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. 2015 Oct 24;8:119. doi: 10.1186/s13045-015-0221-6

Table 1.

Genomic abnormalities of the FGFR pathway in cancer

Gene Cancer Prevalence (%)
FGFR1 Amplification Hormone receptor positive breast cancer 10–15 [20]
Squamous NSCLC 10–20 [21]
Urothelial cancer 9–10 [7]
Squamous cell carcinoma of the head and neck 10–17 [22]
Oesophageal squamous cell carcinoma 9 [23]
Osteosarcoma 5 [11]
FGFR2 Amplification Gastric cancer 5–10 [24]
Triple negative breast cancer 4 [25]
Mutation Squamous NSCLC 3–5 [26]
Endometrial cancers 12 [27]
FGFR3 Amplification Urothelial cancer 3–5 [7]
Translocation Multiple myeloma 20 [28]
Glioblastoma 3–7 [29]
Mutation Non-invasive urothelial cancer 38–66 [6, 9]
Invasive urothelial cancer 15–20 [68]

FGFR fibroblast growth factor receptor, NSCLC non-small-cell lung cancer