Show simple item record

dc.contributor.authorSilvestri, V
dc.contributor.authorBarrowdale, D
dc.contributor.authorMulligan, AM
dc.contributor.authorNeuhausen, SL
dc.contributor.authorFox, S
dc.contributor.authorKarlan, BY
dc.contributor.authorMitchell, G
dc.contributor.authorJames, P
dc.contributor.authorThull, DL
dc.contributor.authorZorn, KK
dc.contributor.authorCarter, NJ
dc.contributor.authorNathanson, KL
dc.contributor.authorDomchek, SM
dc.contributor.authorRebbeck, TR
dc.contributor.authorRamus, SJ
dc.contributor.authorNussbaum, RL
dc.contributor.authorOlopade, OI
dc.contributor.authorRantala, J
dc.contributor.authorYoon, S-Y
dc.contributor.authorCaligo, MA
dc.contributor.authorSpugnesi, L
dc.contributor.authorBojesen, A
dc.contributor.authorPedersen, IS
dc.contributor.authorThomassen, M
dc.contributor.authorJensen, UB
dc.contributor.authorToland, AE
dc.contributor.authorSenter, L
dc.contributor.authorAndrulis, IL
dc.contributor.authorGlendon, G
dc.contributor.authorHulick, PJ
dc.contributor.authorImyanitov, EN
dc.contributor.authorGreene, MH
dc.contributor.authorMai, PL
dc.contributor.authorSinger, CF
dc.contributor.authorRappaport-Fuerhauser, C
dc.contributor.authorKramer, G
dc.contributor.authorVijai, J
dc.contributor.authorOffit, K
dc.contributor.authorRobson, M
dc.contributor.authorLincoln, A
dc.contributor.authorJacobs, L
dc.contributor.authorMachackova, E
dc.contributor.authorForetova, L
dc.contributor.authorNavratilova, M
dc.contributor.authorVasickova, P
dc.contributor.authorCouch, FJ
dc.contributor.authorHallberg, E
dc.contributor.authorRuddy, KJ
dc.contributor.authorSharma, P
dc.contributor.authorKim, S-W
dc.contributor.authorkConFab Investigators,
dc.contributor.authorTeixeira, MR
dc.contributor.authorPinto, P
dc.contributor.authorMontagna, M
dc.contributor.authorMatricardi, L
dc.contributor.authorArason, A
dc.contributor.authorJohannsson, OT
dc.contributor.authorBarkardottir, RB
dc.contributor.authorJakubowska, A
dc.contributor.authorLubinski, J
dc.contributor.authorIzquierdo, A
dc.contributor.authorPujana, MA
dc.contributor.authorBalmaña, J
dc.contributor.authorDiez, O
dc.contributor.authorIvady, G
dc.contributor.authorPapp, J
dc.contributor.authorOlah, E
dc.contributor.authorKwong, A
dc.contributor.authorHereditary Breast and Ovarian Cancer Research Group Netherlands (HEBON),
dc.contributor.authorNevanlinna, H
dc.contributor.authorAittomäki, K
dc.contributor.authorPerez Segura, P
dc.contributor.authorCaldes, T
dc.contributor.authorVan Maerken, T
dc.contributor.authorPoppe, B
dc.contributor.authorClaes, KBM
dc.contributor.authorIsaacs, C
dc.contributor.authorElan, C
dc.contributor.authorLasset, C
dc.contributor.authorStoppa-Lyonnet, D
dc.contributor.authorBarjhoux, L
dc.contributor.authorBelotti, M
dc.contributor.authorMeindl, A
dc.contributor.authorGehrig, A
dc.contributor.authorSutter, C
dc.contributor.authorEngel, C
dc.contributor.authorNiederacher, D
dc.contributor.authorSteinemann, D
dc.contributor.authorHahnen, E
dc.contributor.authorKast, K
dc.contributor.authorArnold, N
dc.contributor.authorVaron-Mateeva, R
dc.contributor.authorWand, D
dc.contributor.authorGodwin, AK
dc.contributor.authorEvans, DG
dc.contributor.authorFrost, D
dc.contributor.authorPerkins, J
dc.contributor.authorAdlard, J
dc.contributor.authorIzatt, L
dc.contributor.authorPlatte, R
dc.contributor.authorEeles, R
dc.contributor.authorEllis, S
dc.contributor.authorEMBRACE,
dc.contributor.authorHamann, U
dc.contributor.authorGarber, J
dc.contributor.authorFostira, F
dc.contributor.authorFountzilas, G
dc.contributor.authorPasini, B
dc.contributor.authorGiannini, G
dc.contributor.authorRizzolo, P
dc.contributor.authorRusso, A
dc.contributor.authorCortesi, L
dc.contributor.authorPapi, L
dc.contributor.authorVaresco, L
dc.contributor.authorPalli, D
dc.contributor.authorZanna, I
dc.contributor.authorSavarese, A
dc.contributor.authorRadice, P
dc.contributor.authorManoukian, S
dc.contributor.authorPeissel, B
dc.contributor.authorBarile, M
dc.contributor.authorBonanni, B
dc.contributor.authorViel, A
dc.contributor.authorPensotti, V
dc.contributor.authorTommasi, S
dc.contributor.authorPeterlongo, P
dc.contributor.authorWeitzel, JN
dc.contributor.authorOsorio, A
dc.contributor.authorBenitez, J
dc.contributor.authorMcGuffog, L
dc.contributor.authorHealey, S
dc.contributor.authorGerdes, A-M
dc.contributor.authorEjlertsen, B
dc.contributor.authorHansen, TVO
dc.contributor.authorSteele, L
dc.contributor.authorDing, YC
dc.contributor.authorTung, N
dc.contributor.authorJanavicius, R
dc.contributor.authorGoldgar, DE
dc.contributor.authorBuys, SS
dc.contributor.authorDaly, MB
dc.contributor.authorBane, A
dc.contributor.authorTerry, MB
dc.contributor.authorJohn, EM
dc.contributor.authorSouthey, M
dc.contributor.authorEaston, DF
dc.contributor.authorChenevix-Trench, G
dc.contributor.authorAntoniou, AC
dc.contributor.authorOttini, L
dc.date.accessioned2018-10-18T10:13:00Z
dc.date.issued2016-02-09
dc.identifier.citationBreast cancer research : BCR, 2016, 18 (1), pp. 15 - ?
dc.identifier.issn1465-5411
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/2900
dc.identifier.eissn1465-542X
dc.identifier.doi10.1186/s13058-016-0671-y
dc.description.abstractBACKGROUND: BRCA1 and, more commonly, BRCA2 mutations are associated with increased risk of male breast cancer (MBC). However, only a paucity of data exists on the pathology of breast cancers (BCs) in men with BRCA1/2 mutations. Using the largest available dataset, we determined whether MBCs arising in BRCA1/2 mutation carriers display specific pathologic features and whether these features differ from those of BRCA1/2 female BCs (FBCs). METHODS: We characterised the pathologic features of 419 BRCA1/2 MBCs and, using logistic regression analysis, contrasted those with data from 9675 BRCA1/2 FBCs and with population-based data from 6351 MBCs in the Surveillance, Epidemiology, and End Results (SEER) database. RESULTS: Among BRCA2 MBCs, grade significantly decreased with increasing age at diagnosis (P = 0.005). Compared with BRCA2 FBCs, BRCA2 MBCs were of significantly higher stage (P for trend = 2 × 10(-5)) and higher grade (P for trend = 0.005) and were more likely to be oestrogen receptor-positive [odds ratio (OR) 10.59; 95 % confidence interval (CI) 5.15-21.80] and progesterone receptor-positive (OR 5.04; 95 % CI 3.17-8.04). With the exception of grade, similar patterns of associations emerged when we compared BRCA1 MBCs and FBCs. BRCA2 MBCs also presented with higher grade than MBCs from the SEER database (P for trend = 4 × 10(-12)). CONCLUSIONS: On the basis of the largest series analysed to date, our results show that BRCA1/2 MBCs display distinct pathologic characteristics compared with BRCA1/2 FBCs, and we identified a specific BRCA2-associated MBC phenotype characterised by a variable suggesting greater biological aggressiveness (i.e., high histologic grade). These findings could lead to the development of gender-specific risk prediction models and guide clinical strategies appropriate for MBC management.
dc.formatElectronic
dc.format.extent15 - ?
dc.languageeng
dc.language.isoeng
dc.publisherBMC
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectkConFab Investigators
dc.subjectHereditary Breast and Ovarian Cancer Research Group Netherlands (HEBON)
dc.subjectEMBRACE
dc.subjectHumans
dc.subjectBreast Neoplasms
dc.subjectBreast Neoplasms, Male
dc.subjectGenetic Predisposition to Disease
dc.subjectBRCA1 Protein
dc.subjectBRCA2 Protein
dc.subjectNeoplasm Staging
dc.subjectMutation
dc.subjectPolymorphism, Single Nucleotide
dc.subjectAdult
dc.subjectAged
dc.subjectMiddle Aged
dc.subjectFemale
dc.subjectMale
dc.titleMale breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2.
dc.typeJournal Article
dcterms.dateAccepted2016-01-06
rioxxterms.versionofrecord10.1186/s13058-016-0671-y
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2016-02-09
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfBreast cancer research : BCR
pubs.issue1
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.volume18
pubs.embargo.termsNot known
icr.researchteamOncogenetics
dc.contributor.icrauthorEeles, Rosalind


Files in this item

Thumbnail

This item appears in the following collection(s)

Show simple item record

https://creativecommons.org/licenses/by/4.0
Except where otherwise noted, this item's license is described as https://creativecommons.org/licenses/by/4.0