FGFR1 AMPLIFICATION

fgfr1扩增是肿瘤中fgfr家族最常见的畸变。一项研究报告4853名患者中有3.5%的人出现了fgfr1异常,其中大多数是fgfr1扩增(Helsten等人,2016年)。临床前,fgfr1扩增也被证明对fgfr1抑制剂具有敏感性(Weiss等人,2010年)。目前正在进行临床研究(如NCT0104224)。
FGFR1 amplifications are the most common aberrations of the FGFR family in cancer. One study reports FGFR1 aberrations in 3.5% of 4,853 patients of which most are FGFR1 amplifications (Helsten et. al., 2016). Preclinically, FGFR1 amplifications have also been shown to confer sensitivity to FGFR1 inhibitors (Weiss et. al., 2010). Clinical studies are currently ongoing (e.g. NCT01004224).

别名


Allele Registry ID:
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突变位点

Ref. Build: GRCh37   Ensembl Version: 75
Chr.StartStopRef. sVar. Bases
83826865638325363
Transcript
ENST00000425967.3

基因序列