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Optimizing the risk stratification of astrocytic tumors by applying the cIMPACT-NOW Update 3 signature: real-word single center experience

Our work reports implementation of a useful genetic diagnosis for the clinical managment of patients with astrocytic tumors. We investigated 313 prospectively recruited diffuse astrocytic tumours by applying the cIMPACT-NOW Update 3 signature. The cIMPACT-NOW Update 3 (cIMPACT-NOW 3) markers, i.e.,...

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Detalles Bibliográficos
Autores principales: Molica, Carmen, Gili, Alessio, Nardelli, Carlotta, Pierini, Tiziana, Arniani, Silvia, Beacci, Donatella, Mavridou, Elena, Mandarano, Martina, Corinaldesi, Rodolfo, Metro, Giulio, Gorello, Paolo, Giovenali, Paolo, Cenci, Nunzia, Castrioto, Corrado, Lupattelli, Marco, Roila, Fausto, Mecucci, Cristina, La Starza, Roberta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10654668/
https://www.ncbi.nlm.nih.gov/pubmed/37973912
http://dx.doi.org/10.1038/s41598-023-46701-z
Descripción
Sumario:Our work reports implementation of a useful genetic diagnosis for the clinical managment of patients with astrocytic tumors. We investigated 313 prospectively recruited diffuse astrocytic tumours by applying the cIMPACT-NOW Update 3 signature. The cIMPACT-NOW Update 3 (cIMPACT-NOW 3) markers, i.e., alterations of TERT promoter, EGFR, and/or chromosome 7 and 10, characterized 96.4% of IDH(wt) cases. Interestingly, it was also found in 48,5% of IDH(mut) cases. According to the genomic profile, four genetic subgroups could be distinguished: (1) ID(wt)/cIMPACT-NOW 3 (n = 270); (2) IDH(wt)/cIMPACT-NOW 3 negative (= 10); (3) IDH(mut)/cIMPACT-NOW 3 (n = 16); and 4) IDH(mut)/cIMPACT-NOW 3 negative (n = 17). Multivariate analysis confirmed that IDH1/2 mutations confer a favorable prognosis (IDH(wt), HR 2.91 95% CI 1.39–6.06), and validated the prognostic value of the cIMPACT-NOW 3 signature (cIMPACT-NOW 3, HR 2.15 95% CI 1.15–4.03). To accurately identify relevant prognostic categories, overcoming the limitations of histopathology and immunohistochemistry, molecular-cytogenetic analyses must be fully integrated into the diagnostic work-up of astrocytic tumors.