We determined that the presence of tumor immune-related cells, such as myeloid dendritic cells, CD4+ memory T cells, CD8+ T cells, endothelial cells, and M2 macrophage, was positively correlated with low risk, while common lymphoid progenitor, M0 macrophages, M1 macrophages, and NK cells were positively associated with high risk (Figure 10A). This evidence concerns the gene CD4 and neoplasm.