# Metformin Renders Survival Advantage to Patients with Glioblastoma Multiforme

**Authors:** Daniel Gonzales-Portillo, Bhavya Vashi, Kirsten Bains Williams, Jorge Cervantes

PMC · DOI: 10.3390/neurolint18030040 · Neurology International · 2026-02-24

## TL;DR

This study finds that metformin may improve survival in patients with glioblastoma multiforme, a deadly brain cancer.

## Contribution

The novel contribution is evidence that metformin, a common diabetes drug, may offer a survival benefit for glioblastoma patients.

## Key findings

- Metformin use was associated with increased median overall survival of up to 18 months in GBM patients.
- The survival advantage was statistically significant compared to controls (p = 0.00197).

## Abstract

Purpose: Glioblastoma multiforme (GBM) is a highly aggressive cancer with limited survival despite current treatments. Rising treatment costs highlight the importance of identifying more affordable therapeutic alternatives. A body of literature has shown that metformin has the potential to act as an antineoplastic agent. Here, we examined the effects of metformin on GBM in humans. Methods: The Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) guidelines were followed to perform the review. A total of 469 studies were screened using comprehensive search terms. Of these, 4 studies were compatible for the meta-analysis. Results: Data analysis demonstrated an increase in median overall survival for GBM patients up to 18 months compared to controls (p = 0.00197). Conclusions: Overall, our findings support the efficacy of metformin as an anti-neoplastic agent, and that it may grant a survival advantage for patients diagnosed with GBM. Further analyses should find dose-dependent relationships between metformin and the targeted survival outcomes in larger, rigorous clinical trials.

## Linked entities

- **Chemicals:** metformin (PubChem CID 4091)
- **Diseases:** Glioblastoma multiforme (MONDO:0018177), GBM (MONDO:0018177)

## Full-text entities

- **Genes:** MGMT (O-6-methylguanine-DNA methyltransferase) [NCBI Gene 4255], Pdcd1 (programmed cell death 1) [NCBI Gene 18566] {aka Ly101, PD-1, Pdc1}, IDH1 (isocitrate dehydrogenase (NADP(+)) 1) [NCBI Gene 3417] {aka HEL-216, HEL-S-26, IDCD, IDH, IDP, IDPC}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}
- **Diseases:** brain tumors (MESH:D001932), diabetic (MESH:D003920), central nervous system tumors (MESH:D016543), injury to (MESH:D014947), Glioblastoma (MESH:D005909), Tumor (MESH:D009369), type 2 diabetes (MESH:D003924)
- **Chemicals:** Metformin (MESH:D008687), MTF (-), TMZ (MESH:D000077204)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13029654/full.md

## References

22 references — full list in the complete paper: https://tomesphere.com/paper/PMC13029654/full.md

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Source: https://tomesphere.com/paper/PMC13029654