Distinguishing glioblastoma progression from treatment-related changes using DTI directionality growth analysis

被引:0
作者
van den Elshout, R. [1 ]
Ariens, B. [2 ,6 ]
Esmaeili, M. [3 ,4 ]
Akkurt, B. [5 ]
Mannil, M. [5 ,6 ]
Meijer, F. J. A. [1 ]
van der Kolk, A. G. [1 ]
Scheenen, T. W. J. [1 ]
Henssen, D. [1 ]
机构
[1] Radboud Univ Nijmegen, Dept Med Imaging, Med Ctr, Geert Grootepl Zuid 10, NL-6525 GA Nijmegen, Netherlands
[2] AmsterdamUMC, Radiol & Nucl Med, Amsterdam, Netherlands
[3] Akershus Univ Hosp, Dept Diagnost Imaging, Lorenskog, Norway
[4] Univ Stavanger, Dept Elect Engn & Comp Sci, Stavanger, Norway
[5] Westfal Wilhelms Univ Muenster, Univ Clin Radiol, Munster, Germany
[6] Univ Hosp Muenster, Munster, Germany
关键词
Glioblastoma; MRI; DTI; Lesion development; Satellitosis; DIFFUSION; BRAIN; PSEUDOPROGRESSION; ANTS;
D O I
10.1007/s00234-024-03450-8
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BackgroundIt is difficult to distinguish between tumor progression (TP) and treatment-related abnormalities (TRA) in treated glioblastoma patients via conventional MRI, but this distinction is crucial for treatment decision making. Glioblastoma is known to exhibit an invasive growth pattern along white matter architecture and vasculature. This study quantified lesion development patterns in treated glioblastoma lesions and their relation to white matter microstructure to distinguish TP from TRA.Materials and methodsGlioblastoma patients with confirmed TP or TRA with T1-weighted contrast-enhanced and DTI MR scans from two posttreatment follow-up timepoints were reviewed. The contrast-enhancing regions were segmented, and the regions were coregistered to the DTI data. Lesion increase vectors were categorized into two groups: parallel (0-20 degrees) and perpendicular (70-90 degrees) to white matter. FA-values were also extracted. To test for a statistically significant difference between the TP and TRA groups, a Mann-Whitney U test was performed.ResultsOf 73 glioblastoma patients, fifteen were diagnosed with TRA, whereas 58 patients suffered TP. TP had a 25.8% (95% CI 24.1%-27.6%) increase in parallel lesions, and TRA had a 25.4% (95% CI 20.9%-29.9%) increase in parallel lesions. The perpendicular increase was 14.7% for TP (95% CI 13.0%-16.4%) and 18.0% (95% CI 13.5%-22.5%) for TRA. These results were not significantly different (p = 0.978). FA value for TP showed to be 0.248 (SD = 0.054) and for TRA it was 0.231 (SD = 0.075), showing no statistically significant difference (p = 0.121).ConclusionsBased on our results, quantifying posttreatment contrast-enhancing lesion development directionality with DTI in glioblastoma patients does not appear to effectively distinguish between TP and TRA.
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收藏
页码:2143 / 2151
页数:9
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