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Verfasst von:Bergmeister-Berghoff, Anna Sophie [VerfasserIn]   i
 Deimling, Andreas von [VerfasserIn]   i
Titel:Predictive molecular markers in metastases to the central nervous system
Titelzusatz:recent advances and future avenues
Verf.angabe:Anna Sophie Berghoff, Rupert Bartsch, Adelheid Wöhrer, Berthold Streubel, Peter Birner, Johan M. Kros, Priscilla K. Brastianos, Andreas von Deimling, Matthias Preusser
E-Jahr:2014
Jahr:07 October 2014
Umfang:13 S.
Fussnoten:Gesehen am 14.10.2020
Titel Quelle:Enthalten in: Acta neuropathologica
Ort Quelle:Berlin : Springer, 1961
Jahr Quelle:2014
Band/Heft Quelle:128(2014), 6, Seite 879-891
ISSN Quelle:1432-0533
Abstract:Metastases to the central nervous system (CNS) are common in several cancer types. For most primary tumors that commonly metastasize to the CNS, molecular biomarker analyses are recommended in the clinical setting for selection of appropriate targeted therapies. Therapeutic efficacy of some of these agents has been documented in patients with brain metastases, and molecular testing of CNS metastases should be considered in the clinical setting. Here, we summarize the clinically relevant biomarker tests that should be considered in neurosurgical specimens based on the current recommendations of the European Society of Medical Oncology (ESMO) or the National Comprehensive Cancer Network (NCCN) for the most relevant primary tumor types: lung cancer (EGFR mutations, ALK rearrangement, BRAF mutations), breast cancer (HER2 amplification, steroid receptor overexpression), melanoma (BRAF mutations), and colorectal cancer (RAS mutations). Furthermore, we discuss emerging therapeutic targets including novel oncogenic alterations (ROS1 rearrangements, FGFR1 amplifications, CMET amplifications, and others) and molecular features of the tumor microenvironment (including immune-checkpoint molecules such as CTLA4 and PD-1/PD-L1). We also discuss the potential role of advanced biomarker tests such as next-generation sequencing and “liquid biopsies” for patients with CNS metastases.
DOI:doi:10.1007/s00401-014-1350-7
URL:Bibliographic entry. University members only receive access to full-texts for open access or licensed publications.

Volltext: https://doi.org/10.1007/s00401-014-1350-7
 DOI: https://doi.org/10.1007/s00401-014-1350-7
Datenträger:Online-Ressource
Sprache:eng
K10plus-PPN:173552963X
Verknüpfungen:→ Journal

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