Deep learning classifier for MGMT promoter methylation status in glioblastoma cancer
Javier Barranco Garcia,
Switzerland
PO-1766
Abstract
Deep learning classifier for MGMT promoter methylation status in glioblastoma cancer
Authors: Javier Barranco Garcia1, Daniel Abler2, Mauricio Reyes3, Diem Voung1, Matthias Guckenberger4, Stephanie Tanadini-Lang4, Adrien Depeursinge5
1USZ, Radio Oncology Clinic, Zurich, Switzerland; 2HES-SO Valais-Wallis, Institute of Information Systems, Sierre, Switzerland; 3University of Bern, ARTORG Center for Biomedical Research, Bern, Switzerland; 4USZ, Radio Oncology Clinic , Zurich, Switzerland; 5HES-SO Valais-Wallis, Institute of Information Systems, Sierre, Switzerland
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Purpose or Objective
O6-methylguanine-DNA-methyltransferase
(MGMT)
promoter methylation status in glioblastoma cancer is accepted as a
promising prognostic and predictive biomarker. We explore the
possibility of deep learning algorithms to predict the presence of
MGMT status in MRI imaging as a non-invasive method.
Material and Methods
The
RSNA and the MICCAI collaboration provided a dataset composed of 582
patients with four MRI modalities included (T1, T1ce, T2, FLAIR).
MGMT status was encoded with 0/1. Out of the 582 patients, 306 were
methylated and 276 not. The dataset was divided into
training/validation (90%) and test (10%). using a random split. Then
training and validation are splitted 80/20. The raw images are pre-processed: a)
bias correction, b) normalization z-score and c) cropping and
resampling to fit the entire brain (across all patients) into
144x144x144 voxels. To build the classifier we used two publicly
available pre-trained image classifiers models to initialize the
weights (ResNet50 and DenseNet121). Prior to training the networks,
the 2D slice with the largest tumor area is selected in the
horizontal view. For the largest tumor size, the surrounding bounding
box is calculated and each image is cropped from the center of mass
of the mask. This ensures that the tumor
surrounding tissue is taken into consideration by the model.
To combine the information of the different modalities the RGB
channels were replaced with 3 modalities. Different techniques of
data augmentation were used to prevent overfitting and improve
performance. Affine transformations including horizontal and vertical
translations and z-rotations were applied to the input images. The
model was evaluated first for each modality independently using
5-fold cross validation.
Results
FLAIR
obtained the best performance with DenseNet121 architecture with
validation and test accuracies (0.7429,0.5953).
We evaluate in groups of 3 modalities obtaining the best performance
for the combination of (T1, T1ce and FLAIR) with validation and test
accuracies of (0.7124, 0.6245) with the others combinations showing
lower but close accuracies. Finally, data augmentation was performed
during each epoch leading to similar results with the best
combination again (T1, T1ce and FLAIR) and accuracies of (0.7035,
0.6355).
Conclusion
Deep
learning classifiers shows promising results to predict the MGMT
status in glioblastoma cancer. Combination of different modalities
and data augmentation techniques improved the accuracy of the model.