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Innovative estimation of survival using log-normal survival modelling on ACCENT database
BACKGROUND: The ACCENT database, with individual patient data for 20 898 patients from 18 colon cancer clinical trials, was used to support Food and Drug Administration (FDA) approval of 3-year disease-free survival as a surrogate for 5-year overall survival. We hypothesised substantive differences...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3590670/ https://www.ncbi.nlm.nih.gov/pubmed/23385733 http://dx.doi.org/10.1038/bjc.2013.34 |
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author | Chapman, J W O'Callaghan, C J Hu, N Ding, K Yothers, G A Catalano, P J Shi, Q Gray, R G O'Connell, M J Sargent, D J |
author_facet | Chapman, J W O'Callaghan, C J Hu, N Ding, K Yothers, G A Catalano, P J Shi, Q Gray, R G O'Connell, M J Sargent, D J |
author_sort | Chapman, J W |
collection | PubMed |
description | BACKGROUND: The ACCENT database, with individual patient data for 20 898 patients from 18 colon cancer clinical trials, was used to support Food and Drug Administration (FDA) approval of 3-year disease-free survival as a surrogate for 5-year overall survival. We hypothesised substantive differences in survival estimation with log-normal modelling rather than standard Kaplan–Meier or Cox approaches. METHODS: Time to relapse, disease-free survival, and overall survival were estimated using Kaplan–Meier, Cox, and log-normal approaches for male subjects aged 60–65 years, with stage III colon cancer, treated with 5-fluorouracil-based chemotherapy regimens (with 5FU), or with surgery alone (without 5FU). RESULTS: Absolute differences between Cox and log-normal estimates with (without) 5FU varied by end point. The log-normal model had 5.8 (6.3)% higher estimated 3-year time to relapse than the Cox model; 4.8 (5.1)% higher 3-year disease-free survival; and 3.2 (2.2)% higher 5-year overall survival. Model checking indicated greater data support for the log-normal than the Cox model, with Cox and Kaplan–Meier estimates being more similar. All three model types indicate consistent evidence of treatment benefit on both 3-year disease-free survival and 5-year overall survival; patients allocated to 5FU had 5.0–6.7% higher 3-year disease-free survival and 5.3–6.8% higher 5-year overall survival. CONCLUSION: Substantive absolute differences between estimates of 3-year disease-free survival and 5-year overall survival with log-normal and Cox models were large enough to be clinically relevant, and warrant further consideration. |
format | Online Article Text |
id | pubmed-3590670 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-35906702014-03-05 Innovative estimation of survival using log-normal survival modelling on ACCENT database Chapman, J W O'Callaghan, C J Hu, N Ding, K Yothers, G A Catalano, P J Shi, Q Gray, R G O'Connell, M J Sargent, D J Br J Cancer Clinical Study BACKGROUND: The ACCENT database, with individual patient data for 20 898 patients from 18 colon cancer clinical trials, was used to support Food and Drug Administration (FDA) approval of 3-year disease-free survival as a surrogate for 5-year overall survival. We hypothesised substantive differences in survival estimation with log-normal modelling rather than standard Kaplan–Meier or Cox approaches. METHODS: Time to relapse, disease-free survival, and overall survival were estimated using Kaplan–Meier, Cox, and log-normal approaches for male subjects aged 60–65 years, with stage III colon cancer, treated with 5-fluorouracil-based chemotherapy regimens (with 5FU), or with surgery alone (without 5FU). RESULTS: Absolute differences between Cox and log-normal estimates with (without) 5FU varied by end point. The log-normal model had 5.8 (6.3)% higher estimated 3-year time to relapse than the Cox model; 4.8 (5.1)% higher 3-year disease-free survival; and 3.2 (2.2)% higher 5-year overall survival. Model checking indicated greater data support for the log-normal than the Cox model, with Cox and Kaplan–Meier estimates being more similar. All three model types indicate consistent evidence of treatment benefit on both 3-year disease-free survival and 5-year overall survival; patients allocated to 5FU had 5.0–6.7% higher 3-year disease-free survival and 5.3–6.8% higher 5-year overall survival. CONCLUSION: Substantive absolute differences between estimates of 3-year disease-free survival and 5-year overall survival with log-normal and Cox models were large enough to be clinically relevant, and warrant further consideration. Nature Publishing Group 2013-03-05 2013-02-05 /pmc/articles/PMC3590670/ /pubmed/23385733 http://dx.doi.org/10.1038/bjc.2013.34 Text en Copyright © 2013 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/3.0/ From twelve months after its original publication, 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 Chapman, J W O'Callaghan, C J Hu, N Ding, K Yothers, G A Catalano, P J Shi, Q Gray, R G O'Connell, M J Sargent, D J Innovative estimation of survival using log-normal survival modelling on ACCENT database |
title | Innovative estimation of survival using log-normal survival modelling on ACCENT database |
title_full | Innovative estimation of survival using log-normal survival modelling on ACCENT database |
title_fullStr | Innovative estimation of survival using log-normal survival modelling on ACCENT database |
title_full_unstemmed | Innovative estimation of survival using log-normal survival modelling on ACCENT database |
title_short | Innovative estimation of survival using log-normal survival modelling on ACCENT database |
title_sort | innovative estimation of survival using log-normal survival modelling on accent database |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3590670/ https://www.ncbi.nlm.nih.gov/pubmed/23385733 http://dx.doi.org/10.1038/bjc.2013.34 |
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