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.
引用
收藏
页数:9
相关论文
共 50 条
  • [41] An Observational Study of Acquired EGFR T790M-Dependent Resistance to EGFR-TKI Treatment in Lung Adenocarcinoma Patients in Taiwan
    Wu, Shang-Gin
    Chiang, Chi-Lu
    Liu, Chien-Ying
    Wang, Chin-Chou
    Su, Po-Lan
    Hsia, Te-Chun
    Shih, Jin-Yuan
    Chang, Gee-Chen
    FRONTIERS IN ONCOLOGY, 2020, 10
  • [42] T790M mutation and c-MET amplification might be correlated to TTP of EGFR-TKI in NSCLC
    Wu, Y.
    Mok, T. S.
    Chen, H.
    Zhang, X.
    Guo, A.
    Jaenne, P. A.
    JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (15)
  • [43] Loss of T790M Mutation is Associated with Early Progression to Osimertinib in Chinese Advanced NSCLC Patients Harboring EGFR T790M
    Zhao, S.
    Jiang, T.
    Li, X.
    Zhao, C.
    Su, C.
    Ren, S.
    Zhou, C.
    JOURNAL OF THORACIC ONCOLOGY, 2018, 13 (10) : S410 - S410
  • [44] Mechanisms of acquired resistance to osimertinib in advanced NSCLC with EGFR T790M mutation (LOGIK1607)
    Yamaguchi, Masafumi
    Osoegawa, Atsushi
    Nakamura, Tomomi
    Morinaga, Ryotaro
    Tanaka, Kentaro
    Kashiwabara, Kosuke
    Miura, Takashi
    Suetsugu, Takayuki
    Taguchi, Kenichi
    Nabeshima, Kazuki
    Kishimoto, Junji
    Sakai, Kazuko
    Nishio, Kazuto
    Sugio, Kenji
    CANCER SCIENCE, 2021, 112 : 567 - 567
  • [45] Dynamics of Plasma EGFR T790M Mutation in Advanced NSCLC: A Multicenter Study
    Zhengquan Yang
    Jialu Li
    Yujie Hu
    Meihua Chen
    Danli Peng
    Dan Zong
    Qingjuan Shang
    Lianqin Tao
    Yanling Zhao
    Yiyun Ni
    Jinyan Ye
    Yupeng Xie
    Li Yang
    Quan Lin
    Chang Cai
    Ning Xu
    Xiaoping Huang
    Xiaoting Dong
    Zhonghui Zhou
    Yali Yu
    Zongxiao Shangguan
    Yangyang Xu
    Weiping Ying
    Meiling Weng
    Zuguo Yuan
    Zhijun Dong
    Jifa Li
    Zhe Zheng
    Jiongwei Pan
    Lu Liu
    Junhui Ye
    Zhan Zhang
    Wenfeng Li
    Junfei Zhu
    Shengnan Jin
    Yuping Li
    Chunming Ding
    Targeted Oncology, 2019, 14 : 719 - 728
  • [46] Strategies to Overcome Acquired Resistance to EGFR-TKI Therapy Based on T790M Specific Substances using Osimertinib as an Example
    Griesinger, F.
    Radke, S.
    Lueers, A.
    Deschler-Baier, B.
    Kimmich, M.
    Sebastian, M.
    Schulz, C.
    Brugger, W.
    Wiewrodt, R.
    Pirker, R.
    Fruh, M.
    Gautschi, O.
    Wolf, J.
    PNEUMOLOGIE, 2018, 72 (11): : 774 - 781
  • [47] Clinical utility of liquid biopsy for EGFR driver, T790M mutation and EGFR amplification in plasma in patients with acquired resistance to afatinib
    Yuko Oya
    Tatsuya Yoshida
    Kazuhiro Asada
    Tetsuya Oguri
    Naoki Inui
    Sayako Morikawa
    Kentaro Ito
    Tomoki Kimura
    Eiji Kunii
    Takashi Matsui
    Akihito Kubo
    Tatsuo Kato
    Takashi Abe
    Takeshi Tsuda
    Toyoaki Hida
    BMC Cancer, 21
  • [48] Economic evaluation of diagnostic platforms for T790M detection in post EGFR-TKI NSCLC in Brazil.
    Ferreira, Carlos G. M.
    Caetano, Rosangela
    Custodio, Marcelo
    Montenegro, Giuliana
    Schluckebier, Luciene
    JOURNAL OF CLINICAL ONCOLOGY, 2018, 36 (15)
  • [49] The significance of micro-EGFR T790M mutation on EGFR-TKI efficacy in patients with NSCLC: The WJOG13119L study.
    Sato, Yuki
    Masuda, Takeshi
    Miura, Satoru
    Tachihara, Motoko
    Hosokawa, Shinobu
    Nakamura, Atsushi
    Miyawaki, Taichi
    Yoshimine, Kohei
    Mori, Masahide
    Shiraishi, Hideaki
    Hamai, Kosuke
    Haratani, Koji
    Maeda, Sumiko
    Tabata, Eriko
    Kitagawa, Chiyoe
    Tanizaki, Junko
    Imai, Takumi
    Yamamoto, Nobuyuki
    Nakagawa, Kazuhiko
    Hattori, Noboru
    JOURNAL OF CLINICAL ONCOLOGY, 2022, 40 (16)
  • [50] The significance of ultra-low EGFR T790M mutations on EGFR-TKI efficacy in patients with NSCLC -the WJOG13119L study
    Masuda, Takeshi
    Miura, Satoru
    Koso, Hidenori
    Yanagihara, Kazuhiro
    Okamoto, Tatsuro
    Shoda, Hiroyasu
    Shimizu, Junichi
    Kanaji, Nobuhiro
    Hara, Satoshi
    Sakata, Shinya
    Tokito, Takaaki
    Kashiwabara, Kosuke
    Nishikawa, Kazuo
    Watanabe, Hiroshi
    Maeno, Ken
    Suzuki, Shigeki
    Hayakawa, Daisuke
    Yamamoto, Nobuyuki
    Nakagawa, Kazuhiko
    Noboru, Hattori
    ANNALS OF ONCOLOGY, 2022, 33 : S470 - S471