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dc.contributor.authorAbubakar, M
dc.contributor.authorChang-Claude, J
dc.contributor.authorAli, HR
dc.contributor.authorChatterjee, N
dc.contributor.authorCoulson, P
dc.contributor.authorDaley, F
dc.contributor.authorBlows, F
dc.contributor.authorBenitez, J
dc.contributor.authorMilne, RL
dc.contributor.authorBrenner, H
dc.contributor.authorStegmaier, C
dc.contributor.authorMannermaa, A
dc.contributor.authorRudolph, A
dc.contributor.authorSinn, P
dc.contributor.authorCouch, FJ
dc.contributor.authorDevilee, P
dc.contributor.authorTollenaar, RAEM
dc.contributor.authorSeynaeve, C
dc.contributor.authorFigueroa, J
dc.contributor.authorLissowska, J
dc.contributor.authorHewitt, S
dc.contributor.authorHooning, MJ
dc.contributor.authorHollestelle, A
dc.contributor.authorFoekens, R
dc.contributor.authorKoppert, LB
dc.contributor.authorkConFab Investigators,
dc.contributor.authorBolla, MK
dc.contributor.authorWang, Q
dc.contributor.authorJones, ME
dc.contributor.authorSchoemaker, MJ
dc.contributor.authorKeeman, R
dc.contributor.authorEaston, DF
dc.contributor.authorSwerdlow, AJ
dc.contributor.authorSherman, ME
dc.contributor.authorSchmidt, MK
dc.contributor.authorPharoah, PD
dc.contributor.authorGarcia-Closas, M
dc.date.accessioned2018-04-17T09:12:42Z
dc.date.issued2018-08-15
dc.identifier.citationInternational journal of cancer, 2018, 143 (4), pp. 746 - 757
dc.identifier.issn0020-7136
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/1647
dc.identifier.eissn1097-0215
dc.identifier.doi10.1002/ijc.31352
dc.description.abstractLimited epidemiological evidence suggests that the etiology of hormone receptor positive (HR+) breast cancer may differ by levels of histologic grade and proliferation. We pooled risk factor and pathology data on 5,905 HR+ breast cancer cases and 26,281 controls from 11 epidemiological studies. Proliferation was determined by centralized automated measures of KI67 in tissue microarrays. Odds ratios (OR), 95% confidence intervals (CI) and p-values for case-case and case-control comparisons for risk factors in relation to levels of grade and quartiles (Q1-Q4) of KI67 were estimated using polytomous logistic regression models. Case-case comparisons showed associations between nulliparity and high KI67 [OR (95% CI) for Q4 vs. Q1 = 1.54 (1.22, 1.95)]; obesity and high grade [grade 3 vs. 1 = 1.68 (1.31, 2.16)] and current use of combined hormone therapy (HT) and low grade [grade 3 vs. 1 = 0.27 (0.16, 0.44)] tumors. In case-control comparisons, nulliparity was associated with elevated risk of tumors with high but not low levels of proliferation [1.43 (1.14, 1.81) for KI67 Q4 vs. 0.83 (0.60, 1.14) for KI67 Q1]; obesity among women ≥50 years with high but not low grade tumors [1.55 (1.17, 2.06) for grade 3 vs. 0.88 (0.66, 1.16) for grade 1] and HT with low but not high grade tumors [3.07 (2.22, 4.23) for grade 1 vs. 0.85 (0.55, 1.30) for grade 3]. Menarcheal age and family history were similarly associated with HR+ tumors of different grade or KI67 levels. These findings provide insights into the etiologic heterogeneity of HR+ tumors.
dc.formatPrint-Electronic
dc.format.extent746 - 757
dc.languageeng
dc.language.isoeng
dc.publisherWILEY
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectkConFab Investigators
dc.subjectHumans
dc.subjectBreast Neoplasms
dc.subjectObesity
dc.subjectContraceptives, Oral, Hormonal
dc.subjectKi-67 Antigen
dc.subjectReceptors, Estrogen
dc.subjectReceptors, Progesterone
dc.subjectBody Mass Index
dc.subjectRisk Factors
dc.subjectCase-Control Studies
dc.subjectParity
dc.subjectCell Proliferation
dc.subjectAdult
dc.subjectAged
dc.subjectMiddle Aged
dc.subjectFemale
dc.subjectNeoplasm Grading
dc.subjectBiomarkers, Tumor
dc.titleEtiology of hormone receptor positive breast cancer differs by levels of histologic grade and proliferation.
dc.typeJournal Article
dcterms.dateAccepted2018-01-26
rioxxterms.versionofrecord10.1002/ijc.31352
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2018-08
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfInternational journal of cancer
pubs.issue4
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/Breast Cancer Research
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research/Aetiological Epidemiology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology/Aetiological Epidemiology
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/Breast Cancer Research
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research/Aetiological Epidemiology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology/Aetiological Epidemiology
pubs.publication-statusPublished
pubs.volume143
pubs.embargo.termsNot known
icr.researchteamAetiological Epidemiology
dc.contributor.icrauthorAbubakar, Mustapha
dc.contributor.icrauthorJones, Michael
dc.contributor.icrauthorSchoemaker, Minouk
dc.contributor.icrauthorSwerdlow, Anthony
dc.contributor.icrauthorGarcia-Closas, Montserrat


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