The results showed that activated dendritic cells (aDCs), B cells, CD8+ T cells, DCs, immature dendritic cells (iDCs), macrophages, mast cells, neutrophils, plasmacytoid dendritic cells (pDCs), T helper cells, T follicular helper (Tfh) cells, T helper type 1 (Th1) cells, tumor-infiltrating lymphocyte (TIL) and T regulatory cells (Tregs) were significantly different in the high- and low-risk groups (Figure 9A). This evidence concerns the gene CD8A and neoplasm.