Liquid Biopsy Profiling with Multiple Tests in Patients with Metastatic Breast Cancer

Nikki Higa, L. Welter, Liya Xu, A. Kolatkar, K. Bramlett, Ole V. Gjoerup, Ryon P Graf, Richard S P Huang, Rebecca J. Leary, Young Lee, Jeremy Perkins, Adam Riker, Angad P Singh, Lorraine Tafra, Carol Kaplan Tweed, C. Shriver, James B. Hicks, Peter Kuhn
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Abstract

The chief goal of the Blood Profiling Atlas in Cancer (BloodPAC) consortium is to promote collaborative efforts that support the development and implementation of liquid biopsy tests. Here, we report the results of a pilot study conducted by three BloodPAC members that aimed to demonstrate a multisite liquid biopsy testing framework using longitudinal blood specimens from 38 patients with metastatic breast cancer. Three laboratories receiving identical samples from two clinical sites each applied a different targeted sequencing platform to analyze mutations in cell-free DNA (cfDNA). The resulting mutational profiles reflected common breast cancer alterations, including clinically actionable mutations for 40% of hormone- receptor-positive patients. In 12 genes with shared target regions across sequencing panels, perfect inter-assay concordance was also observed for mutations detected above the lowest common assay limit of detection. Whole-genome copy number profiling of cfDNA and circulating tumor cells (CTCs) further revealed marked heterogeneity in copy number alterations and cfDNA tumor fractions across patients. Additionally, comparison of tumor fraction and CTC abundance demonstrated the complementary nature of cfDNA and CTC analyses. Overall, the framework described in this study may serve as a resource for future trials aiming to identify multimodal liquid biopsy biomarkers to guide clinical care.
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用多种检测方法对转移性乳腺癌患者进行液体活检分析
癌症血液分析图谱(BloodPAC)联盟的主要目标是促进合作,支持液体活检测试的开发和实施。在此,我们报告了BloodPAC三个成员开展的一项试点研究的结果,该研究旨在利用38名转移性乳腺癌患者的纵向血液标本,展示一个多站点液体活检测试框架。三个实验室从两个临床地点接收了相同的样本,各自采用不同的靶向测序平台分析无细胞DNA(cfDNA)中的突变。结果显示的突变图谱反映了常见的乳腺癌改变,包括40%激素受体阳性患者的临床可操作性突变。在测序板上具有共享靶区的12个基因中,检测到的突变超过了最低通用检测限,也观察到了完美的检测间一致性。对cfDNA和循环肿瘤细胞(CTCs)的全基因组拷贝数分析进一步揭示了不同患者拷贝数改变和cfDNA肿瘤部分的明显异质性。此外,肿瘤部分和 CTC 丰度的比较也证明了 cfDNA 和 CTC 分析的互补性。总之,本研究中描述的框架可作为未来旨在确定多模式液体生物标志物以指导临床治疗的试验的资源。
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