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

被引:46
作者
Herbreteau, Guillaume [1 ]
Vallee, Audrey [1 ]
Charpentier, Sandrine [1 ]
Normanno, Nicola [2 ]
Hofman, Paul [3 ,4 ,5 ]
Denis, Marc G. [1 ]
机构
[1] Nantes Univ Hosp, Dept Biochem, 9 Quai Moncousu, F-44093 Nantes, France
[2] Fdn G Pascale, IRCCS, Ist Nazl Tumori, Cell Biol & Biotherapy Unit, Naples, Italy
[3] Univ Cote Azur, CHU Nice, CNRS 7284, INSERM,Lab Clin & Expt Pathol,U1081, Nice, France
[4] Pasteur Hosp, FHU OncoAge, Nice, France
[5] Pasteur Hosp, Hosp Integrated Biobank BB 0033 00025, Nice, France
关键词
Circulating tumor DNA (ctDNA); non-small cell lung cancer (NSCLC); EGFR mutation; ALK translocation; tumor mutation burden (TMB); minimal residual disease (MRD); MOLECULAR TESTING GUIDELINE; T790M RESISTANCE MUTATION; OF-AMERICAN-PATHOLOGISTS; EGFR MUTATION; LIQUID BIOPSY; ACQUIRED-RESISTANCE; ADENOCARCINOMA PATIENTS; CEREBROSPINAL-FLUID; ALK REARRANGEMENT; BRAF MUTATION;
D O I
10.21037/jtd.2018.12.18
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
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.
引用
收藏
页码:S113 / S126
页数:14
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