Regularized Parameter Identification in the Tumor Growth Model

Mathematics, 2026

Full text Open access: Gold Metadata (CSL-JSON)
DOI 10.3390/math14162962
Data confidence 70 medium
How this score is calculated

It is built from checkable properties of the record itself: whether the article has a DOI, how many independent sources confirmed its data, whether the required fields are filled in, and how recent the latest confirmation is. Disagreement between sources and a missing identifier lower it. A value of 80 or above means the record was published without further checking; 60 to 79 means it is published at reduced confidence, with a manual check advisable. A record verified by an editor by hand is never pushed below 90 by a recalculation. This scores our data about the article, not the article itself.

Abstract

This study addresses the inverse problem of parameter identification in mathematical models of tumor growth under limited and noisy experimental data. Three classical growth models—logistic, Richards, and Gompertz—are investigated in the context of structural and practical identifiability. It is demonstrated that, despite structural identifiability, parameter estimation remains highly unstable due to the ill-posed nature of the inverse problem. A comparative analysis of the Levenberg–Marquardt method and a genetic algorithm shows that improvements in optimization strategies alone do not resolve this instability and may lead to overfitting. To overcome this limitation, a Tikhonov regularization framework is introduced for the Gompertz model, ensuring stable and physically interpretable parameter estimates. The regularized formulation provides a balance between data fidelity and parameter stability, resulting in improved agreement with experimental observations. To further validate the identified parameters, a reaction–diffusion partial differential equation model is employed. Numerical simulations demonstrate that regularized parameters lead to significantly different spatial tumor morphologies, including more compact structures with sharper interfaces, highlighting the impact of inverse problem regularization on forward model predictions. The results confirm that the primary limitation in tumor growth modeling lies in the ill-posedness of the inverse problem rather than in the choice of optimization algorithm. The proposed framework provides a robust approach for parameter identification and improves the reliability of predictive tumor growth models.