In our cohort, the combination of necrosis and brain invasion was the only pathological predictor significantly associated with an increased reoccurrence risk (HR= 4.560, P=0.001); necrosis alone did not reach significance (HR=1.898, P=0.145). Similarly, combined necrosis and brain invasion had the worst cumulative survival relative to any other pathological predictor, including necrosis (P=0.001). This trend was maintained after GTR (P=0.001), whereas necrosis alone and combined necrosis and brain invasion behaved similarly after STR(P=0.001).
RT was administered on clinical criteria. Examination of the factors associated with administered RT identified combined necrosis and brain invasion (HR=3.088, p=0.034) and STR (HR= 3.143, P=0.001). RT was associated with worse survival (P=0.001), especially after GTR (P=0.001). Unlike high mitotic count (P=0.961), necrosis alone (P=0.002) but specially combined necrosis and brain invasion (P=0.001) magnified the apparent deleterious effect of RT.