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Histological, molecular, clinical and outcomes characteristics of Multiple Lesion Glioblastoma. A retrospective monocentric study and review of literature.
Armocida, Daniele; Pesce, Alessandro; Di Giammarco, Federico; Frati, Alessandro; Salvati, Maurizio; Santoro, Antonio.
Afiliación
  • Armocida D; Human Neurosciences Department Neurosurgery Division "Sapienza" University, Italy. Electronic address: danielearmocida@yahoo.it.
  • Pesce A; Human Neurosciences Department Neurosurgery Division "Sapienza" University, Italy.
  • Di Giammarco F; Human Neurosciences Department Neurosurgery Division "Sapienza" University, Italy.
  • Frati A; Human Neurosciences Department Neurosurgery Division "Sapienza" University, Italy.
  • Salvati M; IRCCS "Neuromed" Pozzilli (IS), Italy.
  • Santoro A; Human Neurosciences Department Neurosurgery Division "Sapienza" University, Italy.
Neurocirugia (Astur : Engl Ed) ; 32(3): 114-123, 2021.
Article en En, Es | MEDLINE | ID: mdl-32564972
ABSTRACT

BACKGROUND:

Multiple lesion glioblastoma (M-GBM) represent a group of GBM patients in which there exist multiple foci of tumor enhancement. The prognosis is poorer than that of single-lesion GBM patients, but this actually is a controversial data. Is unknown whether multifocality has a genetic and molecular basis. Our specific aim is to identify the molecular characteristics of M-GBM by performing a comprehensive multidimensional analysis.

METHODS:

The surgical, radiological and clinical outcomes of patients that underwent surgery for GBM at our institution for 2 years have been retrospectively reviewed. We compared the overall survival (OS), progression free survival and extent of resection (EOR) between M-GBM tumors (type I) and S-GBM (single contrast-enhancing lesion, type II).

RESULTS:

A total of 177 patients were included in the final cohort, 12 patients had M-GBM and 165 patients had S-GBM. Although patients with M-GBM had higher tumor volumes and midline location, the EOR was not different between both type of lesions. Higher percentage of tumors with EGFR overexpression was detected in M-GBM. PFS and OS was significantly shorter in M-GBM.

CONCLUSIONS:

Considering no differences in EOR, patients with M-GBM showed shorter PFS and OS in comparison with S-GBM. Evidences about the M-GBM origin as a multifocal lesion because its molecular profile are suggested.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Glioblastoma Tipo de estudio: Observational_studies / Prognostic_studies Límite: Humans Idioma: En / Es Revista: Neurocirugia (Astur : Engl Ed) Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Glioblastoma Tipo de estudio: Observational_studies / Prognostic_studies Límite: Humans Idioma: En / Es Revista: Neurocirugia (Astur : Engl Ed) Año: 2021 Tipo del documento: Article