Yeung Kay T, More Soham, Woodward Brian, Velculescu Victor, Husain Hatim
University of California San Diego Moores Cancer Center, #3011, San Diego, CA, 92093, USA.
Johns Hopkins Sidney Kimmel Cancer Center, Baltimore, MD, 21224, USA.
Mol Diagn Ther. 2017 Aug;21(4):375-384. doi: 10.1007/s40291-017-0260-5.
Targeted therapies have changed the treatment landscape of non-small cell lung cancer over the past decade. Analyses of cell free circulating tumor DNA (ctDNA) provide a non-invasive and robust approach for cancer diagnosis and prognosis, real-time monitoring of treatment response, and the identification of appropriate therapeutic targets based on the detection of tumor genetic aberrations. Recent improvements in the sensitivity, specificity, and feasibility of ctDNA detection assays allow the possibility for implementation into clinical practice. This review will focus on key studies using ctDNA analysis in early lung cancer detection, prediction of treatment response, monitoring minimal residual disease and disease relapse, and the identification of resistance mechanisms. We explore how ctDNA can be used as a surrogate for tissue biopsy and an integral biomarker in the clinical management of patients with non-small cell lung cancer.
在过去十年中,靶向治疗改变了非小细胞肺癌的治疗格局。对游离循环肿瘤DNA(ctDNA)的分析为癌症诊断和预后、治疗反应的实时监测以及基于肿瘤基因畸变检测来确定合适的治疗靶点提供了一种非侵入性且可靠的方法。ctDNA检测分析在灵敏度、特异性和可行性方面的最新进展使得其有可能应用于临床实践。本综述将聚焦于使用ctDNA分析进行早期肺癌检测、预测治疗反应、监测微小残留病和疾病复发以及识别耐药机制的关键研究。我们探讨了ctDNA如何能够用作组织活检的替代物以及非小细胞肺癌患者临床管理中的一个不可或缺的生物标志物。