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Prediction of chemotherapy benefit by EndoPredict in patients with breast cancer who received adjuvant endocrine therapy plus chemotherapy or endocrine therapy alone

PURPOSE: 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...

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Autores principales: Sestak, Ivana, Martín, Miguel, Dubsky, Peter, Kronenwett, Ralf, Rojo, Federico, Cuzick, Jack, Filipits, Martin, Ruiz, Amparo, Gradishar, William, Soliman, Hatem, Schwartzberg, Lee, Buus, Richard, Hlauschek, Dominik, Rodríguez-Lescure, Alvaro, Gnant, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6555778/
https://www.ncbi.nlm.nih.gov/pubmed/31041683
http://dx.doi.org/10.1007/s10549-019-05226-8
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author Sestak, Ivana
Martín, Miguel
Dubsky, Peter
Kronenwett, Ralf
Rojo, Federico
Cuzick, Jack
Filipits, Martin
Ruiz, Amparo
Gradishar, William
Soliman, Hatem
Schwartzberg, Lee
Buus, Richard
Hlauschek, Dominik
Rodríguez-Lescure, Alvaro
Gnant, Michael
author_facet Sestak, Ivana
Martín, Miguel
Dubsky, Peter
Kronenwett, Ralf
Rojo, Federico
Cuzick, Jack
Filipits, Martin
Ruiz, Amparo
Gradishar, William
Soliman, Hatem
Schwartzberg, Lee
Buus, Richard
Hlauschek, Dominik
Rodríguez-Lescure, Alvaro
Gnant, Michael
author_sort Sestak, Ivana
collection PubMed
description PURPOSE: 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. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10549-019-05226-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-65557782019-06-21 Prediction of chemotherapy benefit by EndoPredict in patients with breast cancer who received adjuvant endocrine therapy plus chemotherapy or endocrine therapy alone Sestak, Ivana Martín, Miguel Dubsky, Peter Kronenwett, Ralf Rojo, Federico Cuzick, Jack Filipits, Martin Ruiz, Amparo Gradishar, William Soliman, Hatem Schwartzberg, Lee Buus, Richard Hlauschek, Dominik Rodríguez-Lescure, Alvaro Gnant, Michael Breast Cancer Res Treat Clinical Trial PURPOSE: 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. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10549-019-05226-8) contains supplementary material, which is available to authorized users. Springer US 2019-04-30 2019 /pmc/articles/PMC6555778/ /pubmed/31041683 http://dx.doi.org/10.1007/s10549-019-05226-8 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Clinical Trial
Sestak, Ivana
Martín, Miguel
Dubsky, Peter
Kronenwett, Ralf
Rojo, Federico
Cuzick, Jack
Filipits, Martin
Ruiz, Amparo
Gradishar, William
Soliman, Hatem
Schwartzberg, Lee
Buus, Richard
Hlauschek, Dominik
Rodríguez-Lescure, Alvaro
Gnant, Michael
Prediction of chemotherapy benefit by EndoPredict in patients with breast cancer who received adjuvant endocrine therapy plus chemotherapy or endocrine therapy alone
title Prediction of chemotherapy benefit by EndoPredict in patients with breast cancer who received adjuvant endocrine therapy plus chemotherapy or endocrine therapy alone
title_full Prediction of chemotherapy benefit by EndoPredict in patients with breast cancer who received adjuvant endocrine therapy plus chemotherapy or endocrine therapy alone
title_fullStr Prediction of chemotherapy benefit by EndoPredict in patients with breast cancer who received adjuvant endocrine therapy plus chemotherapy or endocrine therapy alone
title_full_unstemmed Prediction of chemotherapy benefit by EndoPredict in patients with breast cancer who received adjuvant endocrine therapy plus chemotherapy or endocrine therapy alone
title_short Prediction of chemotherapy benefit by EndoPredict in patients with breast cancer who received adjuvant endocrine therapy plus chemotherapy or endocrine therapy alone
title_sort prediction of chemotherapy benefit by endopredict in patients with breast cancer who received adjuvant endocrine therapy plus chemotherapy or endocrine therapy alone
topic Clinical Trial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6555778/
https://www.ncbi.nlm.nih.gov/pubmed/31041683
http://dx.doi.org/10.1007/s10549-019-05226-8
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