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dc.contributor.authorSESTAK, IVANA
dc.contributor.authorCUZICK, J
dc.contributor.authorMartín, M
dc.contributor.authorDubsky, P
dc.contributor.authorKronenwett, R
dc.contributor.authorRojo, F
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.accessioned2019-05-20T12:53:48Z
dc.date.available2019-04-06
dc.date.available2019-05-20T12:53:48Z
dc.date.issued2019-04-30
dc.identifier.citationSestak, I., Martín, M., Dubsky, P. et al. Breast Cancer Res Treat (2019). https://doi.org/10.1007/s10549-019-05226-8en_US
dc.identifier.issn0167-6806
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/57640
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.en_US
dc.description.sponsorshipCancer Research UK (C569/A16891)en_US
dc.description.sponsorshipMyriad Geneticsen_US
dc.language.isoenen_US
dc.publisherSpringer USen_US
dc.relation.ispartofBreast Cancer Research and Treatment
dc.rights“This is a post-peer-review, pre-copyedit version of a protocol published in Breast Cancer Research and Treatment. The final publication is available at link.springer.com: https://doi.org/10.1007/s10549-019-05226-8"
dc.subjectBreast canceren_US
dc.subjectChemotherapyen_US
dc.subjectEndoPredicten_US
dc.subjectPredictionen_US
dc.titlePrediction of chemotherapy benefit by EndoPredict in patients with breast cancer who received adjuvant endocrine therapy plus chemotherapy or endocrine therapy aloneen_US
dc.typeArticleen_US
dc.rights.holder© The Author(s) 2019
dc.identifier.doihttps://doi.org/10.1007/s10549-019-05226-8
pubs.notesNot knownen_US
pubs.publication-statusAccepteden_US
dcterms.dateAccepted2019-04-06
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US


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