Prognostic Value of <i>O</i>-(2-<sup>18</sup>F-Fluoroethyl)-l-Tyrosine PET for Patients with Recurrent Glioblastoma.

Geens, Wietse; Buyck, Félix; Raes, Laurens; Schwarze, Julia Katharina; Awada, Gil; De Sutter, Selene; Bruneau, Michaël; Vandemeulebroucke, Jef et al. · J Nucl Med · 2026

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Abstract

The determination of prognoses for patients with recurrent glioblastoma remains challenging. This study aimed to evaluate the prognostic value of static <i>O</i>-(2-<sup>18</sup>F-fluoroethyl)-l-tyrosine (<sup>18</sup>F-FET) PET parameters in patients with recurrent glioblastoma. <b>Methods:</b> 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 <sup>18</sup>F-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. <b>Results:</b> Both univariate and multivariate analysis revealed that patients with a larger baseline metabolic tumor volume (MTV) and higher mean tumor-to-background ratio (TBR<sub>mean</sub>) had an increased risk of death independent of treatment (MTV per 10 mL: hazard ratio, 1.06; 95% CI, 1.01-1.12; <i>P</i> = 0.023; TBR<sub>mean</sub>: hazard ratio, 1.91; 95% CI, 1.14-3.21; <i>P</i> = 0.014). Receiver-operating-characteristic analysis showed that an MTV and TBR<sub>mean</sub> of more than 27.94 cm<sup>3</sup> and 2.15, respectively, identified patients with worse overall survival in our patient population. <b>Conclusion:</b> Pretreatment MTV and TBR<sub>mean</sub> 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.

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