Outcomes | study | Number for patients | Heterogeneity(I2) | RR/HR | 95%CI | P Value | |
---|---|---|---|---|---|---|---|
Cetuximab | bevacizumab | ||||||
Objective response rate | 2 RCTs | 529 | 480 | 0% | 1.08 | 0.99–1.17 | 0.07 |
Disease control rate | 1 RCT | 237 | 256 | – | 0.92 | 0.86–0.99 | 0.02 |
Complete response | 1 RCT | 297 | 295 | – | 3.23 | 1.06–9.79 | 0.04 |
Partial response | 1 RCT | 171 | 167 | – | 1.02 | 0.88–1.17 | 0.81 |
Stable disease | 1 RCT | 297 | 295 | – | 0.62 | 0.46–0.84 | 0.002 |
Progressive disease | 1 RCT | 297 | 295 | – | 1.30 | 0.69–2.45 | 0.41 |
Early objective response rate | 1 RCT | 157 | 173 | – | 1.40 | 1.16–1.68 | 0.0004 |
Hematologic Adverse Events | 1 RCT | 578 | 559 | – | 1.05 | 0.88–1.26 | 0.58 |
Nonhematologic Adverse Events | 1 RCT | 578 | 559 | – | 1.17 | 0.79–1.72 | 0.43 |
Curative intent metastasectomy | 1 RCT | 578 | 559 | – | 1.29 | 0.98–1.71 | 0.07 |
Overall survival | 2 RCTs | 875 | 854 | 20% | 0.86 | 0.76–0.96 | 0.007 |
Progression free survival | 2 RCTs | 875 | 854 | 19% | 0.97 | 0.88–1.06 | 0.44 |