Trial | Patients | Study design | Primary end-point | Secondary end-point |
---|
ACT I [2] | 560 | CRT vs RT | LC; RFS; CFS; OS | - |
Intergroup [3] | 310 | CRT vs RT | LC; CFS; OS; DFS | - |
EORTC [4] | 110 | CRT vs RT | LC | OS; CFS |
UKCCCR [18] | 856 | CRT vs RT | LC | OS; morbidity |
- LC local control; RFS: relapse free survival, CFS colostomy free survival, OS overall survival, DFS disease free survival.