Table 5.
Entotic-CIC in PDAC and patient outcome (univariate analysis).
Factor | P value | Hazard ratio (95% confidence interval) | ||
---|---|---|---|---|
Clinicopathologic | Entotic-CIC | (Positive vs. negative) | <0.001 | 1.813 (1.323–2.484) |
Age | (>65 vs. < =65) | 0.853 | 1.024 (0.8–1.31) | |
Gender | (Male vs. female) | 0.010 | 1.380 (1.082–1.761) | |
Location | (Primary vs. metastasis) | <0.001 | 0.327 (0–0.423) | |
Histology | (PDA vs. ASQ) | 0.415 | 0.778 (0.425–1.424) | |
Genetic | KRAS | (Mutated vs. WT) | 0.969 | 0.991 (0.646–1.521) |
TP53 | (Mutated vs. WT) | 0.173 | 1.216 (0.918–1.611) | |
CDKN2A | (Mutated vs. WT) | 0.094 | 1.259 (0.962–1.649) | |
SMAD4 | (Mutated vs. WT) | 0.976 | 0.996 (0.746–1.329) | |
CDKN2AP16INK4A | (Mutated vs. WT) | 0.384 | 1.141 (0.848–1.534) | |
ARID1A | (Mutated vs. WT) | 0.395 | 1.179 (0.807–1.725) | |
CDKN2AP14ARF | (Mutated vs. WT) | 0.310 | 1.199 (0.844–1.703) | |
RNF43 | (Mutated vs. WT) | 0.382 | 0.772 (0.433–1.378) | |
KDM6A | (Mutated vs. WT) | 0.828 | 1.062 (0.619–1.82) | |
APC | (Mutated vs. WT) | 0.166 | 1.464 (0.854–2.51) | |
CNA alteration | MYC | (Amplified vs. not amplified) | 0.883 | 0.941 (0.419–2.115) |
AKT2 | (Amplified vs. not amplified) | 0.399 | 1.297 (0.709–2.371) | |
CCNE1 | (Amplified vs. not amplified) | 0.503 | 0.678 (0.217–2.116) | |
KRAS | (Amplified vs. not amplified) | <0.001 | 5.480 (2.419–12.416) | |
FGFR1 | (Amplified vs. not amplified) | 0.117 | 2.490 (0.796–7.788) | |
CDKN2A | (Deep deletion vs. no deletion) | 0.010 | 1.631 (1.122–2.372) | |
CDKN2AP16INK4A | (Deep deletion vs. no deletion) | 0.019 | 1.575 (1.077–2.303) | |
CDKN2AP14ARF | (Deep deletion vs. no deletion) | 0.016 | 1.604 (1.091–2.358) | |
CDKN2B | (Deep deletion vs. no deletion) | 0.216 | 1.291 (0.862–1.934) | |
SMAD4 | (Deep deletion vs. no deletion) | 0.242 | 0.639 (0.302–1.353) |
The bold value means statistically significant P value.