Clinical Outcomes and Prognostic Features of Diffuse Hemispheric Glioma, H3 G34-Mutant: An International Multi-institutional Study.

Clinical cancer research : an official journal of the American Association for Cancer Research
Authors
Abstract

PURPOSE: Knowledge of prognostic factors and long-term survival in patients with diffuse hemispheric glioma, H3 G34-mutant (DHG, H3 G34), remains limited in this tumor with a poor prognosis.EXPERIMENTAL DESIGN: This retrospective, multi-institutional study investigated prognostic variables for patients with DHG, H3 G34, and their association with progression-free survival (PFS) and overall survival (OS). Uni- and multivariable Cox proportional hazard models were applied with multiple imputed datasets.RESULTS: A total of 153 patients (142 G34R, 9 G34V, 2 via DNA methylation) were included. The median age at diagnosis was 17 years (range, 2-45). Initial gross/near total resection (GTR/NTR) was achieved in 43% of patients. Radiation was given in 91% (85% focal irradiation), and initial chemotherapy was given in 87% [70% temozolomide-based (TMZ), 25% TMZ/lomustine, 5% non-TMZ]. Median OS was 24 months [interquartile range (IQR), 22-28] with a median PFS of 14 months (IQR, 12-19). Twelve patients (8%) were found to be long-term survivors (≥5 years). Exploratory multivariable analysis showed that adjuvant radiotherapy [HR, 0.076; 95% confidence interval (CI), 0.033-0.17] and achieving GTR/NTR compared with < NTR (HR, 0.51; 95% CI, 0.33-0.78) were associated with improved PFS. Multivariable analysis showed improved OS with increasing age at diagnosis (HR, 0.70; 95% CI, 0.57-0.87), initial radiotherapy (HR, 0.38; 95% CI, 0.15-0.96), and initial GTR/NTR compared with < NTR (HR, 0.60; 95% CI, 0.37-0.97).CONCLUSIONS: This cohort highlights prognostic factors for patients with DHG, H3 G34, and describes relapse patterns and therapy approaches. Clinical trials and prospective registries are needed to improve outcomes.

Year of Publication
2026
Journal
Clinical cancer research : an official journal of the American Association for Cancer Research
Volume
32
Issue
11
Pages
2243-2254
Date Published
06/2026
ISSN
1557-3265
DOI
10.1158/1078-0432.CCR-25-3764
PubMed ID
41801141
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