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非小细胞肺癌分子靶向治疗中EGFR-TKI的耐药机制研究进展
With a greater understanding of tumor biology, novel molecular-targeted strategies that block cancer progression pathways have been evaluated as a new therapeutic approach for treating non-small cell lung cancer (NSCLC). Epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs), such a...
Formato: | Online Artículo Texto |
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Lenguaje: | English |
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中国肺癌杂志编辑部
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000259/ https://www.ncbi.nlm.nih.gov/pubmed/22336239 http://dx.doi.org/10.3779/j.issn.1009-3419.2012.02.08 |
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collection | PubMed |
description | With a greater understanding of tumor biology, novel molecular-targeted strategies that block cancer progression pathways have been evaluated as a new therapeutic approach for treating non-small cell lung cancer (NSCLC). Epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs), such as gefitinib and erlotinib, show favorable response to EGFR mutant lung cancer in some populations of NSCLC patients. However, the efficacy of EGFR-TKIs is limited by either primary (de novo) or acquired resistance after therapy. This review will focus on recently identified mechanisms of primary and acquired resistance to EGFR TKIs and strategies currently being employed to overcome resistance. |
format | Online Article Text |
id | pubmed-6000259 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | 中国肺癌杂志编辑部 |
record_format | MEDLINE/PubMed |
spelling | pubmed-60002592018-07-06 非小细胞肺癌分子靶向治疗中EGFR-TKI的耐药机制研究进展 Zhongguo Fei Ai Za Zhi 综述 With a greater understanding of tumor biology, novel molecular-targeted strategies that block cancer progression pathways have been evaluated as a new therapeutic approach for treating non-small cell lung cancer (NSCLC). Epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs), such as gefitinib and erlotinib, show favorable response to EGFR mutant lung cancer in some populations of NSCLC patients. However, the efficacy of EGFR-TKIs is limited by either primary (de novo) or acquired resistance after therapy. This review will focus on recently identified mechanisms of primary and acquired resistance to EGFR TKIs and strategies currently being employed to overcome resistance. 中国肺癌杂志编辑部 2012-02-20 /pmc/articles/PMC6000259/ /pubmed/22336239 http://dx.doi.org/10.3779/j.issn.1009-3419.2012.02.08 Text en 版权所有©《中国肺癌杂志》编辑部2012 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 | 综述 非小细胞肺癌分子靶向治疗中EGFR-TKI的耐药机制研究进展 |
title | 非小细胞肺癌分子靶向治疗中EGFR-TKI的耐药机制研究进展 |
title_full | 非小细胞肺癌分子靶向治疗中EGFR-TKI的耐药机制研究进展 |
title_fullStr | 非小细胞肺癌分子靶向治疗中EGFR-TKI的耐药机制研究进展 |
title_full_unstemmed | 非小细胞肺癌分子靶向治疗中EGFR-TKI的耐药机制研究进展 |
title_short | 非小细胞肺癌分子靶向治疗中EGFR-TKI的耐药机制研究进展 |
title_sort | 非小细胞肺癌分子靶向治疗中egfr-tki的耐药机制研究进展 |
topic | 综述 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000259/ https://www.ncbi.nlm.nih.gov/pubmed/22336239 http://dx.doi.org/10.3779/j.issn.1009-3419.2012.02.08 |