About this trial
Glioma is a cancer of glial cells, a class of tissue supporting neuronal function in the brain. As many as 85% of glioma patients experience cognitive impairment. This is not only from direct tumor involvement, but also from therapy such as cranial radiation and chemotherapy, which degrades neuronal function. There is evidence that serotonin selective reuptake inhibitors (SSRIs), such as escitalopram, improve cognition or prevent cognitive decline and may also improve outcomes critical to overall survival including functional independence, psychosocial stability, and quality of life. This pilot study will evaluate the effectiveness of the selective serotonin reuptake inhibitor (SSRI) escitalopram for treating cognitive impairment in newly diagnosed grade IV glioma over a 17 week treatment period.
Eligibility criteria
Qualifiers
Pathologically proven diagnosis of Grade IV glioma
Newly diagnosed disease to receive chemotherapy and/or radiation
Performance status Eastern Cooperative Oncology Group (ECOG) 0-2 or equivalent
19 years of age or older
Disqualifiers
Hemifield defects (obscures visual field necessary to participate in all tests)
Inability to undergo MRI
Severe renal impairment defined as Glomerular Filtration Rate (GFR) <30 mL/minute
Screen positive for depression or anxiety
Trial design
Treatments tested in this trial
- Escitalopram Oral Capsules