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Development after pediatric brain tumor-a longitudinal study

Olsson, Ingrid Tonning LU orcid ; Lundgren, Johan LU ; Hjorth, Lars LU and Perrin, Sean LU orcid (2016) In Neuro-Oncology 18. p.135-135
Abstract
Background: Patients treated for Pediatric Brain Tumors (PBTs) often experience a decline/stagnation in their cognitive functioning.Anumber of potential risk factors for cognitive decline have been identified including gender (female), young age-at-diagnosis, higher baseline IQ, hydrocephalus at diagnosis, treatment with Whole Brain Radiation Therapy (WBRT), and larger radiation field and/or dose. The aim of this longitudinal study was to statistically model the rate of cognitive decline in a large population-based sample of PBT survivors and to find risk factors for a faster decline. Methods: Study participants were patients diagnosed with PBTs between 2001-2013 and/or who turned 18 years of age between 2006 and 2013 (n = 151). Measures... (More)
Background: Patients treated for Pediatric Brain Tumors (PBTs) often experience a decline/stagnation in their cognitive functioning.Anumber of potential risk factors for cognitive decline have been identified including gender (female), young age-at-diagnosis, higher baseline IQ, hydrocephalus at diagnosis, treatment with Whole Brain Radiation Therapy (WBRT), and larger radiation field and/or dose. The aim of this longitudinal study was to statistically model the rate of cognitive decline in a large population-based sample of PBT survivors and to find risk factors for a faster decline. Methods: Study participants were patients diagnosed with PBTs between 2001-2013 and/or who turned 18 years of age between 2006 and 2013 (n = 151). Measures of verbal ability, perceptual reasoning, general cognitive ability, auditory working memory, cognitive processing speed, visual workingmemory and sustained attention were collected longitudinally. Multilevel Linear Modelling (MLM) was used to evaluate the rate of cognitive decline in the sample and to estimate baseline values (risk factors) influencing the rate of decline. Results: A significant decline was found for most cognitive abilities across all patient categories with only elementary verbal skills either stable or improving. Variables predicting lower cognitive performance at baseline were gender (male), age at diagnosis, supratentorial lateral tumor, larger tumor size, and treatment withWBRTor chemotherapy.Conclusions: Pediatric BT survivors experience a decline in age related cognitive performance, regardless of the treatment received. Young age at PBT diagnosis, male, gender, supratentorial lateral tumors, larger tumors and treatment with WBRT or chemotherapy were all correlated with a lowered baseline performance. (Less)
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author
; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
adult, animal model, attention, brain radiation, brain tumor, cancer epidemiology, chemotherapy, child, cognitive defect, controlled study, diagnosis, disease model, drug therapy, female, gender, human, human tissue, longitudinal study, major clinical study, male, population model, risk factor, skill, statistical model, survivor, tumor volume, velocity, working memory, young adult
in
Neuro-Oncology
volume
18
pages
1 pages
publisher
Oxford University Press
ISSN
1523-5866
DOI
10.1093/neuonc/now079.04
language
English
LU publication?
yes
id
3f0f9a60-be1d-4e95-931d-ac029927c3c3
date added to LUP
2016-11-10 17:23:50
date last changed
2019-03-08 03:03:10
@article{3f0f9a60-be1d-4e95-931d-ac029927c3c3,
  abstract     = {{Background: Patients treated for Pediatric Brain Tumors (PBTs) often experience a decline/stagnation in their cognitive functioning.Anumber of potential risk factors for cognitive decline have been identified including gender (female), young age-at-diagnosis, higher baseline IQ, hydrocephalus at diagnosis, treatment with Whole Brain Radiation Therapy (WBRT), and larger radiation field and/or dose. The aim of this longitudinal study was to statistically model the rate of cognitive decline in a large population-based sample of PBT survivors and to find risk factors for a faster decline. Methods: Study participants were patients diagnosed with PBTs between 2001-2013 and/or who turned 18 years of age between 2006 and 2013 (n = 151). Measures of verbal ability, perceptual reasoning, general cognitive ability, auditory working memory, cognitive processing speed, visual workingmemory and sustained attention were collected longitudinally. Multilevel Linear Modelling (MLM) was used to evaluate the rate of cognitive decline in the sample and to estimate baseline values (risk factors) influencing the rate of decline. Results: A significant decline was found for most cognitive abilities across all patient categories with only elementary verbal skills either stable or improving. Variables predicting lower cognitive performance at baseline were gender (male), age at diagnosis, supratentorial lateral tumor, larger tumor size, and treatment withWBRTor chemotherapy.Conclusions: Pediatric BT survivors experience a decline in age related cognitive performance, regardless of the treatment received. Young age at PBT diagnosis, male, gender, supratentorial lateral tumors, larger tumors and treatment with WBRT or chemotherapy were all correlated with a lowered baseline performance.}},
  author       = {{Olsson, Ingrid Tonning and Lundgren, Johan and Hjorth, Lars and Perrin, Sean}},
  issn         = {{1523-5866}},
  keywords     = {{adult; animal model; attention; brain radiation; brain tumor; cancer epidemiology; chemotherapy; child; cognitive defect; controlled study; diagnosis; disease model; drug therapy; female; gender; human; human tissue; longitudinal study; major clinical study; male; population model; risk factor; skill; statistical model; survivor; tumor volume; velocity; working memory; young adult}},
  language     = {{eng}},
  month        = {{06}},
  pages        = {{135--135}},
  publisher    = {{Oxford University Press}},
  series       = {{Neuro-Oncology}},
  title        = {{Development after pediatric brain tumor-a longitudinal study}},
  url          = {{http://dx.doi.org/10.1093/neuonc/now079.04}},
  doi          = {{10.1093/neuonc/now079.04}},
  volume       = {{18}},
  year         = {{2016}},
}