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. 2017 Dec 14;9(14):11465–11476. doi: 10.18632/oncotarget.23222

Table 1. Clinical and pathological characteristics of study participants.

Characteristics No. (%) P (Cox univariate and multivariate analysis for overall survival)
Total No. patients 59 (100%)
MTHFR C677T 0.777 and 0.849
CC 15 (25.4%)
CT 20 (33.9%)
TT 24 (40.7%)
MTHFR A1298C
AA 58 (98.3%)
AC 1 (1.7%)
CC 0 (0.0%)
Age at diagnosis, y 0.416 and 0.909
Median (range) 16.0 (5–52)
Follow-up, mo
Median (range) 39.1 (29.4–69.6)
Gender 0.866 and 0.475
Male 37 (62.7%)
Female 22 (37.3%)
Primary location 0.089 and 0.056
axial skeleton 12 (20.3%)
distal femur 24 (40.7%)
proximal tibia 12 (20.3%)
proximal humerus 8 (13.6%)
proximal femur 1 (1.7%)
distal tibia and fibula 2 (3.4%)
Metastasis at diagnosis 0.004 and 0.033
Absent 39 (66.1%)
Present 20 (33.9%)
Histological subtype 0.059 and 0.052
Common type(osteoblastic, chondroblastic, fibroblastic) 36 (61.0%)
Telangiectatic type 3 (5.1%)
Histological response 0.164 and 0.294
Good (≥90%) 11 (18.6%)
Poor (<90%) 33 (55.9%)
Not evaluable 15 (25.4%)
Death
Yes 28 (47.5%)
No 31 (52.5%)
Progression
Yes 36 (61.0%)
No 23 (39.0%)

Only one patient was tested as heterozygous mutant genotype of A1298C with a mutation frequency of 0.84%, thus no statistical calculation has been done due to its low incidence. As for the incidence of C667T, 15 (25.4%) patients had wild type, 20 (33.9%) had heterozygous mutant genotype and 24 (40.7%) had homozygous mutant genotype with the genic mutation frequency of 57.7%.