Table 2.
MSI status | Monotherapy or combination therapy | PD-1 or PD-L1 inhibitors | Nivolumab, pembrolizumab or others (Nivolumab) | Nivolumab, pembrolizumab or others (pembrolizumab) | |
---|---|---|---|---|---|
ORR | 0* | 0.576 | 0.086 | 0.079 | 0.017* |
DCR | 0.012* | 0.04* | 0.688 | 0.062 | 0.964 |
CR | 0.001* | 0.566 | 0.017* | 0.821 | 0.406 |
PR | 0.001* | 0.567 | 0.076 | 0.044* | 0.009* |
SD | 0.835 | 0.284 | 0.335* | 0.084 | 0.018* |
PD | 0.004* | 0.972 | 0.051 | 0.1 | 0.549 |
AEs | 0.607 | 0.259 | 0.036* | 0.44 | 0.867 |
SAE | 0.51 | 0.151 | 0.058 | 0.958 | 0.606 |
PFS | 0.034* | 0.75 | 0.908 | 0.031* | 0.122 |
OS | 0.029* | 0.962 | 0.025* | 0.188 | 0.188 |
P value < 0.05 means significant statistical differences. ORR objective response rate, DCR disease control rate, CR complete response rate, PR partial response rate, SD stable disease rate, PD progression disease rate, AEs adverse events, SAEs severe adverse events, PFS 1-year progression-free survival rate, OS 1-year overall survival rate (OS)