TP53 oncogenic variants as prognostic factors in individuals with glioblastoma: a systematic review and meta-analysis
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Updated: May 7, 2026

The Clinical Application of Tumor Treating Fields Therapy in Glioblastoma
Published on: April 16, 2019
Diego Esperante1,2, Kena Daza Galicia3, Kalu Gabriel Rivas-Cuervo4
1Combined Studies Plan in Medicine (PECEM), Universidad Nacional Autónoma de México (UNAM), Mexico City, Mexico.
Background:
This systematic review and meta-analysis investigated the relationship between somatic TP53 oncogenic variants and prognosis, specifically with overall survival (OS) and progression-free survival (PFS) in patients diagnosed with supratentorial glioblastoma.
Methods:
We included longitudinal studies and clinical trials involving a minimum of 40 adult participants diagnosed with supratentorial glioblastoma, wherein the status of TP53 variants was assessed. We conducted searches in multiple databases. We assessed bias risk using a modified version of the Quality in Prognosis Studies tool, and the certainty of evidence was evaluated following the principles of the GRADE approach.
Results And Conclusion:
This study encompassed 23 papers involving 2,555 patients, out of which 716 had reported oncogenic variants. TP53 oncogenic variants were associated with a reduced likelihood of 1-year survival (OR 0.52, 95% CI 0.29-0.94). However, our analysis did not reveal any significant impact of TP53 variants on overall survival, progression-free survival, or 2-year survival. Therefore, this comprehensive analysis demonstrates that the presence of genetic variants in TP53 does not provide useful information for the prognosis of glioblastoma.
Systematic Review Registration:
https://www.crd.york.ac.uk/prospero/, identifier CRD42021289496.
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