Abstract
Glioblastoma multiforme (GBM), primary brain tumor, is the most common and most malignant of the glia tumors. It is characterized by the worst prognosis with a median overall survival time of only 9–15 months. The infiltrating character of the tumor, its molecular heterogeneity, as well as the protective effects of the blood-brain barrier are the main causes for the insufficiency of established frontline treatments (surgery, radiotherapy, and chemotherapy).
The best treatment strategy for patients with recurrent GBM is unclear and controversial. Even with established state-of-the-art treatment in almost 90% of patients, the recurrence of disease is observed and median survival after recurrence is less than 6 months.
An alternative method of treatment is to apply the drug locally. It has been shown that GBM overexpresses the of NK-1 receptor and substance P (SP) can be used as a ligand. Alpha emitters, with shorter range and higher energy than beta emitters, offer the new potential for selective irradiation of tumors, with minimizing damage to adjacent tissue.
This chapter describes the use of radiolabeled SP for intratumoral treatment of the glia tumors.
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Acknowledgments
The authors are indebted for use of parts of the 225Ac/213Bi to the US Department of Energy, Office of Nuclear Physics, Isotope Development and Production for Research and Applications Program.
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Kunikowska, J., Morgenstern, A., Bruchertseifer, F., Krolicki, L. (2018). Locoregional Treatment of Brain Tumors. In: Bombardieri, E., Seregni, E., Evangelista, L., Chiesa, C., Chiti, A. (eds) Clinical Applications of Nuclear Medicine Targeted Therapy . Springer, Cham. https://doi.org/10.1007/978-3-319-63067-0_35
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