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dc.contributor.authorSestak, I
dc.contributor.authorMartín, M
dc.contributor.authorDubsky, P
dc.contributor.authorKronenwett, R
dc.contributor.authorRojo, F
dc.contributor.authorCuzick, J
dc.contributor.authorFilipits, M
dc.contributor.authorRuiz, A
dc.contributor.authorGradishar, W
dc.contributor.authorSoliman, H
dc.contributor.authorSchwartzberg, L
dc.contributor.authorBuus, R
dc.contributor.authorHlauschek, D
dc.contributor.authorRodríguez-Lescure, A
dc.contributor.authorGnant, M
dc.date.accessioned2019-05-29T08:45:38Z
dc.date.issued2019-07-01
dc.identifier.citationBreast cancer research and treatment, 2019, 176 (2), pp. 377 - 386
dc.identifier.issn0167-6806
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/3243
dc.identifier.eissn1573-7217
dc.identifier.doi10.1007/s10549-019-05226-8
dc.description.abstractPURPOSE: EndoPredict (EPclin) is a prognostic test validated to inform decisions on adjuvant chemotherapy to endocrine therapy alone for patients with oestrogen receptor-positive, HER2-negative breast cancer. Here, we determine the performance of EPclin for estimating 10-year distant recurrence-free interval (DRFI) rates for those who received adjuvant endocrine therapy (ET) alone compared to those with chemotherapy plus endocrine therapy (ET + C). METHODS: A total of 3746 women were included in this joint analysis. 2630 patients received 5 years of ET alone (ABCSG-6/8, TransATAC) and 1116 patients received ET + C (GEICAM 2003-02/9906). The primary objective was to evaluate the ability of EPclin to provide an estimate of the 10-year DR rate as a continuous function of EPclin separately for ET alone and ET + C. Cox proportional hazard models were used for these analyses. RESULTS: EPclin was highly prognostic for DR in women who received ET alone (HR 2.79 (2.49-3.13), P < 0.0001) as well as in those who received ET + C (HR 2.27 (1.99-2.59), P < 0.0001). Women who received ET + C had significantly smaller increases in 10-year DR rates with the increasing EPclin score than those receiving ET alone (EPclin = 5; 12% ET + C vs. 20% ET alone). We observed a significant positive interaction between EPclin and treatment groups (P-interaction = 0.022). CONCLUSIONS: In this comparative non-randomised analysis, the rate of increase in DR with EPclin score was significantly reduced in women who received ET + C versus ET alone. Our indirect comparisons suggest that a high EPclin score can predict chemotherapy benefit in women with ER-positive, HER2-negative disease.
dc.formatPrint-Electronic
dc.format.extent377 - 386
dc.languageeng
dc.language.isoeng
dc.publisherSPRINGER
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectHumans
dc.subjectBreast Neoplasms
dc.subjectCyclophosphamide
dc.subjectFluorouracil
dc.subjectDoxorubicin
dc.subjectReceptor, erbB-2
dc.subjectReceptors, Estrogen
dc.subjectAntineoplastic Agents, Hormonal
dc.subjectAntineoplastic Combined Chemotherapy Protocols
dc.subjectPrognosis
dc.subjectTreatment Outcome
dc.subjectCombined Modality Therapy
dc.subjectChemotherapy, Adjuvant
dc.subjectProportional Hazards Models
dc.subjectRisk Assessment
dc.subjectRetrospective Studies
dc.subjectPredictive Value of Tests
dc.subjectAged
dc.subjectMiddle Aged
dc.subjectFemale
dc.subjectClinical Trials as Topic
dc.subjectKaplan-Meier Estimate
dc.titlePrediction of chemotherapy benefit by EndoPredict in patients with breast cancer who received adjuvant endocrine therapy plus chemotherapy or endocrine therapy alone.
dc.typeJournal Article
dcterms.dateAccepted2019-04-08
rioxxterms.versionofrecord10.1007/s10549-019-05226-8
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2019-07
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfBreast cancer research and treatment
pubs.issue2
pubs.notesNo embargo
pubs.organisational-group/ICR
pubs.organisational-group/ICR
pubs.publication-statusPublished
pubs.volume176
pubs.embargo.termsNo embargo
dc.contributor.icrauthorBuus, Richard


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