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Comparison of uncommon EGFR exon 21 L858R compound mutations with single mutation
Non-small-cell lung cancer with epidermal growth factor receptor (EGFR) mutation is sensitive to EGFR tyrosine kinase inhibitors (TKIs). But little is known about the response to EGFR TKIs and the prognostic role of compound mutations. This study compared the uncommon EGFR exon 21 L858R compound mut...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4410901/ https://www.ncbi.nlm.nih.gov/pubmed/25960661 http://dx.doi.org/10.2147/OTT.S78984 |
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author | Peng, Liang Song, Zhigang Jiao, Shunchang |
author_facet | Peng, Liang Song, Zhigang Jiao, Shunchang |
author_sort | Peng, Liang |
collection | PubMed |
description | Non-small-cell lung cancer with epidermal growth factor receptor (EGFR) mutation is sensitive to EGFR tyrosine kinase inhibitors (TKIs). But little is known about the response to EGFR TKIs and the prognostic role of compound mutations. This study compared the uncommon EGFR exon 21 L858R compound mutations with single mutation to characterize EGFR compound mutations and investigated their response to EGFR TKI treatment. We retrospectively screened 799 non-small-cell lung cancer patients from August 1, 2009 to June 1, 2012 by EGFR mutation testing. EGFR mutations were detected in 443 patients, with 22 (4.97%) compound mutations. Subsequently, six patients with EGFR exon 21 L858R compound mutations and 18 paired patients with single L858R mutation were well characterized. Finally, we also analyzed the EGFR TKI treatment response and patients’ outcomes of compound or single L858R mutations. There was no differential treatment effect on the disease control rate and objective response rate between the L858R compound mutations and single mutation groups. No significant difference in overall survival or progression-free survival of these two groups was found by log-rank test. In conclusion, we demonstrated that no significant difference was detected in the response to EGFR TKIs and patients’ outcomes in the compound and single mutation groups. |
format | Online Article Text |
id | pubmed-4410901 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-44109012015-05-08 Comparison of uncommon EGFR exon 21 L858R compound mutations with single mutation Peng, Liang Song, Zhigang Jiao, Shunchang Onco Targets Ther Original Research Non-small-cell lung cancer with epidermal growth factor receptor (EGFR) mutation is sensitive to EGFR tyrosine kinase inhibitors (TKIs). But little is known about the response to EGFR TKIs and the prognostic role of compound mutations. This study compared the uncommon EGFR exon 21 L858R compound mutations with single mutation to characterize EGFR compound mutations and investigated their response to EGFR TKI treatment. We retrospectively screened 799 non-small-cell lung cancer patients from August 1, 2009 to June 1, 2012 by EGFR mutation testing. EGFR mutations were detected in 443 patients, with 22 (4.97%) compound mutations. Subsequently, six patients with EGFR exon 21 L858R compound mutations and 18 paired patients with single L858R mutation were well characterized. Finally, we also analyzed the EGFR TKI treatment response and patients’ outcomes of compound or single L858R mutations. There was no differential treatment effect on the disease control rate and objective response rate between the L858R compound mutations and single mutation groups. No significant difference in overall survival or progression-free survival of these two groups was found by log-rank test. In conclusion, we demonstrated that no significant difference was detected in the response to EGFR TKIs and patients’ outcomes in the compound and single mutation groups. Dove Medical Press 2015-04-21 /pmc/articles/PMC4410901/ /pubmed/25960661 http://dx.doi.org/10.2147/OTT.S78984 Text en © 2015 Peng et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Peng, Liang Song, Zhigang Jiao, Shunchang Comparison of uncommon EGFR exon 21 L858R compound mutations with single mutation |
title | Comparison of uncommon EGFR exon 21 L858R compound mutations with single mutation |
title_full | Comparison of uncommon EGFR exon 21 L858R compound mutations with single mutation |
title_fullStr | Comparison of uncommon EGFR exon 21 L858R compound mutations with single mutation |
title_full_unstemmed | Comparison of uncommon EGFR exon 21 L858R compound mutations with single mutation |
title_short | Comparison of uncommon EGFR exon 21 L858R compound mutations with single mutation |
title_sort | comparison of uncommon egfr exon 21 l858r compound mutations with single mutation |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4410901/ https://www.ncbi.nlm.nih.gov/pubmed/25960661 http://dx.doi.org/10.2147/OTT.S78984 |
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