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Boron neutron capture therapy (BNCT) for the treatment of spontaneous nasal planum squamous cell carcinoma in felines
Authors:Verónica A Trivillin  Elisa M Heber  Monica Rao  María A Cantarelli  Maria E Itoiz  David W Nigg  Osvaldo Calzetta  Herman Blaumann  Juan Longhino  Amanda E Schwint
Institution:(1) Department of Radiobiology, National Atomic Energy Commission, Av. General Paz 1499, B1650KNA San Martin, Province Buenos Aires, Argentina;(2) Veterinary Oncology Center, Avenida del Libertador 15013, 1642 Acassuso, Province Buenos Aires, Argentina;(3) Department of Oral Pathology, Faculty of Dentistry, University of Buenos Aires, M.T. de Alvear 2142, 1122 Buenos Aires, Argentina;(4) Idaho National Laboratory, 2525 North Fremont Street, P.O. Box 1625, Idaho Falls, ID 83415, USA;(5) Department of Nuclear Engineering, Bariloche Atomic Center, National Atomic Energy Commission, 8400 San Carlos de Bariloche , Province Río Negro, Argentina
Abstract:Recently, Boron neutron capture therapy (BNCT) was successfully applied to treat experimental squamous cell carcinomas (SCC) of the hamster cheek pouch mucosa, with no damage to normal tissue. It was also shown that treating spontaneous nasal planum SCC in terminal feline patients with low dose BNCT is safe and feasible. In an extension of this work, the present study aimed at evaluation of the response of tumor and dose-limiting normal tissues to potentially therapeutic BNCT doses. Biodistribution studies with 10B-boronophenylalanine (BPA enriched in 10B) as a 10B carrier were performed on three felines that showed advanced nasal planum SCC without any standard therapeutic option. Following the biodistribution studies, BNCT mediated by 10BPA was done using the thermalized epithermal neutron beam at the RA-6 Nuclear Reactor. Follow-up included clinical evaluation, assessment of macroscopic tumor and normal tissue response and biopsies for histopathological analysis. The treated animals did not show any apparent radiation-induced toxicity. All three animals exhibited partial tumor control and an improvement in clinical condition. Enhanced therapeutic efficacy was associated with a high 10B content of the tumor and a small tumor size. BNCT is therefore believed to be potentially effective in the treatment of spontaneous SCC. However, improvement in targeting 10B into all tumor cells and delivering a sufficient dose at a greater depth are still required for the treatment of deep-seated, large tumors. Future studies are needed to evaluate the potential efficacy of the dual mode cellular (e.g. BPA-BNCT) and vascular (e.g. GB-10-BNCT) targeting protocol in a preclinical scenario, employing combinations of 10B compounds with different properties and complementary uptake mechanisms.
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