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. 2022 Aug 19;4(1):vdac133.
doi: 10.1093/noajnl/vdac133. eCollection 2022 Jan-Dec.

Systematic review of diffuse hemispheric glioma, H3 G34-mutant: Outcomes and associated clinical factors

Affiliations

Systematic review of diffuse hemispheric glioma, H3 G34-mutant: Outcomes and associated clinical factors

Cameron Crowell et al. Neurooncol Adv. .

Abstract

Background: A comprehensive review and description of the clinical features that impact prognosis for patients with diffuse hemispheric glioma, H3 G34-mutant (G34-DHG) is needed. Understanding survival and prognostic features is paramount for clinical advancements and patient care.

Methods: PubMed, Embase, and Google Scholar were searched for English articles published between January 1, 2012 and June 30, 2021. Eligible studies included patient(s) of any age diagnosed with an H3 G34-mutant brain tumor with at least one measure of survival or progression. Patient-level data were pooled for analyses. This study was prospectively registered in PROSPERO (CRD42021267764) and Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines were followed.

Results: Twenty-seven studies met the criteria with a total of 135 patients included. Median age at diagnosis was 15.8 years (interquartile range [IQR]: 13.3-22.0) with 90% having localized disease. Co-occurring alterations included ATRX mutation in 93%, TP53 mutation in 88%, and MGMT promoter methylation in 70%. Median time-to-progression was 10.0 months (IQR: 6.0-18.0) and median overall survival was 17.3 months (95% CI: 15.0 to 22.9). The median time from progression to death was 5.0 months (IQR: 3.0-11.7). Factors associated with survival duration were age, as patients ≥18 y/o demonstrated longer survival (hazard ratio [HR] =2.05, 95% CI: 1.16 to 3.62), and degree of upfront resection, as near or gross-total resection demonstrated longer survival compared to those with less than near-total resection (HR = 3.75, 95% CI: 2.11 to 6.62).

Conclusion: This systematic review highlights available clinical data for G34-DHG demonstrating poor outcomes and important prognostic features, while serving as a baseline for future research and clinical trials.

Keywords: H3 G34-mutant; diffuse hemispheric glioma; outcomes; survival.

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Figures

Figure 1
Figure 1
PRISMA flowchart demonstrating study selection process by C.C and C.E.
Figure 2
Figure 2
Kaplan-Meier survival plots demonstrating overall survival. (A) Entire cohort with 95% CI. (B) Age: <18 y/o versus 18 y/o. (C) Sex: female versus male. (D) Tumour histology: HGG versus PNET versus other. (E) Tumor mutation: G34R versus G34V. (F) Degree of up-front surgical resection: <NTR versus GTR/NTR. (G) Presence of MGMT promotor methylation.

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