4.5 Article

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

期刊

出版社

WILEY
DOI: 10.1111/nan.12802

关键词

anaplastic PXA; GBM_midline; glioblastoma RTK; mesenchymal; glioblastomas in adolescents and young adults; methylation class

资金

  1. Health and Medical Research Fund (HMRF)
  2. Food and Health Bureau of Hong Kong [07180736]
  3. Children Cancer Foundation
  4. National Natural Science Foundation of China [82072020, 81702465, U1804172, U1904148]
  5. Shanghai Municipal Science and Technology Major Project, China [2018SHZDZX01]

向作者/读者索取更多资源

This study aimed to characterize glioblastomas in adolescents and young adults (AYAs) and found three distinct methylation classes. The results showed that methylation profiling is a useful tool in the diagnosis and prognosis of AYA glioblastomas.
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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