The determination of prognoses for patients with recurrent glioblastoma remains challenging. This study aimed to evaluate the prognostic value of static O-(2- 18F-fluoroethyl)-l-tyrosine ( 18F-FET) PET parameters in patients with recurrent glioblastoma. Methods: We retrospectively evaluated patients treated in 3 institutional clinical trials examining vascular endothelial growth factor inhibition, immune checkpoint inhibition, or their combination in recurrent glioblastoma. Patients with a baseline 18F-FET PET were included in the analysis and stratified by treatment group. Prognostic value was evaluated using univariate Kaplan-Meier and multivariate Cox regression analyses, with receiver-operating-characteristic analysis to identify optimal thresholds. Results: Both univariate and multivariate analysis revealed that patients with a larger baseline metabolic tumor volume (MTV) and higher mean tumor-to-background ratio (TBR mean) had an increased risk of death independent of treatment (MTV per 10 mL: hazard ratio, 1.06; 95\% CI, 1.01-1.12; P = 0.023; TBR mean: hazard ratio, 1.91; 95\% CI, 1.14-3.21; P = 0.014). Receiver-operating-characteristic analysis showed that an MTV and TBR mean of more than 27.94 cm 3 and 2.15, respectively, identified patients with worse overall survival in our patient population. Conclusion: Pretreatment MTV and TBR mean had a significant prognostic value in patients with recurrent glioblastoma, independent of treatment, and could be useful to stratify and select patients for future clinical trials.
Geens, W, Buyck, F, Raes, L, Schwarze, JK, Awada, G, De Sutter, S, Bruneau, M, Vandemeulebroucke, J, Everaert, H, Neyns, B & Duerinck, J 2026, 'Prognostic Value of O-(2-18F-Fluoroethyl)-l-Tyrosine PET for Patients with Recurrent Glioblastoma.', Journal of Nuclear Medicine, vol. 67, no. 4. https://doi.org/10.2967/jnumed.125.270727
Geens, W., Buyck, F., Raes, L., Schwarze, J. K., Awada, G., De Sutter, S., Bruneau, M., Vandemeulebroucke, J., Everaert, H., Neyns, B., & Duerinck, J. (2026). Prognostic Value of O-(2-18F-Fluoroethyl)-l-Tyrosine PET for Patients with Recurrent Glioblastoma. Journal of Nuclear Medicine, 67(4). https://doi.org/10.2967/jnumed.125.270727
@article{8396f90cc81a4dfc99d9099ff44323a8,
title = "Prognostic Value of O-(2-18F-Fluoroethyl)-l-Tyrosine PET for Patients with Recurrent Glioblastoma.",
abstract = "The determination of prognoses for patients with recurrent glioblastoma remains challenging. This study aimed to evaluate the prognostic value of static O-(2- 18F-fluoroethyl)-l-tyrosine ( 18F-FET) PET parameters in patients with recurrent glioblastoma. Methods: We retrospectively evaluated patients treated in 3 institutional clinical trials examining vascular endothelial growth factor inhibition, immune checkpoint inhibition, or their combination in recurrent glioblastoma. Patients with a baseline 18F-FET PET were included in the analysis and stratified by treatment group. Prognostic value was evaluated using univariate Kaplan-Meier and multivariate Cox regression analyses, with receiver-operating-characteristic analysis to identify optimal thresholds. Results: Both univariate and multivariate analysis revealed that patients with a larger baseline metabolic tumor volume (MTV) and higher mean tumor-to-background ratio (TBR mean) had an increased risk of death independent of treatment (MTV per 10 mL: hazard ratio, 1.06; 95\% CI, 1.01-1.12; P = 0.023; TBR mean: hazard ratio, 1.91; 95\% CI, 1.14-3.21; P = 0.014). Receiver-operating-characteristic analysis showed that an MTV and TBR mean of more than 27.94 cm 3 and 2.15, respectively, identified patients with worse overall survival in our patient population. Conclusion: Pretreatment MTV and TBR mean had a significant prognostic value in patients with recurrent glioblastoma, independent of treatment, and could be useful to stratify and select patients for future clinical trials. ",
author = "Wietse Geens and F{\'e}lix Buyck and Laurens Raes and Schwarze, \{Julia Katharina\} and Gil Awada and \{De Sutter\}, Selene and Micha{\"e}l Bruneau and Jef Vandemeulebroucke and Hendrik Everaert and Bart Neyns and Johnny Duerinck",
note = "{\textcopyright} 2026 by the Society of Nuclear Medicine and Molecular Imaging.",
year = "2026",
month = mar,
day = "26",
doi = "10.2967/jnumed.125.270727",
language = "English",
volume = "67",
journal = "Journal of Nuclear Medicine",
issn = "0161-5505",
publisher = "Society of Nuclear Medicine Inc.",
number = "4",
}