T2 FLAIR Hyperintensity Volume Is Associated With Cognitive Function and Quality of Life in Clinically Stable Patients With Lower Grade Gliomas

Tracy L Luks; Javier E Villanueva-Meyer; Christina Weyer-Jamora; Karin Gehring; Angela Jakary; Shawn L Hervey-Jumper; Steve E Braunstein; Paige M Bracci; Melissa S Brie; Ellen M Smith; Susan M Chang; Jennie W Taylor

doi:10.3389/fneur.2021.769345

T2 FLAIR Hyperintensity Volume Is Associated With Cognitive Function and Quality of Life in Clinically Stable Patients With Lower Grade Gliomas

Front Neurol. 2022 Jan 28:12:769345. doi: 10.3389/fneur.2021.769345. eCollection 2021.

Authors

Affiliations

¹ Department of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, CA, United States.
² Zuckerberg San Francisco General Hospital, San Francisco, CA, United States.
³ Department of Neurological Surgery, University of California, San Francisco, San Francisco, CA, United States.
⁴ Department of Neurosurgery, Elisabeth-TweeSteden Hospital, Tilburg, Netherlands.
⁵ Department of Cognitive Neuropsychology, Tilburg University, Tilburg, Netherlands.
⁶ Department of Radiation Oncology, University of California, San Francisco, San Francisco, CA, United States.
⁷ Department of Epidemiology and Biostatistics, University of California, San Francisco, San Francisco, CA, United States.

Abstract

Survival outcomes for patients with lower grade gliomas (LrGG) continue to improve. However, damage caused both by tumor growth and by the consequences of treatment often leads to significantly impaired cognitive function and quality of life (QoL). While neuropsychological testing is not routine, serial clinical MRIs are standard of care for patients with LrGG. Thus, having a greater understanding of MRI indicators of cognitive and QoL impairment risk could be beneficial to patients and clinicians. In this work we sought to test the hypothesis that in clinically stable LrGG patients, T2 FLAIR hyperintensity volumes at the time of cognitive assessment are associated with impairments of cognitive function and QoL and could be used to help identify patients for cognitive and QoL assessments and interventions. We performed anatomical MR imaging, cognitive testing and QoL assessments cross-sectionally in 30 clinically stable grade 2 and 3 glioma patients with subjective cognitive concerns who were 6 or more months post-treatment. Larger post-surgical T2 FLAIR volume at testing was significantly associated with lower cognitive performance, while pre-surgical tumor volume was not. Older patients had lower cognitive performance than younger patients, even after accounting for normal age-related declines in performance. Patients with Astrocytoma, IDH mutant LrGGs were more likely to show lower cognitive performance than patients with Oligodendroglioma, IDH mutant 1p19q co-deleted LrGGs. Previous treatment with combined radiation and chemotherapy was associated with poorer self-reported QoL, including self-reported cognitive function. This study demonstrates the importance of appreciating that LrGG patients may experience impairments in cognitive function and QoL over their disease course, including during periods of otherwise sustained clinical stability. Imaging factors can be helpful in identifying vulnerable patients who would benefit from cognitive assessment and rehabilitation.

Keywords: cognition; glioma; neuro-oncology; neuroimaging; neuropsychology.

Abstract

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