Neuroblastoma Research and Treatments Open access Peer reviewed

Artificial Intelligence for Diagnosis, Risk Stratification, and Prognosis of Neuroblastoma - A Systematic Review and Meta-Analysis

Daniel Rodrigo Serbena, Isabela Luiza Fraron Cieslack, Renan Cassiano Ratis, Débora Van Putten Chaves and 6 more

Current Oncology Reports | Sep 4, 2026

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Evidence on artificial intelligence performance in neuroblastoma (NB) diagnosis, risk stratification, prognosis, prognosis, and genomic characterization synthesizes and clinical adoption remains premature given persistent gaps in external validation, calibration, dataset size, and pediatric-specific model development.

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PURPOSE: To synthesizes evidence on artificial intelligence (AI) performance in neuroblastoma (NB) diagnosis, risk stratification, prognosis, and genomic characterization. MATERIALS AND METHODS: A systematic review and meta-analysis was conducted following PRISMA 2020 guidelines (PROSPERO: CRD42024539475) across five databases. Meta-analyses used random-effects models with logit-transformed Area Under the Curve (AUCs) and cluster-robust standard errors. AI models were classified as Machine Learning Models (MLM) or Hybrid Nomograms (HN) based on their construction methodology. RESULTS: Of 3,742 articles identified, 53 were included. MLMs demonstrated higher point estimates than radiologists in differential diagnosis (AUC: 0.87 vs. 0.83), though this difference was not statistically significant and carried substantial uncertainty. HNs achieved stronger performance in risk stratification (AUC: 0.87). AI-derived nomograms (AUC: 0.9) and gene signatures (AUC: 0.8) outperformed conventional prognostic markers descriptively. Chemotherapy response prediction remained below clinical utility thresholds across all model types. Only 33.9% of models reported calibration and 24.5% underwent external validation. CONCLUSIONS: AI demonstrates proof-of-concept across multiple NB clinical domains. However, clinical adoption remains premature given persistent gaps in external validation, calibration, dataset size, and pediatric-specific model development. Future studies should test these models prospectively in multicenter pediatric cohorts, ideally through COG or SIOPEN, using shared definitions for diagnosis, risk group, treatment response, and survival outcomes.

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Daniel Rodrigo Serbena

first | Universidade Estadual do Centro-Oeste | ORCID 0000-0001-6885-5919

Isabela Luiza Fraron Cieslack

middle | Universidade Estadual do Centro-Oeste | ORCID 0009-0008-8893-8306

Renan Cassiano Ratis

middle | Universidade Estadual do Centro-Oeste | ORCID 0000-0003-3742-7211

Débora Van Putten Chaves

middle | Brazilian Center for Research in Energy and Materials | ORCID 0009-0000-1118-0228

Silva Oliveira

middle | Brazilian Center for Research in Energy and Materials | ORCID 0000-0001-8588-4324

Henrique Alexsander Ferreira Neves

middle | Universidade Federal do Paraná | ORCID 0000-0003-0988-5282

Fernando Sluchensci dos Santos

middle | Universidade Estadual do Centro-Oeste | ORCID 0000-0001-7114-5264

Daniel R. Cassar

middle | Brazilian Center for Research in Energy and Materials | ORCID 0000-0001-6472-2780

Weber Cláudio Francisco Nunes da Silva

middle | Universidade Estadual do Centro-Oeste | ORCID 0000-0002-4688-3115

Juliana Sartori Bonini

last | Universidade Estadual do Centro-Oeste | ORCID 0000-0001-5144-2253

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BibTeX

@article{Serbena2026Artificial,
  title = {Artificial Intelligence for Diagnosis, Risk Stratification, and Prognosis of Neuroblastoma - A Systematic Review and Meta-Analysis},
  author = {Daniel Rodrigo Serbena and Isabela Luiza Fraron Cieslack and Renan Cassiano Ratis and Débora Van Putten Chaves and Silva Oliveira and Henrique Alexsander Ferreira Neves and Fernando Sluchensci dos Santos and Daniel R. Cassar and Weber Cláudio Francisco Nunes da Silva and Juliana Sartori Bonini},
  journal = {Current Oncology Reports},
  year = {2026},
  doi = {10.1007/s11912-026-01824-0},
  url = {https://doi.org/10.1007/s11912-026-01824-0}
}

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