Adaptive Memetic Particle Swarm Optimization with Variable Local Search Pool Size

We propose an adaptive Memetic Particle Swarm Optimization algorithm where local search is selected from a pool of different algorithms. The choice of local search is based on a probabilistic strategy that uses a simple metric to score the efficiency of local search. Our study investigates whether the pool size affects the memetic algorithm’s performance, as well as the possible benefit of using the adaptive strategy against a baseline static one. For this purpose, we employed the memetic algorithms framework provided in the recent MEMPSODE optimization software, and tested the proposed algorithms on the Benchmarking Black Box Optimization (BBOB 2012) test suite. The obtained results lead to a series of useful conclusions

Personalized radiotherapy design for glioblastoma: Integrating mathematical tumor models, multimodal scans, and bayesian inference.

Glioblastoma (GBM) is a highly invasive brain tumor, whose cells infiltrate surrounding normal brain tissue beyond the lesion outlines visible in the current medical scans. These infiltrative cells are treated mainly by radiotherapy. Existing radiotherapy plans for brain tumors derive from population studies and scarcely account for patient-specific conditions. Here, we provide a Bayesian machine learning framework for the rational design of improved, personalized radiotherapy plans using mathematical modeling and patient multimodal medical scans. Our method, for the first time, integrates complementary information from high-resolution MRI scans and highly specific FET-PET metabolic maps to infer tumor cell density in GBM patients. The Bayesian framework quantifies imaging and modeling uncertainties and predicts patient-specific tumor cell density with credible intervals. The proposed methodology relies only on data acquired at a single time point and, thus, is applicable to standard clinical settings. An initial clinical population study shows that the radiotherapy plans generated from the inferred tumor cell infiltration maps spare more healthy tissue thereby reducing radiation toxicity while yielding comparable accuracy with standard radiotherapy protocols. Moreover, the inferred regions of high tumor cell densities coincide with the tumor radioresistant areas, providing guidance for personalized dose-escalation. The proposed integration of multimodal scans and mathematical modeling provides a robust, non-invasive tool to assist personalized radiotherapy design