Skip to main content
. 2023 Jul 12;5(1):vdad085. doi: 10.1093/noajnl/vdad085

Table 2.

Clinical and Molecular Features in Recurrent Gliomas With and Without MMR Gene Mutations in the Recurrence

Subgroup n Gender (M:F) Age (years) Initial 2021 WHO Grade (2:3:4) Recurrence 2021 WHO Grade (2:3:4) ΔGrade (% Increased at Recurrence) MGMT Promoter* (Methylated: Unmethylated) TMZ Therapy* (Treated Between Samples:Not Treated) ΔTMB, Primary vs. Recurrence* (Mutations/Mb) Median Survival Post-Recurrence (Months)
IDH-mutant astrocytoma
MMR-mutant 12 4:6 36.8 ± 3.0 9:3:0 4:1:7 67% 7:1 10:2 89.3 ± 12.5 17.5
MMR-wild type 50 35:15 34.7 ± 1.3 39:5:6 25:9:16 28% 22:4 16:28 3.6 ± 1.6 43.0
P-value - =0.1429 =0.4908 =0.2224 =0.3434 =0.0119 =0.8975 =0.0073 <0.0001 =0.0022
IDH-wild-type glioblastoma
MMR-mutant 18 10:8 49.9 ± 2.5 0:0:18 0:0:18 - 7:2 16:0 62.7 ± 20.1 7.5
MMR-wild type 104 73:31 55.0 ± 1.1 0:0:104 0:0:104 - 23:49 80:11 3.1 ± 0.4 9.0
  P-value - =0.2746 =0.0753 - - - =0.0111 =0.2110 <0.0001 =0.6229

Note: MMR, mismatch repair; ΔGrade, change in grade between primary and recurrence, TMZ, temozolomide; ΔTMB, change in tumor mutation burden between primary and recrurrence; bold indicates statistical significance to a level of < 0.05;

*not all cases had available MGMT promoter methylation, TMZ therapy data, or paired TMB in primary and recurrent samples.