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Quantifying the natural history of breast cancer

BACKGROUND: Natural history models of breast cancer progression provide an opportunity to evaluate and identify optimal screening scenarios. This paper describes a detailed Markov model characterising breast cancer tumour progression. METHODS: Breast cancer is modelled by a 13-state continuous-time...

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Autores principales: Tan, K H X, Simonella, L, Wee, H L, Roellin, A, Lim, Y-W, Lim, W-Y, Chia, K S, Hartman, M, Cook, A R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3798948/
https://www.ncbi.nlm.nih.gov/pubmed/24084766
http://dx.doi.org/10.1038/bjc.2013.471
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author Tan, K H X
Simonella, L
Wee, H L
Roellin, A
Lim, Y-W
Lim, W-Y
Chia, K S
Hartman, M
Cook, A R
author_facet Tan, K H X
Simonella, L
Wee, H L
Roellin, A
Lim, Y-W
Lim, W-Y
Chia, K S
Hartman, M
Cook, A R
author_sort Tan, K H X
collection PubMed
description BACKGROUND: Natural history models of breast cancer progression provide an opportunity to evaluate and identify optimal screening scenarios. This paper describes a detailed Markov model characterising breast cancer tumour progression. METHODS: Breast cancer is modelled by a 13-state continuous-time Markov model. The model differentiates between indolent and aggressive ductal carcinomas in situ tumours, and aggressive tumours of different sizes. We compared such aggressive cancers, that is, which are non-indolent, to those which are non-growing and regressing. Model input parameters and structure were informed by the 1978–1984 Ostergotland county breast screening randomised controlled trial. Overlaid on the natural history model is the effect of screening on diagnosis. Parameters were estimated using Bayesian methods. Markov chain Monte Carlo integration was used to sample the resulting posterior distribution. RESULTS: The breast cancer incidence rate in the Ostergotland population was 21 (95% CI: 17–25) per 10 000 woman-years. Accounting for length-biased sampling, an estimated 91% (95% CI: 85–97%) of breast cancers were aggressive. Larger tumours, 21–50 mm, had an average sojourn of 6 years (95% CI: 3–16 years), whereas aggressive ductal carcinomas in situ took around half a month (95% CI: 0–1 month) to progress to the invasive ⩽10 mm state. CONCLUSION: These tumour progression rate estimates may facilitate future work analysing cost-effectiveness and quality-adjusted life years for various screening strategies.
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spelling pubmed-37989482013-10-21 Quantifying the natural history of breast cancer Tan, K H X Simonella, L Wee, H L Roellin, A Lim, Y-W Lim, W-Y Chia, K S Hartman, M Cook, A R Br J Cancer Clinical Study BACKGROUND: Natural history models of breast cancer progression provide an opportunity to evaluate and identify optimal screening scenarios. This paper describes a detailed Markov model characterising breast cancer tumour progression. METHODS: Breast cancer is modelled by a 13-state continuous-time Markov model. The model differentiates between indolent and aggressive ductal carcinomas in situ tumours, and aggressive tumours of different sizes. We compared such aggressive cancers, that is, which are non-indolent, to those which are non-growing and regressing. Model input parameters and structure were informed by the 1978–1984 Ostergotland county breast screening randomised controlled trial. Overlaid on the natural history model is the effect of screening on diagnosis. Parameters were estimated using Bayesian methods. Markov chain Monte Carlo integration was used to sample the resulting posterior distribution. RESULTS: The breast cancer incidence rate in the Ostergotland population was 21 (95% CI: 17–25) per 10 000 woman-years. Accounting for length-biased sampling, an estimated 91% (95% CI: 85–97%) of breast cancers were aggressive. Larger tumours, 21–50 mm, had an average sojourn of 6 years (95% CI: 3–16 years), whereas aggressive ductal carcinomas in situ took around half a month (95% CI: 0–1 month) to progress to the invasive ⩽10 mm state. CONCLUSION: These tumour progression rate estimates may facilitate future work analysing cost-effectiveness and quality-adjusted life years for various screening strategies. Nature Publishing Group 2013-10-15 2013-10-01 /pmc/articles/PMC3798948/ /pubmed/24084766 http://dx.doi.org/10.1038/bjc.2013.471 Text en Copyright © 2013 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Clinical Study
Tan, K H X
Simonella, L
Wee, H L
Roellin, A
Lim, Y-W
Lim, W-Y
Chia, K S
Hartman, M
Cook, A R
Quantifying the natural history of breast cancer
title Quantifying the natural history of breast cancer
title_full Quantifying the natural history of breast cancer
title_fullStr Quantifying the natural history of breast cancer
title_full_unstemmed Quantifying the natural history of breast cancer
title_short Quantifying the natural history of breast cancer
title_sort quantifying the natural history of breast cancer
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3798948/
https://www.ncbi.nlm.nih.gov/pubmed/24084766
http://dx.doi.org/10.1038/bjc.2013.471
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