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Table 3 Trials of bevacizumab in early-stage breast cancer: preoperative therapy

From: Antiangiogenic therapy for breast cancer

Reference

Phase

Number of patients

Treatment

Response rate (%)

Hurvitz et al. [30]

II (randomised)

37 of 90 planned (HER2-negative)

A: TAC + B (7.5 mg/kg)

All regimens: RR 95; CR 59; PR 35

   

B: TAC + placebo

A: PR 58; CR 42

   

C: TAC + B (15 mg/kg)

B + D: PR 27; CR 64

   

D: TAC + placebo (2:1:2:1, randomisation)

D: PR 21; CR 71

Makhoul et al. [31]

II

36 (11 HER2-negative)

Bevacizumab + docetaxel + cyclophosphamide (4 cycles) → doxorubicin (4 cycles) → bevacizumab (adjuvant, 9 cycles)

PR 31; CR 39; pCR breast 38; pCR breast + axilla 29

Greil et al. [32]

II

18 (HER2-negative)

Bevacizumab × 5* + (docetaxel + capecitabine) × 6*

pCR 22

Balduzzi et al. [33]

II

30

Epirubicin + cisplatin + fluorouracil × 4* → bevacizumab + paclitaxel × 3*

pCR 33; CR + PR 87

Wedam et al. [34]

II

21 (81% HER2-negative)

Bevacizumab × 1* → bevacizumab + doxorubicin + docetaxel × 6*

PR 67; CR 0

Lyons et al. [35]

II

49 (number of patients receiving bevacizumab not reported)

Docetaxel + bevacizumab or docetaxel

CR 14; PR 65

Raefsky et al. [36]

II

25

Nab-paclitaxel + carboplatin × 6* + trastuzumab + bevacizumab × 23*

pCR 26; PR 16

Locatelli et al. [37]

II (randomised)

23 (19 evaluable; locally advanced)

B → vinorelbine + capecitabine (9 pts)

NR

   

B + vinorelbine + capecitabine (14 pts)

NR

Torrisi et al. [38]

II

37 (36 evaluable; estrogen and/or progesterone positive)

Bevacizumab + capecitabine + vinorelbine + letrozole

RR 86; pCR 0

  1. Studies with ≥15 evaluable patients are included. B, bevacizumab, in combination with chemotherapy preoperatively plus adjuvant for 52 weeks; CR, complete response; NR, not reported; pCR, pathological complete response; PR, partial response; pts, patients; RR, response rate; TAC, docetaxel, doxorubicin, cyclophosphamide (six cycles preoperatively). *Times of treatment.