• Medientyp: E-Artikel
  • Titel: Genomic Signatures in Luminal Breast Cancer
  • Beteiligte: Puppe, Julian; Seifert, Tabea; Eichler, Christian; Pilch, Henryk; Mallmann, Peter; Malter, Wolfram
  • Erschienen: S. Karger AG, 2020
  • Erschienen in: Breast Care
  • Sprache: Englisch
  • DOI: 10.1159/000509846
  • ISSN: 1661-3791; 1661-3805
  • Schlagwörter: Oncology ; Surgery
  • Entstehung:
  • Anmerkungen:
  • Beschreibung: <jats:p>&lt;b&gt;&lt;i&gt;Background:&lt;/i&gt;&lt;/b&gt; Breast cancer is a very heterogeneous disease and luminal breast carcinomas represent the hormone receptor-positive tumors among all breast cancer subtypes. In this context, multigene signatures were developed to gain further prognostic and predictive information beyond clinical parameters and traditional immunohistochemical markers. &lt;b&gt;&lt;i&gt;Summary:&lt;/i&gt;&lt;/b&gt; For early breast cancer patients these molecular tools can guide clinicians to decide on the extension of endocrine therapy to avoid over- and undertreatment by adjuvant chemotherapy. Beside the predictive and prognostic value, a few genomic tests are also able to provide intrinsic subtype classification. In this review, we compare the most frequently used and commercially available molecular tests (OncotypeDX®, MammaPrint®, Prosigna®, EndoPredict®, and Breast Cancer Index&lt;sup&gt;SM&lt;/sup&gt;). Moreover, we discuss the clinical utility of molecular profiling for advanced breast cancer of the luminal subtype. &lt;b&gt;&lt;i&gt;Key Messages:&lt;/i&gt;&lt;/b&gt; Multigene assays can help to de-escalate systemic therapy in early-stage breast cancer. Only the Oncotype DX® and MammaPrint®&lt;sup&gt;&lt;/sup&gt;test are validated by entirely prospective and randomized phase 3 trials. More clinical evidence is needed to support the use of genomic tests in node-positive disease. Recent developments in high-throughput sequencing technology will provide further insights to understand the heterogeneity of luminal breast cancers in early-stage and metastatic disease. </jats:p>
  • Zugangsstatus: Freier Zugang