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A systematic review of amino acid PET in assessing treatment response to temozolomide in glioma
The response assessment in neuro-oncology (RANO) criteria have been the gold standard for monitoring treatment response in glioblastoma (GBM) and differentiating tumor progression from pseudoprogression. While the RANO criteria have played a key role in detecting early tumor progression, their abili...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8923003/ https://www.ncbi.nlm.nih.gov/pubmed/35300149 http://dx.doi.org/10.1093/noajnl/vdac008 |
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author | Prather, Kiana Y O’Neal, Christen M Westrup, Alison M Tullos, Hurtis J Hughes, Kendall L Conner, Andrew K Glenn, Chad A Battiste, James D |
author_facet | Prather, Kiana Y O’Neal, Christen M Westrup, Alison M Tullos, Hurtis J Hughes, Kendall L Conner, Andrew K Glenn, Chad A Battiste, James D |
author_sort | Prather, Kiana Y |
collection | PubMed |
description | The response assessment in neuro-oncology (RANO) criteria have been the gold standard for monitoring treatment response in glioblastoma (GBM) and differentiating tumor progression from pseudoprogression. While the RANO criteria have played a key role in detecting early tumor progression, their ability to identify pseudoprogression is limited by post-treatment damage to the blood-brain barrier (BBB), which often leads to contrast enhancement on MRI and correlates poorly to tumor status. Amino acid positron emission tomography (AA PET) is a rapidly growing imaging modality in neuro-oncology. While contrast-enhanced MRI relies on leaky vascularity or a compromised BBB for delivery of contrast agents, amino acid tracers can cross the BBB, making AA PET particularly well-suited for monitoring treatment response and diagnosing pseudoprogression. The authors performed a systematic review of PubMed, MEDLINE, and Embase through December 2021 with the search terms “temozolomide” OR “Temodar,” “glioma” OR “glioblastoma,” “PET,” and “amino acid.” There were 19 studies meeting inclusion criteria. Thirteen studies utilized [(18)F]FET, five utilized [(11)C]MET, and one utilized both. All studies used static AA PET parameters to evaluate TMZ treatment in glioma patients, with nine using dynamic tracer parameters in addition. Throughout these studies, AA PET demonstrated utility in TMZ treatment monitoring and predicting patient survival. |
format | Online Article Text |
id | pubmed-8923003 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-89230032022-03-16 A systematic review of amino acid PET in assessing treatment response to temozolomide in glioma Prather, Kiana Y O’Neal, Christen M Westrup, Alison M Tullos, Hurtis J Hughes, Kendall L Conner, Andrew K Glenn, Chad A Battiste, James D Neurooncol Adv Review The response assessment in neuro-oncology (RANO) criteria have been the gold standard for monitoring treatment response in glioblastoma (GBM) and differentiating tumor progression from pseudoprogression. While the RANO criteria have played a key role in detecting early tumor progression, their ability to identify pseudoprogression is limited by post-treatment damage to the blood-brain barrier (BBB), which often leads to contrast enhancement on MRI and correlates poorly to tumor status. Amino acid positron emission tomography (AA PET) is a rapidly growing imaging modality in neuro-oncology. While contrast-enhanced MRI relies on leaky vascularity or a compromised BBB for delivery of contrast agents, amino acid tracers can cross the BBB, making AA PET particularly well-suited for monitoring treatment response and diagnosing pseudoprogression. The authors performed a systematic review of PubMed, MEDLINE, and Embase through December 2021 with the search terms “temozolomide” OR “Temodar,” “glioma” OR “glioblastoma,” “PET,” and “amino acid.” There were 19 studies meeting inclusion criteria. Thirteen studies utilized [(18)F]FET, five utilized [(11)C]MET, and one utilized both. All studies used static AA PET parameters to evaluate TMZ treatment in glioma patients, with nine using dynamic tracer parameters in addition. Throughout these studies, AA PET demonstrated utility in TMZ treatment monitoring and predicting patient survival. Oxford University Press 2022-02-13 /pmc/articles/PMC8923003/ /pubmed/35300149 http://dx.doi.org/10.1093/noajnl/vdac008 Text en © The Author(s) 2022. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of Neuro-Oncology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Review Prather, Kiana Y O’Neal, Christen M Westrup, Alison M Tullos, Hurtis J Hughes, Kendall L Conner, Andrew K Glenn, Chad A Battiste, James D A systematic review of amino acid PET in assessing treatment response to temozolomide in glioma |
title | A systematic review of amino acid PET in assessing treatment response to temozolomide in glioma |
title_full | A systematic review of amino acid PET in assessing treatment response to temozolomide in glioma |
title_fullStr | A systematic review of amino acid PET in assessing treatment response to temozolomide in glioma |
title_full_unstemmed | A systematic review of amino acid PET in assessing treatment response to temozolomide in glioma |
title_short | A systematic review of amino acid PET in assessing treatment response to temozolomide in glioma |
title_sort | systematic review of amino acid pet in assessing treatment response to temozolomide in glioma |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8923003/ https://www.ncbi.nlm.nih.gov/pubmed/35300149 http://dx.doi.org/10.1093/noajnl/vdac008 |
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