Literature DB >> 25667490

Prognostic impact of central nervous system metastases after acquired resistance to EGFR-TKI: poorer prognosis associated with T790M-negative status and leptomeningeal metastases.

Akito Hata1, Nobuyuki Katakami2, Hiroshige Yoshioka3, Jumpei Takeshita2, Kosuke Tanaka2, Katsuhiro Masago2, Shiro Fujita2, Reiko Kaji2, Yukihiro Imai2, Kazuya Monden4, Takeshi Matsumoto4, Kazuma Nagata4, Kyoko Otsuka4, Ryo Tachikawa4, Keisuke Tomii4, Kei Kunimasa3, Masahiro Iwasaku3, Akihiro Nishiyama3, Tadashi Ishida3, Yoshihiro Nishimura5.   

Abstract

AIM: The aim of the present study was to investigate the prognostic impact of central nervous system metastases (CNS) after acquired resistance to epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor (TKI) in EGFR-mutant non-small cell lung cancer (NSCLC). PATIENTS AND METHODS: We defined CNS-collapse as death due to uncontrolled and progressive CNS metastases. Post-progression survival (PPS) after initial TKI failure and T790M status were retrospectively compared in 92 patients with or without CNS collapse.
RESULTS: The median PPS in 32 patients with CNS-collapse (16.7 months) was significantly shorter than that of 60 without (26.8 months) (p=0.0002). T790M was detected in four (12%) out of the 32 CNS-collapse patients and in 26 (43%) out of 60 without (p=0.0026). Median PPS in 39 patients with leptomeningeal metastases (LM) (11.4 months) was significantly shorter versus 53 without (26.8 months) (p=0.0006). The median PPS was 25.1 months in 40 patients with brain metastases and 11.2 months in 52 without (p=0.0387). T790M was detected in 4/5 resected brain tumors (80%) and in 1/26 cerebrospinal fluid (CSF) samples (4%) (p=0.0008).
CONCLUSION: CNS-collapse represented poorer prognosis, which was associated with T790M-negative status and LM. Controlling CNS metastases, especially LM, is important to achieve longer survival. Copyright
© 2015 International Institute of Anticancer Research (Dr. John G. Delinassios), All rights reserved.

Entities:  

Keywords:  Central nervous system; T790M; acquired resistance; brain metastases; epidermal growth factor receptor-tyrosine kinase inhibitor; leptomeningeal metastases

Mesh:

Substances:

Year:  2015        PMID: 25667490

Source DB:  PubMed          Journal:  Anticancer Res        ISSN: 0250-7005            Impact factor:   2.480


  8 in total

Review 1.  Treatment Options for EGFR T790M-Negative EGFR Tyrosine Kinase Inhibitor-Resistant Non-Small Cell Lung Cancer.

Authors:  Salvatore Corallo; Ettore D'Argento; Antonia Strippoli; Michele Basso; Santa Monterisi; Sabrina Rossi; Alessandra Cassano; Carlo M Barone
Journal:  Target Oncol       Date:  2017-04       Impact factor: 4.493

2.  Rapid intracranial response to osimertinib, without radiotherapy, in nonsmall cell lung cancer patients harboring the EGFR T790M mutation: Two Case Reports.

Authors:  Taro Koba; Takashi Kijima; Takayuki Takimoto; Haruhiko Hirata; Yujiro Naito; Masanari Hamaguchi; Tomoyuki Otsuka; Muneyoshi Kuroyama; Izumi Nagatomo; Yoshito Takeda; Hiroshi Kida; Atsushi Kumanogoh
Journal:  Medicine (Baltimore)       Date:  2017-02       Impact factor: 1.889

3.  Epidermal growth factor receptor (EGFR) T790M mutation identified in plasma indicates failure sites and predicts clinical prognosis in non-small cell lung cancer progression during first-generation tyrosine kinase inhibitor therapy: a prospective observational study.

Authors:  Shirong Zhang; Lucheng Zhu; Bing Xia; Enguo Chen; Qiong Zhao; Xiaochen Zhang; Xueqin Chen; Xufeng Chen; Shenglin Ma
Journal:  Cancer Commun (Lond)       Date:  2018-05-22

4.  Non-small cell lung cancer leptomeningeal metastases treated with intrathecal therapy plus osimertinib and temozolomide and whole-brain radiation therapy: a case report.

Authors:  Yunmei Wang; Shuguang Liu; Xiaohui Wei; Bin Yan; Jun Li; Zhixiang Su; Aiqin Liu; Yanjun Zhang
Journal:  Onco Targets Ther       Date:  2018-08-10       Impact factor: 4.147

5.  [Clinical Value of Cerebrospinal Fluid ctDNA in Patients 
with Non-small Cell Lung Cancer Meningeal Metastasis].

Authors:  Kunyu Zhang; Zhaoxia Dai; Siya Liu; Dan Li; Dafu Yang; Saiqiong Cui
Journal:  Zhongguo Fei Ai Za Zhi       Date:  2020-12-20

6.  Efficacy of Osimertinib in EGFR-Mutated Advanced Non-small-Cell Lung Cancer With Different T790M Status Following Resistance to Prior EGFR-TKIs: A Systematic Review and Meta-analysis.

Authors:  Xiao-Fang Yi; Jun Song; Ruo-Lin Gao; Li Sun; Zhi-Xuan Wu; Shu-Ling Zhang; Le-Tian Huang; Jie-Tao Ma; Cheng-Bo Han
Journal:  Front Oncol       Date:  2022-06-07       Impact factor: 5.738

7.  Standard-dose osimertinib for refractory leptomeningeal metastases in T790M-positive EGFR-mutant non-small cell lung cancer.

Authors:  Shigeki Nanjo; Akito Hata; Chiyuki Okuda; Reiko Kaji; Hideaki Okada; Daisuke Tamura; Kei Irie; Hiroshi Okada; Shoji Fukushima; Nobuyuki Katakami
Journal:  Br J Cancer       Date:  2017-11-30       Impact factor: 7.640

8.  Osimertinib combined with bevacizumab for leptomeningeal metastasis from EGFR-mutation non-small cell lung cancer: A phase II single-arm prospective clinical trial.

Authors:  Zhi-Qin Lu; Jing Cai; Xia Wang; Jian-Ping Wei; Zhi-Min Zeng; Long Huang; An-Wen Liu
Journal:  Thorac Cancer       Date:  2020-11-17       Impact factor: 3.223

  8 in total

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