We applied multivariate analyses using the Cox proportional hazard regression model, comparing PLXNC1 expression values with other clinical factors (e.g., age, gender, tumor size, tumor stage, number of lymph node metastasis, recurrence status) as covariates, to investigate whether the expression levels of PLXNC1 were an independent prognostic factor in our internal GC cohort (n = 111). The gene discussed is PLXNC1; the disease is neoplasm.