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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Veröffentlicht in:Scientific reports 2023-11, Vol.13 (1), p.20101-20101, Article 20101
Hauptverfasser: 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
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Sprache:eng
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Zusammenfassung: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.
ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-023-46701-z