AUTHOR=Meyerheim Marcel , Panagiotidou Foteini , Georgiadi Eleni , Soudris Dimitrios , Stamatakos Georgios , Graf Norbert 

TITLE=Exploring the in silico adaptation of the Nephroblastoma Oncosimulator to MRI scans, treatment data, and histological profiles of patients from different risk groups

JOURNAL=Frontiers in Physiology

VOLUME=Volume 16 - 2025

YEAR=2025

URL=https://www.frontiersin.org/journals/physiology/articles/10.3389/fphys.2025.1465631

DOI=10.3389/fphys.2025.1465631

ISSN=1664-042X

ABSTRACT=IntroductionNephroblastoma or Wilms’ tumor is the most prevalent type of renal tumor in pediatric oncology. Although the overall survival rate for this condition is excellent today (∼90%), there have been no significant improvements over the past two decades. In silico models aim to simulate tumor progression and treatment responses over time; they hold immense potential for enhancing the predictive accuracy and optimizing treatment protocols as they are inspired by the digital twin paradigm.MethodsThe present study uses T2-weighted magnetic resonance images, chemotherapy treatment plans, and post-surgical histological profiles from three patients enrolled in the SIOP 2001/GPOH clinical trial, where each patient represents a distinct clinically assessed risk group. We investigated the clinical adaptation of the Nephroblastoma Oncosimulator to the datasets from these patients with the goal of deriving appropriate value distributions of the model input parameters that enable accurate prediction of tumor volume reduction in response to preoperative chemotherapy.ResultsOur primary focus was on the total cell kill ratio as a parameter reflecting treatment effectiveness. We derived the distribution of this parameter for one patient from each risk group: low (Mdn = 0.875, IQR [0.750, 0.875], n = 178), intermediate (Mdn = 0.875, IQR [0.750, 0.875], n = 175), and high (Mdn = 0.485, IQR [0.438, 0.532], n = 103). Statistically significant differences were observed between the high-risk group and both the low- and intermediate-risk groups (p < 0.001).DiscussionThe present work establishes a foundation for further studies using available retrospective datasets and additional patients per risk group. These efforts are expected to help validate the findings, advance model development, and extend this mechanistic multiscale discretized cancer model. However, clinical validation is ultimately required to assess the potential uses of the model in clinical decision-support systems.