IDH-wild-type
IDH-wild-type predicts individualized survival probabilities for patients with isocitrate dehydrogenase (IDH)-wild-type glioblastoma (GBM) using clinical and molecular prognostic variables.
Key Features:
- Data-Driven Development: Constructed using data from newly diagnosed GBM patients collected between 2007 and 2017 from the Ohio Brain Tumor Study (OBTS) and the University of California San Francisco (UCSF) cohorts.
- Incorporated Variables: Integrates age at diagnosis, sex, extent of resection, concurrent radiation/temozolomide (TMZ) status, Karnofsky Performance Status (KPS), O6-methylguanine-DNA methyltransferase (MGMT) methylation status, and IDH mutation status.
- Advanced Statistical Methods: Employs Cox proportional hazards regression, random survival forests, and recursive partitioning analysis for prognostic modeling.
- Validation Process: Includes internal validation by 10-fold cross-validation and external validation assessed by plotting calibration curves.
- Clinical Utility: Produces individualized survival probability estimates to inform patient counseling and treatment planning for newly diagnosed IDH-wild-type GBM.
Scientific Applications:
- Prognostication: Provides individualized survival estimates for patients with IDH-wild-type GBM incorporating clinical and molecular factors.
- Treatment planning and counseling: Supports clinical decision-making by quantifying survival probabilities relevant to therapeutic strategy selection and patient discussions.
Methodology:
Model development used Cox proportional hazards regression, random survival forests, and recursive partitioning analysis with internal validation by 10-fold cross-validation and external validation via calibration curves.
Topics
Details
- Tool Type:
- web application
- Added:
- 1/9/2020
- Last Updated:
- 12/14/2020
Operations
Publications
Gittleman H, Cioffi G, Chunduru P, Molinaro AM, Berger MS, Sloan AE, Barnholtz-Sloan JS. An independently validated nomogram for isocitrate dehydrogenase-wild-type glioblastoma patient survival. Neuro-Oncology Advances. 2019;1(1). doi:10.1093/noajnl/vdz007. PMID:31608326. PMCID:PMC6777501.
PMID: 31608326
PMCID: PMC6777501
Funding: - National Institutes of Health: CA217956
- National Cancer Institute: P50CA097257