Liquid biopsy using the supernatant of a pleural effusion for EGFR genotyping in pulmonary adenocarcinoma patients: a comparison between cell-free DNA and extracellular vesicle-derived DNA

被引:65
作者
Lee, Jong Sik [1 ]
Hur, Jae Young [1 ,3 ]
Kim, In Ae [1 ]
Kim, Hee Joung [1 ,2 ]
Choi, Chang Min [4 ,5 ]
Lee, Jae Chol [4 ,5 ]
Kim, Wan Seop [3 ]
Lee, Kye Young [1 ,2 ]
机构
[1] Konkuk Univ, Sch Med, Med Ctr & Med, Lung Canc Ctr,Dept Pulm, 120-1 Hwayang Dong, Seoul 05030, South Korea
[2] Konkuk Univ, Sch Med, Dept Pulm Med, Seoul, South Korea
[3] Konkuk Univ, Sch Med, Dept Pathol, Seoul, South Korea
[4] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Pulm & Crit Care Med, Seoul, South Korea
[5] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Oncol, Seoul, South Korea
来源
BMC CANCER | 2018年 / 18卷
关键词
Pleural effusion; Pulmonary adenocarcinoma; EGFR mutation; Extracellular vesicles; Liquid biopsy; CIRCULATING TUMOR DNA; DOUBLE-STRANDED DNA; LUNG-CANCER; MUTATION; EXOSOMES; BLOOD;
D O I
10.1186/s12885-018-5138-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundEGFR genotyping in pulmonary adenocarcinoma patients who develop pleural effusions is mostly performed using cytology or cell block slides with low sensitivity. Liquid biopsy using the supernatant of pleural effusions may be more effective because they contain many components released by cancer cells. Extracellular vesicles (EVs) are known to carry oncogenic double-stranded DNA that is considered a notable biomarker. Here, we investigate the efficiency of liquid biopsy using cell-free DNA (cfDNA) and extracellular vesicle-derived DNA (EV-derived DNA) from the supernatant of pleural effusions for EGFR genotyping in patients with pulmonary adenocarcinoma.MethodsFifty pleural effusion samples from patients with pulmonary adenocarcinoma were evaluated. The supernatant, after removing the cell pellet by centrifugation, was used for liquid biopsy, and EVs were isolated from the pleural effusion by ultracentrifugation. EV-derived DNA and cfDNA were extracted separately, and EGFR genotyping was performed by the PNA clamping method.ResultsAmong 32 patients who were EGFR-tyrosine kinase inhibitor (TKI) naive with a known tissue EGFR genotype, liquid biopsy using EV-derived DNA from the pleural effusion supernatant showed 100% matching results with tissue EGFR genotyping in 19 EGFR mutant cases and detected three additional EGFR mutations in patients with wild-type (WT) tissue. Liquid biopsy using cfDNA from pleural effusion supernatants missed two cases of tissue-based EGFR mutations and found two additional EGFR mutation cases. In 18 patients who acquired resistance to EGFR-TKI, EGFR genotyping using EV-derived DNA from the pleural effusion supernatant detected the T790M mutation in 13 of 18 (72.2%) patients, and this mutation was detected in 11 (61.1%) patients using cfDNA. By contrast, only three patients were found to present the T790M mutation when using cell block or cytology slides.ConclusionsLiquid biopsy using the supernatant of pleural effusions showed significantly improved results for EGFR genotyping compared to those using conventional cell block or cytology samples. Liquid biopsy using EV-derived DNA is promising for EGFR genotyping, including T790M detection in pulmonary adenocarcinoma patients who develop pleural effusions.
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页数:8
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