Skip to main content
Erschienen in: Breast Cancer Research and Treatment 1/2009

01.03.2009 | Epidemiology

Menstrual and reproductive history, postmenopausal hormone use, and risk of benign proliferative epithelial disorders of the breast: a cohort study

verfasst von: Yan Cui, David L. Page, Dorothy S. Lane, Thomas E. Rohan

Erschienen in: Breast Cancer Research and Treatment | Ausgabe 1/2009

Einloggen, um Zugang zu erhalten

Abstract

Menstrual and reproductive history and postmenopausal hormone use are well-established risk factors for breast cancer. However, previous studies that have assessed these factors in association with risk of benign proliferative epithelial disorders (BPED) of the breast, putative precursors of breast cancer, have yielded inconsistent findings. To investigate these associations, we conducted a cohort study among 68,132 postmenopausal women enrolled in the Women’s Health Initiative randomized clinical trials. Women were prospectively followed and those reporting an open surgical biopsy or a core needle biopsy had histological sections obtained for centralized pathology review. Over an average of 7.8 years of follow-up, we identified 1,792 women with BPED of the breast. We used Cox proportional hazards models to estimate hazard ratios (HRs) and 95% confidence limits (CLs) for the associations of interest. Menstrual and reproductive histories were not associated with risk of BPED of the breast, overall or by histological subtype. Women who had used postmenopausal hormones for 15 years or more had a two-fold increase in risk of BPED of the breast compared to women who had never used postmenopausal hormones (HR = 2.03 95% CL = 1.73, 2.38) and the increase in risk was observed for both BPED of the breast without atypia and for atypical hyperplasia. Furthermore, the risk of BPED of the breast decreased with time since cessation of use so that there was essentially no increase in risk 5 or more years after ending use (HR for stopping ≥5 years earlier = 0.96, 95%CL = 0.79, 1.16; HR for stopping <5 years earlier = 1.32, 95% CL = 1.08,1.61).
Anhänge
Nur mit Berechtigung zugänglich
Literatur
1.
Zurück zum Zitat Rohan TE, Kandel RA (2002) Breast. In: Franco EL, Rohan TE (eds) Cancer precursors: epidemiology, detection, and prevention. Springer-Verlag, New York Rohan TE, Kandel RA (2002) Breast. In: Franco EL, Rohan TE (eds) Cancer precursors: epidemiology, detection, and prevention. Springer-Verlag, New York
2.
Zurück zum Zitat Fitzgibbons PL, Henson DE, Hutter RV (1998) Benign breast changes and the risk for subsequent breast cancer: an update of the 1985 consensus statement. Cancer Committee of the College of American Pathologists. Arch Pathol Lab Med 122:1053–1055PubMed Fitzgibbons PL, Henson DE, Hutter RV (1998) Benign breast changes and the risk for subsequent breast cancer: an update of the 1985 consensus statement. Cancer Committee of the College of American Pathologists. Arch Pathol Lab Med 122:1053–1055PubMed
3.
Zurück zum Zitat Lakhani SR (1999) The transition from hyperplasia to invasive carcinoma of the breast. J Pathol 187:272–278PubMedCrossRef Lakhani SR (1999) The transition from hyperplasia to invasive carcinoma of the breast. J Pathol 187:272–278PubMedCrossRef
4.
5.
Zurück zum Zitat Berkowitz GS, Kelsey JL, LiVolsi VA et al (1984) Exogenous hormone use and fibrocystic breast disease by histopathologic component. Int J Cancer 34:443–449PubMedCrossRef Berkowitz GS, Kelsey JL, LiVolsi VA et al (1984) Exogenous hormone use and fibrocystic breast disease by histopathologic component. Int J Cancer 34:443–449PubMedCrossRef
6.
Zurück zum Zitat Berkowitz GS, Kelsey JL, LiVolsi VA et al (1985) Risk factors for fibrocystic breast disease and its histopathologic components. J Natl Cancer Inst 75:43–50PubMed Berkowitz GS, Kelsey JL, LiVolsi VA et al (1985) Risk factors for fibrocystic breast disease and its histopathologic components. J Natl Cancer Inst 75:43–50PubMed
7.
Zurück zum Zitat Bright RA, Morrison AS, Brisson J et al (1989) Histologic and mammographic specificity of risk factors for benign breast disease. Cancer 64:653–657PubMedCrossRef Bright RA, Morrison AS, Brisson J et al (1989) Histologic and mammographic specificity of risk factors for benign breast disease. Cancer 64:653–657PubMedCrossRef
8.
Zurück zum Zitat Friedenreich C, Bryant H, Alexander F et al (2000) Risk factors for benign proliferative breast disease. Int J Epidemiol 29:637–644PubMedCrossRef Friedenreich C, Bryant H, Alexander F et al (2000) Risk factors for benign proliferative breast disease. Int J Epidemiol 29:637–644PubMedCrossRef
9.
Zurück zum Zitat Hsieh CC, Walker AM, Trapido EJ et al (1984) Age at first birth and breast atypia. Int J Cancer 33:309–312PubMedCrossRef Hsieh CC, Walker AM, Trapido EJ et al (1984) Age at first birth and breast atypia. Int J Cancer 33:309–312PubMedCrossRef
10.
Zurück zum Zitat LiVolsi VA, Stadel BV, Kelsey JL et al (1978) Fibrocystic breast disease in oral-contraceptive users. A histopathological evaluation of epithelial atypia. N Engl J Med 299:381–385PubMedCrossRef LiVolsi VA, Stadel BV, Kelsey JL et al (1978) Fibrocystic breast disease in oral-contraceptive users. A histopathological evaluation of epithelial atypia. N Engl J Med 299:381–385PubMedCrossRef
11.
Zurück zum Zitat Minami Y, Ohuchi N, Taeda Y et al (1998) Risk factors for benign breast disease according to histopathological type: comparisons with risk factors for breast cancer. Jpn J Cancer Res 89:116–123PubMed Minami Y, Ohuchi N, Taeda Y et al (1998) Risk factors for benign breast disease according to histopathological type: comparisons with risk factors for breast cancer. Jpn J Cancer Res 89:116–123PubMed
12.
Zurück zum Zitat Pastides H, Kelsey JL, LiVolsi VA et al (1983) Oral contraceptive use and fibrocystic breast disease with special reference to its histopathology. J Natl Cancer Inst 71:5–9PubMed Pastides H, Kelsey JL, LiVolsi VA et al (1983) Oral contraceptive use and fibrocystic breast disease with special reference to its histopathology. J Natl Cancer Inst 71:5–9PubMed
13.
Zurück zum Zitat Rohan TE, L’Abbe KA, Cook MG (1992) Oral contraceptives and risk of benign proliferative epithelial disorders of the breast. Int J Cancer 50:891–894PubMedCrossRef Rohan TE, L’Abbe KA, Cook MG (1992) Oral contraceptives and risk of benign proliferative epithelial disorders of the breast. Int J Cancer 50:891–894PubMedCrossRef
14.
Zurück zum Zitat Rohan TE, Miller AB (1999) A cohort study of oral contraceptive use and risk of benign breast disease. Int J Cancer 82:191–196PubMedCrossRef Rohan TE, Miller AB (1999) A cohort study of oral contraceptive use and risk of benign breast disease. Int J Cancer 82:191–196PubMedCrossRef
15.
Zurück zum Zitat Rohan TE, Miller AB (1999) Hormone replacement therapy and risk of benign proliferative epithelial disorders of the breast. Eur J Cancer Prev 8:123–130PubMedCrossRef Rohan TE, Miller AB (1999) Hormone replacement therapy and risk of benign proliferative epithelial disorders of the breast. Eur J Cancer Prev 8:123–130PubMedCrossRef
16.
Zurück zum Zitat Soini I, Aine R, Lauslahti K et al (1981) Independent risk factors of benign and malignant breast lesions. Am J Epidemiol 114:507–514PubMed Soini I, Aine R, Lauslahti K et al (1981) Independent risk factors of benign and malignant breast lesions. Am J Epidemiol 114:507–514PubMed
17.
Zurück zum Zitat The Women’s Health Initiative Study Group (1998) Design of the Women’s Health Initiative clinical trial and observational study. Control Clin Trials 19:61–109CrossRef The Women’s Health Initiative Study Group (1998) Design of the Women’s Health Initiative clinical trial and observational study. Control Clin Trials 19:61–109CrossRef
18.
Zurück zum Zitat Jackson RD, LaCroix AZ, Cauley JA et al (2003) The women’s health initiative calcium-vitamin D trial: overview and baseline characteristics of participants. Ann Epidemiol 13:S98–S106PubMedCrossRef Jackson RD, LaCroix AZ, Cauley JA et al (2003) The women’s health initiative calcium-vitamin D trial: overview and baseline characteristics of participants. Ann Epidemiol 13:S98–S106PubMedCrossRef
19.
Zurück zum Zitat Ritenbaugh C, Patterson RE, Chlebowski RT et al (2003) The Women’s Health Initiative Dietary Modification trial: overview and baseline characteristics of participants. Ann Epidemiol 13:S87–S97PubMedCrossRef Ritenbaugh C, Patterson RE, Chlebowski RT et al (2003) The Women’s Health Initiative Dietary Modification trial: overview and baseline characteristics of participants. Ann Epidemiol 13:S87–S97PubMedCrossRef
20.
Zurück zum Zitat Stefanick ML, Cochrane BB, Hsia J et al (2003) The Women’s Health Initiative postmenopausal hormone trials: overview and baseline characteristics of participants. Ann Epidemiol 13:S78–S86PubMedCrossRef Stefanick ML, Cochrane BB, Hsia J et al (2003) The Women’s Health Initiative postmenopausal hormone trials: overview and baseline characteristics of participants. Ann Epidemiol 13:S78–S86PubMedCrossRef
21.
Zurück zum Zitat Hartmann LC, Sellers TA, Frost MH et al (2005) Benign breast disease and the risk of breast cancer. N Engl J Med 353:229–237PubMedCrossRef Hartmann LC, Sellers TA, Frost MH et al (2005) Benign breast disease and the risk of breast cancer. N Engl J Med 353:229–237PubMedCrossRef
22.
Zurück zum Zitat Cui Y, Page DL, Chlebowski RT et al (2007) Cigarette smoking and risk of benign proliferative epithelial disorders of the breast in the Women’s Health Initiative. Cancer Causes Control 18:431–438PubMedCrossRef Cui Y, Page DL, Chlebowski RT et al (2007) Cigarette smoking and risk of benign proliferative epithelial disorders of the breast in the Women’s Health Initiative. Cancer Causes Control 18:431–438PubMedCrossRef
23.
Zurück zum Zitat Cui Y, Page DL, Chlebowski RT et al (2007) Alcohol and folate consumption and risk of benign proliferative epithelial disorders of the breast. Int J Cancer 121:1346–1351PubMedCrossRef Cui Y, Page DL, Chlebowski RT et al (2007) Alcohol and folate consumption and risk of benign proliferative epithelial disorders of the breast. Int J Cancer 121:1346–1351PubMedCrossRef
24.
Zurück zum Zitat Rothman JK, Greenland S (eds) (1998) Modern epidemiology. Lippincott-Raven, Philadelphia (PA) Rothman JK, Greenland S (eds) (1998) Modern epidemiology. Lippincott-Raven, Philadelphia (PA)
25.
Zurück zum Zitat Key T, Appleby P, Barnes I et al (2002) Endogenous sex hormones and breast cancer in postmenopausal women: reanalysis of nine prospective studies. J Natl Cancer Inst 94:606–616PubMed Key T, Appleby P, Barnes I et al (2002) Endogenous sex hormones and breast cancer in postmenopausal women: reanalysis of nine prospective studies. J Natl Cancer Inst 94:606–616PubMed
26.
Zurück zum Zitat Collaborative Group on Hormonal Factors in Breast Cancer (1997) Breast cancer and hormone replacement therapy: collaborative reanalysis of data from 51 epidemiological studies of 52,705 women with breast cancer and 108,411 women without breast cancer. Lancet 350:1047–1059CrossRef Collaborative Group on Hormonal Factors in Breast Cancer (1997) Breast cancer and hormone replacement therapy: collaborative reanalysis of data from 51 epidemiological studies of 52,705 women with breast cancer and 108,411 women without breast cancer. Lancet 350:1047–1059CrossRef
27.
Zurück zum Zitat Rossouw JE, Anderson GL, Prentice RL et al (2002) Risks and benefits of estrogen plus progestin in healthy postmenopausal women: principal results From the Women’s Health Initiative randomized controlled trial. JAMA 288:321–333PubMedCrossRef Rossouw JE, Anderson GL, Prentice RL et al (2002) Risks and benefits of estrogen plus progestin in healthy postmenopausal women: principal results From the Women’s Health Initiative randomized controlled trial. JAMA 288:321–333PubMedCrossRef
28.
Zurück zum Zitat Schairer C, Hill D, Sturgeon SR et al (2005) Serum concentrations of estrogens, sex hormone binding globulin, and androgens and risk of breast hyperplasia in postmenopausal women. Cancer Epidemiol Biomarkers Prev 14:1660–1665PubMedCrossRef Schairer C, Hill D, Sturgeon SR et al (2005) Serum concentrations of estrogens, sex hormone binding globulin, and androgens and risk of breast hyperplasia in postmenopausal women. Cancer Epidemiol Biomarkers Prev 14:1660–1665PubMedCrossRef
29.
Zurück zum Zitat Jacquemier JD, Rolland PH, Vague D et al (1982) Relationships between steroid receptor and epithelial cell proliferation in benign fibrocystic disease of the breast. Cancer 49:2534–2536PubMedCrossRef Jacquemier JD, Rolland PH, Vague D et al (1982) Relationships between steroid receptor and epithelial cell proliferation in benign fibrocystic disease of the breast. Cancer 49:2534–2536PubMedCrossRef
30.
Zurück zum Zitat Giani C, D’Amore E, Delarue JC et al (1986) Estrogen and progesterone receptors in benign breast tumors and lesions: relationship with histological and cytological features. Int J Cancer 37:7–10PubMedCrossRef Giani C, D’Amore E, Delarue JC et al (1986) Estrogen and progesterone receptors in benign breast tumors and lesions: relationship with histological and cytological features. Int J Cancer 37:7–10PubMedCrossRef
31.
Zurück zum Zitat Tan-Chiu E, Wang J, Costantino JP et al (2003) Effects of tamoxifen on benign breast disease in women at high risk for breast cancer. J Natl Cancer Inst 95:302–307PubMedCrossRef Tan-Chiu E, Wang J, Costantino JP et al (2003) Effects of tamoxifen on benign breast disease in women at high risk for breast cancer. J Natl Cancer Inst 95:302–307PubMedCrossRef
32.
Zurück zum Zitat Anderson GL, Limacher M, Assaf AR et al (2004) Effects of conjugated equine estrogen in postmenopausal women with hysterectomy: the Women’s Health Initiative randomized controlled trial. JAMA 291:1701–1712PubMedCrossRef Anderson GL, Limacher M, Assaf AR et al (2004) Effects of conjugated equine estrogen in postmenopausal women with hysterectomy: the Women’s Health Initiative randomized controlled trial. JAMA 291:1701–1712PubMedCrossRef
33.
Zurück zum Zitat Cline JM, Soderqvist G, von Schoultz E et al (1996) Effects of hormone replacement therapy on the mammary gland of surgically postmenopausal cynomolgus macaques. Am J Obstet Gynecol 174:93–100PubMedCrossRef Cline JM, Soderqvist G, von Schoultz E et al (1996) Effects of hormone replacement therapy on the mammary gland of surgically postmenopausal cynomolgus macaques. Am J Obstet Gynecol 174:93–100PubMedCrossRef
34.
Zurück zum Zitat Cook MG, Rohan TE (1985) The patho-epidemiology of benign proliferative epithelial disorders of the female breast. J Pathol 146:1–15PubMedCrossRef Cook MG, Rohan TE (1985) The patho-epidemiology of benign proliferative epithelial disorders of the female breast. J Pathol 146:1–15PubMedCrossRef
Metadaten
Titel
Menstrual and reproductive history, postmenopausal hormone use, and risk of benign proliferative epithelial disorders of the breast: a cohort study
verfasst von
Yan Cui
David L. Page
Dorothy S. Lane
Thomas E. Rohan
Publikationsdatum
01.03.2009
Verlag
Springer US
Erschienen in
Breast Cancer Research and Treatment / Ausgabe 1/2009
Print ISSN: 0167-6806
Elektronische ISSN: 1573-7217
DOI
https://doi.org/10.1007/s10549-008-9973-9

Weitere Artikel der Ausgabe 1/2009

Breast Cancer Research and Treatment 1/2009 Zur Ausgabe

Adjuvante Immuntherapie verlängert Leben bei RCC

25.04.2024 Nierenkarzinom Nachrichten

Nun gibt es auch Resultate zum Gesamtüberleben: Eine adjuvante Pembrolizumab-Therapie konnte in einer Phase-3-Studie das Leben von Menschen mit Nierenzellkarzinom deutlich verlängern. Die Sterberate war im Vergleich zu Placebo um 38% geringer.

Alectinib verbessert krankheitsfreies Überleben bei ALK-positivem NSCLC

25.04.2024 NSCLC Nachrichten

Das Risiko für Rezidiv oder Tod von Patienten und Patientinnen mit reseziertem ALK-positivem NSCLC ist unter einer adjuvanten Therapie mit dem Tyrosinkinase-Inhibitor Alectinib signifikant geringer als unter platinbasierter Chemotherapie.

Bei Senioren mit Prostatakarzinom auf Anämie achten!

24.04.2024 DGIM 2024 Nachrichten

Patienten, die zur Behandlung ihres Prostatakarzinoms eine Androgendeprivationstherapie erhalten, entwickeln nicht selten eine Anämie. Wer ältere Patienten internistisch mitbetreut, sollte auf diese Nebenwirkung achten.

ICI-Therapie in der Schwangerschaft wird gut toleriert

Müssen sich Schwangere einer Krebstherapie unterziehen, rufen Immuncheckpointinhibitoren offenbar nicht mehr unerwünschte Wirkungen hervor als andere Mittel gegen Krebs.

Update Onkologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.