Mathematical modeling of the synergetic effect between radiotherapy and immunotherapy

The synergy between radiotherapy and immunotherapy plays a pivotal role in enhancing tumor control and treatment outcomes. To explore the underlying mechanisms of synergy, we investigated a novel treatment approach known as personalized ultra-fractionated stereotactic adaptive radiation (PULSAR) therapy, which emphasizes the impact of radiation timing. Unlike conventional daily treatments, PULSAR delivers high-dose radiation in spaced intervals over weeks or months, enabling tumors to adapt and potentially enhancing synergy with immunotherapy. Drawing on insights from small-animal radiation studies, we developed a discrete-time model based on multiple difference equations to elucidate the temporal dynamics of tumor control driven by both radiation and the adaptive immune response. By accounting for the migration and infiltration of T cells within the tumor microenvironment, we established a quantitative link between radiation therapy and immunotherapy. Model parameters were estimated using a simulated annealing algorithm applied to training data, and our model achieved high accuracy for the test data with a root mean square error of 287 mm<sup>3</sup>. Notably, our framework replicated the PULSAR effect observed in animal studies, revealing that longer intervals between radiation treatments in the context of immunotherapy yielded enhanced tumor control. Specifically, mice receiving immunotherapy alongside radiation pulses delivered at extended intervals, ten days, showed markedly improved tumor responses, whereas those treated with shorter intervals did not achieve comparable benefits. Moreover, our model offers an in-silico tool for designing future personalized ultra-fractionated stereotactic adaptive radiation trials. Overall, these findings underscore the critical importance of treatment timing in harnessing the synergy between radiotherapy and immunotherapy and highlight the potential of our model to optimize and individualize treatment protocols.

Authors

Institutions

Publication Details

Journal
Mathematical Biosciences & Engineering
Published
2025-01-01
DOI
https://doi.org/10.3934/mbe.2025044
Primary Topic
Mathematical Biology Tumor Growth
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Mathematical modeling of the synergetic effect between radiotherapy and immunotherapy

Steve Jiang, Yixun Xing, Debabrata Saha, Xun Jia et al.
Mathematical Biosciences & Engineering
Mathematical Biology Tumor Growth
article

Mathematical modeling of the synergetic effect between radiotherapy and immunotherapy

Steve Jiang, Yixun Xing, Debabrata Saha, Xun Jia, MaryLena Bleile, Hao Peng, Dan Nguyen, Casey Moore, Robert Timmerman
article en

Abstract

The synergy between radiotherapy and immunotherapy plays a pivotal role in enhancing tumor control and treatment outcomes. To explore the underlying mechanisms of synergy, we investigated a novel treatment approach known as personalized ultra-fractionated stereotactic adaptive radiation (PULSAR) therapy, which emphasizes the impact of radiation timing. Unlike conventional daily treatments, PULSAR delivers high-dose radiation in spaced intervals over weeks or months, enabling tumors to adapt and potentially enhancing synergy with immunotherapy. Drawing on insights from small-animal radiation studies, we developed a discrete-time model based on multiple difference equations to elucidate the temporal dynamics of tumor control driven by both radiation and the adaptive immune response. By accounting for the migration and infiltration of T cells within the tumor microenvironment, we established a quantitative link between radiation therapy and immunotherapy. Model parameters were estimated using a simulated annealing algorithm applied to training data, and our model achieved high accuracy for the test data with a root mean square error of 287 mm<sup>3</sup>. Notably, our framework replicated the PULSAR effect observed in animal studies, revealing that longer intervals between radiation treatments in the context of immunotherapy yielded enhanced tumor control. Specifically, mice receiving immunotherapy alongside radiation pulses delivered at extended intervals, ten days, showed markedly improved tumor responses, whereas those treated with shorter intervals did not achieve comparable benefits. Moreover, our model offers an in-silico tool for designing future personalized ultra-fractionated stereotactic adaptive radiation trials. Overall, these findings underscore the critical importance of treatment timing in harnessing the synergy between radiotherapy and immunotherapy and highlight the potential of our model to optimize and individualize treatment protocols.

Mathematical Biosciences & EngineeringVol. 22(5)
University of North Texas (US), Southern Methodist University (US), The University of Texas Southwestern Medical Center (US)
Openalex Percentile: Top 91%
Mathematical Biology Tumor Growth
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.