Glioblastoma as an age-related neurological disorder in adults.

dc.contributor.author

Kim, Miri

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Ladomersky, Erik

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Mozny, Andreas

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Kocherginsky, Masha

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O'Shea, Kaitlyn

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Reinstein, Zachary Z

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Zhai, Lijie

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Bell, April

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Lauing, Kristen L

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Bollu, Lakshmi

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Rabin, Erik

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Dixit, Karan

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Kumthekar, Priya

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Platanias, Leonidas C

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Hou, Lifang

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Zheng, Yinan

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Wu, Jennifer

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Zhang, Bin

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Hrachova, Maya

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Merrill, Sarah A

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Mrugala, Maciej M

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Prabhu, Vikram C

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Horbinski, Craig

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James, Charles David

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Yamini, Bakhtiar

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Ostrom, Quinn T

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Johnson, Margaret O

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Reardon, David A

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Lukas, Rimas V

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Wainwright, Derek A

dc.date.accessioned

2021-11-01T13:38:08Z

dc.date.available

2021-11-01T13:38:08Z

dc.date.issued

2021-01

dc.date.updated

2021-11-01T13:38:07Z

dc.description.abstract

Background

Advanced age is a major risk factor for the development of many diseases including those affecting the central nervous system. Wild-type isocitrate dehydrogenase glioblastoma (IDHwt GBM) is the most common primary malignant brain cancer and accounts for ≥90% of all adult GBM diagnoses. Patients with IDHwt GBM have a median age of diagnosis at 68-70 years of age, and increasing age is associated with an increasingly worse prognosis for patients with this type of GBM.

Methods

The Surveillance, Epidemiology, and End Results, The Cancer Genome Atlas, and the Chinese Glioma Genome Atlas databases were analyzed for mortality indices. Meta-analysis of 80 clinical trials was evaluated for log hazard ratio for aging to tumor survivorship.

Results

Despite significant advances in the understanding of intratumoral genetic alterations, molecular characteristics of tumor microenvironments, and relationships between tumor molecular characteristics and the use of targeted therapeutics, life expectancy for older adults with GBM has yet to improve.

Conclusions

Based upon the results of our analysis, we propose that age-dependent factors that are yet to be fully elucidated, contribute to IDHwt GBM patient outcomes.
dc.identifier

vdab125

dc.identifier.issn

2632-2498

dc.identifier.issn

2632-2498

dc.identifier.uri

https://hdl.handle.net/10161/23941

dc.language

eng

dc.publisher

Oxford University Press (OUP)

dc.relation.ispartof

Neuro-oncology advances

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10.1093/noajnl/vdab125

dc.subject

CD4

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IDO

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aging

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glioma

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immunotherapy

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senescence

dc.title

Glioblastoma as an age-related neurological disorder in adults.

dc.type

Journal article

duke.contributor.orcid

Ostrom, Quinn T|0000-0003-3469-7558

duke.contributor.orcid

Johnson, Margaret O|0000-0003-1208-622X|0009-0005-5596-3407

pubs.begin-page

vdab125

pubs.issue

1

pubs.organisational-group

School of Medicine

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Duke Cancer Institute

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Neurosurgery

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Neurology, General & Community Neurology

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Duke

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Institutes and Centers

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Clinical Science Departments

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Neurology

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Population Health Sciences

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Basic Science Departments

pubs.publication-status

Published

pubs.volume

3

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