“…As a result, in both unadjusted DFS and overall survival (OS), patients with ≤pT3a were significantly better than those with ≥pT3b. In addition, multivariate analysis revealed that ≥T3b in pathological T stage was a significant risk factor for poor DFS and OS 2 . Increasing evidence suggests that response to immunotherapy in RCC is independent of the CD8 + T cell infiltration, or PD‐L1 expression, 3 therefore, careful patient selection using clinical variables including pathological stage as shown in this article should be performed for determining the treatment.…”