Cargando…

EGFR-TKI原发性耐药的分子机制及其进展——附2例病例分析

Tyrosine kinase inhibitor (TKI) have been proved to be effective in the treatment of advanced non-small cell lung cancer (NSCLC) patients with epidermal growth factor receptor (EGFR) sensitive mutation, which is superior to chemotherapy. However, there are still some patients with sensitive mutation...

Descripción completa

Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 中国肺癌杂志编辑部 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6348160/
https://www.ncbi.nlm.nih.gov/pubmed/30674394
http://dx.doi.org/10.3779/j.issn.1009-3419.2019.01.10
_version_ 1783390042000982016
collection PubMed
description Tyrosine kinase inhibitor (TKI) have been proved to be effective in the treatment of advanced non-small cell lung cancer (NSCLC) patients with epidermal growth factor receptor (EGFR) sensitive mutation, which is superior to chemotherapy. However, there are still some patients with sensitive mutations have primary drug resistance. It may be related to the coexistence of susceptible and resistant mutations of EGFR gene, downstream mutations of EGFR pathway, MET amplification and BIM deletion polymorphism. We present 2 cases of primary drug resistance and analyze the reasons.
format Online
Article
Text
id pubmed-6348160
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher 中国肺癌杂志编辑部
record_format MEDLINE/PubMed
spelling pubmed-63481602019-02-11 EGFR-TKI原发性耐药的分子机制及其进展——附2例病例分析 Zhongguo Fei Ai Za Zhi 病例报道 Tyrosine kinase inhibitor (TKI) have been proved to be effective in the treatment of advanced non-small cell lung cancer (NSCLC) patients with epidermal growth factor receptor (EGFR) sensitive mutation, which is superior to chemotherapy. However, there are still some patients with sensitive mutations have primary drug resistance. It may be related to the coexistence of susceptible and resistant mutations of EGFR gene, downstream mutations of EGFR pathway, MET amplification and BIM deletion polymorphism. We present 2 cases of primary drug resistance and analyze the reasons. 中国肺癌杂志编辑部 2019-01-20 /pmc/articles/PMC6348160/ /pubmed/30674394 http://dx.doi.org/10.3779/j.issn.1009-3419.2019.01.10 Text en 版权所有©《中国肺癌杂志》编辑部2019 https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 3.0) License. See: https://creativecommons.org/licenses/by/3.0/
spellingShingle 病例报道
EGFR-TKI原发性耐药的分子机制及其进展——附2例病例分析
title EGFR-TKI原发性耐药的分子机制及其进展——附2例病例分析
title_full EGFR-TKI原发性耐药的分子机制及其进展——附2例病例分析
title_fullStr EGFR-TKI原发性耐药的分子机制及其进展——附2例病例分析
title_full_unstemmed EGFR-TKI原发性耐药的分子机制及其进展——附2例病例分析
title_short EGFR-TKI原发性耐药的分子机制及其进展——附2例病例分析
title_sort egfr-tki原发性耐药的分子机制及其进展——附2例病例分析
topic 病例报道
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6348160/
https://www.ncbi.nlm.nih.gov/pubmed/30674394
http://dx.doi.org/10.3779/j.issn.1009-3419.2019.01.10
work_keys_str_mv AT egfrtkiyuánfāxìngnàiyàodefēnzijīzhìjíqíjìnzhǎnfù2lìbìnglìfēnxī
AT egfrtkiyuánfāxìngnàiyàodefēnzijīzhìjíqíjìnzhǎnfù2lìbìnglìfēnxī
AT egfrtkiyuánfāxìngnàiyàodefēnzijīzhìjíqíjìnzhǎnfù2lìbìnglìfēnxī
AT egfrtkiyuánfāxìngnàiyàodefēnzijīzhìjíqíjìnzhǎnfù2lìbìnglìfēnxī
AT egfrtkiyuánfāxìngnàiyàodefēnzijīzhìjíqíjìnzhǎnfù2lìbìnglìfēnxī