AUTHOR=Unterrainer Marcus , Ruf Viktoria , von Rohr Katharina , Suchorska Bogdana , Mittlmeier Lena Maria , Beyer Leonie , Brendel Matthias , Wenter Vera , Kunz Wolfgang G. , Bartenstein Peter , Herms Jochen , Niyazi Maximilian , Tonn Jörg C. , Albert Nathalie Lisa 

TITLE=TERT-Promoter Mutational Status in Glioblastoma – Is There an Association With Amino Acid Uptake on Dynamic 18F-FET PET?

JOURNAL=Frontiers in Oncology

VOLUME=11

YEAR=2021

URL=https://www.frontiersin.org/journals/oncology/articles/10.3389/fonc.2021.645316

DOI=10.3389/fonc.2021.645316

ISSN=2234-943X

ABSTRACT=<sec><title>Objective</title><p>The mutation of the ‘telomerase reverse transcriptase gene promoter’ (TERTp) has been identified as an important factor for individual prognostication and tumorigenesis and will be implemented in upcoming glioma classifications. Uptake characteristics on dynamic <sup>18</sup>F-FET PET have been shown to serve as additional imaging biomarker for prognosis. However, data on the correlation of TERTp-mutational status and amino acid uptake on dynamic <sup>18</sup>F-FET PET are missing. Therefore, we aimed to analyze whether static and dynamic <sup>18</sup>F-FET PET parameters are associated with the TERTp-mutational status in de-novo <italic>IDH</italic>-wildtype glioblastoma and whether a TERTp-mutation can be predicted by dynamic <sup>18</sup>F-FET PET.</p></sec><sec><title>Methods</title><p>Patients with de-novo <italic>IDH</italic>-wildtype glioblastoma, WHO grade IV, available TERTp-mutational status and dynamic <sup>18</sup>F-FET PET scan prior to any therapy were included. Here, established clinical parameters maximal and mean tumor-to-background-ratios (TBR<sub>max</sub>/TBR<sub>mean</sub>), the biological-tumor-volume (BTV) and minimal-time-to-peak (TTP<sub>min</sub>) on dynamic PET were analyzed and correlated with the TERTp-mutational status.</p></sec><sec><title>Results</title><p>One hundred <italic>IDH</italic>-wildtype glioblastoma patients were evaluated; 85/100 of the analyzed tumors showed a TERTp-mutation (C228T or C250T), 15/100 were classified as TERTp-wildtype. None of the static PET parameters was associated with the TERTp-mutational status (median TBR<sub>max</sub> 3.41 vs. 3.32 (p=0.362), TBR<sub>mean</sub> 2.09 vs. 2.02 (p=0.349) and BTV 26.1 vs. 22.4 ml (p=0.377)). Also, the dynamic PET parameter TTP<sub>min</sub> did not differ in both groups (12.5 vs. 12.5 min, p=0.411). Within the TERTp-mutant subgroups (i.e., C228T (n=23) &amp; C250T (n=62)), the median TBR<sub>max</sub> (3.33 vs. 3.69, p=0.095), TBR<sub>mean</sub> (2.08 vs. 2.09, p=0.352), BTV (25.4 vs. 30.0 ml, p=0.130) and TTP<sub>min</sub> (12.5 vs. 12.5 min, p=0.190) were comparable, too.</p></sec><sec><title>Conclusion</title><p>Uptake characteristics on dynamic <sup>18</sup>F-FET PET are not associated with the TERTp-mutational status in glioblastoma However, as both, dynamic <sup>18</sup>F-FET PET parameters as well as the TERTp-mutation status are well-known prognostic biomarkers, future studies should investigate the complementary and independent prognostic value of both factors in order to further stratify patients into risk groups.</p></sec>