Mild cognitive impairment in long-term brain tumor survivors following brain irradiation.


Journal

Journal of neuro-oncology
ISSN: 1573-7373
Titre abrégé: J Neurooncol
Pays: United States
ID NLM: 8309335

Informations de publication

Date de publication:
01 2019
Historique:
received: 01 08 2018
accepted: 14 10 2018
pubmed: 9 11 2018
medline: 16 4 2019
entrez: 9 11 2018
Statut: ppublish

Résumé

There is no accepted classification of cognitive impairment in cancer survivors. We assess the extent of mild cognitive impairment (MCI) syndrome in brain tumor survivors using criteria adapted from the National Institute on Aging and the Alzheimer's Association (NIA-AA). We retrospectively reviewed the cognitive data of brain tumor survivors post-radiation therapy (RT) enrolled from 2008 to 2011 in a randomized trial of donepezil versus placebo for cognitive impairment. One hundred and ninety eight adult survivors with primary or metastatic brain tumors who were ≥ 6 months post RT were recruited at 24 sites in the United States. Cognitive function was assessed at baseline, 12 and 24 weeks post-randomization. For this analysis, we used baseline data to identify MCI and possible dementia using adapted NIA-AA criteria. Cases were subtyped into four groups: amnestic MCI-single domain (aMCI-sd), amnestic MCI-multiple domain (aMCI-md), non-amnestic MCI-single domain (naMCI-sd), and non-amnestic MCI-multiple domain (naMCI-md). One hundred and thirty one of 197 evaluable patients (66%) met criteria for MCI. Of these, 13% were classified as aMCI-sd, 58% as aMCI-md, 19% as naMCI-sd, and 10% as naMCI-md. Patients with poorer performance status, less education, lower household income and those not working outside the home were more likely to be classified as MCI. Two-thirds of post-RT brain tumor survivors met NIA-AA criteria for MCI. This taxonomy may be useful when applied to brain tumor survivors because it defines cognitive phenotypes that may be differentially associated with course, treatment response, and risk factor profiles.

Identifiants

pubmed: 30406339
doi: 10.1007/s11060-018-03032-8
pii: 10.1007/s11060-018-03032-8
pmc: PMC6570494
mid: NIHMS1013841
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

235-244

Subventions

Organisme : NIA NIH HHS
ID : P30 AG049638
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA081851
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA189824
Pays : United States
Organisme : NINR NIH HHS
ID : R01 NR009675
Pays : United States

Références

Arch Neurol. 1999 Mar;56(3):303-8
pubmed: 10190820
Psychooncology. 2003 Sep;12(6):612-9
pubmed: 12923801
Arch Neurol. 2003 Oct;60(10):1385-9
pubmed: 14568808
Arch Clin Neuropsychol. 1996;11(4):329-38
pubmed: 14588937
Health Qual Life Outcomes. 2003 Dec 16;1:79
pubmed: 14678568
Arch Neurol. 2004 Jan;61(1):59-66
pubmed: 14732621
J Intern Med. 2004 Sep;256(3):183-94
pubmed: 15324362
J Intern Med. 2004 Sep;256(3):240-6
pubmed: 15324367
Int J Radiat Oncol Biol Phys. 2007 Dec 1;69(5):1496-501
pubmed: 17869448
Ann Intern Med. 2008 Mar 18;148(6):427-34
pubmed: 18347351
Lancet Neurol. 2009 Sep;8(9):810-8
pubmed: 19665931
Alzheimer Dis Assoc Disord. 2010 Jul-Sep;24(3):248-55
pubmed: 20473134
Neurology. 2010 Sep 7;75(10):889-97
pubmed: 20820000
Alzheimers Dement. 2011 May;7(3):270-9
pubmed: 21514249
Alzheimers Dement. 2011 May;7(3):263-9
pubmed: 21514250
J Neurooncol. 2012 Sep;109(2):357-63
pubmed: 22700031
Front Oncol. 2012 Jul 19;2:73
pubmed: 22833841
Neurology. 2013 Feb 19;80(8):747-53
pubmed: 23390169
Neuro Oncol. 2013 Oct;15(10):1429-37
pubmed: 23956241
J Clin Oncol. 2015 May 20;33(15):1653-9
pubmed: 25897156
J Cancer Surviv. 2016 Feb;10(1):176-84
pubmed: 26130292
Alzheimers Dement (Amst). 2016;2:1-11
pubmed: 26949733
JAMA. 2016 Jul 26;316(4):401-409
pubmed: 27458945
Neuro Oncol. 2017 Nov 6;19(suppl_5):v1-v88
pubmed: 29117289
Adv Radiat Oncol. 2017 Aug 30;2(4):624-629
pubmed: 29204530
Alzheimers Dement. 2018 Apr;14(4):535-562
pubmed: 29653606
J Oncol Research. 2017;1(1):null
pubmed: 29873324
Neurology. 1984 Jul;34(7):939-44
pubmed: 6610841
Cancer. 1995 Mar 1;75(5):1151-61
pubmed: 7850714
J Clin Oncol. 1998 Jul;16(7):2522-7
pubmed: 9667273

Auteurs

Christina K Cramer (CK)

Department of Radiation Oncology, Wake Forest School of Medicine, Medical Center Blvd, Winston-Salem, NC, 27157, USA. ccramer@wakehealth.edu.

Neil McKee (N)

Department of Radiation Oncology, Wake Forest School of Medicine, Medical Center Blvd, Winston-Salem, NC, 27157, USA.

L Doug Case (LD)

Department of Biostatistical Sciences, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.

Michael D Chan (MD)

Department of Radiation Oncology, Wake Forest School of Medicine, Medical Center Blvd, Winston-Salem, NC, 27157, USA.

Tiffany L Cummings (TL)

Department of Neurology, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.

Glenn J Lesser (GJ)

Department of Internal Medicine (Hematology and Oncology), Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.

Edward G Shaw (EG)

Department of Internal Medicine (Gerontology and Geriatrics), Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.

Stephen R Rapp (SR)

Department of Psychiatry and Behavioral Medicine, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.

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