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. 2022 Jan 5;7(1):100365. doi: 10.1016/j.esmoop.2021.100365

Table 1.

Patient and disease characteristics

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.