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Published on: December 28, 2017
Targeted Radionuclide Therapy in Glioblastoma
Xiaobin Zhao1,2,3,4,5, Vivianne Jakobsson1,2,3,5, Yucen Tao1,3,5
1Department of Diagnostic Radiology, Yong Loo Lin School of Medicine and College of Design and Engineering, National University of Singapore, Singapore 119074, Singapore.
Abstract:
Despite the development of various novel therapies, glioblastoma (GBM) remains a devastating disease, with a median survival of less than 15 months. Recently, targeted radionuclide therapy has shown significant progress in treating solid tumors, with the approval of Lutathera for neuroendocrine tumors and Pluvicto for prostate cancer by the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA). This achievement has shed light on the potential of targeted radionuclide therapy for other solid tumors, including GBM. This review presents the current status of targeted radionuclide therapy in GBM, highlighting the commonly used therapeutic radionuclides emitting alpha, beta particles, and Auger electrons that could induce potent molecular and cellular damage to treat GBM. We then explore a range of targeting vectors, including small molecules, peptides, and antibodies, which selectively target antigen-expressing tumor cells with minimal or no binding to healthy tissues. Considering that radiopharmaceuticals for GBM are often administered locoregionally to bypass the blood-brain barrier (BBB), we review prominent delivery methods such as convection-enhanced delivery, local implantation, and stereotactic injections. Finally, we address the challenges of this therapeutic approach for GBM and propose potential solutions.
Insights
Targeted radionuclide therapy shows promise for glioblastoma (GBM) treatment. This review explores radionuclides, targeting vectors, and delivery methods to improve outcomes for this aggressive brain cancer.
Area of Science:
- Oncology
- Nuclear Medicine
- Radiochemistry
Background:
- Glioblastoma (GBM) has a poor prognosis despite novel therapies.
- Targeted radionuclide therapy has gained FDA and EMA approval for other cancers.
- This suggests potential for GBM treatment.
Purpose of the Study:
- To review the current status of targeted radionuclide therapy for GBM.
- To highlight therapeutic radionuclides, targeting vectors, and delivery methods.
- To address challenges and propose solutions for GBM radionuclide therapy.
Main Methods:
- Review of therapeutic radionuclides (alpha, beta, Auger electrons).
- Exploration of targeting vectors (small molecules, peptides, antibodies).
- Analysis of locoregional delivery methods (convection-enhanced delivery, local implantation, stereotactic injections).
Main Results:
- Radionuclides can induce potent molecular and cellular damage in GBM.
- Targeting vectors offer selective tumor cell binding.
- Locoregional delivery bypasses the blood-brain barrier effectively.
Conclusions:
- Targeted radionuclide therapy is a promising approach for GBM.
- Further research is needed to overcome existing challenges.
- Optimized strategies can improve patient survival and outcomes.

