好色先生

好色先生

Explore the latest content from across our publications

Log In

Forgot Password?
Create New Account

Loading... please wait

Abstract Details

Depression & Neurotoxicity in a Population of Brain Tumor Patients Treated with a Short Course of Prophylactic Levetiracetam
Neuro-oncology
P1 - Poster Session 1 (9:00 AM-5:00 PM)
432

To evaluate short course levetiracetam therapy by Beck Depression Index (BDI) and neurotoxicity scale scores in a cohort of brain tumor patients, sorted by tumor location.

We evaluated rates of depression & neurotoxic symptoms by tumor location in post resection brain tumor patients treated for 1 week vs 6 weeks of prophylactic levetiracetam.  The overall study goal was to determine optimal post-surgical therapy and minimize negative side effects. 

81 patients were enrolled postoperatively and randomized to one week (40 patients) or six weeks (41 patients) of levetiracetam.  BDI & neurotoxicity scales were performed on postoperative enrollment and at the study exit in 65 subjects.  Tumors were categorized into limbic, frontal, and bilateral frontal locations. P scores were calculated using the Wilcoxon rank sum test.

Higher neurotoxicity (9 vs –3, p=0.0420)  and BDI (4 vs. 0, p= 0.0086) scores were seen with bifrontal tumors vs. other locations, regardless of treatment arm.  Seizure incidence was rare, with 1 patient in each treatment arm (2.9% of total patients) experiencing a seizure during the follow-up period.

Nine patients treated with immediate release levetiracetam due to XR levetiracetam access issues tended to have increased BDI and neurotoxicity scores, but this did not reach significance (P=0.0821).  

Fatigue, slowing & memory difficulties were the predominant symptoms reported in any tumor location subgroup. No difference in BDI or neurotoxicity score was shown by treatment duration, race, or sex.

Increased BDI and neurotoxicity scores observed in post-resection patients with bifrontal tumors on levetiracetam raises concern for optimal postoperative recovery prior to neuro-oncologic therapy but could be confounded by co-administration of high dose corticosteroids and poor prognosis.

Regardless, increased vigilance & intervention in these patients may improve recovery, quality of life and reduce adverse effects of therapy. Future research is warranted to separate the effect of therapy from clinicopathological factors.

Authors/Disclosures
Matthew J. Goldman
PRESENTER
Mr. Goldman has nothing to disclose.
No disclosure on file
No disclosure on file
No disclosure on file
No disclosure on file
Jean E. Cibula, MD, FAAN (University of Florida) Dr. Cibula has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Medical Information Group. Dr. Cibula has received stock or an ownership interest from Merck. Dr. Cibula has received stock or an ownership interest from 3M. Dr. Cibula has received stock or an ownership interest from Steris. Dr. Cibula has received stock or an ownership interest from Baxter. The institution of Dr. Cibula has received research support from UCB Pharma.