul 16;12(7):1917. doi: 10.3390/cancers12071917.
In non-small cell lung cancer (NSCLC) the usage of plasma-derived circulating tumor DNA (ctDNA) have come into focus to obtain a comprehensive genetic profile of a given lung cancer. Despite the usage of specific sampling tubes, archived plasma samples as well as inappropriately treated blood samples still cause a loss of information due to cell lysis and contamination with cellular DNA. Our aim was to establish a reliable protocol to rescue ctDNA from such non-informative samples to monitor the mutational landscape in NSCLC. As a proof-of-concept study we used archived plasma samples derived from whole blood EDTA samples of 51 patients suffering from NSCLC. Analysis of the isolated plasma DNA determined only a small fraction of ctDNA in a range of 90-250 bp. By applying a specific purification procedure, we were able to increase the informative ctDNA content and improve in a cohort of 42 patients the detection of driver mutations from 32% to 79% of the mutations found in tissue biopsies. Thus, we present here an easy to perform, time and cost effective procedure to rescue non-informative ctDNA samples, which is sufficient to detect oncogenic mutations in NGS approaches and is therefore a valuable technical improvement for laboratories handling liquid biopsy samples.
在非小细胞肺癌(NSCLC)中,血浆来源的循环肿瘤DNA(ctDNA)的应用已成为焦点,以获取特定肺癌的全面基因图谱。尽管使用了特定的采样管,但存档的血浆样本以及处理不当的血液样本仍会因细胞裂解和细胞DNA污染而导致信息丢失。我们的目标是建立一种可靠的方案,从此类无信息价值的样本中挽救ctDNA,以监测NSCLC中的突变情况。作为一项概念验证研究,我们使用了来自51例NSCLC患者全血EDTA样本的存档血浆样本。对分离出的血浆DNA进行分析,结果显示只有一小部分ctDNA,其大小在90 - 250 bp范围内。通过应用特定的纯化程序,我们能够提高有信息价值的ctDNA含量,并在42例患者中,将驱动突变的检测率从组织活检中发现的突变的32%提高到79%。因此,我们在此展示了一种易于执行、省时且经济高效的程序,用于挽救无信息价值的ctDNA样本,该程序足以在NGS方法中检测致癌突变,因此对于处理液体活检样本的实验室来说是一项有价值的技术改进。