Risk and prognosis of endometrial cancer after tamoxifen for breast cancer

被引:409
作者
Bergman, L
Beelen, MLR
Gallee, MPW
Hollema, H
Benraadt, J
van Leeuwen, FE
机构
[1] Netherlands Canc Inst, Dept Epidemiol, NL-1066 CX Amsterdam, Netherlands
[2] Netherlands Canc Inst, Dept Pathol, NL-1066 CX Amsterdam, Netherlands
[3] Acad Hosp Groningen, Dept Pathol, Groningen, Netherlands
[4] Ctr Comprehens Canc, Amsterdam, Netherlands
关键词
D O I
10.1016/S0140-6736(00)02677-5
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Background Tamoxifen increases the risk of endometrial cancer. However, few studies have produced reliable risk estimates by duration, dose, and recency of use, or addressed the prognosis of endometrial cancers in tamoxifen-treated women. Methods We did a nationwide case-control study on the risk and prognosis of endometrial cancer after tamoxifen use for breast cancer. Information on tamoxifen use and other risk factors for endometrial cancer was obtained from 309 women with endometrial cancer after breast cancer (cases), and 860 matched controls with breast cancer but without endometrial cancer. For 276 cases, we obtained tissue blocks of endometrial cancer to review the diagnosis, and used immunohistochemistry to examine hormone-receptor status and overexpression of p53, Findings Tamoxifen had been used by 108 (36.1%) of 299 cases and 245 (28.5%) controls (relative risk 1.5 [95% CI 1.1-2.0]). Risk of endometrial cancer increased with longer duration of tamoxifen use (p<0.001), with relative risks of 2.0 (1.2-3.2) for 2-5 years and 6.9 (2.4-19.4) for at least 5 years compared with non-users. Endometrial cancers of stage III and IV occurred more frequently in long-term tamoxifen users (greater than or equal to 2 years) than in non-users (17.4% vs 5.4%, p=0.006). long-term users were more likely than non-users to have had malignant mixed mesodermal tumours or sarcomas of the endometrium (15.4% vs 2.9%, p less than or equal to 0.02), p53-positive tumours (31.4% vs 18.2%, p=0.05), and negative oestrogen-receptor concentrations (60.8% vs 26.2%, p less than or equal to 0.001). 3-year endometrial-cancer-specific survival was significantly worse for long-term tamoxifen users than for non-users (76% for greater than or equal to 5 years, 85% for 2-5 years vs 94% for non-users, p=0.02). Interpretation Long-term tamoxifen users have a worse prognosis of endometrial cancers, which seems to be due to less favourable histology and higher stage. However, the benefit of tamoxifen on breast-cancer survival far outweighs the increased mortality from endometrial cancer. Nevertheless, we seriously question widespread use of tamoxifen as a preventive agent against breast cancer in healthy women.
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页码:881 / 887
页数:7
相关论文
共 36 条
[1]
ROLE OF PROLONGED STIMULATION OF TAMOXIFEN THERAPY IN THE ETIOLOGY OF ENDOMETRIAL SARCOMAS [J].
ALTARAS, MM ;
AVIRAM, R ;
COHEN, I ;
CORDOBA, M ;
YARKONI, S ;
BEYTH, Y .
GYNECOLOGIC ONCOLOGY, 1993, 49 (02) :255-258
[2]
INCIDENCE OF NEW PRIMARY CANCERS AFTER ADJUVANT TAMOXIFEN THERAPY AND RADIOTHERAPY FOR EARLY BREAST-CANCER [J].
ANDERSSON, M ;
STORM, HH ;
MOURIDSEN, HT .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1991, 83 (14) :1013-1017
[3]
The hormonal receptor status of uterine carcinosarcomas (mixed Mullerian tumours): An immunohistochemical study [J].
Ansink, AC ;
Cross, PA ;
Scorer, P ;
Lopes, AD ;
Monaghan, JM .
JOURNAL OF CLINICAL PATHOLOGY, 1997, 50 (04) :328-331
[4]
Tamoxifen and endometrial cancer: most cancers are early stage and highly curable [J].
Barakat, R .
EUROPEAN JOURNAL OF CANCER, 1998, 34 :S49-S50
[5]
TAMOXIFEN USE IN BREAST-CANCER PATIENTS WHO SUBSEQUENTLY DEVELOP CORPUS CANCER IS NOT ASSOCIATED WITH A HIGHER INCIDENCE OF ADVERSE HISTOLOGIC FEATURES [J].
BARAKAT, RR ;
WONG, G ;
CURTIN, JP ;
VLAMIS, V ;
HOSKINS, WJ .
GYNECOLOGIC ONCOLOGY, 1994, 55 (02) :164-168
[6]
Tamoxifen therapy for breast cancer and endometrial cancer risk [J].
Bernstein, L ;
Deapen, D ;
Cerhan, JR ;
Schwartz, SM ;
Liff, J ;
McGann-Maloney, E ;
Perlman, JA ;
Ford, L .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1999, 91 (19) :1654-1662
[7]
UTERINE MULLERIAN ADENOSARCOMA FOLLOWING ADENOMYOMA IN A WOMAN ON TAMOXIFEN THERAPY [J].
BOCKLAGE, T ;
LEE, KR ;
BELINSON, JL .
GYNECOLOGIC ONCOLOGY, 1992, 44 (01) :104-109
[8]
Breslow NE, 1980, STAT METHODS CANC RE, V1, DOI DOI 10.1097/00002030-199912240-00009
[9]
Carmichael PL, 1996, CANCER RES, V56, P1475
[10]
Clarke M, 1998, LANCET, V351, P1451