<i>O</i>-(2-<sup>18</sup>F-Fluoroethyl)-L-Tyrosine PET Predicts Failure of Antiangiogenic Treatment in Patients with Recurrent High-Grade Glioma

Markus Hutterer(Innsbruck Medical University), Martha Nowosielski(Innsbruck Medical University), Daniel Putzer(Innsbruck Medical University), Dietmar Waitz(Innsbruck Medical University), Gerd Tinkhauser(Innsbruck Medical University), H. Kostron(Innsbruck Medical University), Armin Muigg(Innsbruck Medical University), Irene Virgolini(Innsbruck Medical University), Wolfgang Staffen(Paracelsus Medical University), Eugen Trinka(Paracelsus Medical University), T. Gotwald(Innsbruck Medical University), Andreas H. Jacobs(European Molecular Biology Laboratory), Guenther Stockhammer(Innsbruck Medical University)
Journal of Nuclear Medicine
May 27, 2011
Cited by 167Open Access
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Abstract

UNLABELLED: The objective of this study was to compare MRI response assessment with metabolic O-(2-(18)F-fluoroethyl)-L-tyrosine ((18)F-FET) PET response evaluation during antiangiogenic treatment in patients with recurrent high-grade glioma (rHGG). METHODS: Eleven patients with rHGG were treated biweekly with bevacizumab-irinotecan. MR images and (18)F-FET PET scans were obtained at baseline and at follow-up 8-12 wk after treatment onset. MRI treatment response was evaluated by T1/T2 volumetry according to response assessment in neurooncology (RANO) criteria. For (18)F-FET PET evaluation, an uptake reduction of more than 45% calculated with a standardized uptake value of more than 1.6 was defined as a metabolic response (receiver-operating-characteristic curve analysis). MRI and (18)F-FET PET volumetry results and response assessment were compared with each other and in relation to progression-free survival (PFS) and overall survival (OS). RESULTS: At follow-up, MR images showed partial response in 7 of 11 patients (64%), stable disease in 2 of 11 patients (18%), and tumor progression in 2 of 11 patients (18%). In contrast, (18)F-FET PET revealed 5 of 11 metabolic responders (46%) and 6 of 11 nonresponders (54%). MRI and (18)F-FET PET showed that responders survived significantly longer than did nonresponders (10.24 vs. 4.1 mo, P = 0.025, and 7.9 vs. 2.3 mo, P = 0.015, respectively). In 4 patients (36.4%), diagnosis according to RANO criteria and (18)F-FET PET was discordant. In these cases, PET was able to detect tumor progression earlier than was MRI. CONCLUSION: In rHGG patients undergoing antiangiogenic treatment, (18)F-FET PET seems to be predictive for treatment failure in that it contributes important information to response assessment based solely on MRI and RANO criteria.


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