Table 5.
Study | Design | n | Pre-operative treatment | RT | Primary endpoint | Status | Comments |
AXE BEAM trial (NCT00828672) | Randomized | 80 | Concomitant XELOX +/- BV + RT | CT-RT | pCR | Recruiting | |
Phase II | 45 Gy | ||||||
New Beat trial (NCT01554059) | Phase II | 28 | Concomitant FOLFOX + BV + RT | CT-RT | pCR | Recruiting | |
40 Gy/20 fractions | |||||||
NCT01818973 | Phase II | 45 | XELOX + BV for 1 cycle followed by concomitant CT-RT with XELOX + BV for 2 cycles and RT | CT-RT | Tumor regression grade | Recruiting | Adjuvant CT with XELOX for 3 cycles followed by capecitabine for 2 cycles |
50 Gy/25 fractions | |||||||
BACCHUS trial (NCT01650428) | RandomizedPhase II | 60 | FOLFOX + BV for 5 cycles followed by FOLFOX for 1 cycle vs FOLFOXIRI + BV for 5 cycles followed by FOLFOXIRI for 1 cycle | No | pCR | Recruiting | Magnetic resonance imaging-defined poor risk criteria |
NCT01871571 | Phase II | 43 | mFOLFOX7 + BV for 6 cycles | No | pCR | Recruiting | |
NCT00865189 | Randomized Phase II | 91 | FOLFOX + BV for 6 cycles followed by CT-RT with BV and 5-FU vs CT-RT alone | CT-RT | pCR | Ongoing, not recruiting | Not specified RT dose and fractioning |
NCT00462501 | Phase II | 36 | FOLFOX + BV for 4 cycles followed by FOLFOX for 2 cycles with selective use of CT-RT with 5-FU in patients not candidate for R0 resection | CT-RT | R0 resection rate | Ongoing, not recruiting | Not specified RT dose and fractioning |
TRUST trial (EUDRACT 2011-003340-45) | Phase II | 43 | FOLFOXIRI + BV for 6 cycles followed by CTRT with BV and capecitabine or 5-FU | CT-RT 50.4 Gy/28 fractions | DFS rate at 2 yr | Recruiting |
LARC: Locally-advanced rectal cancer; BV: Bevacizumab; RT: Radiotherapy; CT: Chemotherapy; CT-RT: Chemo-radiotherapy; pCR: Pathological complete response; DFS: Disease-free survival; 5-FU: Fluorouracil; XELOX: Capecitabine and oxaliplatin; FOLFOX: 5-FU and oxaliplatin; FOLFOXIRI: 5-FU, oxaliplatin and irinotecan.