Selective serotonin reuptake inhibitors, glioblastoma multiforme, and impact on toxicities and overall survival: The mayo clinic experience

Jonathan S. Caudill, Paul D. Brown, Jane H. Cerhan, Teresa A. Rummans

Research output: Contribution to journalReview articlepeer-review

28 Scopus citations

Abstract

Purpose: The diagnoses of glioblastoma multiforme (GBM) and depression are often found to coexist. The impact of selective serotonin reuptake inhibitors (SSRI) on treatment-related toxicity and outcome in patients with GBM is unclear. Methods and Materials: We retrospectively reviewed 160 patients with GBM who received treatment at our institution between 1999 and 2008. Those taking an SSRI during treatment for GBM were identified and toxicities were assessed. Results: Median survival for the entire cohort was 1.05 years. A total of 35 patients (21.8%) took an SSRI during initial treatment for GBM. There was no statistical difference in the rate of ≥grade 3 toxicity in patients taking an SSRI when compared with those who were not (11.4% vs. 13.6%, respectively; P = 1.00). Two-year survival in the cohort of patients taking an SSRI was 32% versus 17% in those who were not (P = 0.18). After making adjustment for age, recursive partitioning analysis class, and extent of surgery, absence of an SSRI during treatment was associated with a hazard risk of 1.5 (95% confidence interval = 1.00-2.42; P = 0.05). Conclusions: This retrospective review suggests that concomitant use of an SSRI during treatment does not adversely affect survival. There was no increased toxicity with the use of SSRI concurrent with treatment of newly-diagnosed GBM.

Original languageEnglish (US)
Pages (from-to)385-387
Number of pages3
JournalAmerican Journal of Clinical Oncology: Cancer Clinical Trials
Volume34
Issue number4
DOIs
StatePublished - Aug 2011

Keywords

  • citalopram
  • depression
  • glioblastoma multiforme
  • selective serotonin reuptake inhibitor
  • toxicity

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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