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  4. Disease characteristics and clinical specific survival prediction of spinal ependymoma: a genetic and population-based study

Disease characteristics and clinical specific survival prediction of spinal ependymoma: a genetic and population-based study

Frontiers in Neurology, 2024 · DOI: 10.3389/fneur.2024.1454061 · Published: September 13, 2024

OncologyGeneticsResearch Methodology & Design

Simple Explanation

This study explores spinal ependymoma (SP-EP), a common spinal cord tumor. Early diagnosis and treatment improve patient outcomes. The research identifies key genes characteristic of SP-EP by analyzing RNA sequencing data and clinical information. A survival-related nomogram is developed to predict patient survival rates. The researchers used data from the Gene Expression Integrated Database (GEO) to find genes that are expressed differently in SP-EP samples compared to normal samples. Machine learning and the CIBERSORT algorithm helped to identify immune characteristic genes specific to SP-EP patients. This enhances the understanding of target genes. The study used data from the Surveillance, Epidemiology, and End Results (SEER) Database, screening for factors that significantly affect patient outcomes. The developed nomogram visualizes predicted overall survival rates at 3, 5, and 8 years post-diagnosis. The model's reliability was assessed using metrics like the consistency index and ROC curves.

Study Duration
20 Years
Participants
1,696 patients diagnosed with SP-EP
Evidence Level
Not specified

Key Findings

  • 1
    A total of 5,151 differentially expressed genes (DEGs) were identified between SP-EP and normal samples. These DEGs are involved in cellular processes like cell cycle regulation and cell sensitivity mechanisms, according to Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis.
  • 2
    Immune infiltration analysis identified CELF4 as a core gene. The 3-year, 5-year, and 8-year survival rates for SP-EP patients were 72.5%, 57.0%, and 40.8%, respectively. Diagnostic age, gender, and surgical approach were independent prognostic factors for overall survival.
  • 3
    A nomogram model was constructed based on prognostic factors, showing good consistency between predicted and actual results. More extensive surgical resection could extend patients’ overall survival.

Research Summary

The study identified CELF4 as a central gene associated with immune infiltration among DEGs through bioinformatics analysis of microarray datasets. Previous research indicates that CELF4 may play a crucial role in the development of SP-EP. A prognostic prediction model, utilizing the SEER database in the form of a nomogram, was developed and validated. This model enables clinicians to accurately assess treatment risks and benefits. The developed model enhances personalized therapeutic strategies and prognosis predictions for SP-EP patients.

Practical Implications

Personalized Treatment Strategies

The nomogram allows clinicians to assess treatment risks and benefits accurately, leading to more personalized treatment plans.

Improved Prognosis Prediction

The prognostic prediction model enables better estimation of survival rates, aiding in patient counseling and management.

Targeted Research

Identifying CELF4 as a key gene suggests new avenues for targeted therapies and further research into the pathogenesis of SP-EP.

Study Limitations

  • 1
    Retrospective cohort study prone to selection bias.
  • 2
    Validation process limited to internal data; external validation needed.
  • 3
    Lack of detailed data on chemotherapy and radiation in the SEER database.

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