Adjuvant high-dose medroxyprogesterone acetate for early breast cancer: 13 years update in a multicentre randomized trial

被引:15
作者
Focan, C [1 ]
Beauduin, M
Salamon, E
de Greve, J
de Wasch, G
Lobelle, JP
Majois, F
Tagnon, A
Tytgat, J
van Belle, S
Vandervellen, R
Vindevoghel, A
机构
[1] St Joseph Clin, Liege, Belgium
[2] Jolimont Hosp, Haine St Paul, Belgium
[3] St Elisabeth Clin, Namur, Belgium
[4] AZ VUB, Ctr Oncol, Jette, Belgium
[5] Pharmacia & Upjohn Inc, Brussels, Belgium
[6] Inst Medicochirurg, Tournai, Belgium
[7] Heilige Hart Clin, Roeselaere, Belgium
[8] Oncol Ctr Univ, Ghent, Belgium
[9] St Michel Clin, Brussels, Belgium
关键词
D O I
10.1054/bjoc.2001.1829
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The authors updated their report on a randomized trial initiated in 1982 comparing, in early breast cancer, high-dose IM Medroxyprogesterone acetate (HD-MPA) adjuvant hormonotherapy during 6 months with no hormonotherapy; node-positive patients also received 6 courses of IV CMF (day 1, day 8; q.4 weeks). 246 node-negative (NN) and 270 node-positive (NP) patients had been followed for a median duration of 13 years. Previous results were confirmed in this analysis on mature data. In NN patients, relapse-free survival (RFS) was improved in the adjuvant hormonotherapy arm, regardless of age while overall survival (OAS) was also increased in younger (less then 50 years) patients. In the whole group of NP patients, no difference was seen regarding RFS or GAS. However, an age-dependant opposite effect was observed: younger patients (< 50) experienced a worse and significant outcome of relapse-free and overall survivals when receiving adjuvant HD-MPA while older patients (> = 50) enjoyed a significant improvement of their relapse-free survival. For both NN and NP patients, differences in overall survivals observed in older women with a shorter follow-up, were no longer detected. (C) 2001 Cancer Research Campaign.
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页码:1 / 8
页数:8
相关论文
共 47 条
[1]  
Alberts SR, 1996, CANCER-AM CANCER SOC, V78, P764
[2]   DETERMINATION OF ESTROGEN-RECEPTORS IN PARAFFIN-EMBEDDED TISSUE - TECHNIQUES AND THE VALUE IN BREAST-CANCER-TREATMENT [J].
ANDERSEN, J .
ACTA ONCOLOGICA, 1992, 31 (06) :611-627
[3]   Tamoxifen in high-risk premenopausal women with primary breast cancer receiving adjuvant chemotherapy.: Report from the Danish Breast Cancer Co-Operative Group DBCG 82B trial [J].
Andersson, M ;
Kamby, C ;
Jensen, MB ;
Mouridsen, H ;
Ejlertsen, B ;
Dombernowsky, P ;
Rose, C ;
Cold, S ;
Overgaard, M ;
Andersen, J ;
Kjær, M .
EUROPEAN JOURNAL OF CANCER, 1999, 35 (12) :1659-1666
[4]  
[Anonymous], 1996, Lancet, V348, P1189
[5]  
[Anonymous], P ASCO
[6]  
BEEX L, 1987, CANCER TREAT REP, V71, P1151
[7]  
BLOSSEY HC, 1984, CANCER, V54, P1208, DOI 10.1002/1097-0142(19840915)54:1+<1208::AID-CNCR2820541319>3.0.CO
[8]  
2-K
[9]   Tamoxifen added to adjuvant chemotherapy in premenopausal women with early breast cancer: is it standard practice or still a subject for study? [J].
Bramwell, VHC ;
Pritchard, KI .
EUROPEAN JOURNAL OF CANCER, 1999, 35 (12) :1625-1627
[10]   THE PHARMACOKINETICS OF MEDROXYPROGESTERONE ACETATE FOLLOWING 2 DIFFERENT LOADING DOSE SCHEDULES IN ADVANCED-CARCINOMA OF THE BREAST [J].
CANNEY, PA ;
DOWSETT, M ;
PRIESTMAN, TJ .
BRITISH JOURNAL OF CANCER, 1988, 58 (01) :73-76