研究目的
To develop a concurrent Monte Carlo treatment plan optimization platform that optimizes fluence during dose calculation to reduce computational time and memory overhead while maintaining dosimetric accuracy in radiation therapy.
研究成果
The concurrent Monte Carlo optimization platform significantly reduces computational time and memory overhead (50-80% history reduction, ~10% time overhead, minimal memory increase) while achieving conformal dose distributions. It shows promise for next-generation radiation therapy but needs further development for clinical use.
研究不足
The study uses simple cost functions and geometries; clinical applicability requires further validation. The backward difference method introduces truncation error, and step-size parameters are empirically determined. Handling zero bixel intensities and complex clinical objectives are not fully addressed.
1:Experimental Design and Method Selection:
The study uses a novel gradient descent algorithm integrated with Monte Carlo particle transport for concurrent optimization. It includes stochastic gradient descent with momentum and gradient rescaling/renormalization to handle stochasticity and negative gradients.
2:Sample Selection and Data Sources:
Two simple geometrical phantoms (cubic and horseshoe targets in water) and one clinical patient geometry (prostate case) are used. Data includes dose distributions and optimization metrics.
3:List of Experimental Equipment and Materials:
GEANT4 Monte Carlo toolkit for particle transport, in-house forward transport user code, optimization manager class, and computational hardware (not specified).
4:Experimental Procedures and Operational Workflow:
The platform initializes with ray-tracing, allocates memory, and performs iterative sub-beamlet transport. Each iteration updates dose and fluence, calculates gradients, and biases subsequent transport. Optimization terminates when gradient falls below a threshold.
5:Data Analysis Methods:
Metrics include reduction in transported histories, computational time overhead, and memory usage. Convergence is evaluated using cost functions and dose-volume histograms.
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