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EGFR mutational status in a large series of Caucasian European NSCLC patients: data from daily practice

BACKGROUND: The prognosis of metastatic non-small cell lung cancer (NSCLC) is still poor. Activating epithelial growth factor receptor (EGFR) mutations are important genetic alterations with dramatic therapeutical implications. Up to now, in contrast to Asian populations only limited data on the pre...

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Autores principales: Gahr, S, Stoehr, R, Geissinger, E, Ficker, J H, Brueckl, W M, Gschwendtner, A, Gattenloehner, S, Fuchs, F S, Schulz, C, Rieker, R J, Hartmann, A, Ruemmele, P, Dietmaier, W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3790166/
https://www.ncbi.nlm.nih.gov/pubmed/24002608
http://dx.doi.org/10.1038/bjc.2013.511
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author Gahr, S
Stoehr, R
Geissinger, E
Ficker, J H
Brueckl, W M
Gschwendtner, A
Gattenloehner, S
Fuchs, F S
Schulz, C
Rieker, R J
Hartmann, A
Ruemmele, P
Dietmaier, W
author_facet Gahr, S
Stoehr, R
Geissinger, E
Ficker, J H
Brueckl, W M
Gschwendtner, A
Gattenloehner, S
Fuchs, F S
Schulz, C
Rieker, R J
Hartmann, A
Ruemmele, P
Dietmaier, W
author_sort Gahr, S
collection PubMed
description BACKGROUND: The prognosis of metastatic non-small cell lung cancer (NSCLC) is still poor. Activating epithelial growth factor receptor (EGFR) mutations are important genetic alterations with dramatic therapeutical implications. Up to now, in contrast to Asian populations only limited data on the prevalence of those mutations are available from patients with Caucasian and especially European ethnicity. METHODS: In this multicentre study, 1201 unselected NSCLC patients from Southern Germany were tested in the daily clinical routine for EGFR mutation status. RESULTS: Activating EGFR mutations were found in 9.8% of all tumours. Mutations in exons 18, 19 and 21 accounted for 4.2%, 61.9% and 33.1% of all mutations, respectively. Non-smokers had a significantly higher rate of EGFR mutations than smokers or ex-smokers (24.4% vs 4.2% P<0.001). Non-lepidic-non-mucinous adenocarcinomas (G2) accounted for 45.5% of all activating EGFR mutations and 3.5% of all squamous cell carcinomas were tested positive. Thyroid transcription factor 1 protein expression was significantly associated with EGFR mutational status. CONCLUSION: These comprehensive data from clinical routine in Germany add to the knowledge of clinical and histopathological factors associated with EGFR mutational status in NSCLC.
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spelling pubmed-37901662014-10-01 EGFR mutational status in a large series of Caucasian European NSCLC patients: data from daily practice Gahr, S Stoehr, R Geissinger, E Ficker, J H Brueckl, W M Gschwendtner, A Gattenloehner, S Fuchs, F S Schulz, C Rieker, R J Hartmann, A Ruemmele, P Dietmaier, W Br J Cancer Molecular Diagnostics BACKGROUND: The prognosis of metastatic non-small cell lung cancer (NSCLC) is still poor. Activating epithelial growth factor receptor (EGFR) mutations are important genetic alterations with dramatic therapeutical implications. Up to now, in contrast to Asian populations only limited data on the prevalence of those mutations are available from patients with Caucasian and especially European ethnicity. METHODS: In this multicentre study, 1201 unselected NSCLC patients from Southern Germany were tested in the daily clinical routine for EGFR mutation status. RESULTS: Activating EGFR mutations were found in 9.8% of all tumours. Mutations in exons 18, 19 and 21 accounted for 4.2%, 61.9% and 33.1% of all mutations, respectively. Non-smokers had a significantly higher rate of EGFR mutations than smokers or ex-smokers (24.4% vs 4.2% P<0.001). Non-lepidic-non-mucinous adenocarcinomas (G2) accounted for 45.5% of all activating EGFR mutations and 3.5% of all squamous cell carcinomas were tested positive. Thyroid transcription factor 1 protein expression was significantly associated with EGFR mutational status. CONCLUSION: These comprehensive data from clinical routine in Germany add to the knowledge of clinical and histopathological factors associated with EGFR mutational status in NSCLC. Nature Publishing Group 2013-10-01 2013-09-03 /pmc/articles/PMC3790166/ /pubmed/24002608 http://dx.doi.org/10.1038/bjc.2013.511 Text en Copyright © 2013 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/3.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Molecular Diagnostics
Gahr, S
Stoehr, R
Geissinger, E
Ficker, J H
Brueckl, W M
Gschwendtner, A
Gattenloehner, S
Fuchs, F S
Schulz, C
Rieker, R J
Hartmann, A
Ruemmele, P
Dietmaier, W
EGFR mutational status in a large series of Caucasian European NSCLC patients: data from daily practice
title EGFR mutational status in a large series of Caucasian European NSCLC patients: data from daily practice
title_full EGFR mutational status in a large series of Caucasian European NSCLC patients: data from daily practice
title_fullStr EGFR mutational status in a large series of Caucasian European NSCLC patients: data from daily practice
title_full_unstemmed EGFR mutational status in a large series of Caucasian European NSCLC patients: data from daily practice
title_short EGFR mutational status in a large series of Caucasian European NSCLC patients: data from daily practice
title_sort egfr mutational status in a large series of caucasian european nsclc patients: data from daily practice
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3790166/
https://www.ncbi.nlm.nih.gov/pubmed/24002608
http://dx.doi.org/10.1038/bjc.2013.511
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