对临床全面基因组图谱敏感性增加的液体活检测定的验证

Xavier S. Bower , Jan Wignall , Matthew G. Varga , Joyce Zhu , Michael O'Sullivan , Naomi E. Searle , Lenny K. Hong , Turgut Dogruluk , Zeqian Li , Tiffany E. Farmer , Emilio Rosas-Linhard , Jason Luong , Esther Lin , Marie Erica Simon , David S. Tsao , John R. ten Bosch , Gary Palmer , Ajeet Gajra , Chanh Huynh , Wen Zhou
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引用次数: 0

摘要

精确肿瘤学的最新进展证实了对具有更高灵敏度的全面基因组分析(CGP)液体活检分析的需求,特别是在检测低丰度循环肿瘤DNA (ctDNA)脱落的肿瘤中的变化时。这种测试可以解决组织活检的局限性,同时增强对临床可操作变异的检测。该研究包括Northstar Select的分析和临床验证研究,Northstar Select是一种基于血浆的肿瘤初始CGP检测,涵盖84个基因。该方法检测SNV/Indels、cnv(增益和损失)、融合和微卫星不稳定性(MSI-H)。回顾性分析了在美国常规护理期间收集的674例分析患者样本,涵盖了各种实体肿瘤类型,以调查不同肿瘤类型的表现。此外,在182例患者的前瞻性头对头比较研究中进行了临床验证,评估了Northstar Select和市场上的CGP液体活检检测的性能。分析验证表明,SNV/Indels的0.15%变异等位基因频率(VAF)的检出限为95%,数字液滴PCR证实了这一点。Northstar Select在液体中对CNVs的检测灵敏度为2.11拷贝(扩增),1.80拷贝(缺失),0.30%(基因融合),解决了液体活检检测的关键挑战。它优于市场上的CGP检测,鉴定出的致病性SNV/indels多51%,cnv多109%。此外,这导致无致病或可操作结果的无效报告减少了45%。大多数(91%)临床可操作的SNV/indels是在0.5% VAF以下检测到的。Northstar Select显示了分析和临床有效性,在所有变异类别中具有高灵敏度。与现有的商业分析相比,低LOD允许在较低的vaf下可靠地检测变异。因此,Northstar Select可以通过提供识别更多可操作的基因组改变的机会来增强临床决策,这可能对低脱落肿瘤患者特别有益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Validation of a liquid biopsy assay with increased sensitivity for clinical comprehensive genomic profiling
Recent advancements in precision oncology have affirmed the need for comprehensive genomic profiling (CGP) liquid biopsy assays with increased sensitivity, especially for detecting alterations in tumors which shed circulating tumor DNA (ctDNA) at low abundance. Such tests could address the limitations of tissue biopsies while simultaneously enhancing the detection of clinically actionable variants. This study included analytical and clinical validation studies of Northstar Select, a plasma-based, tumor-naive CGP assay covering 84 genes. The assay detects SNV/Indels, CNVs (gain and loss), fusions, and microsatellite instability (MSI-H). A retrospective analysis of 674 analytical patient samples collected during routine care in the United States, covering various solid tumor types, was conducted to investigate performance across tumor types. In addition, clinical validation was conducted in a prospective head-to-head comparison study of 182 patients, assessing the performance of Northstar Select and on-market CGP liquid biopsy assays. Analytical validation demonstrated a 95 % Limit of Detection of 0.15 % variant allele frequency (VAF) for SNV/Indels, which was confirmed by digital droplet PCR. Northstar Select demonstrated sensitive detection of CNVs in liquid down to 2.11 copies for amplifications and 1.80 copies for losses, and 0.30 % for gene fusions, addressing a key challenge in liquid biopsy testing. It outperformed on-market CGP assays, identifying 51 % more pathogenic SNV/indels and 109 % more CNVs. Additionally, this resulted in 45 % fewer null reports with no pathogenic or actionable results. The majority (91 %) of additional clinically actionable SNV/indels found were detected below 0.5 % VAF. Northstar Select demonstrated analytical and clinical validity, with high sensitivity across all variant classes. The low LOD allows for reliable detection of variants at lower VAFs compared to existing commercial assays. Northstar Select can therefore enhance clinical decision-making by providing the opportunity to identify more actionable genomic alterations, which may be especially beneficial for patients with low-shedding tumors.
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