- Author:
Younghee PARK
1
;
Eun Seung YU
;
Boram HA
;
Hyeon Jin PARK
;
Jong Heun KIM
;
Joo Young KIM
Author Information
- Publication Type:Original Article
- Keywords: Brain neoplasms; Germ cell tumor; Cognitive function
- MeSH: Basal Ganglia; Brain Neoplasms; Checklist; Child Behavior; Child*; Cognition; Diagnosis; Follow-Up Studies; Germ Cells*; Humans; Intelligence; Korea; Memory; Neoplasms, Germ Cell and Embryonal*; Pineal Gland; Proton Therapy
- From:Cancer Research and Treatment 2017;49(4):960-969
- CountryRepublic of Korea
- Language:English
- Abstract: PURPOSE: This study was conducted to investigate the neurocognitive functioning of children with intracranial germ cell tumor (IGCT) prior to receiving proton beam therapy (PBT), and to identify differential characteristics of their neurocognitive functioning depending on tumor location. As a secondary object of this study, neurocognitive functions were followed up at 1-2 years after PBT to examine early post-treatment changes. MATERIALS AND METHODS: Between 2008 and 2014, 34 childrenwith IGCT treatedwho received PBT atNational Cancer Center, Korea were enrolled in this study. Standardized neurocognitive tests of intelligence, memory, and executive functioning were performed with baseline psychological assessments using the Child Behavior Checklist (CBCL). Follow-up assessments after PBT were conducted in 20 patients (T2). The results were analyzed based on the locations of tumors, which included the suprasellar, pineal gland, basal ganglia, and bifocal regions. RESULTS: The neurocognitive function of IGCT patients was significantly lower than that of the normal population in performance intelligence quotient (p=0.041), processing speed (p=0.007), memory (p < 0.001), and executive functioning (p=0.010). Patients with basal ganglia tumors had significantly lower scores for most domains of neurocognitive functioning and higher scores for CBCL than both the normal population and patients with IGCT in other locations. There was no significant change in neurocognitive function between T1 and T2 for all types of IGCT patients in first 1-2 years after PBT. CONCLUSION: Tumor location significantly affects the neuropsychological functioning in patients with IGCT. Neuropsychological functioning should be closely monitored from the time of diagnosis in IGCT patients.