Author:
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
Abstract
AbstractOur 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 IDHwt cases. Interestingly, it was also found in 48,5% of IDHmut cases. According to the genomic profile, four genetic subgroups could be distinguished: (1) IDwt/cIMPACT-NOW 3 (n = 270); (2) IDHwt/cIMPACT-NOW 3 negative (= 10); (3) IDHmut/cIMPACT-NOW 3 (n = 16); and 4) IDHmut/cIMPACT-NOW 3 negative (n = 17). Multivariate analysis confirmed that IDH1/2 mutations confer a favorable prognosis (IDHwt, 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.
Publisher
Springer Science and Business Media LLC
Reference26 articles.
1. WHO Classification of Tumours Editorial Board. Central Nervous System Tumours (International Agency for Research on Cancer, 2016).
2. Louis, D. N. et al. World Health Organization Histological Classification of Tumours of the Central Nervous System (International Agency for Research on Cancer, 2016).
3. Louis, D. N. et al. cIMPACT-NOW: A practical summary of diagnostic points from Round 1 updates. Brain Pathol. 29(4), 469–472 (2019).
4. Brito, C. et al. Clinical insights gained by refining the 2016 WHO classification of diffuse gliomas with: EGFR amplification, TERT mutations, PTEN deletion and MGMT methylation. BMC Cancer 19, 968 (2019).
5. Kuwahara, K. et al. Clinical, histopathological, and molecular analyses of IDH-wild-type WHO grade II-III gliomas to establish genetic predictors of poor prognosis. Brain Tumor Pathol. 36, 135–143 (2019).