Immunological Approaches in the Treatment of Metastasized Breast Cancer

被引:7
作者
Mueller, Volkmar [1 ]
Witzel, Isabell [1 ]
Stickeler, Elmar [2 ]
机构
[1] Univ Med Ctr Hamburg Eppendorf, Dept Gynecol, Hamburg, Germany
[2] Univ Freiburg, Dept Obstet & Gynecol, D-7800 Freiburg, Germany
关键词
Breast cancer; Metastasis; Antibody; Therapy; GROWTH-FACTOR RECEPTOR; MULTICENTER PHASE-II; DEPENDENT CELLULAR CYTOTOXICITY; MONOCLONAL-ANTIBODY; 1ST-LINE TREATMENT; OPEN-LABEL; TRASTUZUMAB; EFFICACY; HER2; SAFETY;
D O I
10.1159/000262454
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A better understanding of tumor biology has led to the development of a number of antibody-based targeted therapies in breast cancer. Several of these newer agents, such as trastuzumab and bevacizumab have demonstrated clinical activity and have improved the treatment of patients with metastatic breast cancer (MBC). Trastuzumab is a monoclonal antibody that binds to the extracellular domain of the HER2 receptor. The addition of trastuzumab to chemotherapy and also to endocrine therapy has enhanced efficacy of treatment. New antibody-based strategies directed against HER2 are under development. These new approaches include pertuzumab, an antibody with a different binding epitope that inhibits dimerization of HER2 with other members of the HER receptor family and TDM1, a trastuzumab-based antibody chemotherapeutic conjugate. Another approach to the treatment of solid tumors is inhibition of angiogenesis. The anti-VEGF antibody bevacizumab has been approved for treatment of MBC. Although the mechanism of action is still under investigation, bevacizumab is tested in other clinical settings such as adjuvant therapy, maintenance therapy, and in combination with both chemotherapy and other targeted agents. In this review, we will summarize the most important studies on trastuzumab and bevacizumab, and describe new antibodies currently under clinical development.
引用
收藏
页码:358 / 366
页数:8
相关论文
共 71 条
[1]   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
[2]  
[Anonymous], CLIN BREAST CANC
[3]   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
[4]   Endocytosis and sorting of ErbB2 and the site of action of cancer therapeutics trastuzumab and geldanamycin [J].
Austin, CD ;
De Mazière, AM ;
Pisacane, PI ;
van Dijk, SM ;
Eigenbrot, C ;
Sliwkowski, MX ;
Klumperman, J ;
Scheller, RH .
MOLECULAR BIOLOGY OF THE CELL, 2004, 15 (12) :5268-5282
[5]   Capecitabine and trastuzumab in heavily pretreated metastatic breast cancer [J].
Bartsch, Rupert ;
Wenzel, Catharina ;
Altorjai, Gabriela ;
Pluschnig, Ursula ;
Rudas, Margaretha ;
Mader, Robert M. ;
Gnant, Michael ;
Zielinski, Christoph C. ;
Steger, Guenther G. .
JOURNAL OF CLINICAL ONCOLOGY, 2007, 25 (25) :3853-3858
[6]   A new anti-ErbB2 strategy in the treatment of cancer: Prevention of ligand-dependent ErbB2 receptor heterodimerization [J].
Baselga, J .
CANCER CELL, 2002, 2 (02) :93-95
[7]  
Blowers Elaine, 2009, Br J Nurs, V18, P351
[8]   Trastuzumab and vinorelbine as first-line therapy for HER2-overexpressing metastatic breast cancer: Multicenter phase II trial with clinical outcomes, analysis of serum tumor markers as predictive factors, and cardiac surveillance algorithm [J].
Burstein, HJ ;
Harris, LN ;
Marcom, PK ;
Lambert-Falls, R ;
Havlin, K ;
Overmoyer, B ;
Friedlander, RJ ;
Gargiulo, J ;
Strenger, R ;
Vogel, CL ;
Ryan, PD ;
Ellis, MJ ;
Nunes, RA ;
Bunnell, CA ;
Campos, SM ;
Hallor, M ;
Gelman, R ;
Winer, EP .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (15) :2889-2895
[9]  
CAMERON D, 2009, BREAST CANC RES TREA, V113, P207
[10]   HUMANIZATION OF AN ANTI-P185HER2 ANTIBODY FOR HUMAN CANCER-THERAPY [J].
CARTER, P ;
PRESTA, L ;
GORMAN, CM ;
RIDGWAY, JBB ;
HENNER, D ;
WONG, WLT ;
ROWLAND, AM ;
KOTTS, C ;
CARVER, ME ;
SHEPARD, HM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (10) :4285-4289