Bevacizumab dose adjustment to improve clinical outcomes of glioblastoma.

Glioblastoma (GBM) is one of the most aggressive and vascularized brain tumors in adults, with a median survival of 20.9 months. In newly diagnosed and recurrent GBM, bevacizumab demonstrated an increase in progression-free survival, but not in overall survival. We conducted an in silico analysis of...

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Detalles Bibliográficos
Autores: García-Romero, N, Palacín-Aliana, I, Madurga, R, Carrión-Navarro, J, Esteban-Rubio, Susana, Jiménez, B, Collazo, A, Pérez-Rodríguez, F, Ortiz de Mendivil, A, Fernández-Carballal, C, García-Duque, S, Diamantopoulos-Fernández, J, Belda-Iniesta, Cristobal, Prat-Acín, R, Calvo, E, Ayuso-Sacido, Angel, Sánchez-Gómez, Pilar
Tipo de recurso: artículo
Fecha de publicación:2020
País:España
Institución:Instituto de Salud Carlos III (ISCIII)
Repositorio:Repisalud
Idioma:inglés
OAI Identifier:oai:repisalud.isciii.es:20.500.12105/10986
Acceso en línea:http://hdl.handle.net/20.500.12105/10986
Access Level:acceso abierto
Palabra clave:Angiogenesis
Bevacizumab
Glioblastoma
Neovasculogenesis
VEGFA
Descripción
Sumario:Glioblastoma (GBM) is one of the most aggressive and vascularized brain tumors in adults, with a median survival of 20.9 months. In newly diagnosed and recurrent GBM, bevacizumab demonstrated an increase in progression-free survival, but not in overall survival. We conducted an in silico analysis of VEGF expression, in a cohort of 1082 glioma patients. Then, to determine whether appropriate bevacizumab dose adjustment could increase the anti-angiogenic response, we used in vitro and in vivo GBM models. Additionally, we analyzed VEGFA expression in tissue, serum, and plasma in a cohort of GBM patients before and during bevacizumab treatment. We identified that 20% of primary GBM did not express VEGFA suggesting that these patients would probably not respond to bevacizumab therapy as we proved in vitro and in vivo. We found that a specific dose of bevacizumab calculated based on VEGFA expression levels increases the response to treatment in cell culture and serum samples from mice bearing GBM tumors. Additionally, in a cohort of GBM patients, we observed a correlation of VEGFA levels in serum, but not in plasma, with bevacizumab treatment performance. Our data suggest that bevacizumab dose adjustment could improve clinical outcomes in Glioblastoma treatment.