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. 2019 Jan 1;10(3):697–707. doi: 10.7150/jca.28494

Table 1.

Demographic, clinical and pathological information of TCGA cohort.

TCGA Cohort
No. of patients 408
Age year
Mean 75.0
Range 40~98
Gender n(%)
Male 301(73.8)
Female 107(26.2)
Stage n(%)
I 2(0.5)
II 130(31.9)
III 140(34.3)
134(32.8)
Unknown 2(0.5)
TMIT types n(%)
I 150(36.8)
II 150(36.8)
III 54(13.2)
54(13.2)
FGFR3 n(%)
Mutation 60(14.7)
Wild type 348(85.3)
RB1 n(%)
Mutation 71(17.4)
Wild type 337 (82.6)
Mutation burden x±σ 356.9±384.7
mRNA expression x±σ
CD8A 3.1±5.8
PD-L1 3.1±5.1
IFN-γ 0.6±1.5
Cytolytic activity x±σ 6.6±11.8
Neoantigen number x±σ 45.8±42.8

The cytolytic activity of each sample was calculated using the value of the geometric mean of granzyme and perforin1. The predicted neoantigen number was referenced in a previous report by Chan-Young Ock. TCGA, the Cancer Genome Atlas; TMIT, tumor microenvironment immune type; x±σ, mean ± standard deviation.