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Racial and socioeconomic disparities in glioblastoma outcomes: A single-center, retrospective cohort study.
Estevez-Ordonez, Dagoberto; Abdelrashid, Moaaz; Coffee, Elizabeth; Laskay, Nicholas M B; Atchley, Travis J; Chkheidze, Rati; Fiveash, John B; Markert, James M; Lobbous, Mina; Maveal, Brandon M; Burt Nabors, Louis.
Afiliación
  • Estevez-Ordonez D; Department of Neurosurgery, University of Alabama at Birmingham, Birmingham, Alabama, USA.
  • Abdelrashid M; Department of Neurosurgery, University of Alabama at Birmingham, Birmingham, Alabama, USA.
  • Coffee E; Division of Neuro-Oncology, Department of Neurology, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
  • Laskay NMB; Department of Neurosurgery, University of Alabama at Birmingham, Birmingham, Alabama, USA.
  • Atchley TJ; Department of Neurosurgery, University of Alabama at Birmingham, Birmingham, Alabama, USA.
  • Chkheidze R; Division of Neuropathology, Department of Pathology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
  • Fiveash JB; Department of Radiation Oncology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
  • Markert JM; O'Neal Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, Alabama, USA.
  • Lobbous M; Department of Neurosurgery, University of Alabama at Birmingham, Birmingham, Alabama, USA.
  • Maveal BM; O'Neal Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, Alabama, USA.
  • Burt Nabors L; School of Public Health, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Cancer ; 129(19): 3010-3022, 2023 10 01.
Article en En | MEDLINE | ID: mdl-37246417
BACKGROUND: Glioblastoma (GBM) is the most common malignant primary brain tumor. Emerging reports have suggested that racial and socioeconomic disparities influence the outcomes of patients with GBM. No studies to date have investigated these disparities controlling for isocitrate dehydrogenase (IDH) mutation and O-6-methylguanine-DNA methyltransferase (MGMT) status. METHODS: Adult patients with GBM were retrospectively reviewed at a single institution from 2008 to 2019. Univariable and multivariable complete survival analyses were performed. A Cox proportional hazards model was used to assess the effect of race and socioeconomic status controlling for a priori selected variables with known relevance to survival. RESULTS: In total, 995 patients met inclusion criteria. Of these, 117 patients (11.7%) were African American (AA). The median overall survival for the entire cohort was 14.23 months. In the multivariable model, AA patients had better survival compared with White patients (hazard ratio [HR], 0.37; 95% confidence interval [CI], 0.2-0.69). The observed survival difference was significant in both a complete case analysis model and a multiple imputations model accounting for missing molecular data and controlling for treatment and socioeconomic status. AA patients with low income (HR, 2.17; 95% CI, 1.04-4.50), public insurance (HR, 2.25; 95% CI, 1.04-4.87), or no insurance (HR, 15.63; 95% CI, 2.72-89.67) had worse survival compared with White patients with low income, public insurance, or no insurance, respectively. CONCLUSIONS: Significant racial and socioeconomic disparities were identified after controlling for treatment, GBM genetic profile, and other variables associated with survival. Overall, AA patients demonstrated better survival. These findings may suggest the possibility of a protective genetic advantage in AA patients. PLAIN LANGUAGE SUMMARY: To best personalize treatment for and understand the causes of glioblastoma, racial and socioeconomic influences must be examined. The authors report their experience at the O'Neal Comprehensive Cancer Center in the deep south. In this report, contemporary molecular diagnostic data are included. The authors conclude that there are significant racial and socioeconomic disparities that influence glioblastoma outcome and that African American patients do better.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Glioblastoma Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Humans Idioma: En Revista: Cancer Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Glioblastoma Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Humans Idioma: En Revista: Cancer Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos