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|Title:||Targeted alpha therapy of glioblastoma multiforme with 213Bi-substance P|
|Authors:||MORGENSTERN Alfred; KROLICKI Leszek; KUNIKOWSKA Jolanta; KOCIARA Henryk; KROLICKI B; JAKUCINSKI M; MIKOŁAJCZAK Renata; PAWLAK Dariusz; APOSTOLIDIS Christos; BRUCHERTSEIFER Frank|
|Citation:||Proceedings of the 8th International Symposium on Targeted Alpha Therapy p. 15|
|Publisher:||Oak Ridge National Laboratory|
|Type:||Articles in periodicals and books|
|Abstract:||Glioblastoma multiforme (GBM), the most common primary brain tumor in adults, has a very poor prognosis with a median overall survival of 15 months despite of aggressive therapy including surgery, chemotherapy and radiation therapy. New therapy options are urgently needed. Targeted alpha therapy with the short range, high LET alpha emitter 213Bi offers the potential for selective irradiation of tumors, while minimizing damage to adjacent, functional critical areas of the brain. The peptide carrier substance P is targeting neurokinin type 1 (NK-1) receptors, which are consistently over-expressed on glioblastoma cells. Here we report the first clinical experience with 213Bi-labeled DOTA-Substance P in patients with recurrent GBM.|
|JRC Directorate:||Nuclear Safety and Security|
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