What can we learn from Herceptin® trials in metastatic breast cancer?

被引:35
作者
Bell, R [1 ]
机构
[1] Geelong Hosp, Andrew Love Canc Ctr, Geelong, Vic 3220, Australia
关键词
Herceptin (R); metastatic breast cancer; HER2;
D O I
10.1159/000066200
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Herceptin(R) (trastuzumab), an anti-HER2 monoclonal antibody, is the first oncogene-targeted therapy to be developed for the treatment of metastatic breast cancer. The Herceptin clinical trial program has demonstrated that treatment with Herceptin provides substantial clinical benefits when used either as monotherapy or in combination with a number of chemotherapeutic agents. Of note, accurate assessment of HER2 status is essential to ensure that the patients most likely to benefit from Herceptin are identified: patients with immunohistochemistry (IHC) 3+ or fluorescence in-situ hybridization (FISH)positive disease gain the greatest clinical benefits. In addition, clinical benefits appear to be greater the earlier Herceptin is used, although there is currently no direct clinical evidence to indicate whether an initial strategy of combination therapy is better than monotherapy or vice versa. Herceptin has been shown to be generally well tolerated. The most severe adverse events are rare serious infusion-related reactions and cardiotoxicity. These adverse events can be managed by standard care and patients at risk can often be identified prior to the initiation of Herceptin treatment. Currently, Herceptin should be given until disease progression, but there could be benefit in continuing treatment beyond disease progression. Copyright (C) 2002 S. Karger AG, Basel.
引用
收藏
页码:39 / 46
页数:8
相关论文
共 48 条
[1]
GROWTH-FACTORS AND CANCER [J].
AARONSON, SA .
SCIENCE, 1991, 254 (5035) :1146-1153
[2]
[Anonymous], P AM SOC CLIN ONCOL
[3]
Bangemann N, 2000, ANN ONCOL, V11, P143
[4]
Bangemann N., 2000, Breast Cancer Research and Treatment, V64, P123
[5]
Phase II study of weekly intravenous recombinant humanized Anti-p185(HER2) monoclonal antibody in patients with HER2/neu-overexpressing metastatic breast [J].
Baselga, J ;
Tripathy, D ;
Mendelsohn, J ;
Baughman, S ;
Benz, CC ;
Dantis, L ;
Sklarin, NT ;
Seidman, AD ;
Hudis, CA ;
Moore, J ;
Rosen, PP ;
Twaddell, T ;
Henderson, IC ;
Norton, L .
JOURNAL OF CLINICAL ONCOLOGY, 1996, 14 (03) :737-744
[6]
Baselga J, 1998, CANCER RES, V58, P2825
[7]
BIANCO AR, 2000, P AN M AM SOC CLIN, V19, pA75
[8]
Burris HA, 1999, SEMIN ONCOL, V26, P1
[9]
Clinical activity of trastuzumab and vinorelbine in women with HER2-overexpressing metastatic breast cancer [J].
Burstein, HJ ;
Kuter, I ;
Campos, SM ;
Gelman, RS ;
Tribou, L ;
Parker, LM ;
Manola, J ;
Younger, J ;
Matulonis, U ;
Bunnell, CA ;
Partridge, AH ;
Richardson, PG ;
Clarke, K ;
Shulman, LN ;
Winer, EP .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (10) :2722-2730
[10]
Multinational study of the efficacy and safety of humanized anti-HER2 monoclonal antibody in women who have HER2-overexpressing metastatic breast cancer that has progressed after chemotherapy for metastatic disease [J].
Cobleigh, MA ;
Vogel, CL ;
Tripathy, D ;
Robert, NJ ;
Scholl, S ;
Fehrenbacher, L ;
Wolter, JM ;
Paton, V ;
Shak, S ;
Lieberman, G ;
Slamon, DJ .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (09) :2639-2648