Dose-dependent effect of tamoxifen therapy on endometrial pathologies in postmenopausal breast cancer patients

被引:30
作者
Cohen, I [1 ]
Perel, E
Tepper, R
Flex, D
Figer, A
Shapira, J
Altaras, MM
Fishman, A
Bernheim, J
Cordoba, M
Yigael, D
Beyth, Y
机构
[1] Sapir Med Ctr, Dept Obstet & Gynecol, IL-44281 Kfar Saba, Israel
[2] Sapir Med Ctr, Dept Pathol, IL-44281 Kfar Saba, Israel
[3] Sapir Med Ctr, Dept Med, IL-44281 Kfar Saba, Israel
[4] Sapir Med Ctr, Dept Gynecol Oncol, IL-44281 Kfar Saba, Israel
[5] Tel Aviv Univ, Sackler Sch Med, Rabin Med Ctr, Dept Oncol, IL-69978 Tel Aviv, Israel
关键词
cumulative dose; endometrial pathologies; postmenopausal; tamoxifen;
D O I
10.1023/A:1006142904301
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To assess whether a higher cumulative tamoxifen dose is associated with increased incidence of various types of endometrial pathologies, we compared cumulative dose of tamoxifen treatment as well as demographic characteristics, risk factors for endometrial cancer, transvaginal ultrasonographic endometrial thickness, and various treatments for the primary breast cancer between 159 postmenopausal breast cancer tamoxifen-treated patients without endometrial pathologies (group I) and 67 similar patients with endometrial pathologies (group II). A similar comparison was made between group I patients and similar patients with proliferative endometrium (group IIa), with endometrial hyperplasia (group IIb), with endometrial polyps (group IIc), and with endometrial cancer (group IId). Overall cumulative tamoxifen dose was significantly higher in group II as compared to group I (27.4 +/- 33.4 and 17.4 +/- 20.2, respectively; P < 0.0252). Transvaginal ultrasonographic endometrial thickness was significantly higher in group II than in group I patients (16.3 +/- 11.3 mm and 12.1 +/- 6.3 mm, respectively; P < 0.0147). The frequency of diabetes mellitus, of previous postmenopausal bleeding, and of previous exposure to hormone replacement therapy was significantly higher in group II than in group I patients (P < 0.001; P < 0.0001 and P < 0.001, respectively). There were no significant differences in all parameters tested between group I, group IIa, group IIb, group IIc, and group IId. However, there was an obvious trend for higher cumulative tamoxifen dose in patients with benign endometrial pathologies as compared to those without endometrial pathologies or to those with endometrial cancer (Group I = 17.4 +/- 20.2 g, group IIa = 22.5 +/- 18.5 g, group IIb = 28.1 +/- 20.3 g, group IIc = 31.4 +/- 42.7 g and group IId = 10.4 +/- 12.6 g). Endometrial pathologies, except for endometrial cancer, are associated with a high cumulative dose of tamoxifen in postmenopausal breast cancer patients.
引用
收藏
页码:255 / 262
页数:8
相关论文
共 43 条
[1]  
ABE O, 1992, LANCET, V339, P71
[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]   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
[4]   Comparison of endometrial changes among symptomatic tamoxifen-treated and nontreated premenopausal and postmenopausal breast cancer patients [J].
Cheng, WF ;
Lin, HH ;
Torng, PL ;
Huang, SC .
GYNECOLOGIC ONCOLOGY, 1997, 66 (02) :233-237
[5]   CONTINUOUS TAMOXIFEN TREATMENT IN ASYMPTOMATIC, POSTMENOPAUSAL BREAST-CANCER PATIENTS DOES NOT CAUSE AGGRAVATION OF ENDOMETRIAL PATHOLOGIES [J].
COHEN, I ;
TEPPER, R ;
ROSEN, DJD ;
SHAPIRA, J ;
CORDOBA, M ;
DROR, Y ;
ALTARAS, M ;
BEYTH, Y .
GYNECOLOGIC ONCOLOGY, 1994, 55 (01) :138-143
[6]   Time-dependent effect of tamoxifen therapy on endometrial pathology in asymptomatic postmenopausal breast cancer patients [J].
Cohen, I ;
Altaras, MM ;
Shapira, J ;
Tepper, R ;
Rosen, DJD ;
Cordoba, M ;
Zalel, Y ;
Figer, A ;
Yigael, D ;
Beyth, Y .
INTERNATIONAL JOURNAL OF GYNECOLOGICAL PATHOLOGY, 1996, 15 (02) :152-157
[7]   Different coexisting endometrial histological features in asymptomatic postmenopausal breast cancer patients treated with tamoxifen [J].
Cohen, I ;
Altaras, MM ;
Shapira, J ;
Tepper, R ;
Cordoba, M ;
Figer, A ;
Zalel, Y ;
Dror, Y ;
Beyth, Y .
GYNECOLOGIC AND OBSTETRIC INVESTIGATION, 1997, 43 (01) :60-63
[8]   ENDOMETRIAL CHANGES IN POSTMENOPAUSAL WOMEN TREATED WITH TAMOXIFEN FOR BREAST-CANCER [J].
COHEN, I ;
ROSEN, DJD ;
SHAPIRA, J ;
CORDOBA, M ;
GILBOA, S ;
ALTARAS, MM ;
YIGAEL, D ;
BEYTH, Y .
BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 1993, 100 (06) :567-570
[9]   ENDOMETRIAL CHANGES WITH TAMOXIFEN - COMPARISON BETWEEN TAMOXIFEN-TREATED AND NONTREATED ASYMPTOMATIC, POSTMENOPAUSAL BREAST-CANCER PATIENTS [J].
COHEN, I ;
ROSEN, DJD ;
SHAPIRA, J ;
CORDOBA, M ;
GILBOA, S ;
ALTARAS, MM ;
YIGAEL, D ;
BEYTH, Y .
GYNECOLOGIC ONCOLOGY, 1994, 52 (02) :185-190
[10]   POPULATION-BASED STUDY OF TAMOXIFEN THERAPY AND SUBSEQUENT OVARIAN, ENDOMETRIAL, AND BREAST CANCERS [J].
COOK, LS ;
WEISS, NS ;
SCHWARTZ, SM ;
WHITE, E ;
MCKNIGHT, B ;
MOORE, DE ;
DALING, JR .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1995, 87 (18) :1359-1364