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.
Armocida, D., Pesce, A., Di Giammarco, F., Frati, A., Salvati, M., Santoro, A. (2021). Histological, molecular, clinical and outcomes characteristics of Multiple Lesion Glioblastoma. A retrospective monocentric study and review of literature. NEUROCIRUGIA, 32(3), 114-123 [10.1016/j.neucir.2020.04.003].
Histological, molecular, clinical and outcomes characteristics of Multiple Lesion Glioblastoma. A retrospective monocentric study and review of literature
Pesce, Alessandro;Salvati, Maurizio;Santoro, Antonio
2021-01-01
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.| File | Dimensione | Formato | |
|---|---|---|---|
|
3349923.pdf
solo utenti autorizzati
Tipologia:
Versione Editoriale (PDF)
Licenza:
Copyright dell'editore
Dimensione
4.55 MB
Formato
Adobe PDF
|
4.55 MB | Adobe PDF | Visualizza/Apri Richiedi una copia |
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.


