Skip to main content
. 2024 Apr 26;2:37. doi: 10.1038/s44276-024-00056-8

Table 6.

Univariate and multivariate Cox proportional hazard model recurrence free survival analysis for clinicopathologic features and adaptive T cell and macrophage phenotypes in CLM with preoperative chemotherapy (n-56).

Factor Univariate Multivariate
HR 95% CI p value HR 95% CI p value
Age (year) 0.99 0.961–1.018 0.458
Gender 0.93 0.524–1.665 0.817
Primary tumor location 0.94 0.474–1.859 0.855
Primary tumor T stage (T3-T4) 2.07 0.497–8.577 0.318
Primary nodal status (N1) 1.33 0.687–2.585 0.396
Synchronous liver metastasis 1.25 0.671–2.318 0.485
Preoperative CEA level (>5 ng/mL) 0.81 0.444–1.466 0.482
Post hepatectomy chemotherapy 1.90 0.874–4.123 0.106
Diameter of largest liver metastasis (>5 cm) 0.56 0.236–1.332 0.190
Number of liver metastasis 1.38 0.765–2.475 0.286
Liver resection margin 0.96 0.379–2.448 0.936
Major pathological responsea 1.45 0.792–2.657 0.229
Cell phenotype
 CD68+ 0.63 0.345–1.142 0.127
 CD68+pSMAD3+ 2.01 1.113–3.634 0.021 1.96 1.052–3.655 0.034
 CD68+TGFb+ 0.88 0.490–1.594 0.681
 CD68+FOXP+ 0.91 0.487–1.709 0.776
 CD68+CD163+ (M2) 0.44 0.235–0.833 0.012 0.69 0.262–1.815 0.450
 CD68+CD86+ (M1) 1.67 0.895–3.119 0.107

Factors with a threshold p value < 0.10 were selected for the final model.

HR hazard ratio, CI confidence interval, CEA carcinoembryonic antigen, CLM colorectal liver metastasis.

aData of major pathological response was missing in 3 patients.

Statistically significant p-values are in bold