Table 1.
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) | |
Ⅳ | 134(32.8) | |
Unknown | 2(0.5) | |
TMIT types | n(%) | |
I | 150(36.8) | |
II | 150(36.8) | |
III | 54(13.2) | |
Ⅳ | 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.