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. 2018 Mar 2;13(3):e0193694. doi: 10.1371/journal.pone.0193694

Table 1. Patient demographics, clinical features and cell line designations.

Cell Line Designation Location Histologya,[15] Primary Treatment Treatment at Recurrence Overall Survival (Months)
GS1 Right fronto-temporal Gliosarcoma Surgical resection N/A 4.3
TS1 Left frontal & thalamic Gliomatosis cerebri Biopsy only N/A 1.3
TS6 Right frontal GBM Surgical resection + TMZ +Irradiation PCV 9.2
TS9 Left frontal Recurrent GBM Surgical resection + TMZ +Irradiation Surgical resection +PCV 14.3
TS17 Right occipital GBM Surgical resection N/A 0.9
TS18 Left parietal GBM Surgical resection N/A 5.6
TS20 Left frontal GBM Surgical resection + TMZ +Irradiation N/A 8.4

aHistological diagnoses were made prior to the WHO 2016 re-classification. Gliomatosis cerebri is now referred to as a rare diffuse-pattern glioblastoma and gliosarcoma has been incorporated into the umbrella term IDH-wildtype glioblastoma.