4.5 Article

Meta-Analysis of Diffusion Metrics for the Prediction of Tumor Grade in Gliomas

Journal

AMERICAN JOURNAL OF NEURORADIOLOGY
Volume 36, Issue 2, Pages 302-308

Publisher

AMER SOC NEURORADIOLOGY
DOI: 10.3174/ajnr.A4097

Keywords

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Funding

  1. NCI NIH HHS [R01 CA161404, 1R01CA161404-01A] Funding Source: Medline
  2. NHLBI NIH HHS [R01 HL071944, 2R01HL071944-06] Funding Source: Medline

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BACKGROUND AND PURPOSE: Diffusion-tensor-metrics are potential-in-vivo quantitative neuroimaging biomarkers for the characterization of brain tumor subtype. This meta-analysis analyzes the ability of mean diffusivity and fractional anisotropy to distinguish low-grade from high-grade gliomas in the identifiable tumor core and the region of peripheral edema. MATERIALS AND METHODS: A meta-analysis of articles with mean diffusivity and fractional anisotropy data for World Health Organization low-grade (I, II) and high-grade (III, IV) gliomas, between 2000 and 2013, was performed. Pooled data were analyzed by using the odds ratio and mean difference. Receiver operating characteristic analysis was performed for patient-level data. RESULTS: The minimum mean diffusivity of high-grade gliomas was decreased compared with low-grade gliomas. High-grade gliomas had decreased average mean diffusivity values compared with low-grade gliomas in the tumor core and increased average mean diffusivity values in the peripheral region. High-grade gliomas had increased FA values compared with low-grade gliomas in the tumor core, decreased values in the peripheral region, and a decreased fractional anisotropy difference between the tumor core and peripheral region. CONCLUSIONS: The minimum mean diffusivity differs significantly with respect to the World Health Organization grade of gliomas. Statistically significant effects of tumor grade on average mean diffusivity and fractional anisotropy were observed, supporting the concept that high-grade tumors are more destructive and infiltrative than low-grade tumors. Considerable heterogeneity within the literature may be due to systematic factors in addition to underlying lesion heterogeneity.

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