4.5 Article

MRI radiomics analysis of molecular alterations in low-grade gliomas

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s11548-017-1691-5

Keywords

MRI; Radiomics; Low-grade gliomas; 1p/19q Codeletion; Machine learning classifiers

Ask authors/readers for more resources

Low-grade gliomas (LGG) are classified into three distinct groups based on their IDH1 mutation and 1p/19q codeletion status, each of which is associated with a different clinical expression. The genomic sub-classification of LGG requires tumor sampling via neurosurgical procedures. The aim of this study was to evaluate the radiomics approach for noninvasive classification of patients with LGG and IDH mutation, based on their 1p/19q codeletion status, by testing different classifiers and assessing the contribution of the different MR contrasts. Preoperative MRI scans of 47 patients diagnosed with LGG with IDH1-mutated tumors and a genetic analysis for 1p/19q deletion status were included in this study. A total of 152 features, including size, location and texture, were extracted from fluid-attenuated inversion recovery images, -weighted images (WI) and post-contrast . Classification was performed using 17 machine learning classifiers. Results were evaluated by a fivefold cross-validation analysis. Radiomic analysis differentiated tumors with 1p/19q intact (; astrocytomas) from those with 1p/19q codeleted (; oligodendrogliomas). Best classification was obtained using the Ensemble Bagged Trees classifier, with sensitivity 92%, specificity 83% and accuracy 87%, and with area under the curve 0.87. Tumors with 1p/19q intact were larger than those with 1p/19q codeleted ( vs. cc, respectively; ) and predominantly located to the left insula (). The proposed method yielded good discrimination between LGG with and without 1p/19q codeletion. Results from this study demonstrate the great potential of this method to aid decision-making in the clinical management of patients with LGG.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available