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Logo of bmccancBioMed Centralsearchsubmit a manuscriptregisterthis articleBMC Cancer
BMC Cancer. 2012; 12: 482.
Published online Oct 19, 2012. doi:  10.1186/1471-2407-12-482
PMCID: PMC3488474
Maintenance bevacizumab beyond first-line paclitaxel plus bevacizumab in patients with Her2-negative hormone receptor-positive metastatic breast cancer: efficacy in combination with hormonal therapy
Alessandra Fabi,corresponding author1 Michelangelo Russillo,1 Gianluigi Ferretti,1 Giulio Metro,1 Cecilia Nisticò,1 Paola Papaldo,1 Ferdinando De Vita,2 Giuliana D’Auria,3 Antonello Vidiri,4 Diana Giannarelli,5 and Francesco Cognetti1
1Division of Medical Oncology A, Regina Elena National Cancer Institute, Via Elio Chianesi 53, Rome, Italy
2Division of Medical Oncology, Second University of Naples School of Medicine, II Policlinico, Naples, Italy
3Division of Medical Oncology, Belcolle Hospital, Viterbo, Italy
4Diagnostic Imaging Department, Regina Elena National Cancer Institute, Rome, Italy
5Service of Biostatistics, Regina Elena National Cancer Institute, Rome, Italy
corresponding authorCorresponding author.
Alessandra Fabi: alessandra.fabi/at/; Michelangelo Russillo: michelangelorussillo/at/; Gianluigi Ferretti: gianluigi.ferretti/at/; Giulio Metro: giulio.metro/at/; Cecilia Nisticò: cnistico/at/; Paola Papaldo: p.papaldo/at/; Ferdinando De Vita: devita/at/; Giuliana D’Auria: gdauria/at/; Antonello Vidiri: vidiri/at/; Diana Giannarelli: giannarelli/at/; Francesco Cognetti: cognetti/at/
Received December 27, 2011; Accepted September 22, 2012.
Data on efficacy of bevacizumab (B) beyond first-line taxane -including regimen (BT) as first-line treatment are lacking. Although preclinical results that anti-angiogenic agents combined with hormonal therapy (HT) could be active, no clinical data exist about combination of maintenance Bevacizumab (mBev) with HT.
Thirty-five patients who experienced a response after first-line BT, were given mBev at the dose of 15 mg/kg every 3 weeks. Among 30 pts with hormonal receptor-positive metastatic breast cancer (MBC), 20 (66.6%) received HT with mBev (mHTBev). Objective of the study was the outcome and safety of mBev and in two groups of patients receiving HT or not.
Complete response and partial response was achieved/maintained in 4 (11.4%) and 13 (37.1%) patients, respectively (overall response rate: 48.5%). Clinical benefit was obtained on 23 patients (65.7%). Median of mBev PFS and clinical benefit were 6.8 months (95% CI: 0.8-12.7) and 17.1 months (95% CI :12.2-21.9), respectively. Median PFS of patients who received mHTBev was longer than mBev without HT (13 months and 4.1 months, respectively, p = 0.05). The most common severe toxicities were proteinuria (11.4%) and hypertension (8.5%). No additional toxicity was observed with HTBev.
Maintenance bevacizumab with or without anti-hormonal therapy in patients with hormone receptor positive breast cancer is tolerable and associated with long-term clinical outcome; these results encourage the strategy of prolonging bevacizumab until progression in combination with anti-hormonal agents.
Keywords: Maintenance Bevacizumab, Antiangiogenic agents, HER2 negative metastatic breast cancer
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