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Conference paper · Journal article

PATH-01. Identification of Prognastic Variables Based on Molecular Profiling of Long-Term and Short-Term Surviving Gglioblastoma Patients

From

Rigshospitalet1

Department of Biotechnology and Biomedicine, Technical University of Denmark2

Genomic Epidemiology, Department of Bio and Health Informatics, Technical University of Denmark3

Department of Bio and Health Informatics, Technical University of Denmark4

Danish Cancer Society5

Glioblastoma is a devastating disease and despite extensive treatment, overall survival (OS) for these patients remains poor. Yet, a small proportion of glioblastoma patients present relatively long survival over 3 years, but the underlying molecular background separating these long-term survivors (LTS) from short-term survivors (STS) are still insufficiently understood.

The purpose of this study was to identify independent prognostic variables for survival by examining molecular profiles of LTS and STS in a clinically well characterized cohort of glioblastoma patients. The cohort consisted of 93 patients diagnosed with primary glioblastoma and treated with radiation therapy plus concomitant and adjuvant chemotherapy as well as bevacizumab administered in the first-line setting or at time of recurrence.

Among these, 14 STS (OS36 months) were identified, which were all confirmed being IDHwt. For all patients, RNA had previously been purified from microdissected tumor tissue of the diagnostic specimen and analyzed for expression levels by a customized NanoString platform. This covered 800 genes related to glioblastoma cancer hallmarks, including regulation of angiogenesis and immune response.

When comparing expression of these genes in LTS vs. STS using a Welsh’s t-test, 14 candidate genes ended up significant (P

Language: English
Publisher: Oxford University Press
Year: 2017
Pages: vi170-vi170
Proceedings: 22nd Annual Scientific Meeting and Education Day of the Society for Neuro-Oncology
ISSN: 15235866 and 15228517
Types: Conference paper and Journal article
DOI: 10.1093/neuonc/nox168.692
ORCIDs: Olsen, Lars Rønn

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