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. 2020 May 15;22(11):1614–1624. doi: 10.1093/neuonc/noaa121

Table 1.

Distribution of F3T3 diffuse gliomas according to WHO grading and IDH status

Histological Entity FGFR3-TACC3 Fusions Identified/Samples Tested
Without Prescreening for FGFR3 Immunopositivity Prescreened for FGFR3 Immunopositivity
Diffuse glioma (grade II-IV), IDH mutant 0/187 0/6
Grade II glioma, IDH wildtype 2/24 (8.3%) 4/6 (66.7%)
Grade III glioma, IDH wildtype 1/56 (1.8%) 5/19 (26.3%)
Glioblastoma, IDH wildtype 21/588 (3.6%) 42/84 (50%)
Diffuse glioma NOS, IDH wildtype 0/7 1/60 (1.7%)
Diffuse glioma (grade II-III), IDH NOS 0/7 0/6
Glioblastoma, IDH NOS 0/82 4/30 (13.3%)
Total 24/951 (2.5%) 56/211 (26.5%)

NOS = not otherwise specified. Note. Twenty-four F3T3 cases were identified from a systematic screening of 951 gliomas from Pitié-Salpêtrière tumor bank without FGFR3 IHC pre-screening (frequency of F3T3 fusions among unselected diffuse gliomas, grades II–IV: 2.5%), while 56 F3T3 cases were detected from an additional series of 211 preselected gliomas with FGFR3 protein immunopositivity (frequency of F3T3 fusions among FGFR3-immunopositive tumors: 26.5%).