Table 1.
(B) Characteristics of studies (Antiangiogenic drugs+Chemo) included in network meta-analysis.
Study | ClinicalTrials.gov Identifier | Histology | Arm | No.pts | OS HR (95%CI) | PFS HR (95%CI) | Analysis Timing | AE(≥grade3)of any cause(%pts) |
EYOND | NCT01364012 | Non-Squamous | Bevacizumab + Chemo | 138 | 0.68 (0.5,0.93) | 0.4 (0.29,0.54) | PFS:Final | 67% |
Chemo | 138 | OS:Final | 62.00% | |||||
ECOG-4599 | NCT00021060 | Non-Squamous | Bevacizumab + Chemo | 434 | 0.79 (0.67,0.92) | 0.66 (0.57,0.77) | PFS:Final | NA |
Chemo | 444 | OS:Final | NA | |||||
MONET1 | NCT00460317 | Non-Squamous | Motesanib+Chemo | 541 | 0.9 (0.78,1.04) | 0.79 (0.68,0.9) | PFS:Final | 73.00% |
Chemo | 549 | OS:Final | 59% | |||||
BR29 | NCT00795340 | All | Cediranib+Chemo | 153 | 0.94 (0.69,1.3) | 0.91 (0.71,1.18) | PFS:Final | NA |
Chemo | 153 | OS:Final | NA |
OS, overall survival; PFS, progress free survial.