From: Regulatory withdrawal of medicines marketed with uncertain benefits: the bevacizumab case study
Trial | Line in therapy | Trial years | Number patients enrolled | Comparison | Progression-free survival | Overall survival | ||
---|---|---|---|---|---|---|---|---|
 |  |  |  |  | Median difference (months) | Hazard Ratio (95 % confidence interval, P value) | Median difference (months) | Hazard Ratio (95 % confidence interval, P value) |
AVF2119g trial [63] | Second line (previously treated with anthracycline and taxane) | 2000–2002 | 462 | Bevacizumab plus capecitabine versus capecitabine | 0.7 | 0.98 (0.77–1.25, P < 0.86) | 0.6 | 1.05 (0.86–1.30, P < 0.63) |
First line | 2001–2004 | 722 | Bevacizumab plus paclitaxel versus paclitaxel | 5.5 | 0.48 (0.39–0.61, P < 0.0001) | 1.7 | 0.87 (0.72–1.05, P = 0.137) | |
First line | 2006–2007 | 736 | Bevacizumab plus docetaxel versus docetaxel | 0.9 | 0.62 (0.48–0.79, P = 0.0003) | - 1.7 | 1.00, 0.76–1.32, P = 0.98) | |
First line | 2005–2007 | 622 | Bevacizumab plus taxane/anthracycline versus taxane/anthracycline | 1.2 | 0.64 (0.52–0.80, P < 0.0001) | Not reported | 1.11 (0.86–1.43, P = 0.44) | |
 |  | 2005–2007 | 615 | Bevacizumab plus capecitabine versus capecitabine | 2.9 | 0.69 (0.56–0.84, P =0.0002) | 2.9 | 0.88 (0.69–1.13, P = 0.33) |
RIBBON-2 (AVF3693g) [28] | Second line | 2006–2008 | 684 | Bevacizumab plus taxanes, capecitabine or gemcitabine versus taxanes, capecitabine or gemcitabine | 2.1 | 0.78 (0.64–0.93, P = 0.0072) | Non significant difference |  |