O-(2-18F-fluoroethyl)-L-tyrosine PET Predicts Failure of Antiangiogenic Treatment in Patients with Recurrent High-grade Glioma
Overview
Authors
Affiliations
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.
Galldiks N, Kaufmann T, Vollmuth P, Lohmann P, Smits M, Veronesi M Neuro Oncol. 2024; 26(7):1181-1194.
PMID: 38466087 PMC: 11226881. DOI: 10.1093/neuonc/noae049.
Design of Novel F-Labeled Amino Acid Tracers Using Sulfur F-Fluoride Exchange Click Chemistry.
Huang Y, Chen H, Zhang L, Xie Y, Li C, Yu Z ACS Med Chem Lett. 2024; 15(2):294-301.
PMID: 38352831 PMC: 10860173. DOI: 10.1021/acsmedchemlett.3c00557.
Chaban A, Waschulzik B, Bernhardt D, Delbridge C, Schmidt-Graf F, Wagner A Eur J Nucl Med Mol Imaging. 2024; 51(6):1698-1702.
PMID: 38228970 PMC: 11043199. DOI: 10.1007/s00259-024-06601-4.
Manzarbeitia-Arroba B, Hodolic M, Pichler R, Osipova O, Soriano-Castrejon A, Garcia-Vicente A Cancers (Basel). 2024; 16(1).
PMID: 38201621 PMC: 10778283. DOI: 10.3390/cancers16010195.
Albert N, Galldiks N, Ellingson B, van den Bent M, Chang S, Cicone F Lancet Oncol. 2024; 25(1):e29-e41.
PMID: 38181810 PMC: 11787868. DOI: 10.1016/S1470-2045(23)00525-9.