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Validation of Amplification as a Predictive Biomarker for Anti-Epidermal Growth Factor Receptor Antibody Therapy in Metastatic Colorectal Cancer.扩增作为转移性结直肠癌抗表皮生长因子受体抗体治疗预测生物标志物的验证
JCO Precis Oncol. 2019 Dec;3:1-13. doi: 10.1200/PO.18.00226.
2
"Personalized Cancer Therapy": A Publicly Available Precision Oncology Resource.《个性化癌症治疗》:一个公开可用的精准肿瘤学资源。
Cancer Res. 2017 Nov 1;77(21):e123-e126. doi: 10.1158/0008-5472.CAN-17-0341.
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AACR Project GENIE: Powering Precision Medicine through an International Consortium.美国癌症研究协会(AACR)项目GENIE:通过国际联盟推动精准医学发展。
Cancer Discov. 2017 Aug;7(8):818-831. doi: 10.1158/2159-8290.CD-17-0151. Epub 2017 Jun 1.
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IDH2 Mutation in a Patient with Metastatic Colon Cancer.一名转移性结肠癌患者的异柠檬酸脱氢酶2(IDH2)突变
N Engl J Med. 2017 May 18;376(20):1991-2. doi: 10.1056/NEJMc1701072.
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Collaborating to Compete: Blood Profiling Atlas in Cancer (BloodPAC) Consortium.合作以竞争:癌症血液图谱联盟(BloodPAC)
Clin Pharmacol Ther. 2017 May;101(5):589-592. doi: 10.1002/cpt.666. Epub 2017 Apr 12.
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Acquired RAS or EGFR mutations and duration of response to EGFR blockade in colorectal cancer.结直肠癌中获得性 RAS 或 EGFR 突变与 EGFR 阻断反应持续时间。
Nat Commun. 2016 Dec 8;7:13665. doi: 10.1038/ncomms13665.
7
Heterogeneity of Acquired Resistance to Anti-EGFR Monoclonal Antibodies in Patients with Metastatic Colorectal Cancer.转移性结直肠癌患者对抗 EGFR 单克隆抗体获得性耐药的异质性。
Clin Cancer Res. 2017 May 15;23(10):2414-2422. doi: 10.1158/1078-0432.CCR-16-1863. Epub 2016 Oct 25.
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Genomic Correlates of Immune-Cell Infiltrates in Colorectal Carcinoma.结直肠癌中免疫细胞浸润的基因组关联
Cell Rep. 2016 Oct 18;17(4):1206. doi: 10.1016/j.celrep.2016.10.009.
9
MET amplification in metastatic colorectal cancer: an acquired response to EGFR inhibition, not a de novo phenomenon.转移性结直肠癌中的MET扩增:是对EGFR抑制的一种获得性反应,而非一种从头出现的现象。
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10
Prospective Validation of Rapid Plasma Genotyping for the Detection of EGFR and KRAS Mutations in Advanced Lung Cancer.前瞻性验证快速血浆基因分型检测晚期肺癌中 EGFR 和 KRAS 突变。
JAMA Oncol. 2016 Aug 1;2(8):1014-22. doi: 10.1001/jamaoncol.2016.0173.

结直肠癌患者游离 DNA 的基因组特征

Genomic Landscape of Cell-Free DNA in Patients with Colorectal Cancer.

机构信息

Duke University Medical Center, Durham, North Carolina.

The University of Texas MD Anderson Cancer Center, Houston, Texas.

出版信息

Cancer Discov. 2018 Feb;8(2):164-173. doi: 10.1158/2159-8290.CD-17-1009. Epub 2017 Dec 1.

DOI:10.1158/2159-8290.CD-17-1009
PMID:29196463
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5809260/
Abstract

"Liquid biopsy" approaches analyzing cell-free DNA (cfDNA) from the blood of patients with cancer are increasingly utilized in clinical practice. However, it is not yet known whether cfDNA sequencing from large cohorts of patients with cancer can detect genomic alterations at frequencies similar to those observed by direct tumor sequencing, and whether this approach can generate novel insights. Here, we report next-generation sequencing data from cfDNA of 1,397 patients with colorectal cancer. Overall, frequencies of genomic alterations detected in cfDNA were comparable to those observed in three independent tissue-based colorectal cancer sequencing compendia. Our analysis also identified a novel cluster of extracellular domain (ECD) mutations in , mediating resistance by blocking binding of anti-EGFR antibodies. Patients with ECD mutations displayed striking tumor heterogeneity, with 91% harboring multiple distinct resistance alterations (range, 1-13; median, 4). These results suggest that cfDNA profiling can effectively define the genomic landscape of cancer and yield important biological insights. This study provides one of the first examples of how large-scale genomic profiling of cfDNA from patients with colorectal cancer can detect genomic alterations at frequencies comparable to those observed by direct tumor sequencing. Sequencing of cfDNA also generated insights into tumor heterogeneity and therapeutic resistance and identified novel ectodomain mutations. .

摘要

“液体活检”方法分析癌症患者血液中的游离 DNA(cfDNA)在临床实践中越来越多地被应用。然而,目前尚不清楚来自大量癌症患者的 cfDNA 测序是否能以类似于直接肿瘤测序所观察到的频率检测到基因组改变,以及这种方法是否能产生新的见解。在这里,我们报告了来自 1397 名结直肠癌患者 cfDNA 的下一代测序数据。总的来说,cfDNA 中检测到的基因组改变的频率与在三个独立的基于组织的结直肠癌测序文献中观察到的频率相当。我们的分析还鉴定了一种新的 细胞外结构域(ECD)突变簇,通过阻止抗 EGFR 抗体的结合来介导耐药性。携带 ECD 突变的患者表现出明显的肿瘤异质性,91%的患者存在多种不同的耐药改变(范围为 1-13;中位数为 4)。这些结果表明,cfDNA 分析可以有效地定义癌症的基因组图谱,并产生重要的生物学见解。本研究提供了第一个例子之一,说明如何对结直肠癌患者的 cfDNA 进行大规模基因组分析,可以以类似于直接肿瘤测序所观察到的频率检测到基因组改变。cfDNA 测序还深入了解了肿瘤异质性和治疗耐药性,并鉴定了新的 外显子突变。