Faculty, Staff and Student Publications

Language

English

Publication Date

7-30-2024

Journal

Biomedical Physics & Engineering Express

DOI

10.1088/2057-1976/ad6573

PMID

39029475

PMCID

PMC11288403

PubMedCentral® Posted Date

7-30-2024

PubMedCentral® Full Text Version

Post-print

Abstract

Background. Glioblastoma Multiforme (GBM) is an aggressive form of malignant brain tumor with a generally poor prognosis. O 6-methylguanine-DNA methyltransferase (MGMT) promoter methylation has been shown to be a predictive bio-marker for resistance to treatment of GBM, but it is invasive and time-consuming to determine methylation status. There has been effort to predict the MGMT methylation status through analyzing MRI scans using machine learning, which only requires pre-operative scans that are already part of standard-of-care for GBM patients. Purpose. To improve the performance of conventional transfer learning in the identification of MGMT promoter methylation status, we developed a 3D SpotTune network with adaptive fine-tuning capability. Using the pretrained weights of MedicalNet with the SpotTune network, we compared its performance with a randomly initialized network for different combinations of MR modalities.

Methods. Using a ResNet50 as the base network, three categories of networks are created: (1) A 3D SpotTune network to process volumetric MR images, (2) a network with randomly initialized weights, and (3) a network pre-trained on MedicalNet. These three networks are trained and evaluated using a public GBM dataset provided by the University of Pennsylvania. The MRI scans from 240 patients are used, with 11 different modalities corresponding to a set of perfusion, diffusion, and structural scans. The performance is evaluated using 5-fold cross validation with a hold-out testing dataset.

Results. The SpotTune network showed better performance than the randomly initialized network. The best performing SpotTune model achieved an area under the Receiver Operating Characteristic curve (AUC), average precision of the precision-recall curve (AP), sensitivity, and specificity values of 0.6604, 0.6179, 0.6667, and 0.6061 respectively.

Conclusions. SpotTune enables transfer learning to be adaptive to individual patients, resulting in improved performance in predicting MGMT promoter methylation status in GBM using equivalent MRI modalities as compared to a randomly initialized network.

Keywords

Humans, Promoter Regions, Genetic, Glioblastoma, DNA Methylation, Magnetic Resonance Imaging, Brain Neoplasms, DNA Modification Methylases, Tumor Suppressor Proteins, DNA Repair Enzymes, Machine Learning, ROC Curve, Male, Female, Neural Networks, Computer, Adult, Algorithms, transfer learning, MGMT methylation status, SpotTune, deep learning, adaptive fine-tuning

Published Open-Access

yes

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