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. 2022 Jul 14;4(1):vdac111. doi: 10.1093/noajnl/vdac111

Table 2.

Demographics Table for RPA risk Groups for TCGA Cohort

Group 1 (N = 327) Group2 (N = 75) Group 3 (N = 176) Group 4 (N = 188) Total (N = 766)
Clinical and Demographics Variables
Sex
 Female 128 (39.1%) 38 (51.4%) 68 (41.7%) 73 (42.9%) 307 (41.8%)
 Male 199 (60.9%) 36 (48.6%) 95 (58.3%) 97 (57.1%) 427 (58.2%)
Age at diagnosis
 Mean (SD) 60.5 (11.9) 41.1 (10.6) 42.3 (12.5) 40.0 (12.4) 49.7 (15.4)
 Median 61.0 44.0 40.0 38.5 51.0
 Q1, Q3 54.5, 69.0 34.2, 50.0 33.0, 51.0 30.0, 49.8 37.0, 61.0
 Range 14.0–88.0 10.0–54.0 20.0–75.0 14.0–74.0 10.0–88.0
Grade
 II 6 (1.8%) 10 (13.5%) 52 (31.9%) 113 (66.5%) 181 (24.7%)
 III 38 (11.6%) 19 (25.7%) 91 (55.8%) 57 (33.5%) 205 (27.9%)
 IV 283 (86.5%) 45 (60.8%) 20 (12.3%) 0 (0.0%) 348 (47.4%)
WHO grouping
 IDH-mutant Astrocytoma 0 (0.0%) 0 (0.0%) 86 (48.9%) 117 (62.2%) 203 (29.0%)
 IDH-mutant GBM 0 (0.0%) 0 (0.0%) 20 (11.4%) 0 (0.0%) 20 (2.9%)
 IDH-mutant oligodendroglioma 0(0.0%) 0 (0.0%) 70 (39.8%) 71 (37.8%) 141 (20.1%)
 IDH-wildtype astrocytoma 43 (15.8%) 29 (46.0%) 0 (0.0%) 0 (0.0%) 72 (10.3%)
 IDH-wildtype GBM 230 (84.2%) 34 (54.0%) 0 (0.0%) 0 (0.0%) 264 (37.7%)
IDH status
 Wildtype 273 (100.0%) 63(100.0%) 0 (0.0%) 0 (0.0%) 336 (48.0%)
 Mutant 0 (0.0%) 0 (0.0%) 176 (100.0%) 188 (100.0%) 364 (52.0%)
ATRX status
 Wildtype 170 (52.0%) 36 (48.0%) 98 (55.7%) 105 (55.9%) 409 (53.4%)
 Mutant 9 (2.8%) 3 (4.0%) 67 (38.1%) 83 (44.1%) 162 (21.1%)
Vital status
 Alive 53 (16.2%) 26 (34.7%) 126 (71.6%) 175 (93.1%) 380 (49.6%)
 Deceased 274 (83.8%) 49 (65.3%) 50 (28.4%) 13 (6.9%) 386 (50.4%)
Survival time (years)
 Median 1.03 2.14 5.29 14.14 2.50
 95% CI (0.97 to 1.16) (2.04 to 3.92) (4.21 to 7.64) (9.50 to NA) (2.16 to 3.13)
SDL risk
 Mean (SD) 1.2 (0.7) 0.2 (1.1) −0.2 (0.7) −1.7 (0.6) 0.1 (1.3)
 Median 1.3 0.6 −0.3 −1.6 0.2
 Q1, Q3 1.0, 1.6 0.1, 0.9 −0.7, 0.2 −1.9, −1.3 −1.0, 1.3
 Range −1.4 to 2.8 −4.9 to 1.1 −1.0 to 1.5 −3.9 to -1.0 −4.9 to 2.8

Abbreviations: IDH, isocitrate dehydrogenase 1 or 2 gene; ATRX, α-thalassemia, mental retardation, X-linked protein; 1p19q, deletion status of short arm of chromosome 1 and long arm of chromosome 19; GBM, glioblastoma multiforme; SDL risk, survival deep learning risk; RPA, recursive partitioning analysis.