Background and Purpose: WHO grade II gliomas are divided into three classes: Isocitrate dehydrogenase (IDH)-wildtype, IDH-mutant and no 1p/19q codeletion, and IDH-mutant and 1p/19q-codeleted. Different molecular subtypes have been reported to have prognostic differences and different chemosensitivity. Our aim was to evaluate the predictive value of imaging phenotypes assessed with the Visually AcceSAble Rembrandt Images lexicon for molecular classification of lower grade gliomas. Materialsandmethods: MRimaging scans of 175 patients with lower grade gliomas with known IDH1 mutation and 1p/19q-codeletion status were included (78 grade II and 97 grade III) in the discovery set. MR imaging features were reviewed by using Visually AcceSAble Rembrandt Images (VASARI); their associations with molecular markers were assessed. The predictive power of imaging features for IDH1-wild type tumors was evaluated using the Least Absolute Shrinkage and Selection Operator. We tested the model in a validation set (40 subjects). Results: Various imaging features were significantly different according to IDH1 mutation. Nonlobar location, larger proportion of enhancing tumors, multifocal/multicentric distribution, and poor definition of nonenhancing margins were independent predictors of an IDH1 wild type according to the Least Absolute Shrinkage and Selection Operator. The areas under the curve for the prediction model were 0.859 and 0.778 in the discovery and validation sets, respectively. The IDH1-mutant, 1p/19q-codeleted group frequently had mixed/restricted diffusion characteristics and showed more pial invasion compared with the IDH1-mutant, no codeletion group. Conclusions: Preoperative MR imaging phenotypes are different according to the molecular markers of lower grade gliomas, and they may be helpful in predicting the IDH1-mutation status.
Bibliographical noteFunding Information:
Received May 26, 2017; accepted after revision August 14. From the Department of Radiology (Y.W.P.), Ewha Womans University College of Medicine, Seoul, Korea; and Departments of Radiology and Research Institute of Radiological Science (Y.W.P., K.H., S.-K.L., S.B., Y.S.C., S.S.A.), Neurosurgery (J.H.C., S.-G.K.), and Pathology (S.H.K.), Yonsei University College of Medicine, Seoul, Korea. S.S. Ahn was supported by faculty research grants of the Yonsei University College of Medicine (6-2015-0079).
Disclosures: Yae Won Park—RELATED: Grant: Yonsei University College of Medicine (6-2015-0079), Comments: faculty research grants of the Yonsei University College of Medicine (6-2015-0079)*. *Money paid to the institution.
All Science Journal Classification (ASJC) codes
- Radiology Nuclear Medicine and imaging
- Clinical Neurology