Change in neurocognitive functioning after treatment with cranial radiation in childhood

被引:298
作者
Spiegler, BJ
Bouffet, E
Greenberg, ML
Rutka, JT
Mabbott, DJ
机构
[1] Hosp Sick Children, Dept Psychol, Paediat Brain Tumor Program, Toronto, ON M5G 1X8, Canada
[2] Hosp Sick Children, Dept Surg, Toronto, ON M5G 1X8, Canada
[3] Hosp Sick Children, Dept Pediat, Toronto, ON M5G 1X8, Canada
[4] Hosp Sick Children, Div Hematol Oncol, Toronto, ON M5G 1X8, Canada
[5] Hosp Sick Children, Div Neurosurg, Toronto, ON M5G 1X8, Canada
关键词
D O I
10.1200/JCO.2004.05.186
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose To evaluate the pattern of stability and change over time across multiple domains of neurocognitive function in radiated survivors of posterior fossa (PF) tumors. Patients and Methods Thirty-four children (25 males) treated for malignant PF tumors were observed with serial clinical neuropsychologic assessments. Thirty patients were treated for medulloblastoma and four patients were treated for ependymoma. Twelve patients were treated with reduced-dose and 21 patients were treated with standard-dose cranial radiation. All patients received an additional boost to the PF. One patient was treated with PF radiation only. Standardized neuropsychologic tests were administered at different times after diagnosis for each child. The rate of change in scores was determined using a mixed model regression. Results Results showed a 2- to 4-point decline per year in intelligence scores. For our relatively young sample, intellectual function declined quickly in the first few years after treatment, and then more gradually. Significant declines in visual-motor integration, visual memory, verbal fluency, and executive functioning were also documented. No decline was evident for verbal memory and receptive vocabulary. Conclusion Cranial radiation is associated with a decline in multiple neurocognitive domains, with a few notable exceptions. Our results must be interpreted in the context of common limitations of clinical research, including patient variability, changes in test versions, small sample size, and clinical referral bias. (C) 2004 by American Society of Clinical Oncology.
引用
收藏
页码:706 / 713
页数:8
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