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T2 mapping of the peritumoral infiltration zone of glioblastoma and anaplastic astrocytoma

PURPOSE: To characterise peritumoral zones in glioblastoma and anaplastic astrocytoma evaluating T2 values using T2 mapping sequences. MATERIALS AND METHODS: In this study, 41 patients with histopathologically confirmed World Health Organization high grade gliomas and preoperative magnetic resonance...

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Autores principales: Auer, Timo Alexander, Kern, Maike, Fehrenbach, Uli, Tanyldizi, Yasemin, Misch, Martin, Wiener, Edzard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8551439/
https://www.ncbi.nlm.nih.gov/pubmed/33573473
http://dx.doi.org/10.1177/1971400921989325
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author Auer, Timo Alexander
Kern, Maike
Fehrenbach, Uli
Tanyldizi, Yasemin
Misch, Martin
Wiener, Edzard
author_facet Auer, Timo Alexander
Kern, Maike
Fehrenbach, Uli
Tanyldizi, Yasemin
Misch, Martin
Wiener, Edzard
author_sort Auer, Timo Alexander
collection PubMed
description PURPOSE: To characterise peritumoral zones in glioblastoma and anaplastic astrocytoma evaluating T2 values using T2 mapping sequences. MATERIALS AND METHODS: In this study, 41 patients with histopathologically confirmed World Health Organization high grade gliomas and preoperative magnetic resonance imaging examinations were retrospectively identified and enrolled. High grade gliomas were differentiated: (a) by grade, glioblastoma versus anaplastic astrocytoma; and (b) by isocitrate dehydrogenase mutational state, mutated versus wildtype. T2 map relaxation times were assessed from the tumour centre to peritumoral zones by means of a region of interest and calculated pixelwise by using a fit model. RESULTS: Significant differences between T2 values evaluated from the tumour centre to the peritumoral zone were found between glioblastoma and anaplastic astrocytoma, showing a higher decrease in signal intensity (T2 value) from tumour centre to periphery for glioblastoma (P = 0.0049 – fit-model: glioblastoma –25.02± 19.89 (–54–10); anaplastic astrocytoma –5.57±22.94 (–51–47)). Similar results were found when the cohort was subdivided by their isocitrate dehydrogenase profile, showing an increased drawdown from tumour centre to periphery for wildtype in comparison to mutated isocitrate dehydrogenase (P = 0.0430 – fit model: isocitrate dehydrogenase wildtype –10.35±16.20 (–51) – 0; isocitrate dehydrogenase mutated 12.14±21.24 (–15–47)). A strong statistical proof for both subgroup analyses (P = 0.9987 – glioblastoma R(2) 0.93±0.08; anaplastic astrocytoma R(2) 0.94±0.15) was found. CONCLUSION: Peritumoral T2 mapping relaxation time tissue behaviour of glioblastoma differs from anaplastic astrocytoma. Significant differences in T2 values, using T2 mapping relaxation time, were found between glioblastoma and anaplastic astrocytoma, capturing the tumour centre to the peritumoral zone. A similar curve progression from tumour centre to peritumoral zone was found for isocitrate dehydrogenase wildtype high grade gliomas in comparison to isocitrate dehydrogenase mutated high grade gliomas. This finding is in accordance with the biologically more aggressive behaviour of isocitrate dehydrogenase wildtype in comparison to isocitrate dehydrogenase mutated high grade gliomas. These results emphasize the potential of mapping techniques to reflect the tissue composition of high grade gliomas.
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spelling pubmed-85514392021-10-29 T2 mapping of the peritumoral infiltration zone of glioblastoma and anaplastic astrocytoma Auer, Timo Alexander Kern, Maike Fehrenbach, Uli Tanyldizi, Yasemin Misch, Martin Wiener, Edzard Neuroradiol J Original Articles PURPOSE: To characterise peritumoral zones in glioblastoma and anaplastic astrocytoma evaluating T2 values using T2 mapping sequences. MATERIALS AND METHODS: In this study, 41 patients with histopathologically confirmed World Health Organization high grade gliomas and preoperative magnetic resonance imaging examinations were retrospectively identified and enrolled. High grade gliomas were differentiated: (a) by grade, glioblastoma versus anaplastic astrocytoma; and (b) by isocitrate dehydrogenase mutational state, mutated versus wildtype. T2 map relaxation times were assessed from the tumour centre to peritumoral zones by means of a region of interest and calculated pixelwise by using a fit model. RESULTS: Significant differences between T2 values evaluated from the tumour centre to the peritumoral zone were found between glioblastoma and anaplastic astrocytoma, showing a higher decrease in signal intensity (T2 value) from tumour centre to periphery for glioblastoma (P = 0.0049 – fit-model: glioblastoma –25.02± 19.89 (–54–10); anaplastic astrocytoma –5.57±22.94 (–51–47)). Similar results were found when the cohort was subdivided by their isocitrate dehydrogenase profile, showing an increased drawdown from tumour centre to periphery for wildtype in comparison to mutated isocitrate dehydrogenase (P = 0.0430 – fit model: isocitrate dehydrogenase wildtype –10.35±16.20 (–51) – 0; isocitrate dehydrogenase mutated 12.14±21.24 (–15–47)). A strong statistical proof for both subgroup analyses (P = 0.9987 – glioblastoma R(2) 0.93±0.08; anaplastic astrocytoma R(2) 0.94±0.15) was found. CONCLUSION: Peritumoral T2 mapping relaxation time tissue behaviour of glioblastoma differs from anaplastic astrocytoma. Significant differences in T2 values, using T2 mapping relaxation time, were found between glioblastoma and anaplastic astrocytoma, capturing the tumour centre to the peritumoral zone. A similar curve progression from tumour centre to peritumoral zone was found for isocitrate dehydrogenase wildtype high grade gliomas in comparison to isocitrate dehydrogenase mutated high grade gliomas. This finding is in accordance with the biologically more aggressive behaviour of isocitrate dehydrogenase wildtype in comparison to isocitrate dehydrogenase mutated high grade gliomas. These results emphasize the potential of mapping techniques to reflect the tissue composition of high grade gliomas. SAGE Publications 2021-02-11 2021-10 /pmc/articles/PMC8551439/ /pubmed/33573473 http://dx.doi.org/10.1177/1971400921989325 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Articles
Auer, Timo Alexander
Kern, Maike
Fehrenbach, Uli
Tanyldizi, Yasemin
Misch, Martin
Wiener, Edzard
T2 mapping of the peritumoral infiltration zone of glioblastoma and anaplastic astrocytoma
title T2 mapping of the peritumoral infiltration zone of glioblastoma and anaplastic astrocytoma
title_full T2 mapping of the peritumoral infiltration zone of glioblastoma and anaplastic astrocytoma
title_fullStr T2 mapping of the peritumoral infiltration zone of glioblastoma and anaplastic astrocytoma
title_full_unstemmed T2 mapping of the peritumoral infiltration zone of glioblastoma and anaplastic astrocytoma
title_short T2 mapping of the peritumoral infiltration zone of glioblastoma and anaplastic astrocytoma
title_sort t2 mapping of the peritumoral infiltration zone of glioblastoma and anaplastic astrocytoma
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8551439/
https://www.ncbi.nlm.nih.gov/pubmed/33573473
http://dx.doi.org/10.1177/1971400921989325
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