Skip to main content
. 2022 Jul 8;12:918606. doi: 10.3389/fonc.2022.918606

Table 1.

Correlation between NCAPG2 and clinic-pathological examined by TCGA-LGG database.

Characteristic Low expression of NCAPG2 High expression of NCAPG2 p
n 264 264
WHO grade, n (%) < 0.001
G2 144 (30.8%) 80 (17.1%)
G3 88 (18.8%) 155 (33.2%)
IDH status, n (%) < 0.001
WT 29 (5.5%) 68 (13%)
Mut 233 (44.4%) 195 (37.1%)
1p/19q codeletion, n (%) < 0.001
codel 109 (20.6%) 62 (11.7%)
non-codel 155 (29.4%) 202 (38.3%)
Primary therapy outcome, n (%) < 0.001
PD 34 (7.4%) 76 (16.6%)
SD 69 (15.1%) 77 (16.8%)
PR 40 (8.7%) 24 (5.2%)
CR 84 (18.3%) 54 (11.8%)
Race, n (%) 0.560
Asian 3 (0.6%) 5 (1%)
Black or African American 9 (1.7%) 13 (2.5%)
White 245 (47.4%) 242 (46.8%)
Age, n (%) 0.068
<=40 143 (27.1%) 121 (22.9%)
>40 121 (22.9%) 143 (27.1%)
Histological type, n (%) 0.084
Astrocytoma 86 (16.3%) 109 (20.6%)
Oligoastrocytoma 68 (12.9%) 66 (12.5%)
Oligodendroglioma 110 (20.8%) 89 (16.9%)
OS event, n (%) < 0.001
Alive 222 (42%) 170 (32.2%)
Dead 42 (8%) 94 (17.8%)
DSS event, n (%) < 0.001
Alive 224 (43.1%) 173 (33.3%)
Dead 37 (7.1%) 86 (16.5%)
PFI event, n (%) < 0.001
Alive 186 (35.2%) 132 (25%)
Dead 78 (14.8%) 132 (25%)
Age, meidan (IQR) 39 (31, 50.25) 42.5 (33, 54.25) 0.017

G2, grade II; G3, grade III; PD, progressive disease; SD, stable disease; PR, partial response; CR, complete response; OS event, Overall survival event; DSS event, disease specific survival; and PFI event, progression –free survival.