Association Between Brain Substructure Dose and Cognitive Outcomes in Children With Medulloblastoma Treated on SJMB03: A Step Toward Substructure-Informed Planning

Author:

Acharya Sahaja12ORCID,Guo Yian3ORCID,Patni Tushar3ORCID,Li Yimei3,Wang Chuang1,Gargone Melissa1,Ashford Jason M.4,Wilson Lydia1ORCID,Faught Austin1,Reddick Wilburn E.5,Patay Zoltan5,Gajjar Amar6ORCID,Conklin Heather M.4ORCID,Merchant Thomas E.1ORCID

Affiliation:

1. Department of Radiation Oncology, St Jude Children's Research Hospital, Memphis, TN

2. Department of Radiation Oncology and Molecular Radiation Sciences, Johns Hopkins Medicine, Baltimore, MD

3. Department of Biostatistics, St Jude Children's Research Hospital, Memphis, TN

4. Department of Psychology, St Jude Children's Research Hospital, Memphis, TN

5. Department of Diagnostic Imaging, St Jude Children's Research Hospital, Memphis, TN

6. Division of Neuro-Oncology, St Jude Children's Research Hospital, Memphis, TN

Abstract

PURPOSE To characterize the association between neurocognitive outcomes (memory and processing speed) and radiation (RT) dose to the hippocampus, corpus callosum (CC), and frontal white matter (WM) in children with medulloblastoma treated on a prospective study, SJMB03. PATIENTS AND METHODS Patients age 3-21 years with medulloblastoma were treated at a single institution on a phase III study. The craniospinal RT dose was 23.4 Gy for average-risk patients and 36-39.6 Gy for high-risk patients. The boost dose was 55.8 Gy to the tumor bed. Patients underwent cognitive testing at baseline and once yearly for 5 years. Performance on tests of memory (associative memory and working memory) and processing speed (composite processing speed and perceptual speed) was analyzed. Mixed-effects models were used to estimate longitudinal trends in neurocognitive outcomes. Reliable change index and logistic regression were used to define clinically meaningful neurocognitive decline and identify variables associated with decline. RESULTS One hundred and twenty-four patients were eligible for inclusion, with a median neurocognitive follow-up of 5 years. Mean right and left hippocampal doses were significantly associated with decline in associative memory in patients without posterior fossa syndrome (all P < .05). Mean CC and frontal WM doses were significantly associated with decline in both measures of processing speed (all P < .05). Median brain substructure dose–volume histograms were shifted to the right for patients with a decline in associative memory or processing speed. The odds of decline in associative memory and composite processing speed increased by 23%-26% and by 10%-15% for every 1-Gy increase in mean hippocampal dose and mean CC or frontal WM dose, respectively. CONCLUSION Increasing RT dose to the CC or frontal WM and hippocampus is associated with worse performance on tests of processing speed and associative memory, respectively. Brain substructure–informed RT planning may mitigate neurocognitive impairment.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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