Hiret 2016.
Methods | Phase II randomised study |
Participants | People with KRAS WT mCRC whose disease progressed on first‐line treatment with fluoropyrimidine‐based chemotherapy and bevacizumab |
Interventions | mFOLFOX or FOLFIRI (the one not used in first‐line treatment) with bevacizumab vs mFOLFOX or FOLFIRI (the one not used in first‐line treatment) with cetuximab |
Outcomes | Primary endpoint: PFS at 4 months. Secondary endpoints: response rate, median PFS, OS, safety, quality of life (EORTC QLQ‐C30) |
Notes |