Intratumoral heterogeneity and TERT promoter mutations in progressive/higher-grade meningiomas

• Published in: Oncotarget Vol. 8; no. 65; pp. 109228 - 109237
• Main Authors: Juratli, Tareq A., Thiede, Christian, Koerner, Mara V.A., Tummala, Shilpa S., Daubner, Dirk, Shankar, Ganesh M., Williams, Erik A., Martinez-Lage, Maria, Soucek, Silke, Robel, Katja, Penson, Tristan, Krause, Mechthild, Appold, Steffen, Meinhardt, Matthias, Pinzer, Thomas, Miller, Julie J., Krex, Dietmar, Ely, Heather A., Silverman, Ian M., Christiansen, Jason, Schackert, Gabriele, Wakimoto, Hiroaki, Kirsch, Matthias, Brastianos, Priscilla K., Cahill, Daniel P.
• Format: Journal Article
• Language: English
• Published: United States Impact Journals LLC 12.12.2017
• Subjects: Research Paper; fusion; meningioma; heterogeneity; rearrangements; telomere
• ISSN: 1949-2553; 1949-2553
• DOI: 10.18632/oncotarget.22650

Recent studies have reported mutations in the telomerase reverse transcriptase promoter ( p) in meningiomas. We sought to determine the frequency, clonality and clinical significance of telomere gene alterations in a cohort of patients with progressive/higher-grade meningiomas. We characterized 64 temporally- and regionally-distinct specimens from 26 WHO grade III meningioma patients. On initial diagnoses, the meningiomas spanned all WHO grades (3 grade I, 13 grade II and 10 grade III). The tumor samples were screened for p and mutations, and rearrangements. Additionally, p was sequenced in a separate cohort of 19 patients with radiation-associated meningiomas. We examined the impact of mutational status on patients' progression and overall survival. Somatic p mutations were detected in six patients (6/26 = 23%). Regional intratumoral heterogeneity in p mutation status was noted. In 4 patients, p mutations were detected in recurrent specimens but not in the available specimens of the first surgery. Additionally, a gene fusion ( ) was found in one sample. In contrary, none of the investigated samples harbored an or mutation. In the cohort of radiation-induced meningiomas, p mutation was detected in two patients (10.5%). Importantly, we found that patients with emergence of p mutations had a substantially shorter OS than their p wild-type counterparts (2.7 years, 95% CI 0.9 - 4.5 years versus 10.8 years, 95% CI 7.8 -12.8 years, p=0.003). In progressive/higher-grade meningiomas, p mutations are associated with poor survival, supporting a model in which selection of this alteration is a harbinger of aggressive tumor development. In addition, we observe spatial intratumoral heterogeneity of p mutation status, consistent with this model of late emergence in tumor evolution. Thus, early detection of p mutations may define patients with more aggressive meningiomas. Stratification for alterations should be adopted in future clinical trials of progressive/higher-grade meningiomas.