Brueckl Wolfgang M, Schoeberl Anja, Wirtz Ralph M, Murray Samuel, Hahn Eckhart G, Wiest Gunther H
Department of Medicine 1, University Hospital Erlangen, Ulmenweg 18, 91054 Erlangen, Germany.
J Thorac Oncol. 2008 Mar;3(3):314-6. doi: 10.1097/JTO.0b013e3181654423.
A 37-year-old female never smoker with metastatic large cell carcinoma of the lung had a partial response to a second line palliative therapy with the EGF-R tyrosine kinase inhibitor erlotinib after platinum based first line therapy failed. Molecular analysis of the primary and a liver metastasis did neither find any EGF-R mutation nor an EGF-R amplification. However, both the primary and the metastasis showed an increased gene expression of vascular-endothelial growth factor-A in contrast to normal tissue, which was confirmed by immunohistochemistry. To our knowledge, this is the first report about a high vascular-endothelial growth factor-A expression in the tumor of a patient responding to an EGF-R inhibitor postulating that there might be a link between both tyrosine kinase pathways.
一名37岁从不吸烟的女性,患有转移性肺大细胞癌,在一线铂类治疗失败后,接受表皮生长因子受体(EGF-R)酪氨酸激酶抑制剂厄洛替尼进行二线姑息治疗,出现部分缓解。对原发肿瘤和一处肝转移灶进行分子分析,既未发现任何EGF-R突变,也未发现EGF-R扩增。然而,与正常组织相比,原发肿瘤和转移灶的血管内皮生长因子-A(vascular-endothelial growth factor-A)基因表达均增加,这一点通过免疫组化得以证实。据我们所知,这是关于一名对EGF-R抑制剂有反应的患者肿瘤中血管内皮生长因子-A高表达的首篇报道,推测这两种酪氨酸激酶途径之间可能存在联系。