Prediction of MYCN Gene Amplification in Pediatric Neuroblastomas: Development of a Deep Learning–Based Tool for Automatic Tumor Segmentation and Comparative Analysis of Computed Tomography–Based Radiomics Features Harmonization

Author:

Yeow Ling Yun1,Teh Yu Xuan2,Lu Xinyu3,Srinivasa Arvind Channarayapatna1,Tan Eelin4,Tan Timothy Shao Ern4,Tang Phua Hwee4,KN Bhanu Prakash1

Affiliation:

1. Bioinformatics Institute, Agency for Science, Technology and Research (A*STAR)

2. Division of Mathematical Sciences, School of Physical and Mathematical Sciences, Nanyang Technological University

3. Victoria Junior College

4. Department of Diagnostic & Interventional Imaging, KK Women's and Children's Hospital, Singapore, Singapore.

Abstract

Objective MYCN oncogene amplification is closely linked to high-grade neuroblastoma with poor prognosis. Accurate quantification is essential for risk assessment, which guides clinical decision making and disease management. This study proposes an end-to-end deep-learning framework for automatic tumor segmentation of pediatric neuroblastomas and radiomics features-based classification of MYCN gene amplification. Methods Data from pretreatment contrast-enhanced computed tomography scans and MYCN status from 47 cases of pediatric neuroblastomas treated at a tertiary children's hospital from 2009 to 2020 were reviewed. Automated tumor segmentation and grading pipeline includes (1) a modified U-Net for tumor segmentation; (2) extraction of radiomic textural features; (3) feature-based ComBat harmonization for removal of variabilities across scanners; (4) feature selection using 2 approaches, namely, (a) an ensemble approach and (b) stepwise forward-and-backward selection method using logistic regression classifier; and (5) radiomics features-based classification of MYCN gene amplification using machine learning classifiers. Results Median train/test Dice score for modified U-Net was 0.728/0.680. The top 3 features from the ensemble approach were neighborhood gray-tone difference matrix (NGTDM) busyness, NGTDM strength, and gray-level run-length matrix (GLRLM) low gray-level run emphasis, whereas those from the stepwise approach were GLRLM low gray-level run emphasis, GLRLM high gray-level run emphasis, and NGTDM coarseness. The top-performing tumor classification algorithm achieved a weighted F1 score of 97%, an area under the receiver operating characteristic curve of 96.9%, an accuracy of 96.97%, and a negative predictive value of 100%. Harmonization-based tumor classification improved the accuracy by 2% to 3% for all classifiers. Conclusion The proposed end-to-end framework achieved high accuracy for MYCN gene amplification status classification.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Radiology, Nuclear Medicine and imaging

Reference53 articles.

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