- 作者：Matthias Preusser ; Anna S. Berghoff ; Walter Berger ; Ayseg眉l Ilhan-Mutlu ; Carina Dinhof ; Georg Widhalm ; Karin Dieckmann ; Adelheid W枚hrer ; Monika Hackl ; Andreas von Deimling ; Berthold Streubel ; Peter Birner
- 关键词：FGFR1 ; Gene amplification ; Fluorescent in situ hybridization ; Brain metastases ; Lung cancer
- 刊名：Lung Cancer
- 出版年：January, 2014
- 年：2014
- 卷：83
- 期：1
- 页码：83-89
- 全文大小：473 K
Objectives
FGFR1 amplifications are common in squamous cell carcinoma and rare in adenocarcinoma of the lung, but have not been investigated in brain metastases of non-small cell lung cancer (NSCLC).Materials and methods
We performed fluorescent in situ hybridization (FISH) for FGFR1 and immunohistochemistry for pAKT, PI3K, HIF1a and Ki67 in 175 NSCLC brain metastases and 11 matched primary tumors. ALK gene rearrangement status was available from a previous study. We performed statistical correlations of clinical, histopathological and molecular data.
Results
FGFR1 amplifications were found in a total of 30/175 (17%) brain metastases: 4/21 (19%) squamous cell carcinomas, 20/130 (15.3%) adenocarcinomas, 2/12 (16.6%) adenosquamous carcinomas, 4/9 (44.4%) large cell carcinomas and 0/3 neuroendocrine large cell carcinoma. FGFR1 gene status was identical between primary tumors and brain metastases in 9/11 evaluable cases. In 2/11 cases (1 adenosquamous and 1 large cell carcinoma), FGFR1 amplifications were present only in the brain metastasis and not in the primary tumor. Furthermore, we found a significant positive correlation of ALK and FGFR1 gene amplification status in brain metastases (p < 0.001, Chi square test). Patients with high-level FGFR1 amplifications had significantly higher number of visceral metastases (p < 0.001, Chi square test).
Conclusion
Our findings argue for an enrichment of FGFR1 amplifications in brain metastases of adenocarcinomas (where they were 5-fold more frequent than reported for primary tumors) and possibly also of other non-squamous carcinomas, but not in squamous cell carcinomas of the lung. These results may be relevant for targeted therapy and prophylaxis of NSCLC brain metastases.