secondary glioblastoma

GPTKB entity

Statements (57)
Predicate Object
gptkbp:instance_of gptkb:Oncology
gptkbp:associated_with gptkb:neurofibromatosis_type_1
gptkb:hereditary_nonpolyposis_colorectal_cancer
gptkb:Li-Fraumeni_syndrome
gptkb:Turcot_syndrome
genetic mutations
gptkbp:characterized_by rapid growth
necrosis
infiltrative nature
gptkbp:clinical_trial ongoing
heterogeneous appearance
may have midline shift
may present with edema
often multifocal
gptkbp:death less than 5% at 5 years
gptkbp:diagnosis gptkb:MRI
CT scan
poor
gptkbp:epidemiology higher incidence in Caucasians
increased incidence in women
often arises from low-grade gliomas
gptkbp:genetic_alterations gptkb:TP53_mutation
ATRX loss
EGFR amplification
PTEN loss
IDH1 mutation
https://www.w3.org/2000/01/rdf-schema#label secondary glioblastoma
gptkbp:is_common_in adults
gptkbp:occurs_in 1-2 per 100,000 people
gptkbp:originated_in previous cancer
gptkbp:research_focus gptkb:immunotherapy
biomarkers
targeted therapy
gptkbp:risk_factor age
radiation exposure
previous cancer history
gptkbp:symptoms cognitive decline
headache
nausea
vomiting
seizures
vision problems
weakness
personality changes
gptkbp:treatment gptkb:surgery
palliative care
variable
clinical trials
side effects
supportive care
radiation therapy
chemotherapy
recurrence
resistance to therapy
gptkbp:type gptkb:Oncology
gptkbp:bfsParent gptkb:Oncology
gptkbp:bfsLayer 4