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Machine Learning-Based Classification of Neuroblastoma Risk Groups and MYCN Status

dc.contributor.authorEkmekci, Sumeyye
dc.contributor.authorIpek, Emre
dc.contributor.authorApaydin, Mehmet Serkan
dc.contributor.authorOzer, Erdener
dc.date.accessioned2026-11-05T11:00:33Z
dc.date.issued2026
dc.description.abstractBackground: Artificial intelligence (AI)-based methods have demonstrated considerable promise in identifying histological features in whole slide images (WSIs) and supporting risk classification in tumors. For pediatric cancers such as neuroblastoma, integrating histological findings with molecular data may enhance risk stratification and support clinical management. This study aims to evaluate the performance of a deep learning AI model on WSIs to classify neuroblastoma patients according to risk groups and determine the MYCN amplification status.Methods: Hematoxylin and eosin-stained slides from 10 high-risk MYCN amplified, 10 high risk MYCN non-amplified, 5 intermediate-risk MYCN non-amplified, and 5 low-risk MYCN non-amplified neuroblastoma cases were digitally scanned. WSIs were processed using a deep learning-based segmentation and classification algorithms. Two patch-level datasets were constructed: 1 to predict MYCN amplification status (positive versus negative), and another to classify patients into 4 distinct risk groups (low-risk MYCN-negative, intermediate-risk MYCN-negative, high-risk MYCN-negative, and high-risk MYCN-positive).Results: Our deep learning model achieved 98% accuracy of classifying neuroblastoma patients' risk groups across validation trials on slide-level classification tasks, reflecting robust performance. The accuracy of distinguishing MYCN amplified tumors from MYCN non-amplified tumors was 99%, and even within high-risk neuroblastoma cases, it was 96%.Conclusion: AI models can facilitate accurate risk classification of neuroblastoma patients and may also predict MYCN amplification status. They represent a promising complementary tool for pathologists working on risk stratification, especially when histological examination is limited or molecular testing for MYCN amplification is unavailable.
dc.description.sponsorshipThe authors disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: The authors acknowledge financial support for this research from the Dokuz Eylul University Scientific Research Project Support Program (Project ID: TDK-2022-2770).
dc.identifier.doi10.1177/10935266261474215
dc.identifier.issn1093-5266
dc.identifier.issn1615-5742
dc.identifier.urihttps://doi.org/10.1177/10935266261474215
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/10476
dc.identifier.wosWOS:001846419000001
dc.language.isoen
dc.publisherSAGE PUBLICATIONS INC
dc.relation.fundingdokuz eylul universitesi(Dokuz Eylul University)
dc.relation.fundingdokuz eylul universitesi [TDK-2022-2770]
dc.relation.hasversion10.1177/10935266261474215
dc.relation.ispartofPEDIATRIC AND DEVELOPMENTAL PATHOLOGY
dc.subjectartificial intelligence
dc.subjectmachine learning
dc.subjectMYCN
dc.subjectneuroblastoma
dc.subjectrisk group
dc.subjectBIOLOGY
dc.subjectPathology
dc.subjectPediatrics
dc.titleMachine Learning-Based Classification of Neuroblastoma Risk Groups and MYCN Status
dc.typeArticle
oaire.citation.editionScience Citation Index Expanded (SCI-EXPANDED)
person.identifier.orcid0000-0003-1607-500X
person.identifier.ridACD-6079-2022
person.identifier.ridAAV-5748-2021

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