Cargando…

Multiparameter quantitative histological MRI values in high-grade gliomas: a potential biomarker of tumor progression

BACKGROUND: Conventional MRI poorly distinguishes brain parenchyma microscopically invaded by high-grade gliomas (HGGs) from the normal brain. By contrast, quantitative histological MRI (hMRI) measures brain microstructure in terms of physical MR parameters influenced by histochemical tissue composi...

Descripción completa

Detalles Bibliográficos
Autores principales: Reuter, Gilles, Lommers, Emilie, Balteau, Evelyne, Simon, Jessica, Phillips, Christophe, Scholtes, Felix, Martin, Didier, Lombard, Arnaud, Maquet, Pierre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7716186/
https://www.ncbi.nlm.nih.gov/pubmed/33304600
http://dx.doi.org/10.1093/nop/npaa047
_version_ 1783619109186961408
author Reuter, Gilles
Lommers, Emilie
Balteau, Evelyne
Simon, Jessica
Phillips, Christophe
Scholtes, Felix
Martin, Didier
Lombard, Arnaud
Maquet, Pierre
author_facet Reuter, Gilles
Lommers, Emilie
Balteau, Evelyne
Simon, Jessica
Phillips, Christophe
Scholtes, Felix
Martin, Didier
Lombard, Arnaud
Maquet, Pierre
author_sort Reuter, Gilles
collection PubMed
description BACKGROUND: Conventional MRI poorly distinguishes brain parenchyma microscopically invaded by high-grade gliomas (HGGs) from the normal brain. By contrast, quantitative histological MRI (hMRI) measures brain microstructure in terms of physical MR parameters influenced by histochemical tissue composition. We aimed to determine the relationship between hMRI parameters in the area surrounding the surgical cavity and the presence of HGG recurrence. METHODS: Patients were scanned after surgery with an hMRI multiparameter protocol that allowed for estimations of longitudinal relaxation rate (R1) = 1/T1, effective transverse relaxation rate (R2)*=1/T2*, magnetization transfer saturation (MT(sat)), and proton density. The initial perioperative zone (IPZ) was segmented on the postoperative MRI. Once recurrence appeared on conventional MRI, the area of relapsing disease was delineated (extension zone, EZ). Conventional MRI showing recurrence and hMRI were coregistered, allowing for the extraction of parameters R1, R2*, MT(sat), and PD in 3 areas: the overlap area between the IPZ and EZ (OZ), the peritumoral brain zone, PBZ (PBZ = IPZ – OZ), and the area of recurrence (RZ = EZ – OZ). RESULTS: Thirty-one patients with HGG who underwent gross-total resection were enrolled. MT(sat) and R1 were the most strongly associated with tumor progression. MT(sat) was significantly lower in the OZ and RZ, compared to PBZ. R1 was significantly lower in RZ compared to PBZ. PD was significantly higher in OZ compared to PBZ, and R2* was higher in OZ compared to PBZ or RZ. These changes were detected 4 to 120 weeks before recurrence recognition on conventional MRI. CONCLUSIONS: HGG recurrence was associated with hMRI parameters’ variation after initial surgery, weeks to months before overt recurrence.
format Online
Article
Text
id pubmed-7716186
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-77161862020-12-09 Multiparameter quantitative histological MRI values in high-grade gliomas: a potential biomarker of tumor progression Reuter, Gilles Lommers, Emilie Balteau, Evelyne Simon, Jessica Phillips, Christophe Scholtes, Felix Martin, Didier Lombard, Arnaud Maquet, Pierre Neurooncol Pract Original Articles BACKGROUND: Conventional MRI poorly distinguishes brain parenchyma microscopically invaded by high-grade gliomas (HGGs) from the normal brain. By contrast, quantitative histological MRI (hMRI) measures brain microstructure in terms of physical MR parameters influenced by histochemical tissue composition. We aimed to determine the relationship between hMRI parameters in the area surrounding the surgical cavity and the presence of HGG recurrence. METHODS: Patients were scanned after surgery with an hMRI multiparameter protocol that allowed for estimations of longitudinal relaxation rate (R1) = 1/T1, effective transverse relaxation rate (R2)*=1/T2*, magnetization transfer saturation (MT(sat)), and proton density. The initial perioperative zone (IPZ) was segmented on the postoperative MRI. Once recurrence appeared on conventional MRI, the area of relapsing disease was delineated (extension zone, EZ). Conventional MRI showing recurrence and hMRI were coregistered, allowing for the extraction of parameters R1, R2*, MT(sat), and PD in 3 areas: the overlap area between the IPZ and EZ (OZ), the peritumoral brain zone, PBZ (PBZ = IPZ – OZ), and the area of recurrence (RZ = EZ – OZ). RESULTS: Thirty-one patients with HGG who underwent gross-total resection were enrolled. MT(sat) and R1 were the most strongly associated with tumor progression. MT(sat) was significantly lower in the OZ and RZ, compared to PBZ. R1 was significantly lower in RZ compared to PBZ. PD was significantly higher in OZ compared to PBZ, and R2* was higher in OZ compared to PBZ or RZ. These changes were detected 4 to 120 weeks before recurrence recognition on conventional MRI. CONCLUSIONS: HGG recurrence was associated with hMRI parameters’ variation after initial surgery, weeks to months before overt recurrence. Oxford University Press 2020-08-15 /pmc/articles/PMC7716186/ /pubmed/33304600 http://dx.doi.org/10.1093/nop/npaa047 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Neuro-Oncology and the European Association of Neuro-Oncology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://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 Original Articles
Reuter, Gilles
Lommers, Emilie
Balteau, Evelyne
Simon, Jessica
Phillips, Christophe
Scholtes, Felix
Martin, Didier
Lombard, Arnaud
Maquet, Pierre
Multiparameter quantitative histological MRI values in high-grade gliomas: a potential biomarker of tumor progression
title Multiparameter quantitative histological MRI values in high-grade gliomas: a potential biomarker of tumor progression
title_full Multiparameter quantitative histological MRI values in high-grade gliomas: a potential biomarker of tumor progression
title_fullStr Multiparameter quantitative histological MRI values in high-grade gliomas: a potential biomarker of tumor progression
title_full_unstemmed Multiparameter quantitative histological MRI values in high-grade gliomas: a potential biomarker of tumor progression
title_short Multiparameter quantitative histological MRI values in high-grade gliomas: a potential biomarker of tumor progression
title_sort multiparameter quantitative histological mri values in high-grade gliomas: a potential biomarker of tumor progression
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7716186/
https://www.ncbi.nlm.nih.gov/pubmed/33304600
http://dx.doi.org/10.1093/nop/npaa047
work_keys_str_mv AT reutergilles multiparameterquantitativehistologicalmrivaluesinhighgradegliomasapotentialbiomarkeroftumorprogression
AT lommersemilie multiparameterquantitativehistologicalmrivaluesinhighgradegliomasapotentialbiomarkeroftumorprogression
AT balteauevelyne multiparameterquantitativehistologicalmrivaluesinhighgradegliomasapotentialbiomarkeroftumorprogression
AT simonjessica multiparameterquantitativehistologicalmrivaluesinhighgradegliomasapotentialbiomarkeroftumorprogression
AT phillipschristophe multiparameterquantitativehistologicalmrivaluesinhighgradegliomasapotentialbiomarkeroftumorprogression
AT scholtesfelix multiparameterquantitativehistologicalmrivaluesinhighgradegliomasapotentialbiomarkeroftumorprogression
AT martindidier multiparameterquantitativehistologicalmrivaluesinhighgradegliomasapotentialbiomarkeroftumorprogression
AT lombardarnaud multiparameterquantitativehistologicalmrivaluesinhighgradegliomasapotentialbiomarkeroftumorprogression
AT maquetpierre multiparameterquantitativehistologicalmrivaluesinhighgradegliomasapotentialbiomarkeroftumorprogression