“…Despite the significant and promising results shown in clinical trials for immunotherapy, some reviews have pointed out that PD-L1 is not the ideal biomarker to be used in patients’ selection for anti-PD-L1/anti-PD-1 therapies and the prediction of responses to immunotherapy [ 131 , 132 , 133 ]. Other biomarkers are currently under investigation, such as tumor mutational burden, the presence of tumor-infiltrating lymphocytes, microsatellite instability, LDH levels, the presence of visceral disease, major histocompatibility complex, the detection of circulating tumor DNA, the value of CD274 amplifications, and immune gene expression profiles [ 131 , 132 , 133 , 134 ]. Despite of the search for new and better biomarkers, other forms of immunotherapy are also currently under investigation, which include vaccines, adoptive cell therapies, autologous tumor-infiltrating lymphocytes, oncolytic virus therapies, and cytokine agents [ 14 , 133 , 135 ].…”