Evidence map›Paper›PMID 41144062›Full record

ArticleJournal of neuro-oncology2025

Survival outcomes associated with antidepressant use in glioblastoma: a cohort study.

Yifei Sun, Mohammad Hamo, Travis Atchley, James M Markert, Burt Nabors, Dagoberto Estevez-Ordonez

Abstract read
In one paragraph

Article in Journal of neuro-oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Yifei SunMarnix E. Heersink School of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA. ysun3@uab.edu.
Mohammad HamoMarnix E. Heersink School of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA.
Travis AtchleyDepartment of Neurosurgery, University of Alabama at Birmingham, Birmingham, AL, USA.
James M MarkertDepartment of Neurosurgery, University of Alabama at Birmingham, Birmingham, AL, USA.
Burt NaborsO'Neal Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, AL, USA.
Dagoberto Estevez-OrdonezDepartment of Neurological Surgery, University of Miami & Jackson Health System, 1095 NW 14th Terrace, 2nd FL, Miami, FL, 33136, USA. dagoberto.estevezor@jhsmiami.org.

Funding

UAB Research Education Program for Residents and Fellows in NeuroscienceR25NS079188 · NINDS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI STANDAERT, DAVID G. · 2012 to 2022
$1.1M
National Institute of Neurological Disorders and Stroke of the National Institutes of Health R25NS079188NINDS NIH HHS R25 NS079188
6 · The paper itself

Abstract

purposeGlioblastoma is the most common primary brain malignancy and carries significant mortality. Preclinical studies have highlighted the efficacy of antidepressant therapy in inhibiting glioblastoma progression; however, real-world evidence remains conflicting. We sought to investigate the impact of different commonly utilized antidepressant therapies on survival in patients with glioblastoma.

methodsIn total, 1464 consecutive patients with glioblastoma treated at a single institution from 2008 to 2023 were included for analysis. Multivariate cox regression analysis with antidepressant usage modeled as a time varying covariate was used to assess the effect of antidepressants while controlling for a priori selected clinical variables with known relevance to survival.

resultsThe median age at diagnosis was 62 (IQR 52-70) years with a median overall survival of 13.8 months. Of the cohort, 44% utilized antidepressants after diagnosis, with SSRIs as the most common class utilized (26%). The median duration of any antidepressant therapy was 111 (IQR 9-303) days. In a time varying, multivariate cox regression, usage of SSRIs (HR 1.4, 95%CI 1.21-1.62), SNRIs (HR 1.33, 95%CI 1.03-1.72), serotonin modulators (HR 1.61, 95%CI 1.40-1.86), and atypical antidepressants (HR 1.7, 95%CI 1.28-2.26) were associated with worse survival. Amongst SSRIs, only escitalopram (HR 1.33, 95%CI 1.10-1.60) and citalopram (HR 1.31, 95%CI 1.01-1.70) were associated with worse survival.

conclusionsAntidepressant therapy is associated with worse survival in patients with glioblastoma after adjusting for known factors with relevance to survival. Clinicians should consider the risks and benefits of prescribing antidepressants in patients with glioblastoma. Further evidence is necessary to better understand the impact of antidepressant therapy in glioblastoma survival.

Indexed as

Antidepressive AgentsBrain NeoplasmsDepressionGlioblastomaAgedCohort StudiesFemaleFollow-Up StudiesHumansMaleMiddle AgedPrognosisRetrospective StudiesSurvival RateAntidepressive AgentsAntidepressantsGlioblastomaSurvival

Identifiers

PMID41144062
PMCPMC12559032

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.