The course of neurocognitive functioning in high-grade glioma patients

被引:119
作者
Bosma, Ingeborg
Vos, Maaike J.
Heimans, Jan J.
Taphoorn, Martin J. B.
Aaronson, Neil K.
Postma, Tjeerd J.
van der Ploeg, Henk M.
Muller, Martin
Vandertop, W. Peter
Slotman, Ben. J.
Klein, Martin
机构
[1] Vrije Univ Amsterdam Med Ctr, Dept Neurol, NL-1081 HV Amsterdam, Netherlands
[2] Vrije Univ Amsterdam Med Ctr, Dept Med Psychol, NL-1081 HV Amsterdam, Netherlands
[3] Vrije Univ Amsterdam Med Ctr, Dept Neurosurg, NL-1081 HV Amsterdam, Netherlands
[4] Vrije Univ Amsterdam Med Ctr, Dept Radiat Oncol, NL-1081 HV Amsterdam, Netherlands
[5] Med Ctr Haaglanden, Dept Neurol, NL-2501 CK The Hague, Netherlands
[6] Univ Med Ctr Utrecht, NL-3508 GA Utrecht, Netherlands
[7] Netherlands Canc Inst, Div Psychosocial Res & Epidemiol, NL-1066 CX Amsterdam, Netherlands
关键词
high-grade glioma; neurocognitive functioning; neuropsychological assessment; tumor recurrence; prospective study;
D O I
10.1215/15228517-2006-012
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We evaluated the course of neurocognitive functioning in newly diagnosed high-grade glioma patients and specifically the effect of tumor recurrence. Following baseline assessment (after surgery and before radiotherapy), neurocognitive functioning was evaluated at 8 and 16 months. Neurocognitive summary measures were calculated to detect possible deficits in the domains of (1) information processing, (2) psychomotor function, (3) attention, (4) verbal memory, (5) working memory, and (6) executive functioning. Repeated-measures analyses of covariance were used to evaluate changes over time. Thirty-six patients were tested at baseline only. Follow-up data were obtained for 32 patients: 14 had a follow-up at 8 months, and 18 had an additional follow-up at 16 months. Between baseline and eight months, patients deteriorated in information-processing capacity, psychomotor speed, and attentional functioning. Further deterioration was observed between 8 and 16 months. Of 32 patients, 15 suffered from tumor recurrence before the eight-month follow-up. Compared with recurrence-free patients, not only did patients with recurrence have lower information-processing capacity, psychomotor speed, and executive functioning, but they also exhibited a more pronounced deterioration between baseline and eight-month follow-up. This difference could be attributed to the use of antiepileptic drugs in the patient group with recurrence. This study showed a marked decline in neurocognitive functioning in HGG patients in the course of their disease. Patients with tumor progression performed worse on neurocognitive tests than did patients without progression, which could be attributed to the use of antiepileptic drugs. The possibility of deleterious effects is important to consider when prescribing antiepileptic drug treatment.
引用
收藏
页码:53 / 62
页数:10
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