Table 2

Multivariable Cox regression analysis of prognostic factors in the training cohort and validation cohort

HR* (95% CI)P value
Distant metastasis-free survival
Training cohort (n=194)
 HGB (≥130 vs <130 g/L)0.335 (0.126 to 0.890)0.028
 N category (2–3 vs 0–1)2.522 (1.086 to 5.857)0.031
 Immune signature (high vs low)6.295 (2.886 to 13.729)<0.001
 Validation cohort (n=304)
 Age (≥45 years vs <45 years)3.003 (1.355 to 6.654)0.007
 N stage (N2–3 vs N0–1)3.461 (1.501 to 7.979)0.004
 Immune signature (high vs low)4.297 (2.182 to 8.461)<0.001
Progression-free survival
Training cohort (n=194)
 N category (2–3 vs 0–1)2.136 (1.107 to 4.118)0.024
 Immune signature (high vs low)2.775 (1.484 to 5.189)0.001
 Validation cohort (n=304)
 HGB (≥130 vs <130 g/L)0.535 (0.325 to 0.878)0.013
 Age (≥45 years vs <45 years)2.018 (1.194 to 3.411)0.009
 N stage (N2–3 vs N0–1)1.713 (1.028 to 2.854)0.045
 Immune signature (high vs low)2.115 (1.289 to 3.469)0.003
  • HRs and p values were calculated using an adjusted multivariate Cox proportional hazards regression model, immune signature (high risk vs low risk), gender (male vs female), age (≥45 years vs <45 years), T stage (T3–4 vs T1–2), N stage (N2–3 vs N0–1), overall stage (I–III vs IV), ECOG (0 vs 1 vs 2), LDH (≥245 vs <245 U/L), CRP (≥3 vs <3 mg/L), HGB (≥130 vs <130 g/L), and BMI (≥23 vs <23 kg/m²) were included as covariates. Variables were selected with the backward stepwise approach, and the p value threshold was 0.1 (p>0.1) for removing insignificant variables from the model. Only variables significantly associated with survival were presented, and marginally significant variables (0.05<p<0.1) were remained in the final Cox model but not presented in the table.

  • BMI, body mass index; CRP, serum C reactive protein; ECOG, Eastern Cooperative Oncology Group; HGB, hemoglobin; LDH, serum lactate dehydrogenase.