Conventional MRI features can predict the molecular subtype of adult grade 2–3 intracranial diffuse gliomas.

Purpose: Molecular biomarkers are important for classifying intracranial gliomas, prompting research into correlating imaging with genotype ("radiogenomics"). A limitation of the existing radiogenomics literature is the paucity of studies specifically characterizing grade 2–3 gliomas into the three...

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Publicado en:Neuroradiology Vol. 64; no. 12; pp. 2295 - 2306
Autores principales: Lasocki, Arian, Buckland, Michael E., Drummond, Katharine J., Wei, Heng, Xie, Jing, Christie, Michael, Neal, Andrew, Gaillard, Frank
Formato: diagnostic images research tables/charts Journal Article
Publicado: Springer Nature Dec2022
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Dec2022
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      pub: Springer Nature
      place: New York, New York
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        10.1007/s00234-022-02975-0
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        atl: Conventional MRI features can predict the molecular subtype of adult grade 2–3 intracranial diffuse gliomas.
      aug:
        au:
          Lasocki, Arian
          Buckland, Michael E.
          Drummond, Katharine J.
          Wei, Heng
          Xie, Jing
          Christie, Michael
          Neal, Andrew
          Gaillard, Frank
        affil: Department of Cancer Imaging, Peter MacCallum Cancer Centre, Melbourne, VIC, Australia
      sug:
        subj:
          Glioma Diagnosis
          Magnetic Resonance Imaging
          Pathology, Molecular
          Genotype
          Human
          Tumor Markers, Biological
          Neuroradiography
          Algorithms
      ab: Purpose: Molecular biomarkers are important for classifying intracranial gliomas, prompting research into correlating imaging with genotype ("radiogenomics"). A limitation of the existing radiogenomics literature is the paucity of studies specifically characterizing grade 2–3 gliomas into the three key molecular subtypes. Our study investigated the accuracy of multiple different conventional MRI features for genotype prediction. Methods: Grade 2–3 gliomas diagnosed between 2007 and 2013 were identified. Two neuroradiologists independently assessed nine conventional MRI features. Features with better inter-observer agreement (κ ≥ 0.6) proceeded to consensus assessment. MRI features were correlated with genotype, classified as IDH-mutant and 1p/19q-codeleted (IDHmut/1p19qcodel), IDH-mutant and 1p/19q-intact (IDHmut/1p19qint), or IDH-wildtype (IDHwt). For IDHwt tumors, additional molecular markers of glioblastoma were noted. Results: One hundred nineteen patients were included. T2-FLAIR mismatch (stratified as > 50%, 25–50%, or < 25%) was the most predictive feature across genotypes (p < 0.001). All 30 tumors with > 50% mismatch were IDHmut/1p19qint, and all seven with 25–50% mismatch. Well-defined margins correlated with IDHmut/1p19qint status on univariate analysis (p < 0.001), but this related to correlation with T2-FLAIR mismatch; there was no longer an association when considering only tumors with < 25% mismatch (p = 0.386). Enhancement (p = 0.001), necrosis (p = 0.002), and hemorrhage (p = 0.027) correlated with IDHwt status (especially "molecular glioblastoma"). Calcification correlated with IDHmut/1p19qcodel status (p = 0.003). A simple, step-wise algorithm incorporating these features, when present, correctly predicted genotype with a positive predictive value 91.8%. Conclusion: T2-FLAIR mismatch strongly predicts IDHmut/1p19qint even with a lower threshold of ≥ 25% mismatch and outweighs other features. Secondary features include enhancement, necrosis and hemorrhage (predicting IDHwt, especially "molecular glioblastoma"), and calcification (predicting IDHmut/1p19qcodel).
      pubtype: Academic Journal
      doctype:
        diagnostic images
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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