New hints towards a precision medicine strategy for IDH wild-type glioblastoma

被引:34
作者
White, K. [1 ]
Connor, K. [1 ]
Clerkin, J. [1 ,2 ]
Murphy, B. M. [3 ]
Salvucci, M. [3 ]
O'Farrell, A. C. [1 ]
Rehm, M. [4 ,5 ]
O'Brien, D. [2 ]
Prehn, J. H. M. [3 ]
Niclou, S. P. [6 ]
Lamfers, M. L. M. [7 ]
Verreault, M. [8 ]
Idbaih, A. [8 ]
Verhaak, R. [9 ]
Golebiewska, A. [6 ]
Byrne, A. T. [1 ]
机构
[1] Royal Coll Surgeons Ireland, Dept Physiol & Med Phys, Precis Canc Med Grp, Dublin, Ireland
[2] Beaumont Hosp, Natl Neurosurg Dept, Dublin, Ireland
[3] Royal Coll Surgeons Ireland, Dept Physiol & Med Phys, Ctr Syst Med, Dublin, Ireland
[4] Univ Stuttgart, Inst Cell Biol & Immunol, Stuttgart, Germany
[5] Univ Stuttgart, Stuttgart Res Ctr Syst Biol, Stuttgart, Germany
[6] Luxembourg Inst Hlth, Dept Oncol, NORLUX Neurooncol Lab, Luxembourg, Luxembourg
[7] Erasmus MC, Brain Tumor Ctr, Dept Neurosurg, Univ Med Ctr Rotterdam, Rotterdam, Netherlands
[8] Sorbonne Univ, Inst Cerveau & Moelle Epiniere, Hop Univ La Pitie Salpetriere Charles Foix, Serv Neurol, Paris, France
[9] Jackson Lab Genom Med, Farmington, CT USA
基金
欧盟地平线“2020”;
关键词
IDH-wt glioblastoma; tumour microenvironment; multi-omics; precision therapy; NEWLY-DIAGNOSED GLIOBLASTOMA; CENTRAL-NERVOUS-SYSTEM; PHASE-II; T-CELLS; RECURRENT GLIOBLASTOMA; PD-L1; EXPRESSION; TUMOR EVOLUTION; IMMUNE-SYSTEM; GLIOMA; TEMOZOLOMIDE;
D O I
10.1016/j.annonc.2020.08.2336
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Glioblastoma represents the most common primary malignancy of the central nervous system in adults and remains a largely incurable disease. The elucidation of disease subtypes based on mutational profiling, gene expression and DNA methylation has so far failed to translate into improved clinical outcomes. However, new knowledge emerging from the subtyping effort in the IDH-wild-type setting may provide directions for future precision therapies. Here, we review recent learnings in the field, and further consider how tumour microenvironment differences across subtypes may reveal novel contexts of vulnerability. We discuss recent treatment approaches and ongoing trials in the IDH-wildtype glioblastoma setting, and propose an integrated discovery stratagem incorporating multi-omics, single-cell technologies and computational approaches.
引用
收藏
页码:1679 / 1692
页数:14
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