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Using the molecular classification of glioblastoma to inform personalized treatment

期刊

JOURNAL OF PATHOLOGY
卷 232, 期 2, 页码 165-177

出版社

WILEY
DOI: 10.1002/path.4282

关键词

glioblastoma; pathogenesis; IDH; EGFR; MGMT; FGFR; TACC; 1p; 19q; proneural; mesenchymal

资金

  1. National Institutes of Health/National Cancer Institute (NIH/NCI) [P50CA127001, 5T32CA163185]
  2. NATIONAL CANCER INSTITUTE [T32CA163185, P50CA127001] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Glioblastoma is the most common and most aggressive diffuse glioma, associated with short survival and uniformly fatal outcome, irrespective of treatment. It is characterized by morphological, genetic and gene-expression heterogeneity. The current standard of treatment is maximal surgical resection, followed by radiation, with concurrent and adjuvant chemotherapy. Due to the heterogeneity, most tumours develop resistance to treatment and shortly recur. Following recurrence, glioblastoma is quickly fatal in the majority of cases. Recent genetic molecular advances have contributed to a better understanding of glioblastoma pathophysiology and disease stratification. In this paper we review basic glioblastoma pathophysiology, with emphasis on clinically relevant genetic molecular alterations and potential targets for further drug development. Copyright (c) 2013 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.

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