Long-Term Benefits of 5 Years of Tamoxifen: 10-Year Follow-Up of a Large Randomized Trial in Women at Least 50 Years of Age With Early Breast Cancer

被引:71
作者
Hackshaw, Allan [1 ]
Roughton, Michael
Forsyth, Sharon
Monson, Kathryn
Reczko, Krystyna
Sainsbury, Richard
Baum, Michael
机构
[1] Canc Res UK, London W1T 4TJ, England
关键词
ADJUVANT ENDOCRINE THERAPY; HEART-DISEASE MORTALITY; POSTMENOPAUSAL PATIENTS; OLDER WOMEN; ADHERENCE; DISCONTINUATION; PREDICTORS; BELIEFS;
D O I
10.1200/JCO.2010.32.2933
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose The Cancer Research UK "Over 50s" trial compared 5 and 2 years of tamoxifen in women with early breast cancer. Results are reported after median follow-up of 10 years. Patients and Methods Between 1987 and 1997, 3,449 patients age 50 to 81 years with operable breast cancer who had been taking 20 mg of tamoxifen for 2 years were randomly assigned to either stop or continue for an additional 3 years, if they were alive and recurrence free. Data on recurrences, new tumors, deaths, and cardiovascular events were obtained (April 2010). Results There were 1,103 recurrences, 755 deaths as a result of breast cancer, 621 cardiovascular (CV) events, and 236 deaths as a result of CV events. Fifteen years after starting treatment, for every 100 women who received tamoxifen for 5 years, 5.8 fewer experienced recurrence, compared with those who received tamoxifen for 2 years. The risk of contralateral breast cancer was significantly reduced (hazard ratio, 0.70; 95% CI, 0.48 to 1.00). Among women age 50 to 59 years, there was a 35% reduction in CV events (P = .005) and 59% reduction in death as a result of a CV event (P = .02); in older women, the effect was much smaller and not statistically significant. Conclusion Taking tamoxifen for the recommended 5 years reduces the risk of recurrence or contralateral breast cancer 15 years after starting treatment. It also lowers the risk of CV disease and death as a result of a CV event, particularly among those age 50 to 59 years. Women should therefore be encouraged to complete the full course. Although aromatase inhibitors improve disease-free survival, tamoxifen remains a cheap and highly effective alternative, particularly in developing countries. J Clin Oncol 29:1657-1663. (C) 2011 by American Society of Clinical Oncology
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收藏
页码:1657 / 1663
页数:7
相关论文
共 32 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]   Early discontinuation of tamoxifen - A lesson for oncologists [J].
Barron, Thomas I. ;
Connolly, Roisin M. ;
Bennett, Kathleen ;
Feely, John ;
Kennedy, M. John .
CANCER, 2007, 109 (05) :832-839
[4]   Twelve-year mortality results of a randomized trial of 2 versus 5 years of adjuvant tamoxifen for postmenopausal early-stage breast carcinoma patients (SITAM 01) [J].
Belfiglio, M ;
Valentini, M ;
Pellegrini, F ;
De Berardis, G ;
Franciosi, M ;
Rossi, MCE ;
Sacco, M ;
Nicolucci, A .
CANCER, 2005, 104 (11) :2334-2339
[5]  
*BREASTC ORG, AR INH
[6]  
*BRIT NAT FORM, 59 BRIT NAT FORM
[7]   Adherence to endocrine therapy for breast cancer [J].
Chlebowski, Rowan T. ;
Geller, Michelle L. .
ONCOLOGY, 2006, 71 (1-2) :1-9
[8]  
Clarke M, 1998, LANCET, V351, P1451
[9]  
*CLIN TRIAL SERV U, FACT SHEET QUEST ANS
[10]   Five years of letrozole compared with tamoxifen as initial adjuvant therapy for postmenopausal women with endocrine-responsive early breast cancer:: Update of study BIG 1-98 [J].
Coates, Alan S. ;
Keshaviah, Aparna ;
Thuerlimann, Beat ;
Mouridsen, Henning ;
Mauriac, Louis ;
Forbes, John F. ;
Paridaens, Robert ;
Castiglione-Gertsch, Monica ;
Gelber, Richard D. ;
Colleoni, Marco ;
Lang, Istvan ;
Del Mastro, Lucia ;
Smith, Ian ;
Chirgwin, Jacquie ;
Nogaret, Jean-Marie ;
Pienkowski, Tadeusz ;
Wardley, Andrew ;
Jakobsen, Erik H. ;
Price, Karen N. ;
Goldhirsch, Aron .
JOURNAL OF CLINICAL ONCOLOGY, 2007, 25 (05) :486-492