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晚期肺腺癌患者化疗前后血清EGFR基因突变状态的比较
BACKGROUND AND OBJECTIVE: Non-small cell lung cancer (NSCLC) with mutations in the epidermal growth factor receptor (EGFR) is a distinct subgroup of NSCLC, which is particularly responsive to EGFR tyrosine kinase inhibitors (TKIs). The aim of this study is to detect EGFR mutations in paired serum of...
Formato: | Online Artículo Texto |
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Lenguaje: | English |
Publicado: |
中国肺癌杂志编辑部
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5999769/ https://www.ncbi.nlm.nih.gov/pubmed/21342642 http://dx.doi.org/10.3779/j.issn.1009-3419.2011.02.04 |
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collection | PubMed |
description | BACKGROUND AND OBJECTIVE: Non-small cell lung cancer (NSCLC) with mutations in the epidermal growth factor receptor (EGFR) is a distinct subgroup of NSCLC, which is particularly responsive to EGFR tyrosine kinase inhibitors (TKIs). The aim of this study is to detect EGFR mutations in paired serum of pre- and post-chemotherapy from advanced pulmonary adenocarcinoma patients to evaluate impact of chemotherapy on EGFR mutation status. METHODS: Magnetic beads were used for DNA extraction from paired serum of pre- and post-chemotherapy of 33 advanced pulmonary adenocarcinoma patients. The EGFR exon 19 and 21 were amplified by mutant-enriched nested PCR and analyzed by direct sequencing. RESULTS: EGFR mutations were detected in 39.4% (13/33) and 54.5% (18/33) serum samples of pre- and postchemotherapy, respectively. The EGFR mutation status was consistent in 54.5% (18/33) patients. Among 15 discordant cases, 10 changed from pre-chemo wild-type to post-chemo mutant-type status, while 5 from pre-chemo mutant-type to post-chemo wild-type status. CONCLUSION: Chemotherapy may have influence on serum EGFR mutation status in advanced adenocacinoma patients. |
format | Online Article Text |
id | pubmed-5999769 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | 中国肺癌杂志编辑部 |
record_format | MEDLINE/PubMed |
spelling | pubmed-59997692018-07-06 晚期肺腺癌患者化疗前后血清EGFR基因突变状态的比较 Zhongguo Fei Ai Za Zhi 临床研究 BACKGROUND AND OBJECTIVE: Non-small cell lung cancer (NSCLC) with mutations in the epidermal growth factor receptor (EGFR) is a distinct subgroup of NSCLC, which is particularly responsive to EGFR tyrosine kinase inhibitors (TKIs). The aim of this study is to detect EGFR mutations in paired serum of pre- and post-chemotherapy from advanced pulmonary adenocarcinoma patients to evaluate impact of chemotherapy on EGFR mutation status. METHODS: Magnetic beads were used for DNA extraction from paired serum of pre- and post-chemotherapy of 33 advanced pulmonary adenocarcinoma patients. The EGFR exon 19 and 21 were amplified by mutant-enriched nested PCR and analyzed by direct sequencing. RESULTS: EGFR mutations were detected in 39.4% (13/33) and 54.5% (18/33) serum samples of pre- and postchemotherapy, respectively. The EGFR mutation status was consistent in 54.5% (18/33) patients. Among 15 discordant cases, 10 changed from pre-chemo wild-type to post-chemo mutant-type status, while 5 from pre-chemo mutant-type to post-chemo wild-type status. CONCLUSION: Chemotherapy may have influence on serum EGFR mutation status in advanced adenocacinoma patients. 中国肺癌杂志编辑部 2011-02-20 /pmc/articles/PMC5999769/ /pubmed/21342642 http://dx.doi.org/10.3779/j.issn.1009-3419.2011.02.04 Text en 版权所有©《中国肺癌杂志》编辑部2011 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 | 临床研究 晚期肺腺癌患者化疗前后血清EGFR基因突变状态的比较 |
title | 晚期肺腺癌患者化疗前后血清EGFR基因突变状态的比较 |
title_full | 晚期肺腺癌患者化疗前后血清EGFR基因突变状态的比较 |
title_fullStr | 晚期肺腺癌患者化疗前后血清EGFR基因突变状态的比较 |
title_full_unstemmed | 晚期肺腺癌患者化疗前后血清EGFR基因突变状态的比较 |
title_short | 晚期肺腺癌患者化疗前后血清EGFR基因突变状态的比较 |
title_sort | 晚期肺腺癌患者化疗前后血清egfr基因突变状态的比较 |
topic | 临床研究 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5999769/ https://www.ncbi.nlm.nih.gov/pubmed/21342642 http://dx.doi.org/10.3779/j.issn.1009-3419.2011.02.04 |
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