Table · dataset · 2026
Data Sheet 1_Receptor tyrosine kinase targeted therapies in glioblastoma: a systematic review.docx
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Introduction<p>Glioblastoma is the most common primary central nervous system malignancy and has a median survival of 14.6 months.
Description
Receptor tyrosine kinase (RTKs) signalling consitutes one of the three major pathways driving glioblastoma, implicating them as a therapeutic target. However, no individual study has yet demonstrated significant survival benefit of RTK-directed therapy.
The aim of this systematic review was to synthesise the current evidence on the survival efficacy of RTK-directed therapies in human glioblastoma.</p>Methods<p>Studies reporting survival outcomes for human glioblastoma patients receiving any RTK-directed therapy were included. PRISMA guidelines were followed. MEDLINE, Embase, Web of Science and Scopus were searched from inception to May 2025.
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Citation searching of all included studies was performed for additional eligible studies. Duplicate title/abstract screening, data extraction and risk of bias assessments were conducted.</p>Results<p>A total of 135 studies were included in the review, 66.7% (90/135) of which studied recurrent glioblastoma. Studies included 9,029 patients, 51.1% (4612/9029) of which were male.
A total of 47 different RTK-directed therapies were assessed. Multikinase inhibitors (40.7%, 55/135), EGFR-directed therapies (28.9%, 39/135) and VEGFR inhibitors (20%, 27/135) were the most studied therapies. An additional 6.7% (9/135) of studies investigated combined EGFR-directed therapy and VEGFR inhibition.
A total of 4.4% (6/135) of studies demonstrated a statistically significant survival benefit, whilst therapies appeared beneficial to survival in an additional 11.1% (15/135) of studies. There was no consistent evidence supporting survival efficacy for any RTK-directed therapy.</p>Conclusion<p>Whilst there is no strong evidence for survival benefit of any RTK-directed therapy, there are encouraging results in a small proportion of studies.
Future directions include identifying and validating novel biomarkers, standardising reporting, and improving clinical trial design to produce more robust and interpretable data.</p>Systematic Review Registration<p>PROSPERO CRD42022366607.</p>
Links
Where it is published
- DOI doi.org/10.3389/fmed.2026.1928491.s001 ↗
DOI / persistent id · from figshare com
Catalogue records · 1
- OAI-PMH record api.figshare.com/v2/oai?verb=GetRecord&metadataPrefix=oai_dc&identifier=oai%3Af… ↗
metadata API · from figshare com
Topics
Provenance · 1 source records, 18 field assertions
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