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. 2012 Sep 12;2012:417673. doi: 10.1155/2012/417673

Table 1.

Phase III studies with bevacizumab and chemotherapy as first-line treatment of metastatic breast cancer.

Study Treatment line Arms Patients Response rate Progression-free survival Overall survival Crossover
E2100
(2007)
First Paclitaxel q1w +/− Bev 10 mg/kg q2w 722 36.9% versus 21.2% (P < 0.001) 11.8 versus 5.9 months [HR 0.6 (0.51–0.7)] 26.7 versus 25.2 months [HR 0.88 (P = 0.16)] Not allowed

AVADO
(2008)
First Docetaxel q3w + Bev 15 mg/kg or Bev 7.5 mg/kg or Placebo q3w 736 64% (P < 0.001) versus 55% (P = 0.07) versus 46% 10.1 [HR 0.77 (0.64–0.93)] versus 9.0 [HR 0.86 (0.72–1.04)] versus 8.2 months 30.2 [HR 1.03 (0.7–1.3)] versus 30.8 [HR 1.05 (0.81–1.36)] versus 31.9 months Allowed

RIBBON 1
(2009)
First Capecitabine q3w + Bev 15 mg/kg q3w or Placebo q3w
Anthracycline1/ Taxane2 q3w + Bev 15 mg/kg q3w or Placebo q3w
1,237 35.4% versus 23.6% (P = 0.009)
51.3% versus 37.9% (P = 0.005)
8.6 versus 5.7 months [HR 0.69 (0.56–0.84)]
9.2 versus 8.0 months [HR 0.64 (0.52–0.80)]
29.0 versus 21.2 months [HR 0.85 (0.63–1.14)]
25.2 versus 23.8 months [HR 1.03 (0.77–1.38)]
Allowed

1Adriamycin or Epirubicin + Cyclophosphamide +/− 5-Fluorouracil q3w; 2Docetaxel or nab-Paclitaxel q3w.

Abbreviations: ORR: overall response rate; PFS: progression-free survival; HR: hazard ratio; LD: low dose; HD: high dose.