ARTIfiCIAL INTELLIGENCE IMPROVES THE PREOPERATIVE PREDICTION OF CEREBELLAR MUTISM SYNDROME: A MULTINATIONAL, MULTI-READER STUDY AND PRACTICE RECOMMENDATIONS FROM THE POSTERIOR FOSSA SOCIETY

Abstract AIMS Cerebellar mutism syndrome (pCMS) is a severe complication experienced by up to 40% of children undergoing resection of a primary posterior fossa tumour. Accurate prediction of pCMS risk could improve perioperative patient/parental counselling and surgical decision making. This multinational, multi-reader retrospective study aimed to evaluate the generalisation performance of two previously reported artificial intelligence (AI) models (Rotterdam and GOSH-Colorado-Stanford) for the preoperative prediction of pCMS. METHODS 120 children with primary posterior fossa tumours were enrolled across four participating centres (30 children per centre). Neuroimaging was reviewed by 11 readers blinded to clinical outcome and the risk of each pa- tient developing pCMS predicted with and without AI decision support. Model accuracy and the agreement of predictions between investigators were evaluated. RESULTS Across all 120 patients and 11 readers, the accuracy of clinical pCMS predictions without AI decision support was 62.7% which increased significantly in the second round of assessment with AI decision support from both the Rotterdam model (accuracy 76.7%; P<0.001) and the GOSH-Colorado-Stanford model (accuracy 80.3%; P=0.008). Upon direct comparison, the GOSH-Colorado-Stanford model outperformed the Rotterdam model (P=0.012), demonstrating a higher sensitivity (88% vs. 80%) and positive predictive value (82% vs. 76%). AI decision support was also found to significantly standardise the prediction of pCMS across study readers (Fleiss’ κ=0.021- 0.396 without vs. 0.248-0.643 with AI decision support). Finally, AI decision support was reported as helpful by expert clinical readers in a significant number of cases (64%; P<0.001) and was found to increase reader pre- dictive accuracy independent of experience. CONCLUSION Collectively, these results demonstrate that AI decision support provides more accurate, reproducible, and stan- dardised pCMS risk predictions compared to clinical opinion alone, irrespective of investigator experience, across a large, international real-world dataset. Consensus Posterior Fossa Society practice recommendations on model use will be presented.

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Journal
Neuro-Oncology
Published
2025-09-01
DOI
https://doi.org/10.1093/neuonc/noaf185.014
Primary Topic
Fetal and Pediatric Neurological Disorders
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article
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article

ARTIfiCIAL INTELLIGENCE IMPROVES THE PREOPERATIVE PREDICTION OF CEREBELLAR MUTISM SYNDROME: A MULTINATIONAL, MULTI-READER STUDY AND PRACTICE RECOMMENDATIONS FROM THE POSTERIOR FOSSA SOCIETY

Soniya Pinto, Darren Hargrave, Shivaram Avula, Asim K. Bag et al.
Neuro-Oncology
Fetal and Pediatric Neurological Disorders
article

ARTIfiCIAL INTELLIGENCE IMPROVES THE PREOPERATIVE PREDICTION OF CEREBELLAR MUTISM SYNDROME: A MULTINATIONAL, MULTI-READER STUDY AND PRACTICE RECOMMENDATIONS FROM THE POSTERIOR FOSSA SOCIETY

Soniya Pinto, Darren Hargrave, Shivaram Avula, Asim K. Bag, Adam Marcus, N Menon, C. M. S. Cohen, Kshitij Mankad, Andrew Dapaah, Vítor Nagai Yamaki, Kristian Aquilina, Vejay N. Vakharia, Ulrike Löbel, Jai Sidpra, Sebastian Toescu, Samuel S. McAfee, Christopher Parks, Prof Robert A Dineen, Miss Valentina Lind
article en

Abstract

Abstract AIMS Cerebellar mutism syndrome (pCMS) is a severe complication experienced by up to 40% of children undergoing resection of a primary posterior fossa tumour. Accurate prediction of pCMS risk could improve perioperative patient/parental counselling and surgical decision making. This multinational, multi-reader retrospective study aimed to evaluate the generalisation performance of two previously reported artificial intelligence (AI) models (Rotterdam and GOSH-Colorado-Stanford) for the preoperative prediction of pCMS. METHODS 120 children with primary posterior fossa tumours were enrolled across four participating centres (30 children per centre). Neuroimaging was reviewed by 11 readers blinded to clinical outcome and the risk of each pa- tient developing pCMS predicted with and without AI decision support. Model accuracy and the agreement of predictions between investigators were evaluated. RESULTS Across all 120 patients and 11 readers, the accuracy of clinical pCMS predictions without AI decision support was 62.7% which increased significantly in the second round of assessment with AI decision support from both the Rotterdam model (accuracy 76.7%; P<0.001) and the GOSH-Colorado-Stanford model (accuracy 80.3%; P=0.008). Upon direct comparison, the GOSH-Colorado-Stanford model outperformed the Rotterdam model (P=0.012), demonstrating a higher sensitivity (88% vs. 80%) and positive predictive value (82% vs. 76%). AI decision support was also found to significantly standardise the prediction of pCMS across study readers (Fleiss’ κ=0.021- 0.396 without vs. 0.248-0.643 with AI decision support). Finally, AI decision support was reported as helpful by expert clinical readers in a significant number of cases (64%; P<0.001) and was found to increase reader pre- dictive accuracy independent of experience. CONCLUSION Collectively, these results demonstrate that AI decision support provides more accurate, reproducible, and stan- dardised pCMS risk predictions compared to clinical opinion alone, irrespective of investigator experience, across a large, international real-world dataset. Consensus Posterior Fossa Society practice recommendations on model use will be presented.

Neuro-OncologyVol. 27(Supplement_2)
St. Jude Children's Research Hospital (US), Nottingham University Hospitals NHS Trust (GB), Great Ormond Street Hospital (GB), Great Ormond Street Hospital for Children NHS Foundation Trust (GB), Alder Hey Children's NHS Foundation Trust (GB), National Hospital for Neurology and Neurosurgery (GB), University College London (GB), Imperial College London (GB)
Openalex Percentile: Top 67%
Fetal and Pediatric Neurological Disorders
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