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Risk Factors for Domain-specific Neurocognitive Outcome in Pediatric Survivors of a Brain Tumor in the Posterior Fossa-Results of the HIT 2000 Trial

Abstract

Background: Neurocognition can be severely affected in pediatric brain tumor survivors. We analyzed the association of cognitive functioning with radiotherapy dose, postoperative cerebellar mutism syndrome (pCMS), hydrocephalus, intraventricular methotrexate (MTX) application, tumor localization, and biology in pediatric survivors of a posterior fossa tumor.

Methods: Subdomain-specific neurocognitive outcome data from 279 relapse-free survivors of the HIT-2000 trial (241 medulloblastoma and 38 infratentorial ependymoma) using the Neuropsychological Basic Diagnostic tool based on Cattell-Horn-Carroll's model for intelligence were analyzed.

Results: Cognitive performance 5.14 years (mean; range = 1.52-13.02) after diagnosis was significantly below normal for all subtests. Processing speed and psychomotor abilities were most affected. Influencing factors were domain-specific: CSI-dose had a strong impact on most subtests. pCMS was associated with psychomotor abilities (β = -0.25 to -0.16) and processing speed (β = -0.32). Postoperative hydrocephalus correlated with crystallized intelligence (β = -0.20) and short-term memory (β = -0.15), age with crystallized intelligence (β = 0.15) and psychomotor abilities (β = -0.16 and β = -0.17). Scores for fluid intelligence (β = -0.23), short-term memory (β = -0.17) and visual processing (β = -0.25) declined, and scores for selective attention improved (β = 0.29) with time after diagnosis.

Conclusions: The dose of CSI was strongly associated with neurocognitive outcomes. Low psychomotor abilities and processing speed both in patients treated with and without CSI suggest a strong contribution of the tumor and its surgery on these functions. Future research therefore should analyze strategies to both reduce CSI dose and toxicity caused by other treatment modalities.

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Long-term outcome of the Milano-hyperfractionated accelerated radiotherapy strategy for high-risk medulloblastoma, including the impact of molecular subtype.

Massimino M, Barretta F, Dossena C, Minasi S, Buttarelli F, Biassoni V Neuro Oncol. 2024; 27(1):209-218.

PMID: 39331528 PMC: 11726337. DOI: 10.1093/neuonc/noae189.

References
1.
Mynarek M, von Hoff K, Pietsch T, Ottensmeier H, Warmuth-Metz M, Bison B . Nonmetastatic Medulloblastoma of Early Childhood: Results From the Prospective Clinical Trial HIT-2000 and An Extended Validation Cohort. J Clin Oncol. 2020; 38(18):2028-2040. DOI: 10.1200/JCO.19.03057. View

2.
Oyefiade A, Paltin I, De Luca C, Hardy K, Grosshans D, Chintagumpala M . Cognitive Risk in Survivors of Pediatric Brain Tumors. J Clin Oncol. 2021; 39(16):1718-1726. PMC: 8260914. DOI: 10.1200/JCO.20.02338. View

3.
von Bueren A, Kortmann R, von Hoff K, Friedrich C, Mynarek M, Muller K . Treatment of Children and Adolescents With Metastatic Medulloblastoma and Prognostic Relevance of Clinical and Biologic Parameters. J Clin Oncol. 2016; 34(34):4151-4160. DOI: 10.1200/JCO.2016.67.2428. View

4.
Hocking M, Walsh K, Hardy K, Conklin H . Addressing Neurocognitive Late Effects in Pediatric Cancer Survivors: Current Approaches and Future Opportunities. J Clin Oncol. 2021; 39(16):1824-1832. DOI: 10.1200/JCO.20.02327. View

5.
Traunwieser T, Kandels D, Pauls F, Pietsch T, Warmuth-Metz M, Bison B . Long-term cognitive deficits in pediatric low-grade glioma (LGG) survivors reflect pretreatment conditions-report from the German LGG studies. Neurooncol Adv. 2020; 2(1):vdaa094. PMC: 7497816. DOI: 10.1093/noajnl/vdaa094. View