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. 2021 Apr 29;13:3573–3588. doi: 10.2147/CMAR.S291681

Table 2.

Distributions of Representative Genomic Alterations and Clinical Characteristics Between the Different Pathological Subtypes with Glioma

Variable PA (N=6) A/AA (N=20) O/AO (N=17) GBM (N=32) DMG (N=8) P
TP53 0 13 3 15 3 0.0101
TERT 0 1 6 19 2 0.0005
IDH1/2 0 11 12 4 0 <0.0001
PTEN 0 3 0 12 1 0.0123
EGFR 0 0 0 13 0 <0.0001
ATRX 0 7 1 6 1 0.1318
H3F3A 0 0 0 0 8 <0.0001
NF1 0 2 1 4 1 0.8623
PDGFRA 0 0 1 5 2 0.1627
CIC 0 1 6 0 0 0.0004
PIK3CA 0 0 0 4 3 0.0095
SETD2 1 0 3 3 0 0.2862
MET 0 2 0 4 0 0.41
ATM 0 1 2 1 1 0.6484
BRAF 0 3 1 1 0 0.3771
KIT 0 0 0 4 1 0.2211
APC 0 0 1 3 0 0.5231
ARID1A 0 3 0 0 1 0.0801
CDK4 0 0 1 2 1 0.6393
KDR 0 1 0 2 1 0.6739
BRCA1 0 1 0 1 1 0.5905
CDKN2A 0 0 0 2 1 0.3975
EPCAM 0 1 0 1 1 0.5905
FGFR1 0 0 2 0 1 0.1242
FUBP1 0 0 3 0 0 0.0167
NOTCH1 0 1 1 1 0 0.9234
MGMT 2 13 13 15 0 0.0042
1p19q 0 0 10 0 0 <0.0001
CNV 0 2 2 18 4 0.0004
Age≤40 5 9 7 3 5 0.0007
Age>40 1 11 10 29 3
Male 6 14 13 23 4 0.344
Female 0 6 4 9 4

Note: CNV, the number of glioma patients with CNV events.