Abstract
Background
MYCN gene amplification is associated with poor prognosis in neuroblastoma (NB) patients; however, its detection relies on the invasive fluorescence in situ hybridization technique. Radiomics can non-invasively predict MYCN gene amplification by extracting high-dimensional features from medical images.
Purpose
To systematically review and meta-analyze the performance of radiomics models in predicting MYCN gene amplification status in NB patients.
Material and Methods
As of 18 March 2025, a systematic search was performed for original literature on the prediction of MYCN amplification in NB patients using radiomics models in the following databases: PubMed, Embase, Web of Science, and Cochrane Library. The quality of the literature was assessed using the QUADAS-2 and Radiomics Quality Score (RQS) tools. The meta-analysis was performed using the random-effects model.
Results
This research ultimately included nine articles (899 patients), from which data could be extracted for both radiomics-only models and combined models that integrate radiomic features with other predictors. The radiomics-only model demonstrated pooled sensitivity of 0.85 (95% confidence interval [CI] = 0.77–0.91) and specificity of 0.86 (95% CI = 0.79–0.90), while the combined model showed a sensitivity of 0.81 (95% CI = 0.75–0.87) and specificity of 0.92 (95% CI = 0.87–0.95). Summary receiver operating characteristic (SROC) curve yielded an area under ROC curve of 0.92 ± 0.02 for the radiomics-only model and 0.94 ± 0.02 for the combined model. No evidence of publication bias was found.
Conclusions
Radiomics might be one promising approach for predicting MYCN gene amplification in patients with NB.
Get full access to this article
View all access options for this article.
References
Supplementary Material
Please find the following supplemental material available below.
For Open Access articles published under a Creative Commons License, all supplemental material carries the same license as the article it is associated with.
For non-Open Access articles published, all supplemental material carries a non-exclusive license, and permission requests for re-use of supplemental material or any part of supplemental material shall be sent directly to the copyright owner as specified in the copyright notice associated with the article.
