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EGFR mutational status in a large series of Caucasian European NSCLC patients: data from daily practice
被引:115
作者:
Gahr, S.
[1
,2
]
Stoehr, R.
[3
]
Geissinger, E.
[4
]
Ficker, J. H.
[1
,2
]
Brueckl, W. M.
[1
,2
]
Gschwendtner, A.
[5
,6
]
Gattenloehner, S.
[7
]
Fuchs, F. S.
[8
]
Schulz, C.
[9
]
Rieker, R. J.
[3
]
Hartmann, A.
[3
]
Ruemmele, P.
[10
]
Dietmaier, W.
[10
]
机构:
[1] Klinikum Nuernberg, Dept Resp Med Allergol & Sleep Med, Nurnberg, Germany
[2] Paracelsus Med Univ Nuremberg, Nurnberg, Germany
[3] Univ Erlangen Nurnberg, Inst Pathol, Erlangen, Germany
[4] Univ Wurzburg, Inst Pathol, Wurzburg, Germany
[5] Klinikum Coburg GmbH, Inst Pathol, Coburg, Germany
[6] Klinikum St Marien Amberg, Grp Practice Pathol, Amberg, Germany
[7] Univ Giessen Marburg, Inst Pathol, Giessen, Germany
[8] Univ Erlangen Nurnberg, Dept Med 1, D-91054 Erlangen, Germany
[9] Univ Med Ctr Regensburg, Div Pneumol, Dept Internal Med 2, Regensburg, Germany
[10] Univ Regensburg, Inst Pathol, Mol Pathol Diagnost Unit, D-93053 Regensburg, Germany
关键词:
GROWTH-FACTOR-RECEPTOR;
CELL LUNG-CANCER;
TRANSCRIPTION FACTOR-I;
KRAS MUTATIONS;
1ST-LINE TREATMENT;
CLINICAL-RESPONSE;
TTF-1;
EXPRESSION;
GENE-MUTATIONS;
NEVER-SMOKERS;
OPEN-LABEL;
D O I:
10.1038/bjc.2013.511
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
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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页码:1821 / 1828
页数:8
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