Optimizing normal tissue sparing via spatiotemporal optimization under equivalent tumor-radical efficacy

TL;DR

This paper introduces a spatiotemporal optimization model for radiation therapy that ensures effective tumor cell kill while minimizing damage to healthy tissue by considering tumor proliferation dynamics.

Contribution

It develops a novel optimization framework incorporating tumor lag and doubling time to determine optimal dose fractionation and minimize organ damage.

Findings

Mean BED to target meets tumor kill requirements.

Optimal number of fractions varies with tumor proliferation parameters.

Model supports hyperfractionation and accelerated strategies.

Abstract

Objective: Spatiotemporal optimization in radiation therapy involves determining the optimal number of dose delivery fractions (temporal) and the optimal dose per fraction (spatial). Traditional approaches focus on maximizing the biologically effective dose (BED) to the target while constraining BED to organs-at-risk (OAR), which may lead to insufficient BED for complete tumor cell kill. This work proposes a formulation that ensures adequate BED delivery to the target while minimizing BED to the OAR. Approach: A spatiotemporal optimization model is developed that incorporates an inequality constraint to guarantee sufficient BED for tumor cell kill while minimizing BED to the OAR. The model accounts for tumor proliferation dynamics, including lag time (delay before proliferation begins) and doubling time (time for tumor volume to double), to optimize dose fractionation. Results: The performance of our formulation is evaluated for varying lag and doubling times. The results show that mean BED to the target consistently meets the minimum requirement for tumor cell kill. Additionally, the mean BED to OAR varies based on tumor proliferation dynamics. In the prostate case with lag time of 7 days and doubling time of 2 days, it is observed that mean BED delivered to femoral head is lowest at around 20 fractions, making this an optimal choice. While in the head-and-neck case, mean BED to OAR decreases as the number of fractions increases, suggesting that a higher number of fractions is optimal. Significance: A spatiotemporal optimization model is presented that minimizes BED to the OAR while ensuring sufficient BED for tumor cell kill. By incorporating tumor lag and doubling time, the approach identifies optimal number of fractions. This model can be extended to support hyperfractionation or accelerated fractionation strategies, offering a versatile tool for clinical treatment planning.