Beyond tamoxifen - New endpoints for breast cancer chemoprevention, new drugs for breast cancer prevention

被引:19
作者
Fabian, CJ [1 ]
Kimler, BF [1 ]
机构
[1] Univ Kansas, Med Ctr, Kansas City, KS 66160 USA
来源
CANCER PREVENTION: MOLECULAR MECHANISMS TO CLINICAL APPLICATIONS | 2001年 / 952卷
关键词
tamoxifen; breast cancer; breast cancer prevention agents; selective estrogen receptor modulators; biomarkers;
D O I
10.1111/j.1749-6632.2001.tb02727.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Although tamoxifen appears to markedly reduce breast cancer risk in women with a prior diagnosis of atypical hyperplasia or in situ carcinoma, it is not clear what other groups of women receive substantial benefit. Major breast chemoprevention priorities are to (1) develop new agents that (a) have fewer side effects, (b) are effective in ER- as well as tamoxifen-resistant precancerous tissue, and (c) are compatible with hormone therapy; and (2) develop efficient clinical strategies including prognostic and predictive morphologic and molecular biomarkers. Breast tissue may be repeatedly sampled for evidence of intraepithelial neoplasia by fine needle aspiration, ductal lavage, or needle biopsy to select candidates at highest short-term risk as well as to monitor response in small proof of principle studies prior to a large cancer incidence trial. Molecular marker expression may also be used to select a cohort most likely to respond to a particular agent. A large number of new agents are attractive as potential prevention agents and some are already in clinical prevention testing. Compounds which should be effective in ER+ precancerous tissue but may have a better side-effect profile include new selective estrogen receptor modulators which lack uterine estrogen agonist activity, isoflavones, aromatase inactivators/inhibitors for postmenopausal women, and gonadotropin-releasing hormone regimens for premenopausal women. Retinoids, rexinoids, and deltanoids may be efficacious in ER+ tissue resistant to tamoxifen. Agents which should theoretically have activity in ER- or ER+ precancerous tissue include polyamine synthesis inhibitors, tyrosine kinase inhibitors, combined demethylating agents and histone deacetylase inhibitors, as well as metalloprotease and angiogenesis inhibitors. Sample Phase I and Phase H clinical trial designs are re-viewed using modulation of molecular markers and breast intraepithelial neoplasia as the major endpoints.
引用
收藏
页码:44 / 59
页数:16
相关论文
共 116 条
[1]   INHIBITION OF HUMAN AROMATASE BY MAMMALIAN LIGNANS AND ISOFLAVONOID PHYTOESTROGENS [J].
ADLERCREUTZ, H ;
BANNWART, C ;
WAHALA, K ;
MAKELA, T ;
BRUNOW, G ;
HASE, T ;
AROSEMENA, PJ ;
KELLIS, JT ;
VICKERY, LE .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1993, 44 (02) :147-153
[2]   Biomarkers in benign breast disease: Risk factors for breast cancer [J].
Allred, DC ;
Hilsenbeck, SG .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1998, 90 (17) :1247-1248
[3]  
ANDREWS V, 2000, P AN M AM SOC CLIN, V19, pA150
[4]  
Atkinson C, 1999, CANCER EPIDEM BIOMAR, V8, P863
[5]  
AZIAZI EA, 1999, CANCER RES, V59, P1917
[6]  
Bacus JW, 1997, J CELL BIOCHEM, P21
[7]  
Bischoff ED, 1998, CANCER RES, V58, P479
[8]  
BONANNI B, 2000, SAN ANT BREAST CANC
[9]  
BOONE CW, 1993, J CELL BIOCHEM, P37
[10]  
Boyd NF, 1998, CANCER EPIDEM BIOMAR, V7, P1133