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Data Driven Mathematical Model of FOLFIRI Treatment for Colon Cancer
SIMPLE SUMMARY: Since the micro-environment of colonic tumors, including their immune structure would affect the response to treatments, we study the response of five groups of tumors clustered based on their immune patterns to a common colon cancer treatment. We develop a data driven mathematical m...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8198096/ https://www.ncbi.nlm.nih.gov/pubmed/34071939 http://dx.doi.org/10.3390/cancers13112632 |
Sumario: | SIMPLE SUMMARY: Since the micro-environment of colonic tumors, including their immune structure would affect the response to treatments, we study the response of five groups of tumors clustered based on their immune patterns to a common colon cancer treatment. We develop a data driven mathematical model to investigate the behavior of key players in colonic tumors in each of these clusters in response to the FOLFIRI treatment. Although the model shows clear differences in the behavior of tumors in different clusters, it cannot suggest a unique optimal treatment strategy for each cluster. The results show that there is not much difference in the dynamics of tumors in response to 5-FU alone versus 5-FU plus Leucovorin. However, adding Irinotecan changes the dynamics of T-reg and dendritic cells leading to a remarkably slower tumor recurrence, especially for tumors in a cluster, which has the highest level of T-reg/T-helper ratio compared to the other clusters. ABSTRACT: Many colon cancer patients show resistance to their treatments. Therefore, it is important to consider unique characteristic of each tumor to find the best treatment options for each patient. In this study, we develop a data driven mathematical model for interaction between the tumor microenvironment and FOLFIRI drug agents in colon cancer. Patients are divided into five distinct clusters based on their estimated immune cell fractions obtained from their primary tumors’ gene expression data. We then analyze the effects of drugs on cancer cells and immune cells in each group, and we observe different responses to the FOLFIRI drugs between patients in different immune groups. For instance, patients in cluster 3 with the highest T-reg/T-helper ratio respond better to the FOLFIRI treatment, while patients in cluster 2 with the lowest T-reg/T-helper ratio resist the treatment. Moreover, we use ROC curve to validate the model using the tumor status of the patients at their follow up, and the model predicts well for the earlier follow up days. |
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