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Stochastic norton–simon–massagué tumor growth modeling: controlled and mixed-effect uncontrolled analysis

Stochastic norton–simon–massagué tumor growth modeling: controlled and mixed-effect uncontrolled analysis
Stochastic norton–simon–massagué tumor growth modeling: controlled and mixed-effect uncontrolled analysis
Tumorigenesis is a complex process that is heterogeneous and affected by numerous sources of variability. This article proposes a stochastic extension of a biologically grounded tumor growth model, referred to as the Norton-Simon-Massagué (NSM) model. First, we study the uncontrolled version of the model where the effect of the chemotherapeutic drug agent is absent. Conditions on the model's parameters are derived to guarantee the positivity of the solution of the proposed stochastic NSM model and hence its validity to describe the dynamics of tumor volume. The proof of positivity makes use of a Lyapunov-type method and the classical Feller's test for explosion. To calibrate the proposed model, we utilize a population mixed-effect modeling formulation and a maximum likelihood-based estimation algorithm. The identification algorithm is tested by fitting previously published tumor volume mice data. Second, we study the controlled version of the model, which includes the effect of chemotherapy treatment. Analysis of the influence of adding the control drug agent into the model and how sensitive it is to the stochastic parameters is performed both in open- and closed-loop viewpoints. The designed closed-loop control strategy that solves an optimal cancer therapy scheduling problem relies on the model predictive control (MPC) combined with extended Kalman filter approaches. The simulation results and concluding guiding principles are provided for both the open-and closed-loop control cases.
1063-6536
704-717
Belkhatir, Zehor
de90d742-a58f-4425-837c-20ff960fb9b6
Pavon, Michele
5964ce4f-304e-4930-90a8-b8eb10665304
Matthews, James C.
69b1352a-b07e-47f7-9a4e-f1b518674269
Pouryahya, Maryam
1e19637a-c44f-423d-9476-760d76809224
Deasy, Joseph O.
b7de1a95-3c23-47d7-9652-55a2a18f47bd
Norton, Larry
2d3639c9-925d-4acb-8340-1af418c86464
Belkhatir, Zehor
de90d742-a58f-4425-837c-20ff960fb9b6
Pavon, Michele
5964ce4f-304e-4930-90a8-b8eb10665304
Matthews, James C.
69b1352a-b07e-47f7-9a4e-f1b518674269
Pouryahya, Maryam
1e19637a-c44f-423d-9476-760d76809224
Deasy, Joseph O.
b7de1a95-3c23-47d7-9652-55a2a18f47bd
Norton, Larry
2d3639c9-925d-4acb-8340-1af418c86464

Belkhatir, Zehor, Pavon, Michele, Matthews, James C., Pouryahya, Maryam, Deasy, Joseph O. and Norton, Larry (2021) Stochastic norton–simon–massagué tumor growth modeling: controlled and mixed-effect uncontrolled analysis. IEEE Transactions on Control Systems Technology, 29 (2), 704-717. (doi:10.1109/tcst.2020.2975141).

Record type: Article

Abstract

Tumorigenesis is a complex process that is heterogeneous and affected by numerous sources of variability. This article proposes a stochastic extension of a biologically grounded tumor growth model, referred to as the Norton-Simon-Massagué (NSM) model. First, we study the uncontrolled version of the model where the effect of the chemotherapeutic drug agent is absent. Conditions on the model's parameters are derived to guarantee the positivity of the solution of the proposed stochastic NSM model and hence its validity to describe the dynamics of tumor volume. The proof of positivity makes use of a Lyapunov-type method and the classical Feller's test for explosion. To calibrate the proposed model, we utilize a population mixed-effect modeling formulation and a maximum likelihood-based estimation algorithm. The identification algorithm is tested by fitting previously published tumor volume mice data. Second, we study the controlled version of the model, which includes the effect of chemotherapy treatment. Analysis of the influence of adding the control drug agent into the model and how sensitive it is to the stochastic parameters is performed both in open- and closed-loop viewpoints. The designed closed-loop control strategy that solves an optimal cancer therapy scheduling problem relies on the model predictive control (MPC) combined with extended Kalman filter approaches. The simulation results and concluding guiding principles are provided for both the open-and closed-loop control cases.

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More information

Published date: 19 March 2021

Identifiers

Local EPrints ID: 501271
URI: http://eprints.soton.ac.uk/id/eprint/501271
ISSN: 1063-6536
PURE UUID: 732bddb1-5b82-4166-bd10-b922a198557b
ORCID for Zehor Belkhatir: ORCID iD orcid.org/0000-0001-7277-3895

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Date deposited: 28 May 2025 16:37
Last modified: 31 May 2025 02:11

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Contributors

Author: Zehor Belkhatir ORCID iD
Author: Michele Pavon
Author: James C. Matthews
Author: Maryam Pouryahya
Author: Joseph O. Deasy
Author: Larry Norton

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