With the same method, and highlighting the importance of the tumor immunology, eight immune-related lncRNAs correlated with OS [245] and a six-lncRNA signature could separate two immune risk subgroups, where cohorts of high risk showed reduced levels of CD8-T cells and the immunity-related signature compared to cohorts of low risk, suggesting a role of CD8-T cells as a prognostic feature [246]. This evidence concerns the gene CD8A and neoplasm.