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. 2022 Jan 27;8(3):268–278. doi: 10.1002/cjp2.260

Table 2.

Results of the multivariate Cox regression analyses of Siglec‐15 per clinically important and DDR molecules subgroups.

Siglec‐15 stratified by group Subgroups PFS DSS
Lymph node status Positive HR 0.668, 95% CI 0.425–1.048, p = 0.079 HR 0.622, 95% CI 0.368–1.051, p = 0.076
Negative HR 0.257, 95% CI 0.090–0.740, p = 0.012 HR 0.173, 95% CI 0.040–0.743, p = 0.018
Differentiation (grade) Well and moderate HR 0.556, 95% CI 0.340–0.909, p = 0.019 HR 0.529, 95% CI 0.298–0.939, p = 0.030
Poor HR 0.600, 95% CI 0.282–1.278, p = 0.186 HR 0.491, 95% CI 0.234–1.467, p = 0.253
AJCC stage I–II HR 0.645, 95% CI 0.406–1.023, p = 0.062 HR 0.494, 95% CI 0.277–0.879, p = 0.017
III–IV HR 0.491, 95% CI 0.203–1.186, p = 0.114 HR 0.716, 95% CI 0.297–1.730, p = 0.459
p53 status Wild type HR 0.454, 95% CI 0.193–1.070, p = 0.071 HR 0.244, 95% CI 0.080–0.749, p = 0.014
Mutant HR 0.625, 95% CI 0.392–1.096, p = 0.054 HR 0.680, 95% CI 0.396–1.169, p = 0.163
BRCA1 Low HR 0.642, 95% CI 0.409–1.006, p = 0.053 HR 0.703, 95% CI 0.425–1.165, p = 0.171
High HR 0.215, 95% CI 0.052–0.888, p = 0.034 HR 0.046, 95% CI 0.005–0.429, p = 0.007
BRCA2 Low HR 0.565, 95% CI 0.330–0.967, p = 0.037 HR 0.519, 95% CI 0.280–0.962, p = 0.037
High HR 0.664, 95% CI 0.353–1.248, p = 0.204 HR 0.718, 95% CI 0.329–1.571, p = 0.407