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. 2024 Dec 16;28(24):e70286. doi: 10.1111/jcmm.70286

TABLE 1.

Clinical data and predicted molecular subtypes of ependymoma by predicted sex in Pajtler and COG MCI.

Pajtler N = 492 Male, N = 302 Female, N = 190
Predicted subtypes, n (%)
PF‐EPN‐A 238 154 (65) 84 (35)
PF‐EPN‐B 52 21 (40) 31 (60)
PF‐SE 34 26 (76) 8 (24)
SP‐EPN 21 13 (62) 8 (38)
SP‐MPE 26 14 (54) 12 (46)
ST‐EPN‐RELA 87 56 (64) 31 (36)
ST‐EPN‐YAP1 13 3 (23) 10 (77)
ST‐SE 21 15 (71) 6 (29)
Vital status, n (%)
Alive 273 154 (56) 119 (44)
Death 83 56 (67) 27 (33)
Missing 136 92 44
Progression, n (%)
Not progression 168 87 (52) 81 (48)
Progression 198 127 (64) 71 (36)
Missing 126 88 38
COG MCI N = 103 Male, N = 58 Female, N = 45
Predicted subtypes, n (%)
PF‐EPN‐A 45 23 (51) 22 (49)
PF‐EPN‐B 34 24 (71) 10 (29)
SP‐MPE 14 5 (36) 9 (64)
ST‐EPN‐RELA 10 6 (60) 4 (40)

Note: One case diagnosed with astrocytoma was excluded. Distributions of molecular subtypes of ependymoma in Pajtler and COG APEC14B1‐MCI were statistically significantly different by sex according to Fisher's exact test for count data with simulated p value (based on 2000 replicates).