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Predicting Cognitive Dysfunction After Pediatric Posterior Fossa Tumor Surgery

S

Sichuan University

Status

Completed

Conditions

Posterior Fossa Tumors
Pediatric Tumor of Brain

Treatments

Other: Not applicable- observational study

Study type

Observational

Funder types

Other

Identifiers

NCT07350382
WestChinaH-HX-2025-012

Details and patient eligibility

About

The goal of this observational study is to develop and validate a clinical prediction model to identify risk factors for long-term cognitive dysfunction in children (ages 0-18 years) who have undergone surgical resection of a posterior fossa tumor. The main questions it aims to answer are:

Can a combination of preoperative and postoperative clinical, surgical, and neuroimaging factors accurately predict which children will develop long-term cognitive dysfunction after posterior fossa tumor surgery? Is white matter integrity-specifically fractional anisotropy (FA) of the superior cerebellar peduncle (SCP)-a key independent predictor of cognitive outcomes? Researchers will compare children who developed long-term cognitive dysfunction (cases) to those who did not (controls) to see if differences in imaging biomarkers (e.g., SCP FA, fMRI abnormalities), tumor characteristics (e.g., location, volume, histology), treatment factors (e.g., radiotherapy, surgical approach), and demographic variables (e.g., age) are associated with cognitive outcomes.

Participants were not asked to perform any tasks or receive any interventions as part of this study, because it is a retrospective analysis of existing medical records and imaging data. Data collected included:

Preoperative and postoperative brain MRI and DTI scans Tumor pathology and surgical reports Treatment details (e.g., radiation, chemotherapy) Neuropsychological assessment results at 1-year follow-up

Enrollment

600 patients

Sex

All

Ages

Under 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 0-18 years at time of surgery
  • Histopathologically confirmed primary posterior fossa tumor (e.g., medulloblastoma, ependymoma, pilocytic astrocytoma)
  • Underwent surgical resection of the tumor at the hospital
  • Availability of preoperative brain MRI and diffusion tensor imaging (DTI)
  • Completed standardized neuropsychological assessment at approximately 1 year post-surgery

Exclusion criteria

  • Pre-existing neurological or neurodevelopmental disorders (e.g., autism, intellectual disability, cerebral palsy)
  • History of prior cranial irradiation or chemotherapy before posterior fossa surgery
  • Incomplete clinical, imaging, or follow-up data required for model variables
  • Tumor recurrence or progression before 1-year cognitive assessment
  • Non-posterior fossa primary brain tumors (e.g., supratentorial gliomas)

Trial design

600 participants in 1 patient group

pediatric patients who underwent surgical resection of a posterior fossa tumor
Description:
Stratify this cohort into two subgroups based on outcome: Those with long-term cognitive dysfunction (n=172) Those without (n=428)
Treatment:
Other: Not applicable- observational study

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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