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Quantitative mathematical modeling of clinical brain metastasis dynamics in non-small cell lung cancer
Brain metastases (BMs) are associated with poor prognosis in non-small cell lung cancer (NSCLC), but are only visible when large enough. Therapeutic decisions such as whole brain radiation therapy would benefit from patient-specific predictions of radiologically undetectable BMs. Here, we propose a...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6736889/ https://www.ncbi.nlm.nih.gov/pubmed/31506498 http://dx.doi.org/10.1038/s41598-019-49407-3 |
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author | Bilous, M. Serdjebi, C. Boyer, A. Tomasini, P. Pouypoudat, C. Barbolosi, D. Barlesi, F. Chomy, F. Benzekry, S. |
author_facet | Bilous, M. Serdjebi, C. Boyer, A. Tomasini, P. Pouypoudat, C. Barbolosi, D. Barlesi, F. Chomy, F. Benzekry, S. |
author_sort | Bilous, M. |
collection | PubMed |
description | Brain metastases (BMs) are associated with poor prognosis in non-small cell lung cancer (NSCLC), but are only visible when large enough. Therapeutic decisions such as whole brain radiation therapy would benefit from patient-specific predictions of radiologically undetectable BMs. Here, we propose a mathematical modeling approach and use it to analyze clinical data of BM from NSCLC. Primary tumor growth was best described by a gompertzian model for the pre-diagnosis history, followed by a tumor growth inhibition model during treatment. Growth parameters were estimated only from the size at diagnosis and histology, but predicted plausible individual estimates of the tumor age (2.1–5.3 years). Multiple metastatic models were further assessed from fitting either literature data of BM probability (n = 183 patients) or longitudinal measurements of visible BMs in two patients. Among the tested models, the one featuring dormancy was best able to describe the data. It predicted latency phases of 4.4–5.7 months and onset of BMs 14–19 months before diagnosis. This quantitative model paves the way for a computational tool of potential help during therapeutic management. |
format | Online Article Text |
id | pubmed-6736889 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67368892019-09-20 Quantitative mathematical modeling of clinical brain metastasis dynamics in non-small cell lung cancer Bilous, M. Serdjebi, C. Boyer, A. Tomasini, P. Pouypoudat, C. Barbolosi, D. Barlesi, F. Chomy, F. Benzekry, S. Sci Rep Article Brain metastases (BMs) are associated with poor prognosis in non-small cell lung cancer (NSCLC), but are only visible when large enough. Therapeutic decisions such as whole brain radiation therapy would benefit from patient-specific predictions of radiologically undetectable BMs. Here, we propose a mathematical modeling approach and use it to analyze clinical data of BM from NSCLC. Primary tumor growth was best described by a gompertzian model for the pre-diagnosis history, followed by a tumor growth inhibition model during treatment. Growth parameters were estimated only from the size at diagnosis and histology, but predicted plausible individual estimates of the tumor age (2.1–5.3 years). Multiple metastatic models were further assessed from fitting either literature data of BM probability (n = 183 patients) or longitudinal measurements of visible BMs in two patients. Among the tested models, the one featuring dormancy was best able to describe the data. It predicted latency phases of 4.4–5.7 months and onset of BMs 14–19 months before diagnosis. This quantitative model paves the way for a computational tool of potential help during therapeutic management. Nature Publishing Group UK 2019-09-10 /pmc/articles/PMC6736889/ /pubmed/31506498 http://dx.doi.org/10.1038/s41598-019-49407-3 Text en © The Author(s) 2019 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 Bilous, M. Serdjebi, C. Boyer, A. Tomasini, P. Pouypoudat, C. Barbolosi, D. Barlesi, F. Chomy, F. Benzekry, S. Quantitative mathematical modeling of clinical brain metastasis dynamics in non-small cell lung cancer |
title | Quantitative mathematical modeling of clinical brain metastasis dynamics in non-small cell lung cancer |
title_full | Quantitative mathematical modeling of clinical brain metastasis dynamics in non-small cell lung cancer |
title_fullStr | Quantitative mathematical modeling of clinical brain metastasis dynamics in non-small cell lung cancer |
title_full_unstemmed | Quantitative mathematical modeling of clinical brain metastasis dynamics in non-small cell lung cancer |
title_short | Quantitative mathematical modeling of clinical brain metastasis dynamics in non-small cell lung cancer |
title_sort | quantitative mathematical modeling of clinical brain metastasis dynamics in non-small cell lung cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6736889/ https://www.ncbi.nlm.nih.gov/pubmed/31506498 http://dx.doi.org/10.1038/s41598-019-49407-3 |
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