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T790M突变的非小细胞肺癌研究现状与前景
Targeted therapy with epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKIs) is regarded as the main accepted first-line treatment on EGFR mutation in non-small cell lung cancer (NSCLC). Although targeted therapy for the first and two generation of TKIs may lead to longer progression...
Formato: | Online Artículo Texto |
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Lenguaje: | English |
Publicado: |
中国肺癌杂志编辑部
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5973297/ https://www.ncbi.nlm.nih.gov/pubmed/28302223 http://dx.doi.org/10.3779/j.issn.1009-3419.2017.03.09 |
_version_ | 1783326588261105664 |
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collection | PubMed |
description | Targeted therapy with epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKIs) is regarded as the main accepted first-line treatment on EGFR mutation in non-small cell lung cancer (NSCLC). Although targeted therapy for the first and two generation of TKIs may lead to longer progression-free survival (PFS) and better tolerance for patients, the long-term treatment will inevitably lead to drug resistance. Among them, more than 50% of acquired resistance is associated with T790M mutation. The latest guidelines from the National Comprehensive Cancer Network (NCCN) have been proposed that the three generation of TKI (Osimertinib) can be used in first-line TKI therapy progress with detecting T790M mutations in patients. Encouraged by the treatment time of the median PFS up to 13 months and sequential EGFR-TKIs treatment which brought from the three generation of TKI, we also face serious challenges, such as how to achieve the detecting and the dynamic monitoring of T790M, the research progress, mechanism of drug resistance and subsequent treatment of the existing three generation TKI etc. This article will revolve around the above hot issues. |
format | Online Article Text |
id | pubmed-5973297 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | 中国肺癌杂志编辑部 |
record_format | MEDLINE/PubMed |
spelling | pubmed-59732972018-07-06 T790M突变的非小细胞肺癌研究现状与前景 Zhongguo Fei Ai Za Zhi 综述 Targeted therapy with epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKIs) is regarded as the main accepted first-line treatment on EGFR mutation in non-small cell lung cancer (NSCLC). Although targeted therapy for the first and two generation of TKIs may lead to longer progression-free survival (PFS) and better tolerance for patients, the long-term treatment will inevitably lead to drug resistance. Among them, more than 50% of acquired resistance is associated with T790M mutation. The latest guidelines from the National Comprehensive Cancer Network (NCCN) have been proposed that the three generation of TKI (Osimertinib) can be used in first-line TKI therapy progress with detecting T790M mutations in patients. Encouraged by the treatment time of the median PFS up to 13 months and sequential EGFR-TKIs treatment which brought from the three generation of TKI, we also face serious challenges, such as how to achieve the detecting and the dynamic monitoring of T790M, the research progress, mechanism of drug resistance and subsequent treatment of the existing three generation TKI etc. This article will revolve around the above hot issues. 中国肺癌杂志编辑部 2017-03-20 /pmc/articles/PMC5973297/ /pubmed/28302223 http://dx.doi.org/10.3779/j.issn.1009-3419.2017.03.09 Text en 版权所有©《中国肺癌杂志》编辑部2017 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 T790M突变的非小细胞肺癌研究现状与前景 |
title | T790M突变的非小细胞肺癌研究现状与前景 |
title_full | T790M突变的非小细胞肺癌研究现状与前景 |
title_fullStr | T790M突变的非小细胞肺癌研究现状与前景 |
title_full_unstemmed | T790M突变的非小细胞肺癌研究现状与前景 |
title_short | T790M突变的非小细胞肺癌研究现状与前景 |
title_sort | t790m突变的非小细胞肺癌研究现状与前景 |
topic | 综述 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5973297/ https://www.ncbi.nlm.nih.gov/pubmed/28302223 http://dx.doi.org/10.3779/j.issn.1009-3419.2017.03.09 |
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