Neuropsychological functioning following surgery for pediatric low-grade glioma: a prospective longitudinal study.

BRIEF = Behavior Rating Inventory of Executive Function CPT = Continuous Performance Test D-KEFS = Delis-Kaplan Executive Function System FSIQ = Full Scale IQ LGG = low-grade glioma PRI = Perceptual Reasoning Index PSI = Processing Speed Index VCI = Verbal Comprehension Index WISC-V = Wechsler Intelligence Scale for Children, Fifth Edition WMI = Working Memory Index brain tumor executive functioning low-grade glioma neuropsychology oncology pediatric surgery only

Journal

Journal of neurosurgery. Pediatrics
ISSN: 1933-0715
Titre abrégé: J Neurosurg Pediatr
Pays: United States
ID NLM: 101463759

Informations de publication

Date de publication:
06 Dec 2019
Historique:
received: 18 06 2019
accepted: 16 09 2019
entrez: 8 12 2019
pubmed: 8 12 2019
medline: 8 12 2019
Statut: aheadofprint

Résumé

High survival rates have led to an increased emphasis on the functional outcomes of children diagnosed with low-grade glioma. Most outcomes research has focused on risks associated with radiotherapy, but less is known about neuropsychological risks for patients treated with surgery alone. Here, the authors sought to examine the neuropsychological trajectories of children diagnosed with a low-grade glioma and monitored up to 6 years postsurgery. Secondarily, they explored demographic and clinical predictors of neuropsychological performance. The neuropsychological functioning of 32 patients (median age at diagnosis 10.0 years) was prospectively assessed annually for up to 6 years after surgery (median days from surgery at baseline = 72). Tumor location was predominately supratentorial (65.6%). A combination of performance-based and parent-reported measures was used to assess intelligence, memory, executive functioning, and fine motor control in all patients. Binomial tests at the postoperative baseline revealed that the proportion of children falling below the average range (< 16th percentile) was significantly higher than the rate expected among healthy peers on measures of verbal memory, processing speed, executive functioning, and fine motor control (p < 0.05). Even so, linear mixed models indicated that neuropsychological functioning at the postoperative baseline did not significantly change over time for up to 6 years after surgery across all domains. A larger tumor size was associated with a slower reaction time (p < 0.01). A supratentorial tumor location and history of seizures were associated with more parent-reported executive difficulties (p < 0.01). While radiotherapy is a known risk factor for neuropsychological deficits in pediatric brain tumor patients, findings in this study indicate that children treated for low-grade glioma with surgery alone (without radiotherapy or chemotherapy) remain susceptible to difficulties with memory, executive functioning, and motor functioning that persist over time. Over half of the children in the study sample required school support services to address neuropsychological weaknesses. Although low-grade glioma is often conceptualized as a benign tumor, children treated for this lesion require ongoing monitoring and intervention to address neuropsychological weaknesses resulting from the tumor itself as well as the surgery.

Identifiants

pubmed: 31812134
doi: 10.3171/2019.9.PEDS19357
pii: 2019.9.PEDS19357
pmc: PMC9040333
mid: NIHMS1794945
doi:
pii:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-9

Subventions

Organisme : NCI NIH HHS
ID : K07 CA157923
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA187202
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA221197
Pays : United States

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Auteurs

Andrew M Heitzer (AM)

1Department of Pediatrics, Section of Psychology, Baylor College of Medicine.

Kimberly Raghubar (K)

1Department of Pediatrics, Section of Psychology, Baylor College of Medicine.

M Douglas Ris (MD)

1Department of Pediatrics, Section of Psychology, Baylor College of Medicine.

Charles G Minard (CG)

2Dan L. Duncan Institute for Clinical and Translational Research, Baylor College of Medicine.

Marsha N Gragert (MN)

1Department of Pediatrics, Section of Psychology, Baylor College of Medicine.

Heather H Stancel (HH)

1Department of Pediatrics, Section of Psychology, Baylor College of Medicine.

Jessica Orobio (J)

1Department of Pediatrics, Section of Psychology, Baylor College of Medicine.

Judy Xue (J)

1Department of Pediatrics, Section of Psychology, Baylor College of Medicine.
3Rice University, Houston, Texas.

William Whitehead (W)

5Department of Neurosurgery, Division of Pediatric Neurosurgery, Baylor College of Medicine; and.

M Fatih Okcu (MF)

4Department of Pediatrics, Section of Hematology Oncology, Baylor College of Medicine.

Murali Chintagumpala (M)

4Department of Pediatrics, Section of Hematology Oncology, Baylor College of Medicine.

Lisa S Kahalley (LS)

1Department of Pediatrics, Section of Psychology, Baylor College of Medicine.

Classifications MeSH