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. 2021 Dec 10;35(1):77–85. doi: 10.1007/s10334-021-00982-5

Table 1.

Demographics, tumor location, tumor type, molecular tumor profile and progression-free survival for all patients

ID Gender, age Tumor location Tumor type Molecular status BBB break down Recurrency/progressive disease (months)
1 M, 70 R parietal GBM °IV IDH1/2 WT, ATRX retention, MGMT non-methylated Yes 21
2 F, 61 L parieto-temporal GBM °IV IDH1/2 WT, ATRX retention, MGMT non-methylated No 3
3 F, 54 R temporal Giant cell GBM °IV IDH1/2 WT, ATRX retention, MGMT intermediate methylated Yes
4 F, 46 R Temporo-insular Diffuse astro-cytoma °II IDH1 pos, 1p/19q no LoH, ATRX retention No
5 F, 29 L frontal Diffuse astro-cytoma °II IDH1 pos, 1p/19q no LoH, ATRX loss (Yes)
6 M, 70 R temporo-insular-frontal Anaplastic astro-cytoma °III IDH1/2 WT, ATRX retention, MGMT methylated No 11
7 F, 63 L insular GBM °IV IDH1/2 WT, ATRX retention, MGMT non-methylated Yes
8 F, 52 R occipital GBM °IV IDH1/2 WT, ATRX retention, MGMT non-methylated Yes 15
9 F, 58 R parieto-insular GBM °IV IDH1/2 WT, ATRX retention, MGMT non-methylated Yes 7
10 M, 69 L parietal GBM °IV IDH1/2 WT, ATRX retention, MGMT methylated Yes 1
11 M, 43 L fronto-insular LGG N/A (Yes)

BBB blood–brain barrier (= contrast enhancement), F female, GBM glioblastoma multiforme, IDH isocitrate dehydrogenase, L left, LGG low-grade glioma, LoH loss of heterozygosity, M male, MGMT O-6-methylguanine-DNA-methyltransferase, R right, WT wild type, (Yes) faint contrast enhancement