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. 2021 Mar 4;152(3):541–549. doi: 10.1007/s11060-021-03723-9

Table 5.

Analysis of MGMT methylation and TP53 expression status versus recurrence rate in glioblastoma patients receiving different chemotherapies

Recurrence interval P-value Adjusted P-value
Before 1 year After 1 year
n (%) n (%)
MGMT status
 Non-methylated
  Temozolomide 8 (61.5) 5 (38.5) 0.007b 0.041c
  Temozolomide + other 0 (0.0) 8 (100.0)
 Methylated
  Temozolomide 6 (37.5) 10 (62.5) 0.667b
  Temozolomide + other 2 (25.0) 6 (75.0)
TP53 expression
 Negative
  Temozolomide 7 (63.6) 4 (36.4) 0.040a 0.035c
  Temozolomide + other 1 (14.3) 6 (85.7)
 Positive
  Temozolomide 7 (38.9) 11 (61.1) 0.201b
  Temozolomide + other 1 (11.1) 8 (88.9)

All patients with non-methylated MGMT who received temozolomide plus other chemotherapies had delayed recurrence, after at least 1 year (P-value = 0.007) compared with patients who received TZM alone. Around 86% of patients with non-TP53 expressing tumors who received TZM plus other chemotherapies had recurrence after 1 year (P-value = 0.040)

TMZ Temozolomide

aChi-Square Test; bFisher’s Exact Test; cMantel–Haenszel Chi-square test