|
|
||||||||
Articles |
HER-2 is a member of the c-erbB family of receptor tyrosine kinases and is overexpressed by 20-30% of human breast cancers. HER-2 overexpression is an independent adverse prognostic factor and may also predict for response to both chemotherapy and endocrine agents. Trastuzumab is a humanised monoclonal antibody that binds with high affinity to the extracellular domain of HER-2. In HER-2-overexpressing preclinical models trastuzumab has been shown to have a marked antiproliferative effect and demonstrates synergy with a number of cytotoxic drugs. Several phase II and phase III clinical trials have now been performed in patients with advanced breast cancer that overexpress HER-2. Trastuzumab was initially shown to be active and well tolerated as a single agent in heavily pretreated women. Subsequently, studies of first-line treatment for metastatic breast cancer have demonstrated an improvement in survival for trastuzumab when used in combination with either paclitaxel or an anthracycline-cyclophosphamide regimen compared with chemotherapy alone. Unexpectedly, the combination of trastuzumab and the anthracycline-containing regimen was associated with a significant incidence of cardiac dysfunction. The benefit of trastuzumab is generally confined to patients whose tumours have gene amplification as detected by fluorescence in situ hybridisation (FISH) and this is tightly associated with immunohistochemical (IHC) staining at the highest (3+) level. A small number of patients have IHC 2+ tumours together with FISH evidence of gene amplification and may also derive benefit from treatment. Trastuzumab has also been shown to be effective when used as first-line monotherapy for advanced breast cancer. Trials to date have employed trastuzumab in a weekly schedule, but there is emerging evidence that a three-weekly regimen may be as effective. Trastuzumab has shown encouraging activity when used with other agents including docetaxel and vinorelbine. The combination of trastuzumab, docetaxel, and platinum salts also appears to be very active. The role of trastuzumab as adjuvant therapy for early breast cancer is being tested in a number of large randomised trials.
This article has been cited by other articles:
![]() |
A. Vazquez-Martin, C. Oliveras-Ferraros, R. Colomer, J. Brunet, and J. A. Menendez Low-scale phosphoproteome analyses identify the mTOR effector p70 S6 kinase 1 as a specific biomarker of the dual-HER1/HER2 tyrosine kinase inhibitor lapatinib (Tykerb(R)) in human breast carcinoma cells Ann. Onc., June 1, 2008; 19(6): 1097 - 1109. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. E Hynes ErbB Receptors in Cancer: HER2/ErbB2 as a Therapeutic Target Am. Assoc. Cancer Res. Educ. Book, April 12, 2008; 2008(1): 123 - 130. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Yamaguchi, T. Oyama, E. Ito, H. Satoh, S. Azuma, M. Hayashi, K. Shimizu, R. Honma, Y. Yanagisawa, A. Nishikawa, et al. NOTCH3 Signaling Pathway Plays Crucial Roles in the Proliferation of ErbB2-Negative Human Breast Cancer Cells Cancer Res., March 15, 2008; 68(6): 1881 - 1888. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Bartsch, C. Wenzel, G. Altorjai, U. Pluschnig, M. Rudas, R. M. Mader, M. Gnant, C. C. Zielinski, and G. G. Steger Capecitabine and Trastuzumab in Heavily Pretreated Metastatic Breast Cancer J. Clin. Oncol., September 1, 2007; 25(25): 3853 - 3858. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Jiang, W. Shi, Q. Zhang, X. Wang, M. Guo, Z. Cui, C. Su, Q. Yang, Y. Li, J. Sham, et al. Gene Therapy Using Adenovirus-Mediated Full-length Anti-HER-2 Antibody for HER-2 Overexpression Cancers. Clin. Cancer Res., October 15, 2006; 12(20): 6179 - 6185. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Li-Ning-T, R. Ronchetti, C. Torres-Cabala, and M. J. Merino Role of Chromogenic in Situ Hybridization (CISHTM) in the Evaluation of HER2 Status in Breast Carcinoma: Comparison with Immunohistochemistry and Fish International Journal of Surgical Pathology, October 1, 2005; 13(4): 343 - 351. [Abstract] [PDF] |
||||
![]() |
J. A. Menendez, L. Vellon, and R. Lupu Antitumoral actions of the anti-obesity drug orlistat (XenicalTM) in breast cancer cells: blockade of cell cycle progression, promotion of apoptotic cell death and PEA3-mediated transcriptional repression of Her2/neu (erbB-2) oncogene Ann. Onc., August 1, 2005; 16(8): 1253 - 1267. [Abstract] [Full Text] [PDF] |
||||
![]() |
R Duncan, M J Vicent, F Greco, and R I Nicholson Polymer-drug conjugates: towards a novel approach for the treatment of endrocine-related cancer Endocr. Relat. Cancer, July 1, 2005; 12(Supplement_1): S189 - S199. [Abstract] [Full Text] [PDF] |
||||
![]() |
Z. Suo, K. U. Daehli, C. Fr. Lindboe, E. Borgen, A. Bassarova, and J. M. Nesland Real-Time PCR Quantification of c-erbB-2 Gene is an Alternative for Fish in the Clinical Management of Breast Carcinoma Patients International Journal of Surgical Pathology, October 1, 2004; 12(4): 311 - 318. [Abstract] [PDF] |
||||
![]() |
D. K. Biswas, Q. Shi, S. Baily, I. Strickland, S. Ghosh, A. B. Pardee, and J. D. Iglehart NF-{kappa}B activation in human breast cancer specimens and its role in cell proliferation and apoptosis PNAS, July 6, 2004; 101(27): 10137 - 10142. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. F. V. Woude, G. J. Kelloff, R. W. Ruddon, H.-M. Koo, C. C. Sigman, J. C. Barrett, R. W. Day, A. P. Dicker, R. S. Kerbel, D. R. Parkinson, et al. Reanalysis of Cancer Drugs: Old Drugs, New Tricks Clin. Cancer Res., June 1, 2004; 10(11): 3897 - 3907. [Full Text] [PDF] |
||||
![]() |
J. Caldwell Pharmacogenetics and Individual Variation in the Range of Amino Acid Adequacy: The Biological Aspects J. Nutr., June 1, 2004; 134(6): 1600S - 1604S. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Zhou, N. Fernandes, I. L. Dodge, A. L. Reddi, N. Rao, H. Safran, T. A. DiPetrillo, D. E. Wazer, V. Band, and H. Band ErbB2 Degradation Mediated by the Co-chaperone Protein CHIP J. Biol. Chem., April 11, 2003; 278(16): 13829 - 13837. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |