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Table 1 Clinical data, histology, and tumor marker expression of primary GBM vs. secondary GSM

From: Secondary gliosarcoma: the clinicopathological features and the development of a patient-derived xenograft model of gliosarcoma

Tumor

Tumor genetic and molecular profile

Histological features

Treatment

Primary GBM

GFAP positive

Olig2 positive

ATRX preserved

IDH-1/IDH-2 WT

1p/19q no LOH

MGMT promoter unmethylated

STAG2 R216 mutation

Ki-67 15–20%

Moderate neoplastic cellularity on eosinophilic fibrillary background.

Surgery + Concurrent chemoRT + Chemotherapy with TMZ

Bevacizumab, carboplatin, olaparib

Secondary GSM

GFAP positive

Olig2 positive

Ki-67 ≤ 20%

P53 heterogenous expression

Spindle cell morphology, distinct glial and sarcomatous component.

Surgery + bevacizumab only

  1. GBM glioblastoma multiforme, GSM gliosarcoma, WT Wild type, LOH loss of heterozygosity, RT radiotherapy, TMZ temozolomide