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Published on: September 27, 2024
The challenges associated with molecular targeted therapies for glioblastoma
Toni Rose Jue1, Kerrie L McDonald2
1Cure Brain Cancer Foundation Biomarkers and Translational Research Group, University of NSW, Kensington, Australia.
Abstract:
Glioblastoma (GBM) is the most aggressive malignant brain tumor in adults. Improvements in the treatment of GBM have remained static since the advent of the standard therapy which includes radiation with concurrent and adjuvant temozolomide treatment. Developing treatment and diagnostic or companion biomarker combinations is transforming the way we treat numerous cancers. However, can this emerging paradigm be also effective for GBM? Can GBM be treated the same way as other cancers? Here we review the challenges for a personalized molecular targeted therapeutic approach in GBM. The specific challenges for establishing a personalized molecular targeted medicine program for GBM patients include overcoming the blood brain barrier, unravelling the intra- and inter-heterogeneity that exists and the importance of developing more relevant animal models that recapitulate a patient's GBM tumor.
Insights
Personalized medicine shows promise for glioblastoma (GBM) treatment, but significant challenges remain. Overcoming the blood-brain barrier and understanding tumor heterogeneity are key to developing effective targeted therapies for this aggressive brain cancer.
Area of Science:
- Neuro-oncology
- Cancer Therapeutics
- Molecular Medicine
Background:
- Glioblastoma (GBM) is the most aggressive adult malignant brain tumor.
- Current standard treatment (radiation with temozolomide) has shown limited improvement.
- Personalized medicine approaches are revolutionizing cancer care in other malignancies.
Purpose of the Study:
- To review the challenges in applying personalized molecular targeted therapy to GBM.
- To assess the feasibility of GBM treatment mirroring strategies used for other cancers.
Main Methods:
- Literature review of existing challenges and potential solutions for GBM personalized therapy.
- Analysis of factors hindering targeted treatment development in GBM.
Main Results:
- Significant hurdles exist for personalized GBM treatment, including the blood-brain barrier.
- Intra- and inter-tumoral heterogeneity presents a major obstacle.
- The need for more accurate and patient-representative animal models is critical.
Conclusions:
- Personalized molecular targeted medicine for GBM faces substantial challenges.
- Addressing the blood-brain barrier, tumor heterogeneity, and model relevance is essential for advancing GBM treatment.
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