Table 4.
Clinical and genomic characteristics of study population according to subsequent SubRT, ROBO1, and KAT2B somatic mutation status.
Characteristic | No SubRT+mutated (n = 2) | SubRT +nonmutated (n = 6) | No SubRT+nonmutated (n = 10) | P value |
---|---|---|---|---|
AGE (mean ± SD) | 65.5 ± 16.3 | 70.3 ± 6.6 | 65.5 ± 6.9 | 0.500 |
SEX (male) | 1 (50.0%) | 5 (83.3%) | 2 (20.0%) | 0.027 |
ROBO1 | 2 (100.0%) | 0 (0.0%) | 0 (0.0%) | 0.007 |
KAT2B | 2 (100.0%) | 0 (0.0%) | 0 (0.0%) | 0.007 |
APBA1 | 1 (50.0%) | 0 (0.0%) | 1 (10.0%) | 0.314 |
GNA13 | 1 (50.0%) | 1 (16.7%) | 0 (0.0%) | 0.085 |
MYD88 | 2 (100.0%) | 1 (16.7%) | 3 (30.0%) | 0.193 |
SETD1B | 1 (50.0%) | 0 (0.0%) | 1 (10.0%) | 0.314 |
IniRT | 0 (0.0%) | 0 (0.0%) | 2 (20.0%) | 0.608 |
IniST | 1 (50.0%) | 6 (100.0%) | 6 (60.0%) | 0.212 |
SubRT | 0 (0.0%) | 6 (100.0%) | 0 (0.0%) | <0.001 |
SubST | 0 (0.0%) | 2 (33.3%) | 1 (10.0%) | 0.669 |
OS | 1 (50.0%) | 6 (100.0%) | 9 (90.0%) | 0.314 |
P value is estimated using the Wilcoxon rank-sum test or Fisher's exact test.