Cargando…
A QSP model of prostate cancer immunotherapy to identify effective combination therapies
Immunotherapy, by enhancing the endogenous anti-tumor immune responses, is showing promising results for the treatment of numerous cancers refractory to conventional therapies. However, its effectiveness for advanced castration-resistant prostate cancer remains unsatisfactory and new therapeutic str...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7270132/ https://www.ncbi.nlm.nih.gov/pubmed/32493951 http://dx.doi.org/10.1038/s41598-020-65590-0 |
_version_ | 1783541856816070656 |
---|---|
author | Coletti, Roberta Leonardelli, Lorena Parolo, Silvia Marchetti, Luca |
author_facet | Coletti, Roberta Leonardelli, Lorena Parolo, Silvia Marchetti, Luca |
author_sort | Coletti, Roberta |
collection | PubMed |
description | Immunotherapy, by enhancing the endogenous anti-tumor immune responses, is showing promising results for the treatment of numerous cancers refractory to conventional therapies. However, its effectiveness for advanced castration-resistant prostate cancer remains unsatisfactory and new therapeutic strategies need to be developed. To this end, systems pharmacology modeling provides a quantitative framework to test in silico the efficacy of new treatments and combination therapies. In this paper we present a new Quantitative Systems Pharmacology (QSP) model of prostate cancer immunotherapy, calibrated using data from pre-clinical experiments in prostate cancer mouse models. We developed the model by using Ordinary Differential Equations (ODEs) describing the tumor, key components of the immune system, and seven treatments. Numerous combination therapies were evaluated considering both the degree of tumor inhibition and the predicted synergistic effects, integrated into a decision tree. Our simulations predicted cancer vaccine combined with immune checkpoint blockade as the most effective dual-drug combination immunotherapy for subjects treated with androgen-deprivation therapy that developed resistance. Overall, the model presented here serves as a computational framework to support drug development, by generating hypotheses that can be tested experimentally in pre-clinical models. |
format | Online Article Text |
id | pubmed-7270132 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72701322020-06-05 A QSP model of prostate cancer immunotherapy to identify effective combination therapies Coletti, Roberta Leonardelli, Lorena Parolo, Silvia Marchetti, Luca Sci Rep Article Immunotherapy, by enhancing the endogenous anti-tumor immune responses, is showing promising results for the treatment of numerous cancers refractory to conventional therapies. However, its effectiveness for advanced castration-resistant prostate cancer remains unsatisfactory and new therapeutic strategies need to be developed. To this end, systems pharmacology modeling provides a quantitative framework to test in silico the efficacy of new treatments and combination therapies. In this paper we present a new Quantitative Systems Pharmacology (QSP) model of prostate cancer immunotherapy, calibrated using data from pre-clinical experiments in prostate cancer mouse models. We developed the model by using Ordinary Differential Equations (ODEs) describing the tumor, key components of the immune system, and seven treatments. Numerous combination therapies were evaluated considering both the degree of tumor inhibition and the predicted synergistic effects, integrated into a decision tree. Our simulations predicted cancer vaccine combined with immune checkpoint blockade as the most effective dual-drug combination immunotherapy for subjects treated with androgen-deprivation therapy that developed resistance. Overall, the model presented here serves as a computational framework to support drug development, by generating hypotheses that can be tested experimentally in pre-clinical models. Nature Publishing Group UK 2020-06-03 /pmc/articles/PMC7270132/ /pubmed/32493951 http://dx.doi.org/10.1038/s41598-020-65590-0 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Coletti, Roberta Leonardelli, Lorena Parolo, Silvia Marchetti, Luca A QSP model of prostate cancer immunotherapy to identify effective combination therapies |
title | A QSP model of prostate cancer immunotherapy to identify effective combination therapies |
title_full | A QSP model of prostate cancer immunotherapy to identify effective combination therapies |
title_fullStr | A QSP model of prostate cancer immunotherapy to identify effective combination therapies |
title_full_unstemmed | A QSP model of prostate cancer immunotherapy to identify effective combination therapies |
title_short | A QSP model of prostate cancer immunotherapy to identify effective combination therapies |
title_sort | qsp model of prostate cancer immunotherapy to identify effective combination therapies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7270132/ https://www.ncbi.nlm.nih.gov/pubmed/32493951 http://dx.doi.org/10.1038/s41598-020-65590-0 |
work_keys_str_mv | AT colettiroberta aqspmodelofprostatecancerimmunotherapytoidentifyeffectivecombinationtherapies AT leonardellilorena aqspmodelofprostatecancerimmunotherapytoidentifyeffectivecombinationtherapies AT parolosilvia aqspmodelofprostatecancerimmunotherapytoidentifyeffectivecombinationtherapies AT marchettiluca aqspmodelofprostatecancerimmunotherapytoidentifyeffectivecombinationtherapies AT colettiroberta qspmodelofprostatecancerimmunotherapytoidentifyeffectivecombinationtherapies AT leonardellilorena qspmodelofprostatecancerimmunotherapytoidentifyeffectivecombinationtherapies AT parolosilvia qspmodelofprostatecancerimmunotherapytoidentifyeffectivecombinationtherapies AT marchettiluca qspmodelofprostatecancerimmunotherapytoidentifyeffectivecombinationtherapies |