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  •   University of Thessaly Institutional Repository
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
  • View Item
  •   University of Thessaly Institutional Repository
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
  • View Item
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Advanced Non-linear Mathematical Model for the Prediction of the Activity of a Putative Anticancer Agent in Human-to-mouse Cancer Xenografts

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Author
Liliopoulos S.G., Stavrakakis G.S., Dimas K.S.
Date
2020
Language
en
DOI
10.21873/anticanres.14521
Keyword
antineoplastic agent
gemcitabine
antineoplastic agent
animal experiment
Article
cancer inhibition
human
human cell
in vivo study
male
mathematical model
mouse
nonhuman
nonlinear system
pancreas adenocarcinoma
pharmacodynamic parameters
pharmacokinetic parameters
priority journal
solid malignant neoplasm
tumor growth
tumor xenograft
algorithm
animal
cell proliferation
disease model
drug effect
drug screening
pancreas carcinoma
pancreas tumor
pathology
theoretical model
Algorithms
Animals
Antineoplastic Agents
Carcinoma, Pancreatic Ductal
Cell Proliferation
Disease Models, Animal
Humans
Mice
Models, Theoretical
Nonlinear Dynamics
Pancreatic Neoplasms
Xenograft Model Antitumor Assays
International Institute of Anticancer Research
Metadata display
Abstract
Background/Aim: Mathematical models have long been considered as important tools in cancer biology and therapy. Herein, we present an advanced non-linear mathematical model that can predict accurately the effect of an anticancer agent on the growth of a solid tumor. Materials and Methods: Advanced non-linear mathematical optimization techniques and human-to-mouse experimental data were used to develop a tumor growth inhibition (TGI) estimation model. Results: Using this mathematical model, we could accurately predict the tumor mass in a human-to-mouse pancreatic ductal adenocarcinoma (PDAC) xenograft under gemcitabine treatment up to five time periods (points) ahead of the last treatment. Conclusion: The ability of the identified TGI dynamic model to perform satisfactory short-term predictions of the tumor growth for up to five time periods ahead was investigated, evaluated and validated for the first time. Such a prediction model could not only assist the pre-clinical testing of putative anticancer agents, but also the early modification of a chemotherapy schedule towards increased efficacy. © 2020 International Institute of Anticancer Research. All rights reserved.
URI
http://hdl.handle.net/11615/75924
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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