The Value of FET PET/CT in Recurrent Glioma with a Different IDH Mutation Status: The Relationship between Imaging and Molecular Biomarkers

The evaluation of treatment response remains a challenge in glioma cases because the neuro oncological therapy can lead to the development of treatment-related changes (TRC) that mimic true progression (TP). Positron emission tomography (PET) using O-(2-[<sup>18</sup>F] fluoroethyl-)-L-t...

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Main Authors: Marija Skoblar Vidmar, Andrej Doma, Uroš Smrdel, Katarina Zevnik, Andrej Studen
Format: Article
Language:English
Published: MDPI AG 2022-06-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/23/12/6787
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author Marija Skoblar Vidmar
Andrej Doma
Uroš Smrdel
Katarina Zevnik
Andrej Studen
author_facet Marija Skoblar Vidmar
Andrej Doma
Uroš Smrdel
Katarina Zevnik
Andrej Studen
author_sort Marija Skoblar Vidmar
collection DOAJ
description The evaluation of treatment response remains a challenge in glioma cases because the neuro oncological therapy can lead to the development of treatment-related changes (TRC) that mimic true progression (TP). Positron emission tomography (PET) using O-(2-[<sup>18</sup>F] fluoroethyl-)-L-tyrosine (<sup>18</sup>F-FET) has been shown to be a useful tool for detecting TRC and TP. We assessed the diagnostic performance of different <sup>18</sup>F-FET PET segmentation approaches and different imaging biomarkers for differentiation between late TRC and TP in glioma patients. Isocitrate dehydrogenase (IDH) status was evaluated as a predictor of disease outcome. In our study, the proportion of TRC in IDH wild type (IDHwt) and IDH mutant (IDHm) subgroups was without significant difference. We found that the diagnostic value of static and dynamic biomarkers of <sup>18</sup>F-FET PET for discrimination between TRC and TP depends on the IDH mutation status of the tumor. Dynamic <sup>18</sup>F-FET PET acquisition proved helpful in the IDH wild type (IDHwt) subgroup, as opposed to the IDH mutant (IDHm) subgroup, providing an early indication to discontinue dynamic imaging in the IDHm subgroup.
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spelling doaj.art-2cf54a3ecc0d4a82a323abc1d60ffeaa2023-11-23T17:06:46ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672022-06-012312678710.3390/ijms23126787The Value of FET PET/CT in Recurrent Glioma with a Different IDH Mutation Status: The Relationship between Imaging and Molecular BiomarkersMarija Skoblar Vidmar0Andrej Doma1Uroš Smrdel2Katarina Zevnik3Andrej Studen4Division of Radiotherapy, Institute of Oncology Ljubljana, 1000 Ljubljana, SloveniaDepartment of Nuclear Medicine, Institute of Oncology Ljubljana, 1000 Ljubljana, SloveniaDivision of Radiotherapy, Institute of Oncology Ljubljana, 1000 Ljubljana, SloveniaDepartment of Nuclear Medicine, Institute of Oncology Ljubljana, 1000 Ljubljana, SloveniaExperimental Particle Physics Department, Jožef Stefan Institute, 1000 Ljubljana, SloveniaThe evaluation of treatment response remains a challenge in glioma cases because the neuro oncological therapy can lead to the development of treatment-related changes (TRC) that mimic true progression (TP). Positron emission tomography (PET) using O-(2-[<sup>18</sup>F] fluoroethyl-)-L-tyrosine (<sup>18</sup>F-FET) has been shown to be a useful tool for detecting TRC and TP. We assessed the diagnostic performance of different <sup>18</sup>F-FET PET segmentation approaches and different imaging biomarkers for differentiation between late TRC and TP in glioma patients. Isocitrate dehydrogenase (IDH) status was evaluated as a predictor of disease outcome. In our study, the proportion of TRC in IDH wild type (IDHwt) and IDH mutant (IDHm) subgroups was without significant difference. We found that the diagnostic value of static and dynamic biomarkers of <sup>18</sup>F-FET PET for discrimination between TRC and TP depends on the IDH mutation status of the tumor. Dynamic <sup>18</sup>F-FET PET acquisition proved helpful in the IDH wild type (IDHwt) subgroup, as opposed to the IDH mutant (IDHm) subgroup, providing an early indication to discontinue dynamic imaging in the IDHm subgroup.https://www.mdpi.com/1422-0067/23/12/6787gliomatreatment-related changestrue progressionpseudoprogressionradiation necrosisbiomarkers
spellingShingle Marija Skoblar Vidmar
Andrej Doma
Uroš Smrdel
Katarina Zevnik
Andrej Studen
The Value of FET PET/CT in Recurrent Glioma with a Different IDH Mutation Status: The Relationship between Imaging and Molecular Biomarkers
International Journal of Molecular Sciences
glioma
treatment-related changes
true progression
pseudoprogression
radiation necrosis
biomarkers
title The Value of FET PET/CT in Recurrent Glioma with a Different IDH Mutation Status: The Relationship between Imaging and Molecular Biomarkers
title_full The Value of FET PET/CT in Recurrent Glioma with a Different IDH Mutation Status: The Relationship between Imaging and Molecular Biomarkers
title_fullStr The Value of FET PET/CT in Recurrent Glioma with a Different IDH Mutation Status: The Relationship between Imaging and Molecular Biomarkers
title_full_unstemmed The Value of FET PET/CT in Recurrent Glioma with a Different IDH Mutation Status: The Relationship between Imaging and Molecular Biomarkers
title_short The Value of FET PET/CT in Recurrent Glioma with a Different IDH Mutation Status: The Relationship between Imaging and Molecular Biomarkers
title_sort value of fet pet ct in recurrent glioma with a different idh mutation status the relationship between imaging and molecular biomarkers
topic glioma
treatment-related changes
true progression
pseudoprogression
radiation necrosis
biomarkers
url https://www.mdpi.com/1422-0067/23/12/6787
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