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dc.contributor.authorSchrijver, LH
dc.contributor.authorOlsson, H
dc.contributor.authorPhillips, K-A
dc.contributor.authorTerry, MB
dc.contributor.authorGoldgar, DE
dc.contributor.authorKast, K
dc.contributor.authorEngel, C
dc.contributor.authorMooij, TM
dc.contributor.authorAdlard, J
dc.contributor.authorBarrowdale, D
dc.contributor.authorDavidson, R
dc.contributor.authorEeles, R
dc.contributor.authorEllis, S
dc.contributor.authorEvans, DG
dc.contributor.authorFrost, D
dc.contributor.authorIzatt, L
dc.contributor.authorPorteous, ME
dc.contributor.authorSide, LE
dc.contributor.authorWalker, L
dc.contributor.authorBerthet, P
dc.contributor.authorBonadona, V
dc.contributor.authorLeroux, D
dc.contributor.authorMouret-Fourme, E
dc.contributor.authorVenat-Bouvet, L
dc.contributor.authorBuys, SS
dc.contributor.authorSouthey, MC
dc.contributor.authorJohn, EM
dc.contributor.authorChung, WK
dc.contributor.authorDaly, MB
dc.contributor.authorBane, A
dc.contributor.authorvan Asperen, CJ
dc.contributor.authorGómez Garcia, EB
dc.contributor.authorMourits, MJE
dc.contributor.authorvan Os, TAM
dc.contributor.authorRoos-Blom, M-J
dc.contributor.authorFriedlander, ML
dc.contributor.authorMcLachlan, S-A
dc.contributor.authorSinger, CF
dc.contributor.authorTan, YY
dc.contributor.authorForetova, L
dc.contributor.authorNavratilova, M
dc.contributor.authorGerdes, A-M
dc.contributor.authorCaldes, T
dc.contributor.authorSimard, J
dc.contributor.authorOlah, E
dc.contributor.authorJakubowska, A
dc.contributor.authorArver, B
dc.contributor.authorOsorio, A
dc.contributor.authorNoguès, C
dc.contributor.authorAndrieu, N
dc.contributor.authorEaston, DF
dc.contributor.authorvan Leeuwen, FE
dc.contributor.authorHopper, JL
dc.contributor.authorMilne, RL
dc.contributor.authorAntoniou, AC
dc.contributor.authorRookus, MA
dc.contributor.authorEMBRACE, GENEPSO, BCFR, HEBON, kConFab, and IBCCS,
dc.date.accessioned2019-09-17T09:48:41Z
dc.date.issued2018-04-01
dc.identifier.citationJNCI cancer spectrum, 2018, 2 (2), pp. pky023 - ?
dc.identifier.issn2515-5091
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/3342
dc.identifier.eissn2515-5091
dc.identifier.doi10.1093/jncics/pky023
dc.description.abstractBACKGROUND: For BRCA1 and BRCA2 mutation carriers, the association between oral contraceptive preparation (OCP) use and breast cancer (BC) risk is still unclear. METHODS: Breast camcer risk associations were estimated from OCP data on 6030 BRCA1 and 3809 BRCA2 mutation carriers using age-dependent Cox regression, stratified by study and birth cohort. Prospective, left-truncated retrospective and full-cohort retrospective analyses were performed. RESULTS: For BRCA1 mutation carriers, OCP use was not associated with BC risk in prospective analyses (hazard ratio [HR] = 1.08, 95% confidence interval [CI] = 0.75 to 1.56), but in the left-truncated and full-cohort retrospective analyses, risks were increased by 26% (95% CI = 6% to 51%) and 39% (95% CI = 23% to 58%), respectively. For BRCA2 mutation carriers, OCP use was associated with BC risk in prospective analyses (HR = 1.75, 95% CI = 1.03 to 2.97), but retrospective analyses were inconsistent (left-truncated: HR = 1.06, 95% CI = 0.85 to 1.33; full cohort: HR = 1.52, 95% CI = 1.28 to 1.81). There was evidence of increasing risk with duration of use, especially before the first full-term pregnancy (BRCA1: both retrospective analyses, P < .001 and P = .001, respectively; BRCA2: full retrospective analysis, P = .002). CONCLUSIONS: Prospective analyses did not show that past use of OCP is associated with an increased BC risk for BRCA1 mutation carriers in young middle-aged women (40-50 years). For BRCA2 mutation carriers, a causal association is also not likely at those ages. Findings between retrospective and prospective analyses were inconsistent and could be due to survival bias or a true association for younger women who were underrepresented in the prospective cohort. Given the uncertain safety of long-term OCP use for BRCA1/2 mutation carriers, indications other than contraception should be avoided and nonhormonal contraceptive methods should be discussed.
dc.formatElectronic-eCollection
dc.format.extentpky023 - ?
dc.languageeng
dc.language.isoeng
dc.publisherOXFORD UNIV PRESS
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectEMBRACE, GENEPSO, BCFR, HEBON, kConFab, and IBCCS
dc.titleOral Contraceptive Use and Breast Cancer Risk: Retrospective and Prospective Analyses From a BRCA1 and BRCA2 Mutation Carrier Cohort Study.
dc.typeJournal Article
dcterms.dateAccepted2018-04-24
rioxxterms.versionofrecord10.1093/jncics/pky023
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by-nc/4.0
rioxxterms.licenseref.startdate2018-04
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfJNCI cancer spectrum
pubs.issue2
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology/Oncogenetics
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Oncogenetics
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology/Oncogenetics
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Oncogenetics
pubs.publication-statusPublished
pubs.volume2
pubs.embargo.termsNot known
icr.researchteamOncogenetics
dc.contributor.icrauthorEeles, Rosalind


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