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. 2023 Mar 9;15:40. doi: 10.1186/s13148-023-01456-2

Table 2.

Clinicopathological features for patients after re-evaluation

HGG (n = 25) AT/RT (n = 8) CNS NB-FOXR2 (n = 7) ETMR (n = 6) EPN (n = 6) OTHER (n = 14)
Age at diagnosis, median (years) 12.7 2.6 5.3 2.8 5.9 3.3
Gender
 Male 12 (48%) 4 (50%) 3 (43%) 6 (100%) 3 (50%) 9 (64%)
 Female 13 (52%) 4 (50%) 4 (57%) ¨ 3 (50%) 5 (36%)
Location of primary tumor
Hemisphere 18 (72%) 7 (88%) 7 (100%) 5 (83%) 6 (100%) 9 (64%)
Central/Midline 7 (28%) 1 (12%) ¨ 1 (17%) ¨ 2 (14%)
Details unknown 3 (22%)
Metastatic status
M0 24 (96%) 7 (88%) 6 (86%) 6 (100%) 6 (100%) 13 (93%)
M1-3 1 (4%) ¨ 1 (14%) ¨ ¨ 1 (7%)
Details unknown 1 (12%)
Tumor resection
GTR 8 (32%) 3 (38%) 5 (71%) 2 (33%) 4 (67%) 7 (50%)
Partial resection 9 (36%) 1 (12%) 2 (29%) 1 (17%) 1 (17%) 2 (14%)
Biopsy 4 (16%)
Details unknown 4 (16%) 4 (50%) 3 (50%) 1 (17%) 5 (36%)
Radiotherapy received
Yes 19 (76%) 2 (25%) 7 (100%) 1 (17%) 5 (83%) 7 (50%)
No 6 (20%) 6 (75%) ¨ 5 (83%) 1 (17%) 7 (50%)
Chemotherapy received
Yes 21 (84%) 8 (100%) 7 (100%) 5 (83%) 6 (100%) 12 (85%)
No 3 (12%) ¨ ¨ 1 (17%) ¨ 2 (15%)
High-dose chemotherapy with stemcell rescue ¨ 1 (12%) 2 (29%) 2 (33%) ¨ 2 (14%)
Details unknown 1 (4%) ¨ ¨ ¨ ¨ ¨
Survival data
5-year progression free survival 17% ± 17% 25% ± 37% 100% 17% ± 48% 83% ± 21% 36% ± 27%
5-year overall survival 20% ± 16% 25% ± 27% 100% 33% ± 35% 100% 50% ± 26%

HGG, High-grade glioma; AT/RT, atypical teratoid rhabdoid tumour; EPN, ependymoma