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Overcoming EGFR-mediated osimertinib resistance through unique binding characteristics of second-generation EGFR inhibitors.克服 EGFR 介导的奥希替尼耐药性:第二代 EGFR 抑制剂的独特结合特性。
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Landscape of Acquired Resistance to Osimertinib in -Mutant NSCLC and Clinical Validation of Combined EGFR and RET Inhibition with Osimertinib and BLU-667 for Acquired Fusion.奥希替尼获得性耐药的非小细胞肺癌的全景及奥希替尼联合 BLU-667 对获得性融合的 EGFR 和 RET 联合抑制的临床验证
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Landscape of EGFR-Dependent and -Independent Resistance Mechanisms to Osimertinib and Continuation Therapy Beyond Progression in -Mutant NSCLC.奥希替尼治疗及进展后延续治疗中 EGFR 依赖性和非依赖性耐药机制的全景:-突变 NSCLC 患者的研究
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CNS Response to Osimertinib Versus Standard Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors in Patients With Untreated EGFR-Mutated Advanced Non-Small-Cell Lung Cancer.未经治疗的表皮生长因子受体(EGFR)突变型晚期非小细胞肺癌患者中,中枢神经系统(CNS)对奥希替尼与标准表皮生长因子受体酪氨酸激酶抑制剂的反应。
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A method for treatment monitoring using circulating tumour DNA in cancer patients without targetable mutations.一种在无可靶向突变的癌症患者中使用循环肿瘤DNA进行治疗监测的方法。
Oncotarget. 2018 Jul 24;9(57):31066-31076. doi: 10.18632/oncotarget.25779.
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Simultaneous detection of lung fusions using a multiplex RT-PCR next generation sequencing-based approach: a multi-institutional research study.基于多重 RT-PCR 下一代测序的方法同时检测肺融合:一项多机构研究。
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Early Reduction in ctDNA Predicts Survival in Patients with Lung and Bladder Cancer Treated with Durvalumab.早期 ctDNA 降低可预测杜伐鲁单抗治疗的肺癌和膀胱癌患者的生存情况。
Clin Cancer Res. 2018 Dec 15;24(24):6212-6222. doi: 10.1158/1078-0432.CCR-18-0386. Epub 2018 Aug 9.
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Blood-based tumor mutational burden as a predictor of clinical benefit in non-small-cell lung cancer patients treated with atezolizumab.基于血液的肿瘤突变负担可预测接受阿替利珠单抗治疗的非小细胞肺癌患者的临床获益。
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Assessment of Resistance Mechanisms and Clinical Implications in Patients With EGFR T790M-Positive Lung Cancer and Acquired Resistance to Osimertinib.评估 EGFR T790M 阳性肺癌患者对奥希替尼获得性耐药的耐药机制及临床意义。
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Correlation between progression-free survival, tumor burden, and circulating tumor DNA in the initial diagnosis of advanced-stage EGFR-mutated non-small cell lung cancer.晚期 EGFR 突变型非小细胞肺癌初始诊断中无进展生存期、肿瘤负担与循环肿瘤 DNA 的相关性。
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非小细胞肺癌中的循环游离肿瘤DNA:临床应用与未来展望

Circulating free tumor DNA in non-small cell lung cancer (NSCLC): clinical application and future perspectives.

作者信息

Herbreteau Guillaume, Vallée Audrey, Charpentier Sandrine, Normanno Nicola, Hofman Paul, Denis Marc G

机构信息

Department of Biochemistry, Nantes University Hospital, 9 quai Moncousu, F-44093 Nantes Cedex, France.

Cell Biology and Biotherapy Unit, Istituto Nazionale Tumori, IRCCS, "Fondazione G. Pascale", Naples, Italy.

出版信息

J Thorac Dis. 2019 Jan;11(Suppl 1):S113-S126. doi: 10.21037/jtd.2018.12.18.

DOI:10.21037/jtd.2018.12.18
PMID:30775034
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6353745/
Abstract

Major advances in the treatment of non-small cell lung cancer (NSCLC) patients have been obtained during the last decade. Molecular testing of tumor samples is therefore mandatory in routine clinical practice. Tumor DNA is also present as cell-free molecules in blood, which is therefore a very useful and convenient source of tumor DNA. In this review, we discuss pre-analytical and analytical aspects of circulating tumor DNA (ctDNA) analysis. We also describe the use of ctDNA analysis in routine clinical practice, and discuss the potential use of ctDNA monitoring both to identify minimal residual disease and as a potential tool to early identify patients' response to treatment.

摘要

在过去十年中,非小细胞肺癌(NSCLC)患者的治疗取得了重大进展。因此,肿瘤样本的分子检测在常规临床实践中是必不可少的。肿瘤DNA也以游离分子的形式存在于血液中,因此血液是肿瘤DNA非常有用且方便的来源。在本综述中,我们讨论了循环肿瘤DNA(ctDNA)分析的分析前和分析方面。我们还描述了ctDNA分析在常规临床实践中的应用,并讨论了ctDNA监测在识别微小残留病以及作为早期识别患者治疗反应的潜在工具方面的潜在用途。