Letrozole as adjuvant endocrine therapy in postmenopausal women with breast cancer

被引:2
作者
Koeberle, Dieter [1 ]
Thuerlimann, Beat
机构
[1] Kantonsspital, Dept Hematol Oncol, CH-9007 St Gallen, Switzerland
[2] Kantonsspital, Senol Ctr Eastern Switzerland, CH-9007 St Gallen, Switzerland
关键词
adjuvant treatment; aromatase inhibitors; breast cancer letrozole;
D O I
10.1586/14737140.6.1.5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The third-generation aromatase inhibitor letrozole offers a promising approach to treating hormone-sensitive breast cancer for postmenopausal women, through potent and specific inhibition of estrogen synthesis. In neoadjuvant and first-line treatment, letrozole demonstrated superior efficacy compared with tamoxifen in randomized Phase III trials. Initial results of Breast InterGroup 1-98, a large ongoing randomized trial investigating primary adjuvant endocrine treatment with either letrozole or tamoxifen, have recently been presented. Patients treated with letrozole demonstrated a 19% improvement in disease-free survival and a significant reduced risk of distant recurrences, holding out the prospect of a survival advantage over tamoxifen treatment with further maturation of the trial. For patients who have already completed 5 years of tamoxifen, extended endocrine therapy with letrozole is a new therapeutic option based on the results of the MA-17 trial. The optimal use of aromatase inhibitors remains an open question, at least until results from randomized trials (BIG 1-98, TEAM) investigating the sequential use of an aromatase inhibitor and tamoxifen in comparison with continuous monotherapy become available.
引用
收藏
页码:5 / 10
页数:6
相关论文
共 38 条
[1]  
Abe O, 2005, LANCET, V366, P2087, DOI 10.1016/s0140-6736(05)66544-0
[2]  
Abram P, 1996, J NATL CANCER I, V88, P1834
[3]   A REALISTIC ASSESSMENT OF THE ASSOCIATION BETWEEN TAMOXIFEN AND ENDOMETRIAL CANCER [J].
ASSIKIS, VJ ;
JORDAN, VC .
ENDOCRINE-RELATED CANCER, 1995, 2 (03) :235-241
[4]  
Baum M, 2002, LANCET, V359, P2131
[5]  
BAUM M, 2005, P AM SOC CLIN ONCOL
[6]   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
[7]   Switching to anastrozole versus continued tamoxifen treatment of early breast cancer: Preliminary results of the Italian Tamoxifen Anastrozole trial [J].
Boccardo, F ;
Rubagotti, A ;
Puntoni, M ;
Guglielmini, P ;
Amoroso, D ;
Fini, A ;
Paladini, G ;
Mesiti, M ;
Romeo, D ;
Rinaldini, M ;
Scali, S ;
Porpiglia, M ;
Benedetto, C ;
Restuccia, N ;
Buzzi, F ;
Franchi, R ;
Massidda, B ;
Distante, V ;
Amadori, D ;
Sismondi, P .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (22) :5138-5147
[8]   Tamoxifen-treated breast carcinoma patients and the risk of acute myocardial infarction and newly-diagnosed angina [J].
Bradbury, BD ;
Lash, TL ;
Kaye, JA ;
Jick, SS .
CANCER, 2005, 103 (06) :1114-1121
[9]   Meta-analysis of vascular and neoplastic events associated with tamoxifen [J].
Braithwaite, RS ;
Chlebowski, RT ;
Lau, J ;
George, S ;
Hess, R ;
Col, NF .
JOURNAL OF GENERAL INTERNAL MEDICINE, 2003, 18 (11) :937-947
[10]   A randomized trial of exemestane after two to three years of tamoxifen therapy in postmenopausal women with primary breast cancer [J].
Coombes, RC ;
Hall, E ;
Gibson, LJ ;
Paridaens, R ;
Jassem, J ;
Delozier, T ;
Jones, SE ;
Alvarez, I ;
Bertelli, G ;
Ortmann, O ;
Coates, AS ;
Bajetta, E ;
Dodwell, D ;
Coleman, RE ;
Fallowfield, LJ ;
Mickiewicz, E ;
Andersen, J ;
Lonning, PE ;
Cocconi, G ;
Stewart, A ;
Stuart, N ;
Snowdon, CF ;
Carpentieri, M ;
Massimini, G ;
Bliss, JM .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (11) :1081-1092