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dc.contributor.authorSestak, Ien_US
dc.contributor.authorBuus, Ren_US
dc.contributor.authorCuzick, Jen_US
dc.contributor.authorDubsky, Pen_US
dc.contributor.authorKronenwett, Ren_US
dc.contributor.authorDenkert, Cen_US
dc.contributor.authorFerree, Sen_US
dc.contributor.authorSgroi, Den_US
dc.contributor.authorSchnabel, Cen_US
dc.contributor.authorBaehner, FLen_US
dc.contributor.authorMallon, Een_US
dc.contributor.authorDowsett, Men_US
dc.date.accessioned2018-04-26T11:08:34Z
dc.date.available2017-12-06en_US
dc.date.issued2018-04-01en_US
dc.date.submitted2018-02-19T11:17:47.546Z
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/36519
dc.description.abstractImportance: Multiple molecular signatures are available for managing estrogen receptor (ER)-positive breast cancer but with little direct comparative information to guide the patient's choice. Objective: To conduct a within-patient comparison of the prognostic value of 6 multigene signatures in women with early ER-positive breast cancer who received endocrine therapy for 5 years. Design, Setting, and Participants: This retrospective biomarker analysis included 774 postmenopausal women with ER-positive ERBB2 (formerly HER2)-negative breast cancer. This analysis was performed as a preplanned secondary study of data from the Anastrozole or Tamoxifen Alone or Combined randomized clinical trial comparing 5-year treatment with anastrozole vs tamoxifen with 10-year follow-up data. The signatures included the Oncotype Dx recurrence score, PAM50-based Prosigna risk of recurrence (ROR), Breast Cancer Index (BCI), EndoPredict (EPclin), Clinical Treatment Score, and 4-marker immunohistochemical score. Data were collected from January 2009, through April 2015. Main Outcomes and Measures: The primary objective was to compare the prognostic value of these signatures in addition to the Clinical Treatment Score (nodal status, tumor size, grade, age, and endocrine treatment) for distant recurrence for 0 to 10 years and 5 to 10 years after diagnosis. Likelihood ratio (LR) statistics were used with the χ2 test and C indexes to assess the prognostic value of each signature. Results: In this study of 774 postmenopausal women with ER-positive, ERBB2-negative disease (mean [SD] age, 64.1 [8.1] years), 591 (mean [SD] age, 63.4 [7.9] years) had node-negative disease. The signatures providing the most prognostic information were the ROR (hazard ratio [HR], 2.56; 95% CI, 1.96-3.35), followed by the BCI (HR, 2.46; 95% CI, 1.88-3.23) and EPclin (HR, 2.14; 95% CI, 1.71-2.68). Each provided significantly more information than the Clinical Treatment Score (HR, 1.99; 95% CI, 1.58-2.50), the recurrence score (HR, 1.69; 95% CI, 1.40-2.03), and the 4-marker immunohistochemical score (HR, 1.95; 95% CI, 1.55-2.45). Substantially less information was provided by all 6 molecular tests for the 183 patients with 1 to 3 positive nodes, but the BCI (ΔLR χ2 = 9.2) and EPclin (ΔLR χ2 = 7.4) provided more additional prognostic information than the other signatures. Conclusions and Relevance: For women with node-negative disease, the ROR, BCI, and EPclin were significantly more prognostic for overall and late distant recurrence. For women with 1 to 3 positive nodes, limited independent information was available from any test. These data might help oncologists and patients to choose the most appropriate test when considering chemotherapy use and/or extended endocrine therapy. Trial Registration: isrctn.com Identifier: ISRCTN18233230.en_US
dc.description.sponsorshipThis study was supported by grant CTR-Q4-Y1 from the Royal Marsden, National Institute of Health Biomedical Research Centre, Breast Cancer Now and grant C569/A16891 from Cancer Research UK.en_US
dc.format.extent545 - 553en_US
dc.languageengen_US
dc.language.isoenen_US
dc.relation.ispartofJAMA Oncolen_US
dc.rightsThis is an open access article distributed under the terms of the Creative Commons CC BY license, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
dc.titleComparison of the Performance of 6 Prognostic Signatures for Estrogen Receptor-Positive Breast Cancer: A Secondary Analysis of a Randomized Clinical Trial.en_US
dc.typeArticle
dc.rights.holder© 2018 Sestak I et al. JAMA Oncology.
dc.identifier.doi10.1001/jamaoncol.2017.5524en_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/29450494en_US
pubs.issue4en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume4en_US


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