In IDH-wildtype glioblastomas which meet the histopathological or molecular diagnosis criteria, it remains unclear whether the presence of TERT promotor mutations provides additional prognostic information. Based on a multicenter cohort of 466 IDH-wildtype glioblastomas (including 396 with and 70 patients without TERT promotor mutations), we found that TERT promotor mutations were neither associated with progression-free survival nor overall survival. This held true in various treatment-based or molecular subgroups. This argues against standardized analysis for TERT promotor mutation status for the purpose of prognostic or therapeutic relevance in newly diagnosed IDH-wildtype glioblastoma that otherwise meets the histopathological and molecular diagnosis criteria.
TERT promotor status does not add prognostic information in IDH-wildtype glioblastomas fulfilling other diagnostic WHO criteria: A report of the RANO resect group / P. Karschnia, J.S. Young, A. Dono, L. Häni, S.T. Juenger, T. Sciortino, F. Bruno, N. Teske, R.A. Morshed, A.F. Haddad, Y. Zhang, S. Stoecklein, M.A. Vogelbaum, J. Beck, N. Tandon, S. Hervey-Jumper, A.M. Molinaro, R. Rudà, L. Bello, O. Schnell, Y. Esquenazi, M.I. Ruge, S.J. Grau, M. Van Den Bent, M. Weller, M.S. Berger, S.M. Chang, J. Tonn. - In: NEURO-ONCOLOGY ADVANCES. - ISSN 2632-2498. - 4:1(2022), pp. vdac158.1-vdac158.3. [10.1093/noajnl/vdac158]
TERT promotor status does not add prognostic information in IDH-wildtype glioblastomas fulfilling other diagnostic WHO criteria: A report of the RANO resect group
T. Sciortino;L. Bello;
2022
Abstract
In IDH-wildtype glioblastomas which meet the histopathological or molecular diagnosis criteria, it remains unclear whether the presence of TERT promotor mutations provides additional prognostic information. Based on a multicenter cohort of 466 IDH-wildtype glioblastomas (including 396 with and 70 patients without TERT promotor mutations), we found that TERT promotor mutations were neither associated with progression-free survival nor overall survival. This held true in various treatment-based or molecular subgroups. This argues against standardized analysis for TERT promotor mutation status for the purpose of prognostic or therapeutic relevance in newly diagnosed IDH-wildtype glioblastoma that otherwise meets the histopathological and molecular diagnosis criteria.| File | Dimensione | Formato | |
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