Molecular landscape of IDH-wild-type, H3-wild-type glioblastomas of adolescents and young adults

被引:4
作者
Zhi-Feng Shi [1 ,2 ]
Li, Kay Ka-Wai [2 ,3 ]
Huang, Queenie Jun-Qi [3 ]
Wei-Wei Wang [4 ]
Kwan, Johnny Sheung-Him [3 ]
Chen, Hong [5 ]
Xiang-Zhi Liu [6 ]
Wen-Cai Li [4 ]
Tat-Ming Chan, Danny [7 ]
Zhen-Yu Zhang [6 ]
Mao, Ying [1 ]
Ho-Keung Ng [2 ,3 ]
机构
[1] Fudan Univ, Huashan Hosp, Dept Neurosurg, Shanghai, Peoples R China
[2] Hong Kong & Shanghai Brain Consortium HSBC, Hong Kong, Peoples R China
[3] Chinese Univ Hong Kong, Dept Anat & Cellular Pathol, Hong Kong, Peoples R China
[4] Zhengzhou Univ, Dept Pathol, Affiliated Hosp 1, Zhengzhou, Peoples R China
[5] Fudan Univ, Huashan Hosp, Dept Pathol, Shanghai, Peoples R China
[6] Zhengzhou Univ, Dept Neurosurg, Affiliated Hosp 1, Zhengzhou, Peoples R China
[7] Chinese Univ Hong Kong, Dept Surg, Div Neurosurg, Hong Kong, Peoples R China
基金
中国国家自然科学基金;
关键词
anaplastic PXA; GBM_midline; glioblastoma RTK; mesenchymal; glioblastomas in adolescents and young adults; methylation class; PEDIATRIC HIGH-GRADE; CENTRAL-NERVOUS-SYSTEM; GENOMIC LANDSCAPE; TUMORS; GLIOMAS; EXPRESSION; MUTATIONS; CLASSIFICATION; SUBGROUPS; H3K27ME3;
D O I
10.1111/nan.12802
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective We aimed to characterise glioblastomas of adolescents and young adults (AYAs) that were isocitrate dehydrogenase (IDH) wild type (wt) and H3wt. Materials and Methods Fifty such patients (aged 16-32) were studied by methylation profiling, targeted sequencing and targeted RNA-seq. Results Tumours predominantly clustered into three methylation classes according to the terminology of Capper et al. (2018): (anaplastic) pleomorphic xanthoastrocytoma (PXA) (21 cases), GBM_midline (15 cases) and glioblastoma RTK/mesenchymal (seven cases). Two cases clustered with ANA_PA, four cases with LGG classes and one with GBM_MYCN. Only fifteen cases reached a calibrated score >0.84 when the cases were uploaded to DKFZ Classifier. GBM_midline-clustered tumours had a poorer overall survival (OS) compared with the PXA-clustered tumours (p = 0.030). LGG-clustered cases had a significantly better survival than GBM_midline-clustered tumours and glioblastoma RTK/mesenchymal-clustered tumours. Only 13/21 (62%) of PXA-clustered cases were BRAF V600E mutated. Most GBM_midline-clustered cases were not located in the midline. GBM_midline-clustered cases were characterised by PDGFRA amplification/mutation (73.3%), mutations of mismatch repair genes (40.0%), and all showed H3K27me3 and EZH1P loss, and an unmethylated MGMT promoter. Across the whole cohort, MGMT promoter methylation and wt TERT promoter were favourable prognosticators. Mismatch repair gene mutations were poor prognosticators and together with methylation class and MGMT methylation, maintained their significance in multivariate analyses. BRAF mutation was a good prognosticator in the PXA-clustered tumours. Conclusion Methylation profiling is a useful tool in the diagnosis and prognostication of AYA glioblastomas, and the methylation classes have distinct molecular characteristics. The usual molecular diagnostic criteria for adult IDHwt glioblastoma should be applied with caution within the AYA age group.
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