From: Validating ORR and PFS as surrogate endpoints in phase II and III clinical trials for NSCLC patients: difference exists in the strength of surrogacy in various trial settings
Surrogate endpoint
True endpoint
No. of arms
rs
95%CI
ORR
Median OS
254
0.700
0.631,0.758
Median PFS
271
0.831
0.790,0.864
306
0.755
0.702,0.799