Aromatase inhibitors in the treatment and prevention of breast cancer

被引:232
作者
Goss, PE [1 ]
Strasser, K [1 ]
机构
[1] Princess Margaret Hosp, Div Hematol Oncol, Toronto, ON M5G 2M9, Canada
关键词
D O I
10.1200/JCO.2001.19.3.881
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: The purpose of this article is to provide an overview of the current clinical status and possible future applications of aromatase inhibitors in breast cancer. Methods: A review of the literature on the third-generation aromatase inhibitors was conducted. Some data that have been presented but not published are included. In addition, the designs of ongoing trials with aromatase inhibitors are outlined and the implications of possible results discussed. Results: All of the third-generation oral aromatase inhibitors-lefrazole, anastrozole, and vorozole (nonsteroidal, type II) and exemestane (steroidal, type I) have now been tested in phase III trials as second-line treatment of postmenopausal hormone-dependent breast cancer. They have shown clear superiority compared with the conventional therapies and are there-fore considered established second-line hormonal agents. Currently, they are being tested as first-line therapy in the metastatic, adjuvant, and neoadjuvant settings. preliminary results suggest that the inhibitors might displace tamoxifen as first-line treatment, but further studies are needed to determine this. Conclusion: The role of aromatase inhibitors in premenopausal breast cancer and in combination with chemotherapy and other anticancer treatments are areas of future exploration. The ongoing adjuvant trials will provide important data on the long-term safety of aromatase inhibitors, which will help to determine their suitability for use as chemopreventives in healthy women at risk of developing breast cancer, (C) 2001 by American Society of Clinical Oncology.
引用
收藏
页码:881 / 894
页数:14
相关论文
共 116 条
[1]   RANDOMIZED TRIAL OF TAMOXIFEN VERSUS AMINOGLUTETHIMIDE AND VERSUS COMBINED TAMOXIFEN AND AMINOGLUTETHIMIDE IN ADVANCED POSTMENOPAUSAL BREAST-CANCER [J].
ALONSOMUNOZ, MC ;
OJEDAGONZALEZ, MB ;
BELTRANFABREGAT, M ;
DORCARIBUGENT, J ;
LOPEZLOPEZ, L ;
BORRASBALADA, J ;
CARDENALALEMANV, F ;
GOMEZBATISTE, X ;
FABREGATMAYOL, J ;
VILADIUQUEMADA, P .
ONCOLOGY, 1988, 45 (05) :350-353
[2]  
[Anonymous], BREAST CANC RES TREA
[3]  
BENGTSSON NO, 1997, EUR J CANCER, V33, P148
[4]  
BERGH J, 1997, P AN M AM SOC CLIN, V16, pA155
[5]   HIGHLY SELECTIVE-INHIBITION OF ESTROGEN BIOSYNTHESIS BY CGS-20267, A NEW NONSTEROIDAL AROMATASE INHIBITOR [J].
BHATNAGAR, AS ;
HAUSLER, A ;
SCHIEWECK, K ;
LANG, M ;
BOWMAN, R .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1990, 37 (06) :1021-1027
[6]  
BHATNAGAR AS, 1999, ESTROGENS ANTIESTROG, V2, P223
[7]  
BOCCARDO F, 2000, P AN M AM SOC CLIN, V19, pA71
[8]   AROMATASE-ACTIVITY AND ESTRADIOL IN HUMAN BREAST-CANCER - ITS RELATIONSHIP TO ESTRADIOL AND EPIDERMAL GROWTH-FACTOR RECEPTORS AND TO TUMOR-NODE-METASTASIS STAGING [J].
BOLUFER, P ;
RICART, E ;
LLUCH, A ;
VAZQUEZ, C ;
RODRIGUEZ, A ;
RUIZ, A ;
LLOPIS, F ;
GARCIACONDE, J ;
ROMERO, R .
JOURNAL OF CLINICAL ONCOLOGY, 1992, 10 (03) :438-446
[9]   QUANTITATIVE CLASSIFICATION OF MAMMOGRAPHIC DENSITIES AND BREAST-CANCER RISK - RESULTS FROM THE CANADIAN NATIONAL BREAST SCREENING STUDY [J].
BOYD, NF ;
BYNG, JW ;
JONG, RA ;
FISHELL, EK ;
LITTLE, LE ;
MILLER, AB ;
LOCKWOOD, GA ;
TRITCHLER, DL ;
YAFFE, MJ .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1995, 87 (09) :670-675
[10]  
BRADLOW HL, 1982, CANCER RES, V42, P3382