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Table 1 Phase II trials of bevacizumab in combination with chemotherapy in metastatic breast cancer

From: Antiangiogenic therapy for breast cancer

Reference

Number of patients

Therapy

ORR (%)

PFS (months)

Ramaswamy et al. [6]

27 (78% HER2-negative)

B + docetaxel

52 (1st + 2nd line)

8

Chan et al. [7]

43 (21 evaluable)

B + docetaxel

Approximately 40 (1st line)

NR

Hurvitz et al. [8]

69 (67 evaluable; HER2-negative)

B + docetaxel

48 (1st line)

8 (TTP)

Perez et al. [9]

45 (HER2-negative)

B + docetaxel + capecitabine

49 (1st line)

11

   

69 (CBR)

 

Hoelzer et al. [10]

61 (57 evaluable)

B + paclitaxel

42 (1st line)

15

 

58 (54 evaluable)

B + paclitaxel + gemcitabine

48

20

Guardino et al. [11]

21 (17 evaluable)

B + paclitaxel + gemcitabine

88 (CBR)

NR

Rugo et al. [12]

46

B + ixabepilone (weekly)

50 (1st line)

NR

 

45

B + ixabepione (q3w)

71

NR

 

32

B + paclitaxel

56

NR

Danso et al. [13]

49 (27 evaluable; HER2-negative)

B + nab-paclitaxel

30 (1st line)

9

Conlin et al. [14]

72

B + nab-paclitaxel (three dosing schedules)

42 (1st line)

9 (TTP)

 

54

 

42

6

 

76

 

42

8

Sledge et al. [15]

103

B + capecitabine

39 (1st line)

NR

Traina et al. [16]

29

B + capecitabine

31 (various; 10 pts with SD >6 months)

NR

Dellapasqua et al. [17]

46

B + capecitabine + cyclophosphamide

48 (1st to 3rd line)

10 (TTP)

Rochlitz et al. [18]

41

B + pegylated liposomal doxorubicin

23 (1st line)

8

  1. Studies with ≥15 evaluable patients are included. B, bevacizumab; CBR, clinical benefit rate; NR, not reported; ORR, overall response rate; PFS, progression free survival; pts, patients; q3w, every third week; SD, stable disease; TTP, time to progression.