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FET-PET radiomics in recurrent glioblastoma: prognostic value for outcome after re-irradiation?

PURPOSE: The value of O-(2-[18F]fluoroethyl)-L-tyrosine (FET)-positron emission tomography (PET)-radiomics in the outcome assessment of patients with recurrent glioblastoma (rGBM) has not been evaluated until now. The aim of this study was to evaluate whether a prognostic model based on FET-PET radi...

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Autores principales: Carles, Montserrat, Popp, Ilinca, Starke, Michael Maximilian, Mix, Michael, Urbach, Horst, Schimek-Jasch, Tanja, Eckert, Franziska, Niyazi, Maximilian, Baltas, Dimos, Grosu, Anca L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7931514/
https://www.ncbi.nlm.nih.gov/pubmed/33658069
http://dx.doi.org/10.1186/s13014-020-01744-8
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author Carles, Montserrat
Popp, Ilinca
Starke, Michael Maximilian
Mix, Michael
Urbach, Horst
Schimek-Jasch, Tanja
Eckert, Franziska
Niyazi, Maximilian
Baltas, Dimos
Grosu, Anca L.
author_facet Carles, Montserrat
Popp, Ilinca
Starke, Michael Maximilian
Mix, Michael
Urbach, Horst
Schimek-Jasch, Tanja
Eckert, Franziska
Niyazi, Maximilian
Baltas, Dimos
Grosu, Anca L.
author_sort Carles, Montserrat
collection PubMed
description PURPOSE: The value of O-(2-[18F]fluoroethyl)-L-tyrosine (FET)-positron emission tomography (PET)-radiomics in the outcome assessment of patients with recurrent glioblastoma (rGBM) has not been evaluated until now. The aim of this study was to evaluate whether a prognostic model based on FET-PET radiomics features (RF) is feasible and can identify rGBM patients that would most benefit from re-irradiation. METHODS: We prospectively recruited rGBM patients who underwent FET-PET before re-irradiation (GLIAA-Pilot trial, DRKS00000633). Tumor volume was delineated using a semi-automatic method with a threshold of 1.8 times the standardized-uptake-value of the background. 135 FET-RF (histogram parameters, shape and texture features) were extracted. The analysis involved the characterization of tumor and non-tumor tissue with FET-RF and the evaluation of the prognostic value of FET-RF for time-to-progression (TTP), overall survival (OS) and recurrence location (RL). RESULTS: Thirty-two rGBM patients constituted our cohort. FET-RF discriminated significantly between tumor and non-tumor. The texture feature Small-Zone-Low-Gray-Level-Emphasis (SZLGE) showed the best performance for the prediction of TTP (p = 0.001, satisfying Bonferroni-multiple-test significance level). Additionally, two radiomics signatures could predict TTP (TTP-radiomics-signature, p = 0.001) and OS (OS-radiomics-signature, p = 0.038). SZLGE and the TTP-radiomics-signature additionally predicted RL. Specifically, high values for TTP-radiomics-signature and for SZLGE indicated not only earlier progression, but also a RL within the initial FET-PET active volume. CONCLUSION: Our findings suggest that FET-PET radiomics could contribute to the prognostic assessment and selection of rGBM-patients benefiting from re-irradiation. Trial registration DRKS00000633. Registered on 8th of December in 2010. https://www.drks.de/drks_web/navigate.do?navigationId=trial.HTML&TRIAL_ID=DRKS00000633.
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spelling pubmed-79315142021-03-05 FET-PET radiomics in recurrent glioblastoma: prognostic value for outcome after re-irradiation? Carles, Montserrat Popp, Ilinca Starke, Michael Maximilian Mix, Michael Urbach, Horst Schimek-Jasch, Tanja Eckert, Franziska Niyazi, Maximilian Baltas, Dimos Grosu, Anca L. Radiat Oncol Research PURPOSE: The value of O-(2-[18F]fluoroethyl)-L-tyrosine (FET)-positron emission tomography (PET)-radiomics in the outcome assessment of patients with recurrent glioblastoma (rGBM) has not been evaluated until now. The aim of this study was to evaluate whether a prognostic model based on FET-PET radiomics features (RF) is feasible and can identify rGBM patients that would most benefit from re-irradiation. METHODS: We prospectively recruited rGBM patients who underwent FET-PET before re-irradiation (GLIAA-Pilot trial, DRKS00000633). Tumor volume was delineated using a semi-automatic method with a threshold of 1.8 times the standardized-uptake-value of the background. 135 FET-RF (histogram parameters, shape and texture features) were extracted. The analysis involved the characterization of tumor and non-tumor tissue with FET-RF and the evaluation of the prognostic value of FET-RF for time-to-progression (TTP), overall survival (OS) and recurrence location (RL). RESULTS: Thirty-two rGBM patients constituted our cohort. FET-RF discriminated significantly between tumor and non-tumor. The texture feature Small-Zone-Low-Gray-Level-Emphasis (SZLGE) showed the best performance for the prediction of TTP (p = 0.001, satisfying Bonferroni-multiple-test significance level). Additionally, two radiomics signatures could predict TTP (TTP-radiomics-signature, p = 0.001) and OS (OS-radiomics-signature, p = 0.038). SZLGE and the TTP-radiomics-signature additionally predicted RL. Specifically, high values for TTP-radiomics-signature and for SZLGE indicated not only earlier progression, but also a RL within the initial FET-PET active volume. CONCLUSION: Our findings suggest that FET-PET radiomics could contribute to the prognostic assessment and selection of rGBM-patients benefiting from re-irradiation. Trial registration DRKS00000633. Registered on 8th of December in 2010. https://www.drks.de/drks_web/navigate.do?navigationId=trial.HTML&TRIAL_ID=DRKS00000633. BioMed Central 2021-03-03 /pmc/articles/PMC7931514/ /pubmed/33658069 http://dx.doi.org/10.1186/s13014-020-01744-8 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Carles, Montserrat
Popp, Ilinca
Starke, Michael Maximilian
Mix, Michael
Urbach, Horst
Schimek-Jasch, Tanja
Eckert, Franziska
Niyazi, Maximilian
Baltas, Dimos
Grosu, Anca L.
FET-PET radiomics in recurrent glioblastoma: prognostic value for outcome after re-irradiation?
title FET-PET radiomics in recurrent glioblastoma: prognostic value for outcome after re-irradiation?
title_full FET-PET radiomics in recurrent glioblastoma: prognostic value for outcome after re-irradiation?
title_fullStr FET-PET radiomics in recurrent glioblastoma: prognostic value for outcome after re-irradiation?
title_full_unstemmed FET-PET radiomics in recurrent glioblastoma: prognostic value for outcome after re-irradiation?
title_short FET-PET radiomics in recurrent glioblastoma: prognostic value for outcome after re-irradiation?
title_sort fet-pet radiomics in recurrent glioblastoma: prognostic value for outcome after re-irradiation?
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7931514/
https://www.ncbi.nlm.nih.gov/pubmed/33658069
http://dx.doi.org/10.1186/s13014-020-01744-8
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