Monoclonal antibody-based targeted therapy in breast cancer: Current status and future directions

被引:60
作者
Bernard-Marty, Chantal [1 ]
Lebrun, Fabienne [1 ]
Awada, Ahmad [1 ]
Piccart, Martine J. [1 ]
机构
[1] Inst Jules Bordet, Dept Med Oncol, B-1000 Brussels 125, Belgium
关键词
D O I
10.2165/00003495-200666120-00004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The recent development of monoclonal antibodies targeting growth factor receptors in cancer treatment represents a milestone for both researchers and physicians. Advances in the understanding of key molecular pathways for tumour growth and survival have facilitated the development of these targeted therapies, in particular in breast cancer. This review focuses on the three most important recombinant humanised monoclonal antibodies that have shown activity in women with breast cancer: trastuzumab, pertuzumab and bevacizumab. Trastuzumab, an anti-erbB2 (human epidermal growth factor receptor) monoclonal antibody, is currently routinely used in both the metastatic and adjuvant settings for patients with erbB2-positive tumours. Pertuzumab, a monoclonal antibody binding to a different epitope on erbB2 than trastuzumab, is under early clinical evaluation. This drug has been developed for breast cancer, patients, whether overexpressing erbB2 or not. Bevacizumab, a monoclonal antibody directed against vascular endothelial growth factor-A, is being evaluated in the metastatic setting for its antiangiogenic properties, and is showing promising results.
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收藏
页码:1577 / 1591
页数:15
相关论文
共 162 条
[1]   Phase I clinical study of pertuzumab, a novel HER dimerization inhibitor, in patients with advanced cancer [J].
Agus, DB ;
Gordon, MS ;
Taylor, C ;
Natale, RB ;
Karlan, B ;
Mendelson, DS ;
Press, MF ;
Allison, DE ;
Sliwkowski, MX ;
Lieberman, G ;
Kelsey, SM ;
Fyfe, G .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (11) :2534-2543
[2]   Targeting ligand-activated ErbB2 signaling inhibits breast and prostate tumor growth [J].
Agus, DB ;
Akita, RW ;
Fox, WD ;
Lewis, GD ;
Higgins, B ;
Pisacane, PI ;
Lofgren, JA ;
Tindell, C ;
Evans, DP ;
Maiese, K ;
Scher, HI ;
Sliwkowski, MX .
CANCER CELL, 2002, 2 (02) :127-137
[3]  
Allison DE, 2003, P AN M AM SOC CLIN, V22, P197
[4]   Trastuzumab-based treatment of HER2-positive breast cancer: an antibody-dependent cellular cytotoxicity mechanism? [J].
Arnould, L ;
Gelly, M ;
Penault-Llorca, F ;
Benoit, L ;
Bonnetain, F ;
Migeon, C ;
Cabaret, V ;
Fermeaux, V ;
Bertheau, P ;
Garnier, J ;
Jeannin, JF ;
Coudert, B .
BRITISH JOURNAL OF CANCER, 2006, 94 (02) :259-267
[5]  
ARTEAGA CL, 1994, CANCER RES, V54, P3758
[6]  
ATTARD G, 2005, P AN M AM SOC CLIN, V23, P3166
[7]  
Bangemann N, 2000, ANN ONCOL, V11, P143
[8]  
Baselga J, 1999, SEMIN ONCOL, V26, P78
[9]  
Baselga J, 1998, CANCER RES, V58, P2825
[10]  
Bauer-Kosinska B., 2003, EJC Supplements, V1, pS141, DOI 10.1016/S1359-6349(03)90496-4