Oral contraceptive use and risk of melanoma in premenopausal women

被引:48
作者
Feskanich, D
Hunter, DJ
Willett, WC
Spiegelman, D
Stampfer, MJ
Speizer, FE
Colditz, GA
机构
[1] Brigham & Womens Hosp, Channing Lab, Dept Med, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA 02115 USA
[3] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
[4] Harvard Univ, Sch Publ Hlth, Harvard Ctr Canc Prevent, Boston, MA 02115 USA
[5] Harvard Univ, Sch Publ Hlth, Dept Nutr, Boston, MA 02115 USA
[6] Harvard Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02115 USA
[7] Harvard Univ, Sch Publ Hlth, Dept Environm Hlth, Boston, MA 02115 USA
关键词
melanoma; oral contraceptives; oestrogen; premenopausal;
D O I
10.1038/sj.bjc.6690787
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Melanoma has been increasing in white populations. Incidence rates rise steeply in women until about age 50, suggesting oestrogen as a possible risk factor. Oestrogens can increase melanocyte count and melanin content and cause hyperpigmentation of the skin. We examined prospectively the association between oral contraceptive (OC) use and diagnoses of superficial spreading and nodular melanoma among 183 693 premenopausal white women in the Nurses' Health Study (NHS)and the Nurses' Health Study Il (NHS II) cohorts. One hundred and forty six cases were confirmed in NHS during follow-up from 1976 to 1994, and 106 cases were confirmed in NHS II from 1989 to 1995. Skin reaction to sun exposure, sunburn history. mole counts, hair colour, family history of melanoma, parity, height and body mass index were also assessed and included in logistic regression models. A significant twofold increase in risk of melanoma (relative risk (RR) = 2.0, 95% confidence interval (CI) 1.23.4) was observed among current OC users compared to never users. Risk was further increased among current users with 10 or more years of use (RR = 3.4, 95% CI 1.7-7.0). Risk did not appear elevated among past OC users, even among those with longer durations of use, and risk did not decline linearly with time since last use. In conclusion, risk of premenopausal melanoma may be increased among women who are current OC users, particularly among those with longer durations of use. Further research is needed to determine whether low-dose oestrogen pills in particular are associated with an increase in risk and to describe possible interactions between OC use and sun exposure or other risk factors for melanoma.
引用
收藏
页码:918 / 923
页数:6
相关论文
共 39 条
  • [1] [Anonymous], CANC EPIDEMIOLOGY PR
  • [2] BAIN C, 1982, J NATL CANCER I, V68, P537
  • [3] ORAL-CONTRACEPTIVE USE AND MALIGNANT-MELANOMA IN AUSTRALIA
    BERAL, V
    EVANS, S
    SHAW, H
    MILTON, G
    [J]. BRITISH JOURNAL OF CANCER, 1984, 50 (05) : 681 - 685
  • [4] MALIGNANT-MELANOMA AND ORAL-CONTRACEPTIVE USE AMONG WOMEN IN CALIFORNIA
    BERAL, V
    RAMCHARAN, S
    FARIS, R
    [J]. BRITISH JOURNAL OF CANCER, 1977, 36 (06) : 804 - 809
  • [5] Calle EE, 1996, LANCET, V347, P1713, DOI 10.1016/S0140-6736(96)90806-5
  • [6] INCIDENCE OF ESTROGEN-RECEPTOR IN BENIGN NEVI AND HUMAN-MALIGNANT MELANOMA
    CHAUDHURI, PK
    WALKER, MJ
    BRIELE, HA
    BEATTIE, CW
    GUPTA, TKD
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1980, 244 (08): : 791 - 793
  • [7] COCCONI G, 1992, NEW ENGL J MED, V327, P517
  • [8] The Nurses' Health Study: 20-year contribution to the understanding of health among women
    Colditz, GA
    Manson, JE
    Hankinson, SE
    [J]. JOURNAL OF WOMENS HEALTH, 1997, 6 (01) : 49 - 62
  • [9] RELATION OF POOLED LOGISTIC-REGRESSION TO TIME-DEPENDENT COX REGRESSION-ANALYSIS - THE FRAMINGHAM HEART-STUDY
    DAGOSTINO, RB
    LEE, ML
    BELANGER, AJ
    CUPPLES, LA
    ANDERSON, K
    KANNEL, WB
    [J]. STATISTICS IN MEDICINE, 1990, 9 (12) : 1501 - 1515
  • [10] METAANALYSIS IN CLINICAL-TRIALS
    DERSIMONIAN, R
    LAIRD, N
    [J]. CONTROLLED CLINICAL TRIALS, 1986, 7 (03): : 177 - 188