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dc.contributor.authorUrban Men_AU
dc.contributor.authorBanks Een_AU
dc.contributor.authorEgger Sen_AU
dc.contributor.authorCanfell Ken_AU
dc.contributor.authorO'Connell DLen_AU
dc.contributor.authorBeral Ven_AU
dc.contributor.authorSitas Fen_AU
dc.date.issued2012
dc.date.issued2012en
dc.identifier.urihttps://hdl.handle.net/2123/30298
dc.description.abstractBACKGROUND: Oral contraceptives are known to influence the risk of cancers of the female reproductive system. Evidence regarding the relationship between injectable contraceptives and these cancers is limited, especially in black South Africans, among whom injectable contraceptives are used more commonly than oral contraceptives. METHODS AND FINDINGS: We analysed data from a South African hospital-based case-control study of black females aged 18-79 y, comparing self-reported contraceptive use in patients with breast (n = 1,664), cervical (n = 2,182), ovarian (n = 182), and endometrial (n = 182) cancer, with self-reported contraceptive use in 1,492 control patients diagnosed with cancers with no known relationship to hormonal contraceptive use. We adjusted for potential confounding factors, including age, calendar year of diagnosis, education, smoking, alcohol, parity/age at first birth, and number of sexual partners. Among controls, 26% had used injectable and 20% had used oral contraceptives. For current and more recent users versus never users of oral or injectable contraceptives, the odds ratios (ORs) for breast cancer were significantly increased in users of oral and/or injectable contraceptives (OR 1.66, 95% CI 1.28-2.16, p<0.001) and separately among those exclusively using oral (1.57, 1.03-2.40, p = 0.04) and exclusively using injectable (OR 1.83, 1.31-2.55, p<0.001) contraceptives; corresponding ORs for cervical cancer were 1.38 (1.08-1.77, p = 0.01), 1.01 (0.66-1.56, p = 0.96), and 1.58 (1.16-2.15, p = 0.004). There was no significant increase in breast or cervical cancer risk among women ceasing hormonal contraceptive use >/=10 y previously (p = 0.3 and p = 0.9, respectively). For durations of use >/=5 y versus never use, the ORs of ovarian cancer were 0.60 (0.36-0.99, p = 0.04) for oral and/or injectable contraceptive use and 0.07 (0.01-0.49, p = 0.008) for injectable use exclusively; corresponding ORs for endometrial cancer were 0.44 (0.22-0.86, p = 0.02) and 0.36 (0.11-1.26, p = 0.1). CONCLUSIONS: In this study, use of oral and of injectable hormonal contraceptives was associated with a transiently increased risk of breast and cervical cancer and, for long durations of use, with a reduced risk of ovarian and endometrial cancer. The observed effects of injectable and of oral contraceptives on cancer risk in this study did not appear to differ substantially. Please see later in the article for the Editors' Summaryen_AU
dc.publisherPLoS Medicineen_AU
dc.subjectAfricaen_AU
dc.subjecteducationen_AU
dc.subjectepidemiologyen_AU
dc.subjectFemaleen_AU
dc.subjectmethodsen_AU
dc.subjectOdds Ratioen_AU
dc.subjectoral contraceptivesen_AU
dc.subjectResearchen_AU
dc.subjectRisken_AU
dc.subjectSmokingen_AU
dc.subjectSouth Africaen_AU
dc.subjectAgeden_AU
dc.subjectWomenen_AU
dc.subjectbreasten_AU
dc.subjectcanceren_AU
dc.subjectCase-Control Studiesen_AU
dc.subjectcervicalen_AU
dc.subjectCervical Canceren_AU
dc.subjectCervixen_AU
dc.subjectdiagnosisen_AU
dc.subject.otherCancer Type - Breast Canceren_AU
dc.subject.otherCancer Type - Cervical Canceren_AU
dc.subject.otherCancer Type - Endometrial Canceren_AU
dc.subject.otherCancer Type - Ovarian Canceren_AU
dc.subject.otherEtiology - Exogenous Factors in the Origin and Cause of Canceren_AU
dc.titleInjectable and oral contraceptive use and cancers of the breast, cervix, ovary, and endometrium in black South african women: case-control studyen_AU
dc.typeArticleen_AU
dc.identifier.doi10.1371/journal.pmed.1001182
dc.relation.otherThe NHLS/MRC Cancer Epidemiology Research Group at the National Health Laboratory Service is currently funded by the South African Medical Research Council and the (South African) National Health Laboratory Service; previous funding was received from the University of the Witwatersrand, CANSA (Cancer Association of South Africa), and Cancer Research UK. The Cancer Epidemiology Research Unit at The Cancer Council NSW is funded in the main by The Cancer Council New South Wales. The Cancer Research UK Epidemiology Unit is supported by Cancer Research UK. EB and KC are supported by the Australian National Health and Medical Research Council. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.en_AU


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