Since several studies showed a significant correlation between a baseline T-cell infiltration in the tumor microenvironment and the clinical responses to immune-checkpoint inhibitors [41-43], it may be hypothesized that the first group of tumors, with an inflamed tumor microenvironment, will benefit more from anti-PD-1/PD-L1 directed therapies, compared to those with an oncogene-driven PD-L1 expression status, in absence of T-cell infiltration in the tumor microenvironment. Here, CD274 is linked to neoplasm.