Hormone replacement therapy in relation to breast carcinoma incidence rate ratios -: A prospective Danish cohort study

被引:71
作者
Tjonneland, A
Christensen, J
Thomsen, BL
Olsen, A
Overvad, K
Ewertz, M
Mellemkjær, L
机构
[1] Danish Canc Soc, Inst Canc Epidemiol, DK-2100 Copenhagen, Denmark
[2] Aalborg Hosp, Dept Clin Epidemiol, Aalborg, Denmark
[3] Aarhus Univ Hosp, Dept Clin Epidemiol, Aarhus, Denmark
[4] Univ Aarhus, Dept Epidemiol & Social Med, Aarhus, Denmark
[5] Aalborg Hosp, Dept Oncol, Aalborg, Denmark
[6] Danish Breast Canc Cooperat Grp, Copenhagen, Denmark
关键词
hormone replacement therapy; estrogen receptor status; postmenopausal breast carcinoma; lobular carcinoma;
D O I
10.1002/cncr.20250
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. The goal of the current study was to investigate the relation between hormone replacement therapy (HRT) and breast carcinoma in a prospective study cohort. Particular attention was paid to the type of HRT used and to the association of HRT type with estrogen receptor status and tumor histology. METHODS. Between 1993 and 1997, a total of 29,875 women were enrolled in the Danish Cancer Society's prospective "Diet, Cancer and Health" study. Among 23,618 women who were assumed to be postmenopausal and for whom information on HRT use was available, we identified 423 cases of breast carcinoma over a median follow-tip period of 4.8 years. Statistical analyses were based on the Cox proportional hazards model, with age serving as the time parameter. RESULTS. The breast carcinoma incidence rate ratio (IRR) was 2.22 (95% confidence interval [CI], 1.80-2.75) for users of HRT at baseline compared with women who never received HRT. Among HRT users (relative to nonusers), the IRR for estrogen receptor-positive tumors (2.38; 95% CI, 1.84-3.06) was greater than the IRR for estrogen receptor-negative tumors (1.56; 95% CI, 1.00-2.43). HRT use at baseline also was analyzed in relation to the incidence of lobular carcinoma and the incidence of ductal carcinoma; the adjusted IRR associated with HRT use was 3.53 (95% CI, 1.94-6.41) for lobular carcinoma and 2.10 (95% CI, 1.64-2.70) for ductal carcinoma. The likelihood of developing estrogen receptor-positive breast carcinoma was found to depend significantly on the type of HRT regimen used (P = 0.03), with women receiving continuous therapy having the greatest probability of developing estrogen receptor-positive disease. CONCLUSIONS. An increased breast carcinoma IRR was found to be associated with current HRT use. In addition, relative to other types of HRT regimens, continuous estrogen + progestin regimens were found to be associated with an increased risk of breast carcinoma, and particularly estrogen receptor-positive breast carcinoma. (C) 2004 American Cancer Society.
引用
收藏
页码:2328 / 2337
页数:10
相关论文
共 38 条
  • [1] Beral V, 1997, LANCET, V350, P1047, DOI 10.1016/S0140-6736(97)08233-0
  • [2] Beral Valerie, 2003, Lancet, V362, P419, DOI 10.1016/S0140-6736(03)14065-2
  • [3] Hormone replacement therapy in relation to breast cancer
    Chen, CL
    Weiss, NS
    Newcomb, P
    Barlow, WN
    White, E
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 287 (06): : 734 - 741
  • [4] Relation of regimens of combined hormone replacement therapy to lobular, ductal, and other histologic types of breast carcinoma
    Daling, JR
    Malone, KE
    Doody, DR
    Voigt, LF
    Bernstein, L
    Coates, RJ
    Marchbanks, PA
    Norman, SA
    Weiss, LK
    Ursin, G
    Berlin, JA
    Burkman, RT
    Deapen, D
    Folger, SG
    McDonald, JA
    Simon, MS
    Strom, BL
    Wingo, PA
    Spirtas, R
    [J]. CANCER, 2002, 95 (12) : 2455 - 2464
  • [5] Prognosis of breast cancers detected in women receiving hormone replacement therapy
    Delgado, RC
    Lopez, DML
    [J]. MATURITAS, 2001, 38 (02) : 147 - 156
  • [6] DANISH-BREAST-CANCER-COOPERATIVE-GROUP (DBCG) - STRUCTURE AND RESULTS OF THE ORGANIZATION
    FISCHERMAN, K
    MOURIDSEN, HT
    [J]. ACTA ONCOLOGICA, 1988, 27 (6A) : 593 - 596
  • [7] Estradiol and progesterone regulate the proliferation of human breast epithelial cells
    Foidart, JM
    Colin, C
    Denoo, X
    Desreux, J
    Béliard, A
    Fournier, S
    de Lignières, B
    [J]. FERTILITY AND STERILITY, 1998, 69 (05) : 963 - 969
  • [8] Hormonal regulation of apoptosis in breast cells and tissues
    Gompel, A
    Somai, S
    Chaouat, M
    Kazem, A
    Kloosterboer, HJ
    Beusman, I
    Forgez, P
    Mimoun, M
    Rostène, W
    [J]. STEROIDS, 2000, 65 (10-11) : 593 - 598
  • [9] DOSE-RESPONSE AND TREND ANALYSIS IN EPIDEMIOLOGY - ALTERNATIVES TO CATEGORICAL ANALYSIS
    GREENLAND, S
    [J]. EPIDEMIOLOGY, 1995, 6 (04) : 356 - 365
  • [10] Noncardiovascular disease outcomes during 6.8 years of hormone therapy - Heart and Estrogen/progestin Replacement Study follow-up (HERS II)
    Hulley, S
    Furberg, C
    Barrett-Connor, E
    Cauley, J
    Grady, D
    Haskell, W
    Knopp, R
    Lowery, M
    Satterfield, S
    Schrott, H
    Vittinghoff, E
    Hunninghake, D
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 288 (01): : 58 - 66