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Current Development of Glioblastoma Therapeutic Agents

Journal

MOLECULAR CANCER THERAPEUTICS
Volume 20, Issue 9, Pages 1521-1532

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1535-7163.MCT-21-0159

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GBM is the most common and aggressive malignant primary brain tumor in humans, with limited success in treatment. Identifying and understanding key molecules and barriers for treatment resistance is crucial for discovering new potential therapeutic targets.
Glioblastoma multiforme (GBM) is themost common and aggressive malignant primary brain tumor in humans. Over the past several decades, despite improvements in neurosurgical techniques, development of powerful chemotherapeutic agents, advances in radiotherapy, and comprehensive genomic profiling and molecular characterization, treatment of GBM has achieved very limited success in increasing overall survival. Thus, identifying and understanding the key molecules and barriers responsible for the malignant phenotypes and treatment resistance of GBM will yield new potential therapeutic targets. We review the most recent development of receptor tyrosine kinase targeted therapy for GBM and discuss the current status of several novel strategies with the emphasis on blood-brain barrier penetration as a major obstacle for small-molecule drugs to achieve their therapeutic goals. Likewise, a major opportunity for the treatment of GBM lies in the use of biomarkers for the discovery and development of new receptor tyrosine kinase targeted therapy.

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