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dc.date.accessioned2023-03-29T15:08:52Z
dc.date.available2023-03-29T15:08:52Z
dc.date.created2023-03-24T15:55:43Z
dc.date.issued2022
dc.identifier.citationGrootes, Isabelle Keeman, Renske Blows, Fiona M. Milne, Roger L. Giles, Graham G. Swerdlow, Anthony J. Kristensen, Vessela N. Fasching, Peter A. Abubakar, Mustapha Andrulis, Irene L. Anton-Culver, Hoda Beckmann, Matthias W. Blomqvist, Carl Oliver Bojesen, Stig E. Bolla, Manjeet K. Bonanni, Bernardo Briceno, Ignacio Burwinkel, Barbara Camp, Nicola J. Castelao, Jose E. Choi, Ji-Yeob Clarke, Christine L. Couch, Fergus J. Cox, Angela Cross, Simon S. Czene, Kamila Devilee, Peter Dörk, Thilo Dunning, Alison M. Dwek, Miriam Easton, Douglas F. Eccles, Diana M. Eriksson, Mikael Ernst, Kristina Evans, D. Gareth Figueroa, Jonine D. Fink, Visnja Floris, Giuseppe Fox, Stephen Gabrielson, Marike Gago-Dominguez, Manuela García-Sáenz, José A González-Neira, Anna Haeberle, Lothar Haiman, Christopher A. Hall, Peter Hamann, Ute Harkness, Elaine F. Hartman, Mikael Hein, Alexander Hooning, Maartje J. Hou, Ming-Feng García-Closas, Montserrat Pharoah, Paul D.P. . Incorporating progesterone receptor expression into the PREDICT breast prognostic model. European Journal of Cancer. 2022, 173, 178-193
dc.identifier.urihttp://hdl.handle.net/10852/101859
dc.description.abstractBackground Predict Breast (www.predict.nhs.uk) is an online prognostication and treatment benefit tool for early invasive breast cancer. The aim of this study was to incorporate the prognostic effect of progesterone receptor (PR) status into a new version of PREDICT and to compare its performance to the current version (2.2). Method The prognostic effect of PR status was based on the analysis of data from 45,088 European patients with breast cancer from 49 studies in the Breast Cancer Association Consortium. Cox proportional hazard models were used to estimate the hazard ratio for PR status. Data from a New Zealand study of 11,365 patients with early invasive breast cancer were used for external validation. Model calibration and discrimination were used to test the model performance. Results Having a PR-positive tumour was associated with a 23% and 28% lower risk of dying from breast cancer for women with oestrogen receptor (ER)-negative and ER-positive breast cancer, respectively. The area under the ROC curve increased with the addition of PR status from 0.807 to 0.809 for patients with ER-negative tumours (p = 0.023) and from 0.898 to 0.902 for patients with ER-positive tumours (p = 2.3 × 10−6) in the New Zealand cohort. Model calibration was modest with 940 observed deaths compared to 1151 predicted. Conclusion The inclusion of the prognostic effect of PR status to PREDICT Breast has led to an improvement of model performance and more accurate absolute treatment benefit predictions for individual patients. Further studies should determine whether the baseline hazard function requires recalibration.
dc.languageEN
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleIncorporating progesterone receptor expression into the PREDICT breast prognostic model
dc.title.alternativeENEngelskEnglishIncorporating progesterone receptor expression into the PREDICT breast prognostic model
dc.typeJournal article
dc.creator.authorGrootes, Isabelle
dc.creator.authorKeeman, Renske
dc.creator.authorBlows, Fiona M.
dc.creator.authorMilne, Roger L.
dc.creator.authorGiles, Graham G.
dc.creator.authorSwerdlow, Anthony J.
dc.creator.authorKristensen, Vessela N.
dc.creator.authorFasching, Peter A.
dc.creator.authorAbubakar, Mustapha
dc.creator.authorAndrulis, Irene L.
dc.creator.authorAnton-Culver, Hoda
dc.creator.authorBeckmann, Matthias W.
dc.creator.authorBlomqvist, Carl Oliver
dc.creator.authorBojesen, Stig E.
dc.creator.authorBolla, Manjeet K.
dc.creator.authorBonanni, Bernardo
dc.creator.authorBriceno, Ignacio
dc.creator.authorBurwinkel, Barbara
dc.creator.authorCamp, Nicola J.
dc.creator.authorCastelao, Jose E.
dc.creator.authorChoi, Ji-Yeob
dc.creator.authorClarke, Christine L.
dc.creator.authorCouch, Fergus J.
dc.creator.authorCox, Angela
dc.creator.authorCross, Simon S.
dc.creator.authorCzene, Kamila
dc.creator.authorDevilee, Peter
dc.creator.authorDörk, Thilo
dc.creator.authorDunning, Alison M.
dc.creator.authorDwek, Miriam
dc.creator.authorEaston, Douglas F.
dc.creator.authorEccles, Diana M.
dc.creator.authorEriksson, Mikael
dc.creator.authorErnst, Kristina
dc.creator.authorEvans, D. Gareth
dc.creator.authorFigueroa, Jonine D.
dc.creator.authorFink, Visnja
dc.creator.authorFloris, Giuseppe
dc.creator.authorFox, Stephen
dc.creator.authorGabrielson, Marike
dc.creator.authorGago-Dominguez, Manuela
dc.creator.authorGarcía-Sáenz, José A
dc.creator.authorGonzález-Neira, Anna
dc.creator.authorHaeberle, Lothar
dc.creator.authorHaiman, Christopher A.
dc.creator.authorHall, Peter
dc.creator.authorHamann, Ute
dc.creator.authorHarkness, Elaine F.
dc.creator.authorHartman, Mikael
dc.creator.authorHein, Alexander
dc.creator.authorHooning, Maartje J.
dc.creator.authorHou, Ming-Feng
dc.creator.authorGarcía-Closas, Montserrat
dc.creator.authorPharoah, Paul D.P.
cristin.unitcode185,53,18,10
cristin.unitnameAvdeling for medisinsk genetikk
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.cristin2136785
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=European Journal of Cancer&rft.volume=173&rft.spage=178&rft.date=2022
dc.identifier.jtitleEuropean Journal of Cancer
dc.identifier.volume173
dc.identifier.startpage178
dc.identifier.endpage193
dc.identifier.doihttps://doi.org/10.1016/j.ejca.2022.06.011
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn0959-8049
dc.type.versionPublishedVersion
dc.relation.projectNFR/193387/V50, 193387/ H10
dc.relation.projectHSØ/39346


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