Mellert Hestia, Reese Jordan, Jackson Leisa, Maxwell Victoria, Tschida Chérie, Pestano Gary A
Biodesix Inc., 2970 Wilderness Place Suite 100, Boulder, CO 80301, USA.
Diagnostics (Basel). 2021 Jan 21;11(2):155. doi: 10.3390/diagnostics11020155.
Liquid biopsy tests have become an integral part of the molecular diagnosis of patients with non-small cell lung cancer (NSCLC). We describe a new test panel that uses very low input (20 ng) of cell-free nucleic acids extracted from human plasma, which is designed to yield results in less than 72 h. In this study, we performed novel amplicon-based targeted next-generation sequencing with a semiconductor-based system, the Ion GeneStudio S5 Prime. The analytic performance of the assay was evaluated using contrived and retrospectively collected clinical specimens. The cumulative percent coefficient of variation for the new test process was very precise at 8.4% for inter-day, 4.0% for inter-operator and 3.4% for inter-instrument. We also observed significant agreement (95.7-100%) with an orthogonal, high-sensitivity droplet digital™ Polymerase Chain Reaction (ddPCR) test. This method offers a valuable supplement to assessing targeted mutations from blood while conserving specimens and maintaining sensitivity, with rapid turn-around times to actionable results.
液体活检检测已成为非小细胞肺癌(NSCLC)患者分子诊断的一个组成部分。我们描述了一种新的检测方法,该方法使用从人血浆中提取的极低输入量(20 ng)的游离核酸,旨在在不到72小时内得出结果。在本研究中,我们使用基于半导体的系统Ion GeneStudio S5 Prime进行了基于新型扩增子的靶向新一代测序。使用人工合成和回顾性收集的临床标本评估了该检测方法的分析性能。新检测过程的累积变异系数百分比在日间非常精确,为8.4%,操作员间为4.0%,仪器间为3.4%。我们还观察到与正交的高灵敏度液滴数字™聚合酶链反应(ddPCR)检测有显著一致性(95.7 - 100%)。这种方法为从血液中评估靶向突变提供了有价值的补充,同时保留标本并保持灵敏度,能快速获得可指导治疗的结果。