2013
DOI: 10.1055/s-0033-1350831
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Multigene Assays for Classification, Prognosis, and Prediction in Breast Cancer: a Critical Review on the Background and Clinical Utility

Abstract: Gene signatures which are based on multigene profiling assays have been developed for the purpose to better define the prognosis and prediction of therapy results in early-stage breast cancer. These assays were designed to be more specific than conventional clinico-pathologic parameters in the selection of patients for (neo-)adjuvant treatment and in effect help to avoid unnecessary cytotoxic… Show more

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Cited by 63 publications
(58 citation statements)
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“…Clinicopathological parameters alone do not inform about chemotherapy benefit because they do not adequately represent tumor's biological makeup. The need for support in treatment choice has been mirrored in the explosion of prognostic tests on the market . Two of the most widely used in Germany are uPA/PAI‐1 and EPclin, which we compared in this study.…”
Section: Discussionmentioning
confidence: 99%
“…Clinicopathological parameters alone do not inform about chemotherapy benefit because they do not adequately represent tumor's biological makeup. The need for support in treatment choice has been mirrored in the explosion of prognostic tests on the market . Two of the most widely used in Germany are uPA/PAI‐1 and EPclin, which we compared in this study.…”
Section: Discussionmentioning
confidence: 99%
“…Biomarkers are defined as measurable cellular, biochemical or molecular alternations in biological media such as blood or tissue. Several FDA-approved multi-gene panel tests are now approved for risk prediction and diagnosis of various cancers; however, no similar biomarker tests exist for patient risk stratification of NMSC [92]. At present, there are no skin cancer screening guidelines in the United States.…”
Section: Biomarkers As a Novel Tool In Monitoring Ultraviolet Skin Damentioning
confidence: 99%
“…It was developed to improve discrimination between Luminal A and B subtypes. [40] The accuracy of subtype classification with MammaTyper has not yet been compared with PAM50 or IHC, and it is not currently approved for use by the FDA.…”
Section: Genomic Assaysmentioning
confidence: 99%