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Table 1 Phase 3 trial results, to date, of anti-angiogenic agents in the treatment of advanced breast cancer

From: Angiogenesis - still a worthwhile target for breast cancer therapy?

Trial name and design

Treatment

type

Progression free survival (months)a

Overall survival (months)a

Response ratea

Capecitabine ± bevacizumab

Refractory

4.86 versus 4.17

(HR 0.98; P = 0.857)

15.1 versus 14.5

19.8% versus 9.1%

(P = 0.001)

RIBBON-2: second line chemotherapy ± bevacizumab

Second line

7.2 versus 5.1

(HR 0.775; P = 0.0072)

18.0 versus 16.4

(P = 0.372)

39.5% versus 29.6%

(P = 0.0193)

E2100: paclitaxel ± bevacizumab

First line

11.8 versus 5.9

(HR 0.60; P = <0.001)

26.7 versus 25.2

(HR 0.88; P = 0.16)

36.9% versus 21.2%

(P < 0.001)

AVADO: docetaxel ± bevacizumab

First line

8.8 versus 8.0

(HR 0.61; P = 0.0001)

Not published

44.4% versus 63.1%

(P = 0.0001)

RIBBON-1: capecitabine (C) or taxane (T) or anthracycline (A) ± bevacizumab or placebo

Second line

C: 8.6 versus 5.7

(HR 0.688; P = 0.0002)

A + Tb: 9.2 versus 8.0

(HR 0.644; P ≤ 0.0001)

C: 29.0 versus 21.2

(HR 0.847; P = 0.2706)

A + Tb: 25.2 versus 23.8

(HR 1.032; P = 0.8298)

C: 35.4% versus 23.6%

(P = 0.0097)

A + Tb: 51.3% versus 37.9%

(P = 0.0054)

Capecitabine ± sunitinib

Refractory

5.5 versus 5.9

(HR 1.224)

16.4 versus 16.5

(HR 0.995)

18.6% versus 16.3%

Capecitabine versus sunitinib

Refractory

2.8 versus 4.2

(HR 1.473; P < 0.001)

Not published

9.1% versus 12.9%

Docetaxel ± sunitinib

First line

8.6 versus 8.3

(HR 0.922)

24.8 versus 25.5

(HR 1.207)

51% versus 39%

(P = 0.0018)

  1. aAnti-angiogenic treatment group first. bAnthracycline and taxane cohorts analysed as a pooled group. HR, hazard ratio.