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Extent of resection and survival in IDH-wildtype glioblastoma: interaction with MGMT status and chemoradiation

delete2026-07-23
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OA
AI
N
Noah Drewes *
L
Lara Koutah
R
Rishi Jain
J
Jack Carnduff
K
Kayla Chin
K
Kristin Delfino
J
Jeffrey W. Cozzens
B
Bruce Frankel
DOI:10.1007/s11060-026-05725-xdelete
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Abstract

Abstract

En 中文
Whether gross total resection (GTR) remains associated with survival among MGMT-methylated IDH-wildtype glioblastoma patients receiving chemoradiation remains uncertain. We evaluated whether GTR versus less-than-GTR (< GTR) was associated with overall survival across MGMT promoter methylation and chemoradiation strata. We retrospectively reviewed 261 patients undergoing biopsy or resection for newly diagnosed IDH-wildtype glioblastoma at a single institution from 2010 to 2024. Extent of resection was dichotomized as GTR versus < GTR, and chemoradiation was coded as receipt of postoperative radiation and temozolomide. Overall survival was assessed using Kaplan-Meier analysis and multivariable Cox models with prespecified EOR × MGMT × chemoradiation interaction testing, adjusted for age, KPS, tumor location, and mFI-5. GTR was associated with longer overall survival than < GTR in the overall cohort and within all four MGMT × chemoradiation strata. MGMT-methylated patients receiving chemoradiation had a median overall survival of 17.02 months after GTR versus 10.65 months after < GTR (log-rank p = 0.001), and the model-derived adjusted hazard ratio for < GTR versus GTR was 2.12 (95% CI 1.27–3.54; p = 0.004). The three-way EOR × MGMT × chemoradiation interaction was not significant (likelihood-ratio p = 0.309). In a 6-week sensitivity analysis, all survival associations remained, but EOR × chemoradiation was no longer significant. GTR was associated with longer survival across all MGMT and chemoradiation-defined subgroups, including MGMT-methylated patients receiving chemoradiation. These findings are consistent with maximal safe resection when feasible but should be interpreted cautiously because of small subgroups as well as treatment-selection and immortal-time biases.
Keywords:
Glioblastoma
IDH-wildtype
Extent of resection
MGMT promoter methylation
Chemoradiation
Overall survival

Journal

J
Journal of Neuro-Oncology
IF:
3.1
Papers:
8.1K
Citations:
1.5W

Organization

C
Center for Clinical Research
Scholars:
19
Papers: 15
Citations: 1.4K
F
Feinberg School of Medicine
Scholars:
1.8W
Papers: 1.5W
Citations: 34
D
department of surgery
Scholars:
1.7K
Papers: 516
Citations: 0
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