Recent advances in hormonal treatment of breast cancer

被引:3
作者
Brodowicz, T [1 ]
Wiltschke, C [1 ]
Zielinski, C [1 ]
机构
[1] Univ Vienna, Klin Abt Onkol Extraordinariat Internist Expt Onk, AKH Wien,Innere Med Klin 1, Ludwig Boltzmann Inst Klin Expt Onkol, A-1090 Vienna, Austria
来源
ONKOLOGIE | 1998年 / 21卷 / 05期
关键词
breast cancer; hormonal treatment; antiestrogens; aromatase inhibitors;
D O I
10.1159/000026866
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hormonal therapy in patients with breast cancer is based on estrogen blockade of tumor cell growth. In postmenopausal patients tamoxifen still represents the hormonal agent of first choice and has shown to induce remission in patients with metastatic disease, to reduce recurrence, and to improve overall survival in the adjuvant setting. However, side effects such as slightly increased incidence of endometrial cancer have stimulated the search for other substances. Substantial progress in the development of anti-estrogens have yielded in substances with different antagonistic/agonistic profils (Toremifen, Raloxifen, Droloxifen, Idoxifen, ICI 182,780), which are currently tested in phase II and III studies. In the group of the aromatase inhibitors, which are mostly used in second-line protocols, new compounds are on the market (Formestan, Anastrazol, Letrozol, Vorozol, Fadrozol) which circumvent the main problem of inhibition of the glucocorticoid synthesis of the first-generation drugs (glutethimide) by better specificity. These already are widely used in patients with tamoxifen-resistant tumors. Whether these substances can also improve the outcome in first-line therapy is currently under clinical evaluation. An additional therapeutic intervention is the pharmacological castration (Goserelin), which orginates from the optimistic result of the surgical castration earlier days. This concept is used in premenopausal patients and currently studied alternatively and in addition to tamoxifen. In general there is hope to improve efficacy and to reduce side effects of endocrine treatment with these new compounds in the near future.
引用
收藏
页码:429 / 433
页数:5
相关论文
共 38 条
[11]   Effects of raloxifene on bone mineral density, serum cholesterol concentrations, and uterine endometrium in postmenopausal women [J].
Delmas, PD ;
Bjarnason, NH ;
Mitlak, BH ;
Ravoux, AC ;
Shah, AS ;
Huster, WJ ;
Draper, M ;
Christiansen, C .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (23) :1641-1647
[12]   EFFECTS OF FADROZOLE (CGS-16949A) AND LETROZOLE (CGS-20267) ON THE INHIBITION OF AROMATASE-ACTIVITY IN BREAST-CANCER PATIENTS [J].
DEMERS, LM .
BREAST CANCER RESEARCH AND TREATMENT, 1994, 30 (01) :95-102
[13]   Letrozole, a new oral aromatase inhibitor for advanced breast cancer: Double-blind randomized trial showing a dose effect and improved efficacy and tolerability compared with megestrol acetate [J].
Dombernowsky, P ;
Smith, I ;
Falkson, G ;
Leonard, R ;
Panasci, L ;
Bellmunt, J ;
Bezwoda, W ;
Gardin, G ;
Gudgeon, A ;
Morgan, M ;
Fornasiero, A ;
Hoffmann, W ;
Michel, J ;
Hatschek, T ;
Tjabbes, T ;
Chaudri, HA ;
Hornberger, U ;
Trunet, PF .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (02) :453-461
[14]   2ND GENERATION AROMATASE INHIBITOR - 4-HYDROXYANDROSTENEDIONE [J].
DOWSETT, M ;
COOMBES, RC .
BREAST CANCER RESEARCH AND TREATMENT, 1994, 30 (01) :81-87
[15]   FADROZOLE HYDROCHLORIDE, A NEW NONTOXIC AROMATASE INHIBITOR FOR THE TREATMENT OF PATIENTS WITH METASTATIC BREAST-CANCER [J].
FALKSON, G ;
RAATS, JI ;
FALKSON, HC .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1992, 43 (1-3) :161-165
[16]   Five versus more than five years of tamoxifen therapy for breast cancer patients with negative lymph nodes and estrogen receptor-positive tumors [J].
Fisher, B ;
Dignam, J ;
Bryant, J ;
DeCillis, A ;
Wickerham, DL ;
Wolmark, N ;
Costantino, J ;
Redmond, C ;
Fisher, ER ;
Bowman, DM ;
Deschenes, L ;
Dimitrov, NV ;
Margolese, RG ;
Robidoux, A ;
Shibata, H ;
Terz, J ;
Paterson, AHG ;
Feldman, MI ;
Farrar, W ;
Evans, J ;
Lickley, HL .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1996, 88 (21) :1529-1542
[17]   ENDOMETRIAL CANCER IN TAMOXIFEN-TREATED BREAST-CANCER PATIENTS - FINDINGS FROM THE NATIONAL SURGICAL ADJUVANT BREAST AND BOWEL PROJECT (NSABP) B-14 [J].
FISHER, B ;
COSTANTINO, JP ;
REDMOND, CK ;
FISHER, ER ;
WICKERHAM, DL ;
CRONIN, WM ;
BOWMAN, D ;
COUTURE, J ;
DIMITROV, NV ;
EVANS, J ;
FARRAR, W ;
KAVANAH, M ;
LICKLEY, HL ;
MARGOLESE, R ;
PATERSON, AHG ;
ROBIDOUX, A ;
SHIBATA, H ;
TERZ, J .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1994, 86 (07) :527-537
[18]   ADJUVANT THERAPY FOR BREAST-CANCER - UNDERSTANDING THE OVERVIEW [J].
GELBER, RD ;
GOLDHIRSCH, A ;
COATES, AS .
JOURNAL OF CLINICAL ONCOLOGY, 1993, 11 (03) :580-585
[19]  
GOSS PE, 1995, CLIN CANCER RES, V1, P287
[20]   SEQUENCE AND EXPRESSION OF HUMAN ESTROGEN-RECEPTOR COMPLEMENTARY-DNA [J].
GREENE, GL ;
GILNA, P ;
WATERFIELD, M ;
BAKER, A ;
HORT, Y ;
SHINE, J .
SCIENCE, 1986, 231 (4742) :1150-1154