Regorafenib in adult patients with recurrent glioblastoma: a single-arm meta-analysis.

J ChemotherNov 20, 2025 (epub)

Marcos Henrique da Silva Mezzari, Natan Lucca Lima, Bárbara Ghizoni Maggi et al.

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In 30 seconds

This systematic review and single-arm meta-analysis pooled outcomes from ten studies of regorafenib in 724 adults with recurrent glioblastoma. Median overall survival was 7.2 months and median progression-free survival was 2.6 months; 12-month overall survival was 22.5% and 6-month progression-free survival was 14.9%. Disease control was reported in 36.1%, while grade 3–4 adverse events occurred in 31.4%. Meta-regression associated MGMT methylation with better survival and disease-control outcomes, and male sex with better overall survival and stable disease.

Key findings

  • Across ten studies and 724 patients, median overall survival was 7.2 months and median progression-free survival was 2.6 months.
  • The 12-month overall survival rate was 22.5%, and the 6-month progression-free survival rate was 14.9%.
  • Disease control rate was 36.1%; grade 3-4 adverse events occurred in 31.4%.
  • Meta-regression associated MGMT methylation with improved outcomes; male sex was associated with better overall survival and stable disease.

Why it matters

The pooled estimates provide a summary of reported survival, disease control, and higher-grade toxicity with regorafenib in recurrent glioblastoma, where treatment options are limited. The biomarker and sex associations may help frame questions for further study, but they are meta-regression findings and do not establish which patients will benefit.

What to keep in mind

The analysis was single-arm, pooling studies without a comparator; its findings cannot establish regorafenib's benefit relative to other treatments.

Source

Published in J Chemother. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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