Table 3. Phase-III data for bevacizumab in adjuvant setting and recurrent ovarian cancer.
| TRIAL | ARMS | Setting | PFS (HR, p value) | OS (HR, p value) |
|---|---|---|---|---|
| ICON 7 [21] N = 1528 |
CP versus CP + B → B (7.5 mg/kg) 12 cycles |
Adjuvant | At 36 months follow-up 17.4 versus 19.8 [0.87; 0.004] |
Restricted mean survival time 44.6 versus 44.5 p = 0.85 |
| GOG 218 [20] N = 1873 |
CP versus CP + B versus CP + B → B (15 mg/kg) 22 cycles |
Adjuvant | 10.3 versus 11.2 versus 14.1 [0.908; 0.16] [0.717; < 0.001] |
39.3 versus 38.7 versus 39.7 [1.036; 0.76] [0.915; 0.45] |
| OCEANS [23] n = 484 |
CG + placebo versus CG + B |
Recurrent ovarian cancer | 8.4 versus 12.4 [0.484; < 0.0001] |
33.7c versus 33.4c [0.960; 0.736] |
| AURELIA [24] n = 361 |
CT (PLD, P or Top) versus CT + Bev |
Recurrent ovarian cancer | 3.4 versus 6.7 [0.48; < 0.001] |
13.3 versus 16.6 [0.85; 0.174] |
CP – carboplatin and paclitaxel, B – Bevacizumab, CG – carboplatin and gemcitabine,
CT – chemotherapy, PLD – liposomal doxorubicin, P – pacliltaxel, top – topotecan,
PFS – progression-free survival, OS – overall survival, HR – hazard ratio.