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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...
Formato: | Online Artículo Texto |
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Lenguaje: | English |
Publicado: |
中国肺癌杂志编辑部
2019
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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 |
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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 |
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