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. 2021 Oct 4;15:736891. doi: 10.3389/fnins.2021.736891

TABLE 1.

Patient demographics and genetic information.

Parameter All patients Patients with LGG Patients with GBM
WHO tumor grade 91 48 (52.7%) 43 (47.2%)
Mean age (y)* 47.1 ± 12.6 44.3 ± 11.7 50.3 ± 12.9
No. of women 45 (49.4%) 28 (58.3%) 17 (39.5%)
IDH gene status
Mutated 38 (41.7%) 31 (64.5%) 7 (16.2%)
Wild type 48 (52.7%) 15 (31.2%) 33 (76.7%)
NA 5 (5.4%) 2 (4.1%) 3 (6.9%)
MGMT promoter methylation
Methylated 34 (37.3%) 22 (45.8%) 12 (27.9%)
Unmethylated 55 (60.4%) 26 (54.1%) 29 (67.4%)
NA 2 (2.1%) 0 (0) 2 (4.6%)
RTKs alterations (amplification, mutation)
No. of patients 53 (58.2%) 26 (49.0%) 27 (50.9%)
EGFR 28 (52.8%) 7 (26.9%) 21 (77.8%)
PDGFRA 8 (15.1%) 2 (7.7%) 6 (22.2%)
MET 9 (17.0%) 4 (15.4%) 5 (18.5%)
VEGFR2 7 (13.2%) 3 (11.5%) 4 (14.8%)

Unless otherwise indicated, data are number of patients, with percentages in parentheses. Data are means ± standard deviations.

NA, not applicable; LGG, lower-grade glioma; WHO, World Health Organization; IDH, isocitrate dehydrogenase; MGMT, O6-methylguanine-DNA-methyltransferase; RTKs, receptor tyrosine kinases; CNV, copy number variation.