Table 1.
Patient | Age at diagnosis, years | Gender | EGFR amplification | IDH mutation | LOH 1p/19q | Methylation class | MGMT-promoter methylation |
---|---|---|---|---|---|---|---|
1 | 59 | Male | Yes | IDH wt | No | RTK II | Methylated |
2 | 44 | Female | Yes | IDH wt | No | RTK II | Not methylated |
3 | 50 | Male | Yes | IDH wt | No | RTK II | Not methylated |
4 | 64 | Male | Yes | IDH wt | No | RTK II | Not methylated |
5 | 60 | Female | Yes | IDH wt | No | RTK II | Methylated |
6 | 63 | Male | Yes | IDH wt | No | Mesenchymal | Methylated |
7 | 61 | Male | Yes | IDH wt | No | Unclear | Not methylated |
8 | 58 | Male | Yes | IDH wt | No | Mesenchymal | Not methylated |
9 | 50 | Male | Yes | IDH wt | No | Mesenchymal | Methylated |
EGFR, epidermal growth factor receptor; IDH, isocitrate dehydrogenase; LOH 1p/19q, loss of heterozygosity on chromosome 1 (1p) and 19 (19q); MGMT, O6-methylguanine-DNA methyltransferase; RTK, receptor tyrosine kinase; wt, wild type.