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Relationship between Glioblastoma Dose Volume Parameters Measured by Dual Time Point Fluoroethylthyrosine-PET and Clinical Outcomes

Glioblastoma multiforme (GBM) is highly invasive. Despite irradiation with wide margins, GBM usually recurs in-field. Recent in vitro data have suggested that progression might be promoted by sublethal irradiation. Fluoroethylthyrosine-PET (FET-PET) can be used to detect glioblastoma invasion not ap...

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Autores principales: Harat, Maciej, Małkowski, Bogdan, Wiatrowska, Izabela, Makarewicz, Roman, Roszkowski, Krzysztof
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5786516/
https://www.ncbi.nlm.nih.gov/pubmed/29403428
http://dx.doi.org/10.3389/fneur.2017.00756
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author Harat, Maciej
Małkowski, Bogdan
Wiatrowska, Izabela
Makarewicz, Roman
Roszkowski, Krzysztof
author_facet Harat, Maciej
Małkowski, Bogdan
Wiatrowska, Izabela
Makarewicz, Roman
Roszkowski, Krzysztof
author_sort Harat, Maciej
collection PubMed
description Glioblastoma multiforme (GBM) is highly invasive. Despite irradiation with wide margins, GBM usually recurs in-field. Recent in vitro data have suggested that progression might be promoted by sublethal irradiation. Fluoroethylthyrosine-PET (FET-PET) can be used to detect glioblastoma invasion not apparent on MRI. We therefore performed a retrospective analysis of a prospective clinical study to examine whether glioblastoma outcomes depend on dose volume parameters measured by MRI and FET-PET. Twenty-three patients were prospectively recruited to a study examining the role of dual time point FET-PET in the treatment planning of GBM radiotherapy. The dose delivered to the site of recurrence was subdivided into suboptimal-dose (SOD) and high-dose (HD) areas. Types of progression were defined for correlation with dosimetric parameters including V100% of gross tumor volume (GTV)(PET), GTV(PETMRI), and GTV(MRI). The HD area did not cover the entire GTV(PETMRI) in any case. Recurrences were significantly more frequent in the SubD area (chi-squared test, p = 0.004). There was no relationship between increasing dose volume and progression. The V100% for GTV(PET) and progression-free survival (PFS) was positively correlated (Spearman’s rho 0.417; p = 0.038). Progression is more common in areas with suboptimal dosing. Dose heterogeneity within GTV(PET) may be responsible for shorter PFS.
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spelling pubmed-57865162018-02-05 Relationship between Glioblastoma Dose Volume Parameters Measured by Dual Time Point Fluoroethylthyrosine-PET and Clinical Outcomes Harat, Maciej Małkowski, Bogdan Wiatrowska, Izabela Makarewicz, Roman Roszkowski, Krzysztof Front Neurol Neuroscience Glioblastoma multiforme (GBM) is highly invasive. Despite irradiation with wide margins, GBM usually recurs in-field. Recent in vitro data have suggested that progression might be promoted by sublethal irradiation. Fluoroethylthyrosine-PET (FET-PET) can be used to detect glioblastoma invasion not apparent on MRI. We therefore performed a retrospective analysis of a prospective clinical study to examine whether glioblastoma outcomes depend on dose volume parameters measured by MRI and FET-PET. Twenty-three patients were prospectively recruited to a study examining the role of dual time point FET-PET in the treatment planning of GBM radiotherapy. The dose delivered to the site of recurrence was subdivided into suboptimal-dose (SOD) and high-dose (HD) areas. Types of progression were defined for correlation with dosimetric parameters including V100% of gross tumor volume (GTV)(PET), GTV(PETMRI), and GTV(MRI). The HD area did not cover the entire GTV(PETMRI) in any case. Recurrences were significantly more frequent in the SubD area (chi-squared test, p = 0.004). There was no relationship between increasing dose volume and progression. The V100% for GTV(PET) and progression-free survival (PFS) was positively correlated (Spearman’s rho 0.417; p = 0.038). Progression is more common in areas with suboptimal dosing. Dose heterogeneity within GTV(PET) may be responsible for shorter PFS. Frontiers Media S.A. 2018-01-22 /pmc/articles/PMC5786516/ /pubmed/29403428 http://dx.doi.org/10.3389/fneur.2017.00756 Text en Copyright © 2018 Harat, Małkowski, Wiatrowska, Makarewicz and Roszkowski. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Harat, Maciej
Małkowski, Bogdan
Wiatrowska, Izabela
Makarewicz, Roman
Roszkowski, Krzysztof
Relationship between Glioblastoma Dose Volume Parameters Measured by Dual Time Point Fluoroethylthyrosine-PET and Clinical Outcomes
title Relationship between Glioblastoma Dose Volume Parameters Measured by Dual Time Point Fluoroethylthyrosine-PET and Clinical Outcomes
title_full Relationship between Glioblastoma Dose Volume Parameters Measured by Dual Time Point Fluoroethylthyrosine-PET and Clinical Outcomes
title_fullStr Relationship between Glioblastoma Dose Volume Parameters Measured by Dual Time Point Fluoroethylthyrosine-PET and Clinical Outcomes
title_full_unstemmed Relationship between Glioblastoma Dose Volume Parameters Measured by Dual Time Point Fluoroethylthyrosine-PET and Clinical Outcomes
title_short Relationship between Glioblastoma Dose Volume Parameters Measured by Dual Time Point Fluoroethylthyrosine-PET and Clinical Outcomes
title_sort relationship between glioblastoma dose volume parameters measured by dual time point fluoroethylthyrosine-pet and clinical outcomes
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5786516/
https://www.ncbi.nlm.nih.gov/pubmed/29403428
http://dx.doi.org/10.3389/fneur.2017.00756
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