Minimizing metastatic risk in radiotherapy fractionation schedules

Metastasis is the process by which cells from a primary tumor disperse and form new tumors at distant anatomical locations. The treatment and prevention of metastatic cancer remains an extremely challenging problem. This work introduces a novel biologically motivated objective function to the radiation optimization community that takes into account metastatic risk instead of the status of the primary tumor. In this work, we consider the problem of developing fractionated irradiation schedules that minimize production of metastatic cancer cells while keeping normal tissue damage below an acceptable level. A dynamic programming framework is utilized to determine the optimal fractionation scheme. We evaluated our approach on a breast cancer case using the heart and the lung as organs-at-risk (OAR). For small tumor alpha/beta values, hypo-fractionated schedules were optimal, which is consistent with standard models. However, for relatively larger alpha/beta values, we found the type of schedule depended on various parameters such as the time when metastatic risk was evaluated, the alpha/beta values of the OARs, and the normal tissue sparing factors. Interestingly, in contrast to standard models, hypo-fractionated and semi-hypo-fractionated schedules (large initial doses with doses tapering off with time) were suggested even with large tumor alpha/beta values. Numerical results indicate the potential for significant reduction in metastatic risk.