DREAP
DREAP analyzes radiation-induced biological responses by estimating surviving fraction (SF), relative biological effectiveness (RBE), normal tissue complication probability (NTCP), and tumor control probability (TCP) from clonogenic assay and treatment-plan data across cell population and organ scales.
Key Features:
- Surviving Fraction (SF) Models: Incorporates five established cell population SF models to estimate SF and RBE from clonogenic assay data.
- NTCP and TCP Models: Implements two established models to calculate NTCP and TCP from radiation treatment plans.
- Quantitative Analyses and Graphical Representation: Provides quantitative analyses and graphical outputs to verify and interpret model results.
- Comparative Plan Analysis: Compares NTCP, TCP, uncomplicated TCP (UCP), and user-dependent weight-based UCP (UUCP) across up to three rival treatment plans.
- Uncertainty Verification: Verifies estimated SF, model parameters, RBE, and associated uncertainties.
Scientific Applications:
- Radiation Biology Research: Enables analysis of cellular and tissue responses to ionizing radiation using SF and RBE estimates from clonogenic assays.
- Cancer Treatment Planning: Supports evaluation and comparison of treatment plans by computing NTCP, TCP, UCP, and UUCP metrics.
- Clinical and Academic Studies: Facilitates validation and quantitative assessment of radiobiological models and therapy outcomes across tested cell lines and plans.
Methodology:
DREAP uses deterministic models validated across tested cell lines, reporting averaged mean relative errors (MREs) not exceeding 0.3% for SF models and below 0.1% for NTCP/TCP calculations, with computations for SF, RBE, NTCP, and TCP completed in under 1.5 seconds.
Topics
Details
- Added:
- 11/14/2019
- Last Updated:
- 12/22/2020
Operations
Publications
Lee K, Jung W. Dose response analysis program (DREAP): A user-friendly program for the analyses of radiation-induced biological responses utilizing established deterministic models at cell population and organ scales. Physica Medica. 2019;64:132-144. doi:10.1016/j.ejmp.2019.06.013. PMID:31515012.