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dc.contributor.authorMuranen, TA
dc.contributor.authorMorra, A
dc.contributor.authorKhan, S
dc.contributor.authorBarnes, DR
dc.contributor.authorBolla, MK
dc.contributor.authorDennis, J
dc.contributor.authorKeeman, R
dc.contributor.authorLeslie, G
dc.contributor.authorParsons, MT
dc.contributor.authorWang, Q
dc.contributor.authorAhearn, TU
dc.contributor.authorAittomäki, K
dc.contributor.authorAndrulis, IL
dc.contributor.authorArun, BK
dc.contributor.authorBehrens, S
dc.contributor.authorBialkowska, K
dc.contributor.authorBojesen, SE
dc.contributor.authorCamp, NJ
dc.contributor.authorChang-Claude, J
dc.contributor.authorCzene, K
dc.contributor.authorDevilee, P
dc.contributor.authorHEBON investigators,
dc.contributor.authorDomchek, SM
dc.contributor.authorDunning, AM
dc.contributor.authorEngel, C
dc.contributor.authorEvans, DG
dc.contributor.authorGago-Dominguez, M
dc.contributor.authorGarcía-Closas, M
dc.contributor.authorGerdes, A-M
dc.contributor.authorGlendon, G
dc.contributor.authorGuénel, P
dc.contributor.authorHahnen, E
dc.contributor.authorHamann, U
dc.contributor.authorHanson, H
dc.contributor.authorHooning, MJ
dc.contributor.authorHoppe, R
dc.contributor.authorIzatt, L
dc.contributor.authorJakubowska, A
dc.contributor.authorJames, PA
dc.contributor.authorKristensen, VN
dc.contributor.authorLalloo, F
dc.contributor.authorLindeman, GJ
dc.contributor.authorMannermaa, A
dc.contributor.authorMargolin, S
dc.contributor.authorNeuhausen, SL
dc.contributor.authorNewman, WG
dc.contributor.authorPeterlongo, P
dc.contributor.authorPhillips, K-A
dc.contributor.authorPujana, MA
dc.contributor.authorRantala, J
dc.contributor.authorRønlund, K
dc.contributor.authorSaloustros, E
dc.contributor.authorSchmutzler, RK
dc.contributor.authorSchneeweiss, A
dc.contributor.authorSinger, CF
dc.contributor.authorSuvanto, M
dc.contributor.authorTan, YY
dc.contributor.authorTeixeira, MR
dc.contributor.authorThomassen, M
dc.contributor.authorTischkowitz, M
dc.contributor.authorTripathi, V
dc.contributor.authorWappenschmidt, B
dc.contributor.authorZhao, E
dc.contributor.authorEaston, DF
dc.contributor.authorAntoniou, AC
dc.contributor.authorChenevix-Trench, G
dc.contributor.authorPharoah, PDP
dc.contributor.authorSchmidt, MK
dc.contributor.authorBlomqvist, C
dc.contributor.authorNevanlinna, H
dc.coverage.spatialUnited States
dc.date.accessioned2023-08-15T14:22:09Z
dc.date.available2023-08-15T14:22:09Z
dc.date.issued2023-05-12
dc.identifierARTN 37
dc.identifier10.1038/s41523-023-00546-x
dc.identifier.citationnpj Breast Cancer, 2023, 9 (1), pp. 37 -
dc.identifier.issn2374-4677
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5941
dc.identifier.eissn2374-4677
dc.identifier.eissn2374-4677
dc.identifier.doi10.1038/s41523-023-00546-x
dc.description.abstractWe assessed the PREDICT v 2.2 for prognosis of breast cancer patients with pathogenic germline BRCA1 and BRCA2 variants, using follow-up data from 5453 BRCA1/2 carriers from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA) and the Breast Cancer Association Consortium (BCAC). PREDICT for estrogen receptor (ER)-negative breast cancer had modest discrimination for BRCA1 carrier patients overall (Gönen & Heller unbiased concordance 0.65 in CIMBA, 0.64 in BCAC), but it distinguished clearly the high-mortality group from lower risk categories. In an analysis of low to high risk categories by PREDICT score percentiles, the observed mortality was consistently lower than the expected mortality, but the confidence intervals always included the calibration slope. Altogether, our results encourage the use of the PREDICT ER-negative model in management of breast cancer patients with germline BRCA1 variants. For the PREDICT ER-positive model, the discrimination was slightly lower in BRCA2 variant carriers (concordance 0.60 in CIMBA, 0.65 in BCAC). Especially, inclusion of the tumor grade distorted the prognostic estimates. The breast cancer mortality of BRCA2 carriers was underestimated at the low end of the PREDICT score distribution, whereas at the high end, the mortality was overestimated. These data suggest that BRCA2 status should also be taken into consideration with tumor characteristics, when estimating the prognosis of ER-positive breast cancer patients.
dc.formatElectronic
dc.format.extent37 -
dc.languageeng
dc.language.isoeng
dc.publisherNATURE PORTFOLIO
dc.relation.ispartofnpj Breast Cancer
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectHEBON investigators
dc.titlePREDICT validity for prognosis of breast cancer patients with pathogenic BRCA1/2 variants.
dc.typeJournal Article
dcterms.dateAccepted2023-04-28
dc.date.updated2023-08-15T14:21:20Z
rioxxterms.versionVoR
rioxxterms.versionofrecord10.1038/s41523-023-00546-x
rioxxterms.licenseref.startdate2023-05-12
rioxxterms.typeJournal Article/Review
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/37173335
pubs.issue1
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/Integrative Cancer Epidemiology
pubs.publication-statusPublished online
pubs.publisher-urlhttp://dx.doi.org/10.1038/s41523-023-00546-x
pubs.volume9
icr.provenanceDeposited by Mr Arek Surman on 2023-08-15. Deposit type is initial. No. of files: 1. Files: PREDICT validity for prognosis of breast cancer patients with pathogenic BRCA12 variants.pdf


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