Plasma EGFR T790M ctDNA status is associated with clinical outcome in advanced NSCLC patients with acquired EGFR-TKI resistance

被引:175
|
作者
Zheng, D. [1 ,4 ]
Ye, X. [2 ]
Zhang, M. Z. [3 ]
Sun, Y. [2 ]
Wang, J. Y. [1 ,4 ]
Ni, J. [1 ,4 ]
Zhang, H. P. [1 ,4 ]
Zhang, L. [1 ,4 ]
Luo, J. [1 ,4 ]
Zhang, J. [1 ,5 ]
Tang, L. [1 ,5 ]
Su, B. [1 ,5 ]
Chen, G. [1 ,6 ]
Zhu, G. [2 ,7 ]
Gu, Y. [2 ]
Xu, J. F. [1 ,4 ]
机构
[1] Tongji Univ, Sch Med, Shanghai Pulm Hosp, Shanghai 200092, Peoples R China
[2] AstraZeneca R&D, Asia & Emerging Markets Innovat Med, Shanghai, Peoples R China
[3] AstraZeneca, Res & Dev Informat, Shanghai, Peoples R China
[4] Shanghai Pulm Hosp, Dept Med Oncol, Xiamen, Peoples R China
[5] Shanghai Pulm Hosp, Cent Lab, Xiamen, Peoples R China
[6] Shanghai Pulm Hosp, Dept Pathol, Xiamen, Peoples R China
[7] Amoy Diagnost, Xiamen, Peoples R China
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
关键词
CELL LUNG-CANCER; GROWTH-FACTOR-RECEPTOR; CIRCULATING TUMOR DNA; INTRATUMOR HETEROGENEITY; NONINVASIVE DETECTION; 1ST-LINE TREATMENT; OPEN-LABEL; MUTATION; GEFITINIB; ERLOTINIB;
D O I
10.1038/srep20913
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
EGFR T790M mutation occurs in half of non-small cell lung cancer (NSCLC) patients with acquired EGFR-TKI (TKI) resistance, based on tumor re-biopsies using an invasive clinical procedure. Here, we dynamically monitored T790M mutation in circulating tumor DNA (ctDNA) using serial plasma samples from NSCLC patients receiving TKI through Droplet Digital PCR (ddPCR) method and the associations between overall survival (OS) starting from initial TKI treatment and the T790M ctDNA status detected in plasma were analyzed. Among 318 patients, 117 who acquired TKI resistance were eligible for the analysis. T790M ctDNA was detected in the plasma of 55/117 (47%) patients. Almost half of the T790M ctDNA positive patients were identified at a median time of 2.2 months prior to clinically progressive disease (PD). Furthermore, within the patients receiving TKI treatment at 2nd line or later, the T790M ctDNA positive group had significantly shorter OS than the negative group (median OS: 26.9 months versus NA, P = 0.0489). Our study demonstrates the feasibility of monitoring EGFR mutation dynamics in serial plasma samples from NSCLC patients receiving TKI therapy. T790M ctDNA can be detected in plasma before and after PD as a poor prognostic factor.
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页数:9
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