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EGFR, KRAS, BRAF, and HER-2 molecular status in brain metastases from 77 NSCLC patients

The aim of this study was to determine the frequency of EGFR, KRAS, BRAF, and HER-2 mutations in brain metastases from non-small cell lung carcinomas (BM-NSCLC). A total of 77 samples of BM-NSCLC were included and 19 samples of BM from breast, kidney, and colorectal tumors were also studied as contr...

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Autores principales: Villalva, Claire, Duranton-Tanneur, Valérie, Guilloteau, Karline, Burel-Vandenbos, Fanny, Wager, Michel, Doyen, Jérôme, Levillain, Pierre Marie, Fontaine, Denys, Blons, Hélène, Pedeutour, Florence, Karayan-Tapon, Lucie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3699841/
https://www.ncbi.nlm.nih.gov/pubmed/23930206
http://dx.doi.org/10.1002/cam4.82
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author Villalva, Claire
Duranton-Tanneur, Valérie
Guilloteau, Karline
Burel-Vandenbos, Fanny
Wager, Michel
Doyen, Jérôme
Levillain, Pierre Marie
Fontaine, Denys
Blons, Hélène
Pedeutour, Florence
Karayan-Tapon, Lucie
author_facet Villalva, Claire
Duranton-Tanneur, Valérie
Guilloteau, Karline
Burel-Vandenbos, Fanny
Wager, Michel
Doyen, Jérôme
Levillain, Pierre Marie
Fontaine, Denys
Blons, Hélène
Pedeutour, Florence
Karayan-Tapon, Lucie
author_sort Villalva, Claire
collection PubMed
description The aim of this study was to determine the frequency of EGFR, KRAS, BRAF, and HER-2 mutations in brain metastases from non-small cell lung carcinomas (BM-NSCLC). A total of 77 samples of BM-NSCLC were included and 19 samples of BM from breast, kidney, and colorectal tumors were also studied as controls. These samples were collected from patients followed between 2008 and 2011 at Poitiers and Nice University Hospitals in France. The frequencies of EGFR, KRAS, BRAF, and HER-2 mutations in BM-NSCLC were 2.6, 38.5, 0, and 0% respectively. The incidence of KRAS mutation was significantly higher in female and younger patients (P < 0.05). No mutations of the four genes were found in BM from breast or kidney. However, among six BM from colorectal tumors, we identified KRAS mutations in three cases and BRAF mutations in two other cases. This study is the largest analysis on genetic alterations in BM-NSCLC performed to date. Our results suggest a low frequency of EGFR mutations in BM-NSCLC whereas KRAS mutations are as frequent in BM-NSCLC as in primitive NSCLC. These results raise the question of the variability of the brain metastatic potential of NSCLC cells in relation to the mutation pattern.
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spelling pubmed-36998412013-08-08 EGFR, KRAS, BRAF, and HER-2 molecular status in brain metastases from 77 NSCLC patients Villalva, Claire Duranton-Tanneur, Valérie Guilloteau, Karline Burel-Vandenbos, Fanny Wager, Michel Doyen, Jérôme Levillain, Pierre Marie Fontaine, Denys Blons, Hélène Pedeutour, Florence Karayan-Tapon, Lucie Cancer Med Cancer Biology The aim of this study was to determine the frequency of EGFR, KRAS, BRAF, and HER-2 mutations in brain metastases from non-small cell lung carcinomas (BM-NSCLC). A total of 77 samples of BM-NSCLC were included and 19 samples of BM from breast, kidney, and colorectal tumors were also studied as controls. These samples were collected from patients followed between 2008 and 2011 at Poitiers and Nice University Hospitals in France. The frequencies of EGFR, KRAS, BRAF, and HER-2 mutations in BM-NSCLC were 2.6, 38.5, 0, and 0% respectively. The incidence of KRAS mutation was significantly higher in female and younger patients (P < 0.05). No mutations of the four genes were found in BM from breast or kidney. However, among six BM from colorectal tumors, we identified KRAS mutations in three cases and BRAF mutations in two other cases. This study is the largest analysis on genetic alterations in BM-NSCLC performed to date. Our results suggest a low frequency of EGFR mutations in BM-NSCLC whereas KRAS mutations are as frequent in BM-NSCLC as in primitive NSCLC. These results raise the question of the variability of the brain metastatic potential of NSCLC cells in relation to the mutation pattern. Blackwell Publishing Ltd 2013-06 2013-04-23 /pmc/articles/PMC3699841/ /pubmed/23930206 http://dx.doi.org/10.1002/cam4.82 Text en © 2013 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Cancer Biology
Villalva, Claire
Duranton-Tanneur, Valérie
Guilloteau, Karline
Burel-Vandenbos, Fanny
Wager, Michel
Doyen, Jérôme
Levillain, Pierre Marie
Fontaine, Denys
Blons, Hélène
Pedeutour, Florence
Karayan-Tapon, Lucie
EGFR, KRAS, BRAF, and HER-2 molecular status in brain metastases from 77 NSCLC patients
title EGFR, KRAS, BRAF, and HER-2 molecular status in brain metastases from 77 NSCLC patients
title_full EGFR, KRAS, BRAF, and HER-2 molecular status in brain metastases from 77 NSCLC patients
title_fullStr EGFR, KRAS, BRAF, and HER-2 molecular status in brain metastases from 77 NSCLC patients
title_full_unstemmed EGFR, KRAS, BRAF, and HER-2 molecular status in brain metastases from 77 NSCLC patients
title_short EGFR, KRAS, BRAF, and HER-2 molecular status in brain metastases from 77 NSCLC patients
title_sort egfr, kras, braf, and her-2 molecular status in brain metastases from 77 nsclc patients
topic Cancer Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3699841/
https://www.ncbi.nlm.nih.gov/pubmed/23930206
http://dx.doi.org/10.1002/cam4.82
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