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T2/FLAIR Abnormity Could be the Sign of Glioblastoma Dissemination

PURPOSE: Newly emerged or constantly enlarged contrast-enhancing (CE) lesions were the necessary signs for the diagnosis of glioblastoma (GBM) progression. This study aimed to investigate whether the T2-weighted-Fluid-Attenuated Inversion Recovery (T2/FLAIR) abnormal transformation could predict and...

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Autores principales: Li, Mingxiao, Huang, Wei, Chen, Hongyan, Jiang, Haihui, Yang, Chuanwei, Shen, Shaoping, Cui, Yong, Dong, Gehong, Ren, Xiaohui, Lin, Song
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8849106/
https://www.ncbi.nlm.nih.gov/pubmed/35185770
http://dx.doi.org/10.3389/fneur.2022.819216
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author Li, Mingxiao
Huang, Wei
Chen, Hongyan
Jiang, Haihui
Yang, Chuanwei
Shen, Shaoping
Cui, Yong
Dong, Gehong
Ren, Xiaohui
Lin, Song
author_facet Li, Mingxiao
Huang, Wei
Chen, Hongyan
Jiang, Haihui
Yang, Chuanwei
Shen, Shaoping
Cui, Yong
Dong, Gehong
Ren, Xiaohui
Lin, Song
author_sort Li, Mingxiao
collection PubMed
description PURPOSE: Newly emerged or constantly enlarged contrast-enhancing (CE) lesions were the necessary signs for the diagnosis of glioblastoma (GBM) progression. This study aimed to investigate whether the T2-weighted-Fluid-Attenuated Inversion Recovery (T2/FLAIR) abnormal transformation could predict and assess progression for GBMs, especially for tumor dissemination. METHODS: A consecutive cohort of 246 GBM patients with regular follow-up and sufficient radiological data was included in this study. The series of T2/FLAIR and T1CE images were retrospectively reviewed. The patients were separated into T2/FLAIR and T1CE discordant and accordant subgroups based on the initial progression images. RESULTS: A total of 170 qualified patients were finally analyzed. The incidence of discordant T2/FLAIR and T1CE images was 25.9% (44/170). The median time-span of T2/FLAIR indicated tumor progression was 119.5 days (ranging from 57 days-unreached) prior to T1CE. Nearly half of patients (20/44, 45.5%) in the discordant subgroup suffered from tumor dissemination, substantially higher than accordant patients (23/126, 20.6%, p < 0.001). The median time to progression (TTP), post-progression survival (PPS), and overall survival (OS) were not statistically different (all p > 0.05) between discordant and accordant patients. CONCLUSIONS: T2/FLAIR abnormity could be the sign of GBM progression, especially for newly emerged lesions disseminating from the primary cavity. Physicians should cast more attention on the dynamic change of T2/FLAIR images, which might be of great significance for progression assessment and subsequent clinical decision-making.
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spelling pubmed-88491062022-02-17 T2/FLAIR Abnormity Could be the Sign of Glioblastoma Dissemination Li, Mingxiao Huang, Wei Chen, Hongyan Jiang, Haihui Yang, Chuanwei Shen, Shaoping Cui, Yong Dong, Gehong Ren, Xiaohui Lin, Song Front Neurol Neurology PURPOSE: Newly emerged or constantly enlarged contrast-enhancing (CE) lesions were the necessary signs for the diagnosis of glioblastoma (GBM) progression. This study aimed to investigate whether the T2-weighted-Fluid-Attenuated Inversion Recovery (T2/FLAIR) abnormal transformation could predict and assess progression for GBMs, especially for tumor dissemination. METHODS: A consecutive cohort of 246 GBM patients with regular follow-up and sufficient radiological data was included in this study. The series of T2/FLAIR and T1CE images were retrospectively reviewed. The patients were separated into T2/FLAIR and T1CE discordant and accordant subgroups based on the initial progression images. RESULTS: A total of 170 qualified patients were finally analyzed. The incidence of discordant T2/FLAIR and T1CE images was 25.9% (44/170). The median time-span of T2/FLAIR indicated tumor progression was 119.5 days (ranging from 57 days-unreached) prior to T1CE. Nearly half of patients (20/44, 45.5%) in the discordant subgroup suffered from tumor dissemination, substantially higher than accordant patients (23/126, 20.6%, p < 0.001). The median time to progression (TTP), post-progression survival (PPS), and overall survival (OS) were not statistically different (all p > 0.05) between discordant and accordant patients. CONCLUSIONS: T2/FLAIR abnormity could be the sign of GBM progression, especially for newly emerged lesions disseminating from the primary cavity. Physicians should cast more attention on the dynamic change of T2/FLAIR images, which might be of great significance for progression assessment and subsequent clinical decision-making. Frontiers Media S.A. 2022-02-02 /pmc/articles/PMC8849106/ /pubmed/35185770 http://dx.doi.org/10.3389/fneur.2022.819216 Text en Copyright © 2022 Li, Huang, Chen, Jiang, Yang, Shen, Cui, Dong, Ren and Lin. https://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) and the copyright owner(s) 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 Neurology
Li, Mingxiao
Huang, Wei
Chen, Hongyan
Jiang, Haihui
Yang, Chuanwei
Shen, Shaoping
Cui, Yong
Dong, Gehong
Ren, Xiaohui
Lin, Song
T2/FLAIR Abnormity Could be the Sign of Glioblastoma Dissemination
title T2/FLAIR Abnormity Could be the Sign of Glioblastoma Dissemination
title_full T2/FLAIR Abnormity Could be the Sign of Glioblastoma Dissemination
title_fullStr T2/FLAIR Abnormity Could be the Sign of Glioblastoma Dissemination
title_full_unstemmed T2/FLAIR Abnormity Could be the Sign of Glioblastoma Dissemination
title_short T2/FLAIR Abnormity Could be the Sign of Glioblastoma Dissemination
title_sort t2/flair abnormity could be the sign of glioblastoma dissemination
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8849106/
https://www.ncbi.nlm.nih.gov/pubmed/35185770
http://dx.doi.org/10.3389/fneur.2022.819216
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