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Age-stratified comorbid and pharmacologic analysis of patients with glioblastoma.
Rabin, Erik E; Huang, Jonathan; Kim, Miri; Mozny, Andreas; Lauing, Kristen L; Penco-Campillo, Manon; Zhai, Lijie; Bommi, Prashant; Mi, Xinlei; Power, Erica A; Prabhu, Vikram C; Anderson, Douglas E; Barton, Kevin P; Walunas, Theresa L; Schiltz, Gary E; Amidei, Christina; Sanchez-Gomez, Pilar; Thakkar, Jigisha P; Lukas, Rimas V; Wainwright, Derek A.
Afiliação
  • Rabin EE; Department of Neurological Surgery at Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Huang J; Department of Neurological Surgery at Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Kim M; Department of Neurological Surgery at Loyola University Chicago Stritch School of Medicine, Maywood, IL, USA.
  • Mozny A; Department of Neurological Surgery at Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Lauing KL; Department of Cancer Biology, Loyola University Chicago Stritch School of Medicine, Maywood, IL, USA.
  • Penco-Campillo M; Department of Cancer Biology, Loyola University Chicago Stritch School of Medicine, Maywood, IL, USA.
  • Zhai L; Department of Cancer Biology, Loyola University Chicago Stritch School of Medicine, Maywood, IL, USA.
  • Bommi P; Department of Cancer Biology, Loyola University Chicago Stritch School of Medicine, Maywood, IL, USA.
  • Mi X; Department of Preventive Medicine-Division of Biostatistics at Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Power EA; Department of Cancer Biology, Loyola University Chicago Stritch School of Medicine, Maywood, IL, USA.
  • Prabhu VC; Department of Neurological Surgery at Loyola University Chicago Stritch School of Medicine, Maywood, IL, USA.
  • Anderson DE; Department of Neurological Surgery at Loyola University Chicago Stritch School of Medicine, Maywood, IL, USA.
  • Barton KP; Department of Medicine - Hematology/Oncology at Loyola University Chicago Stritch School of Medicine, Maywood, IL, USA.
  • Walunas TL; Department of Medicine - Division of General Internal Medicine and Geriatrics at Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Schiltz GE; Department of Preventive Medicine-Division of Health and Biomedical Informatics at Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Amidei C; Department of Chemistry at Northwestern University, Evanston, IL, USA.
  • Sanchez-Gomez P; Department of Neurological Surgery at Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Thakkar JP; Neurooncology Unit, Unidad Funcional de Investigación en Enfermedades Crónicas (UFIEC), Instituto de Salud Carlos III (ISCIII), Madrid, Spain.
  • Lukas RV; Department of Neurology at Loyola University Chicago Stritch School of Medicine, Maywood, IL, USA.
  • Wainwright DA; Department of Neurology at Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Brain Behav Immun Health ; 38: 100753, 2024 Jul.
Article em En | MEDLINE | ID: mdl-38600951
ABSTRACT

Background:

Increased age is a strong and unfavorable prognostic factor for patients with glioblastoma (GBM). However, the relationships between stratified patient age, comorbidities, and medications have yet to be explored in GBM patient survival analyses.

Objective:

To evaluate co-morbid conditions, tumor-related symptoms, medication prescriptions, and subject age for patients with GBM and to establish potential targets for prospective studies.

Methods:

Electronic health records for 565 patients with IDHwt GBM were evaluated at a single center between January 1, 2000 and August 9, 2021 were retrospectively assessed. Data were stratified by MGMT promoter methylation status when available and were used to construct multivariable time-dependent cox models and intra-cohort hazards.

Results:

Younger (<65 years of age) but not older (≥65 years) GBM patients demonstrated a worse prognosis with movement related disabilities (P < 0.0001), gait/balance difficulty (P = 0.04) and weakness (P = 0.007), as well as psychiatric conditions, mental health disorders (P = 0.002) and anxiety (P = 0.001). In contrast, older but not younger GBM patients demonstrated a worse prognosis with epilepsy (P = 0.039). Both groups had worse survival with confusion/altered mental status (P = 0.023 vs < 0.000) and an improved survival with a Temozolomide prescription. Older but not younger GBM patients experienced an improved hazard with a prescription of ace-inhibitor medications (P = 0.048).

Conclusion:

Age-dependent novel associations between clinical symptoms and medications prescribed for co-morbid conditions were demonstrated in patients with GBM. The results of the current work support future mechanistic studies that investigate the negative relationship(s) between increased age, comorbidities, and drug therapies for differential clinical decision-making across the lifespan of patients with GBM.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article