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dc.contributor.authorPenault-Llorca, F
dc.contributor.authorDalenc, F
dc.contributor.authorChabaud, S
dc.contributor.authorCottu, P
dc.contributor.authorAllouache, D
dc.contributor.authorCameron, D
dc.contributor.authorGrenier, J
dc.contributor.authorVenat Bouvet, L
dc.contributor.authorJegannathen, A
dc.contributor.authorCampone, M
dc.contributor.authorDebled, M
dc.contributor.authorHardy-Bessard, A-C
dc.contributor.authorGiacchetti, S
dc.contributor.authorBarthelemy, P
dc.contributor.authorKaluzinski, L
dc.contributor.authorMailliez, A
dc.contributor.authorMouret-Reynier, M-A
dc.contributor.authorLegouffe, E
dc.contributor.authorCayre, A
dc.contributor.authorMartinez, M
dc.contributor.authorDelbaldo, C
dc.contributor.authorMollon-Grange, D
dc.contributor.authorMacaskill, EJ
dc.contributor.authorSephton, M
dc.contributor.authorStefani, L
dc.contributor.authorBelgadi, B
dc.contributor.authorWinter, M
dc.contributor.authorOrfeuvre, H
dc.contributor.authorLacroix-Triki, M
dc.contributor.authorBonnefoi, H
dc.contributor.authorBliss, J
dc.contributor.authorCanon, J-L
dc.contributor.authorLemonnier, J
dc.contributor.authorAndre, F
dc.contributor.authorBachelot, T
dc.coverage.spatialEngland
dc.date.accessioned2024-08-02T13:50:13Z
dc.date.available2024-08-02T13:50:13Z
dc.date.issued2024-05-01
dc.identifierARTN 103443
dc.identifierS2059-7029(24)01211-0
dc.identifier.citationESMO Open, 2024, 9 (5), pp. 103443 -en_US
dc.identifier.issn2059-7029
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/6338
dc.identifier.eissn2059-7029
dc.identifier.eissn2059-7029
dc.identifier.doi10.1016/j.esmoop.2024.103443
dc.identifier.doi10.1016/j.esmoop.2024.103443
dc.description.abstractBACKGROUND: The purpose of this study was to evaluate the prognostic value of the multigene EndoPredict test in prospectively collected data of patients screened for the randomized, double-blind, phase III UNIRAD trial, which evaluated the addition of everolimus to adjuvant endocrine therapy in high-risk, hormone receptor-positive, human epidermal growth factor receptor 2 (HER2)-negative early breast cancer. PATIENTS AND METHODS: Patients were classified into low or high risk according to the EPclin score, consisting of a 12-gene molecular score combined with tumor size and nodal status. Association of the EPclin score with disease-free survival (DFS) and distant metastasis-free survival (DMFS) was evaluated using Kaplan-Meier estimates. The independent prognostic added value of EPclin score was tested in a multivariate Cox model after adjusting on tumor characteristics. RESULTS: EndoPredict test results were available for 768 patients: 663 patients classified as EPclin high risk (EPCH) and 105 patients as EPclin low risk (EPCL). Median follow-up was 70 months (range 1-172 months). For the 429 EPCH randomized patients, there was no significant difference in DFS between treatment arms. The 60-month relapse rate for patients in the EPCL and EPCH groups was 0% and 7%, respectively. Hazard ratio (HR) supposing continuous EPclin score was 1.87 [95% confidence interval (CI) 1.4-2.5, P < 0.0001]. This prognostic effect remained significant when assessed in a Cox model adjusting on tumor size, number of positive nodes and tumor grade (HR 1.52, 95% CI 1.09-2.13, P = 0.0141). The 60-month DMFS for patients in the EPCL and EPCH groups was 100% and 94%, respectively (adjusted HR 8.10, 95% CI 1.1-59.1, P < 0.0001). CONCLUSIONS: The results confirm the value of EPclin score as an independent prognostic parameter in node-positive, hormone receptor-positive, HER2-negative early breast cancer patients receiving standard adjuvant treatment. EPclin score can be used to identify patients at higher risk of recurrence who may warrant additional systemic treatments.
dc.formatPrint-Electronic
dc.format.extent103443 -
dc.languageeng
dc.language.isoengen_US
dc.publisherELSEVIERen_US
dc.relation.ispartofESMO Open
dc.subjectEndoPredict
dc.subjectbreast cancer
dc.subjectendocrine therapy
dc.subjectprognostic biomarker
dc.subjectrisk stratification
dc.subjectHumans
dc.subjectFemale
dc.subjectBreast Neoplasms
dc.subjectMiddle Aged
dc.subjectPrognosis
dc.subjectReceptor, ErbB-2
dc.subjectDouble-Blind Method
dc.subjectAged
dc.subjectAdult
dc.subjectReceptors, Estrogen
dc.subjectReceptors, Progesterone
dc.subjectEverolimus
dc.subjectDisease-Free Survival
dc.subjectBiomarkers, Tumor
dc.titlePrognostic value of EndoPredict test in patients with hormone receptor-positive, human epidermal growth factor receptor 2-negative primary breast cancer screened for the randomized, double-blind, phase III UNIRAD trial.en_US
dc.typeJournal Article
dcterms.dateAccepted2024-04-04
dc.date.updated2024-08-02T13:47:12Z
rioxxterms.versionVoRen_US
rioxxterms.versionofrecord10.1016/j.esmoop.2024.103443en_US
rioxxterms.licenseref.urihttp://creativecommons.org/licenses/by/4.0/en_US
rioxxterms.licenseref.startdate2024-05-01
rioxxterms.typeJournal Article/Reviewen_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/38692082
pubs.issue5
pubs.organisational-groupICR
pubs.organisational-groupICR/Primary Group
pubs.organisational-groupICR/Primary Group/ICR Divisions
pubs.organisational-groupICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-groupICR/Primary Group/ICR Divisions/Clinical Studies/Clinical Trials & Statistics Unit
pubs.publication-statusPublished
pubs.publisher-urlhttp://dx.doi.org/10.1016/j.esmoop.2024.103443
pubs.volume9
icr.researchteamClin Trials & Stats Uniten_US
dc.contributor.icrauthorBliss, Judith
icr.provenanceDeposited by Mr Arek Surman on 2024-08-02. Deposit type is initial. No. of files: 1. Files: Prognostic value of EndoPredict test in patients with hormone receptor-positive, human epidermal growth factor receptor 2-ne.pdf


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