Tamoxifen to raloxifene and beyond

被引:34
作者
O'Regan, RM
Jordan, VC
机构
[1] Northwestern Univ, Sch Med, Robert H Lurie Comprehens Canc Ctr, Chicago, IL 60611 USA
[2] Northwestern Univ, Div Hematol Oncol, Chicago, IL 60611 USA
关键词
D O I
10.1053/sonc.2001.23492
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Tamoxifen, a selective estrogen receptor modulator (SERM), is the treatment of choice for all stages of hormone-responsive breast cancer and has been shown to prevent breast cancer in high-risk women. Despite acting as an antiestrogen on the breast, tamoxifen has partial estrogenic effects on other target tissues. These partial estrogen agonistic actions produce beneficial effects on bones and the lipid profile in postmenopausal women. However, tamoxifen is associated with an increase in endometrial cancer. Additionally, its antiestrogenic effects in the central nervous system result in hot flashes in postmenopausal women. Raloxifene is another SERM approved for the prevention of osteoporosis in postmenopausal women. Like tamoxifen, raloxifene appears to prevent breast cancer in high-risk women and has not, to date, been noted to increase the incidence of endometrial cancer. The Study of Tamoxifen and Raloxifene will compare the effects of the two agents on breast cancer prevention and endometrial cancer risk. A number of new agents are being developed for breast cancer treatment and prevention and osteoporosis prevention. These include other SERMs, selective estrogen receptor downregulators (SERDs), and aromatase inhibitors. It is hoped that one of these new agents will be the ideal agent, acting as an antiestrogen on breast and endometrium while having estrogenic effects on bones, the lipid profile, and the central nervous system. © 2001 by W.B. Saunders Company.
引用
收藏
页码:260 / 273
页数:14
相关论文
共 122 条
[51]   ANTIESTROGENS .2. STRUCTURE ACTIVITY STUDIES IN A SERIES OF 3-AROYL-2-ARYLBENZO[B]THIOPHENE DERIVATIVES LEADING TO [6-HYDROXY-2-(4-HYDROXYPHENYL)BENZO[B]THIEN-3-YL][4-[2-(1-PIPERIDINYL)ETHOXY]-PHENYL]METHANONE HYDROCHLORIDE (LY156758), A REMARKABLY EFFECTIVE ESTROGEN ANTAGONIST WITH ONLY MINIMAL INTRINSIC ESTROGENICITYO[ [J].
JONES, CD ;
JEVNIKAR, MG ;
PIKE, AJ ;
PETERS, MK ;
BLACK, LJ ;
THOMPSON, AR ;
FALCONE, JF ;
CLEMENS, JA .
JOURNAL OF MEDICINAL CHEMISTRY, 1984, 27 (08) :1057-1066
[52]  
JORDAN VC, 1980, CANCER TREAT REP, V64, P745
[53]   EFFECTS OF ANTIESTROGENS ON BONE IN CASTRATED AND INTACT FEMALE RATS [J].
JORDAN, VC ;
PHELPS, E ;
LINDGREN, JU .
BREAST CANCER RESEARCH AND TREATMENT, 1987, 10 (01) :31-35
[54]   SUPPRESSION OF MOUSE MAMMARY TUMORIGENESIS BY LONG-TERM TAMOXIFEN THERAPY [J].
JORDAN, VC ;
LABABIDI, MK ;
LANGANFAHEY, S .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1991, 83 (07) :492-496
[55]   ANTITUMOR ACTIVITY OF ANTIESTROGEN ICI 46,474 (TAMOXIFEN) IN DIMETHYLBENZANTHRACENE (DMBA)-INDUCED RAT MAMMARY-CARCINOMA MODEL [J].
JORDAN, VC .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1974, 5 (04) :354-354
[57]   INHIBITION OF THE UTEROTROPIC ACTIVITY OF ESTROGENS AND ANTI-ESTROGENS BY THE SHORT-ACTING ANTIESTROGEN-LY117018 [J].
JORDAN, VC ;
GOSDEN, B .
ENDOCRINOLOGY, 1983, 113 (02) :463-468
[58]   EVALUATION OF THE ANTI-TUMOR ACTIVITY OF THE NON-STEROIDAL ANTIOESTROGEN MONOHYDROXYTAMOXIFEN IN THE DMBA-INDUCED RAT MAMMARY-CARCINOMA MODEL [J].
JORDAN, VC ;
ALLEN, KE .
EUROPEAN JOURNAL OF CANCER, 1980, 16 (02) :239-251
[59]   EFFECT OF TAMOXIFEN (ICI 46,474) ON INITIATION AND GROWTH OF DMBA - INDUCED RAT MAMMARY CARCINOMATA [J].
JORDAN, VC .
EUROPEAN JOURNAL OF CANCER, 1976, 12 (06) :419-424
[60]  
JORDAN VC, 1998, P AM SOC CLIN ONCOL, V466, pA122