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早期乳腺癌循环肿瘤DNA与配对肿瘤组织靶向测序的一致性

Concordance of Targeted Sequencing from Circulating Tumor DNA and Paired Tumor Tissue for Early Breast Cancer.

作者信息

Huang Chi-Cheng, Tsai Yi-Fang, Liu Chun-Yu, Lien Pei-Ju, Lin Yen-Shu, Chao Ta-Chung, Feng Chin-Jung, Chen Yen-Jen, Lai Jiun-I, Cheng Han-Fang, Chen Bo-Fang, Hsu Chih-Yi, Chiu Jen-Hwey, Tseng Ling-Ming

机构信息

Comprehensive Breast Health Center, Department of Surgery, Taipei Veterans General Hospital, Taipei 11217, Taiwan.

Division of Breast Surgery, Department of Surgery, Taipei Veterans General Hospital, Taipei 11217, Taiwan.

出版信息

Cancers (Basel). 2023 Sep 8;15(18):4475. doi: 10.3390/cancers15184475.

Abstract

In this study, we evaluated the concordance of targeted sequencing between paired ctDNA and matched tumor samples from early breast cancers treated with curative intention. Molecular profiling was performed using the Oncomine Comprehensive Assay v3 and the Oncomine Breast cfDNA Assay v2. The liquid biopsy detection rate was 39% (all-stage breast cancers, n = 612). Among 246 early-stage patients assayed for both ctDNA and matched tumor, the cfDNA assay detected 73 (29.6%) and the comprehensive assay detected 201 (81.7%) breast cancers with at least one alteration (χ test, = 0.001). In total, 67 (25.6%) cases tested positive on both platforms, while the cfDNA and comprehensive assays detected an additional 10 (4%) and 138 (56%) cases, respectively. The most prevalent mutant genes were (68.3%) and (53.5%), while the (39.4%), (45.9%), and (17.1%) mutations constituted biomarkers for FDA-approved therapeutics. Our study showed that tumor tissue should be the source of actionable mutation detection for early breast cancers, considering that the concordance rate between tumor and liquid biopsy was only one-quarter.

摘要

在本研究中,我们评估了配对的循环肿瘤DNA(ctDNA)与接受根治性治疗的早期乳腺癌患者匹配肿瘤样本之间靶向测序的一致性。使用Oncomine综合检测v3和Oncomine乳腺癌游离DNA检测v2进行分子谱分析。液体活检检测率为39%(所有阶段乳腺癌,n = 612)。在246例同时检测ctDNA和匹配肿瘤的早期患者中,游离DNA检测法检测到73例(29.6%),综合检测法检测到201例(81.7%)至少有一处改变的乳腺癌(χ检验,P = 0.001)。总共有67例(25.6%)在两个平台上检测均呈阳性,而游离DNA检测法和综合检测法分别额外检测到10例(4%)和138例(56%)。最常见的突变基因是[基因名称1](68.3%)和[基因名称2](53.5%),而[基因名称3](39.4%)、[基因名称4](45.9%)和[基因名称5](17.1%)的突变构成了美国食品药品监督管理局(FDA)批准疗法的生物标志物。我们的研究表明,考虑到肿瘤与液体活检之间的一致率仅为四分之一,肿瘤组织应作为早期乳腺癌可操作突变检测的来源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c12/10526508/59d4d2a0e56d/cancers-15-04475-g001.jpg

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