Scientific Reports (Oct 2024)

Differentiating MYCN-amplified RB1 wild-type retinoblastoma from biallelic RB1 mutant retinoblastoma using MR-based radiomics: a retrospective multicenter case–control study

  • Christiaan M. de Bloeme ,
  • Robin W. Jansen,
  • Liesbeth Cardoen,
  • Sophia Göricke,
  • Sabien van Elst,
  • Jaime Lyn Jessen,
  • Aparna Ramasubramanian,
  • Alison H. Skalet,
  • Audra K. Miller,
  • Philippe Maeder,
  • Ogul E. Uner,
  • G. Baker Hubbard,
  • Hans Grossniklaus,
  • H. Culver Boldt,
  • Kim E. Nichols,
  • Rachel C. Brennan,
  • Saugata Sen,
  • Mériam Koob,
  • Selma Sirin,
  • Hervé J. Brisse,
  • Paolo Galluzzi,
  • Charlotte J. Dommering,
  • Matthijs Cysouw,
  • Ronald Boellaard,
  • Josephine C. Dorsman,
  • Annette C. Moll,
  • Marcus C. de Jong,
  • Pim de Graaf,
  • European Retinoblastoma Imaging Collaboration

DOI
https://doi.org/10.1038/s41598-024-76933-6
Journal volume & issue
Vol. 14, no. 1
pp. 1 – 8

Abstract

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Abstract MYCN-amplified RB1 wild-type (MYCN amp RB1 +/+) retinoblastoma is a rare and aggressive subtype, often resistant to standard therapies. Identifying unique MRI features is crucial for diagnosing this subtype, as biopsy is not recommended. This study aimed to differentiate MYCN amp RB1 +/+ from the most prevalent RB1 -/- retinoblastoma using pretreatment MRI and radiomics. Ninety-eight unilateral retinoblastoma patients (19 MYCN cases and 79 matched controls) were included. Tumors on T2-weighted MR images were manually delineated and validated by experienced radiologists. Radiomics analysis extracted 120 features per tumor. Several combinations of feature selection methods, oversampling techniques and machine learning (ML) classifiers were evaluated in a repeated fivefold cross-validation machine learning pipeline to yield the best-performing prediction model for MYCN. The best model used univariate feature selection, data oversampling (duplicating MYCN cases), and logistic regression classifier, achieving a mean AUC of 0.78 (SD 0.12). SHAP analysis highlighted lower sphericity, higher flatness, and greater gray-level heterogeneity as predictive for MYCN amp RB1 +/+ status, yielding an AUC of 0.81 (SD 0.11). This study shows the potential of MRI-based radiomics to distinguish MYCN amp RB1 +/+ and RB1 -/- retinoblastoma subtypes.

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