RANDOMIZED TRIAL OF ADJUVANT TAMOXIFEN IN NODE NEGATIVE POSTMENOPAUSAL BREAST-CANCER

被引:21
作者
RUTQVIST, LE
CEDERMARK, B
GLAS, U
JOHANSSON, H
ROTSTEIN, S
SKOOG, L
SOMELL, A
THEVE, T
WILKING, N
ASKERGREN, J
HJALMAR, ML
RINGBORG, U
机构
[1] KAROLINSKA HOSP,DEPT SURG,S-10401 STOCKHOLM 60,SWEDEN
[2] SODER SJUKHUSET,DEPT ONCOL,S-10064 STOCKHOLM,SWEDEN
[3] KAROLINSKA HOSP,CTR ONCOL,S-10401 STOCKHOLM 60,SWEDEN
[4] DANDERYD HOSP,DEPT ONCOL,S-18288 DANDERYD,SWEDEN
[5] KAROLINSKA HOSP,DEPT TUMOUR PATHOL,DIV CYTOL,S-10401 STOCKHOLM 60,SWEDEN
[6] SODER SJUKHUSET,DEPT SURG,S-10064 STOCKHOLM,SWEDEN
[7] SABBATSBERGS HOSP,DEPT SURG,S-11382 STOCKHOLM,SWEDEN
[8] DANDERYD HOSP,DEPT SURG,S-18288 DANDERYD,SWEDEN
关键词
BREAST CANCER; ADJUVANT TAMOXIFEN; NODE-NEGATIVE; ESTROGEN RECEPTORS;
D O I
10.3109/02841869209088913
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The paper presents long-term results of a randomized trial of adjuvant tamoxifen (40 mg daily for 2 or 5 years) versus surgery alone including 1 347 postmenopausal patients with histologically negative axillary nodes and a tumour diameter less-than-or-equal-to 30 mm. Data on the estrogen receptor status of the primary tumour were available in 1 136 patients (84%). At a median follow-up of 7 years (range 1.7-13.0 years) there was a significant prolongation of the recurrence-free survival among those allocated to tamoxifen (p < 0.01), significantly fewer deaths due to breast cancer (p = 0.02) and a trend towards improved overall survival (p = 0.11). The treatment benefit was restricted to patients with ER-positive tumours. There was no significant reduction of breast cancer recurrences in the tamoxifen group among patients whose tumours were classified as ER-negative. The results support and extend previous studies in showing a long-term benefit of tamoxifen in postmenopausal breast cancer patients with node-negative, estrogen receptor positive disease.
引用
收藏
页码:265 / 270
页数:6
相关论文
共 19 条
[2]  
CUTLER S J, 1958, J Chronic Dis, V8, P699, DOI 10.1016/0021-9681(58)90126-7
[3]  
Early Breast Cancer Trialists' Collaborative Group, 1990, TREATMENT EARLY BREA, V1
[4]   A RANDOMIZED CLINICAL-TRIAL EVALUATING TAMOXIFEN IN THE TREATMENT OF PATIENTS WITH NODE-NEGATIVE BREAST-CANCER WHO HAVE ESTROGEN-RECEPTOR POSITIVE TUMORS [J].
FISHER, B ;
COSTANTINO, J ;
REDMOND, C ;
POISSON, R ;
BOWMAN, D ;
COUTURE, J ;
DIMITROV, NV ;
WOLMARK, N ;
WICKERHAM, DL ;
FISHER, ER ;
MARGOLESE, R ;
ROBIDOUX, A ;
SHIBATA, H ;
TERZ, J ;
PATERSON, AHG ;
FELDMAN, MI ;
FARRAR, W ;
EVANS, J ;
LICKLEY, HL ;
KETNER, M .
NEW ENGLAND JOURNAL OF MEDICINE, 1989, 320 (08) :479-484
[5]  
FORNANDER T, 1989, LANCET, V1, P177
[6]  
HAYBITTLE JL, 1979, LECTURE NOTES MED IN, V4, P28
[7]  
Jordan VC, 1978, REV ENDOCRINOL REL S, P49
[8]   TAMOXIFEN IN ADVANCED BREAST-CANCER [J].
MOURIDSEN, H ;
PALSHOF, T ;
PATTERSON, J ;
BATTERSBY, L .
CANCER TREATMENT REVIEWS, 1978, 5 (03) :131-141
[9]   DESIGN AND ANALYSIS OF RANDOMIZED CLINICAL-TRIALS REQUIRING PROLONGED OBSERVATION OF EACH PATIENT .2. ANALYSIS AND EXAMPLES [J].
PETO, R ;
PIKE, MC ;
ARMITAGE, P ;
BRESLOW, NE ;
COX, DR ;
HOWARD, SV ;
MANTEL, N ;
MCPHERSON, K ;
PETO, J ;
SMITH, PG .
BRITISH JOURNAL OF CANCER, 1977, 35 (01) :1-39
[10]   DESIGN AND ANALYSIS OF RANDOMIZED CLINICAL-TRIALS REQUIRING PROLONGED OBSERVATION OF EACH PATIENT .1. INTRODUCTION AND DESIGN [J].
PETO, R ;
PIKE, MC ;
ARMITAGE, P ;
BRESLOW, NE ;
COX, DR ;
HOWARD, SV ;
MANTEL, N ;
MCPHERSON, K ;
PETO, J ;
SMITH, PG .
BRITISH JOURNAL OF CANCER, 1976, 34 (06) :585-612