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. 2018 Sep 26;8(1):e1515612. doi: 10.1080/2162402X.2018.1515612

Table 2.

Multivariate survival analyses of the immunological biomarkers affecting crude survival in the total cohort and Lynch syndrome subset using Cox propotional hazard model.

  Total cohort (= 236)*
Lynch syndrome (= 141)**
 
Variable HR 95% CI P HR 95% CI P  
CD3              
 Low vs. high 2.5 1.4–4.6 0.002 3.4 1.6–7.3 0.002  
CD8              
 Low vs. high 1.6 0.9–2.8 0.122 2.0 1.0–4.2 0.058  
CD68              
 Intermediate vs. high 1.9 0.9–4.1 0.065 3.4 0.9–12.3 0.083  
 Low vs. high 2.1 1.0–4.4 0.043 6.5 1.8–23.3 0.004  
B2M              
 Normal vs. loss 3.4 1.4–8.7 0.009 3.5 1.2–10.1 0.022  
 Normal vs. loss*** 3.7 1.3–10.1 0.012  
PD-L1+ TC              
 5–9% vs. ≥ 10% 1.0 0.2–4.9 0.953  
 < 5% vs. ≥ 10% 1.5 0.3–7.3 0.635  
PD-L1+ TIIC              
 5–9% vs. ≥ 10% 3.5 0.7–17.3 0.117  
 < 5% vs. ≥ 10% 4.7 0.9–23.7 0.059  
 5–9% vs. ≥ 10%*** 3.5 0.6–19.0 0.146  
 < 5% vs. ≥ 10%*** 7.9 1.5–40-4 0.013  

Abbreviations: HR, hazard ratio; CI, confidence intervals; TC, tumor cells; TIIC, tumor-infiltrating immune cells; MMR, mismatch repair; TNM, tumor node metastasis.

*Analyses were adjusted for MMR status, TNM stage, sex and age.

**Subset analyses in the Lynch syndrome cohort were adjusted for TNM stage, sex and age.

***Analyses were adjusted for MMR status, TNM stage, sex, age and CD8 expression levels.