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Modelling prognostic factors in advanced pancreatic cancer
Pancreatic cancer is the fifth most common cause of cancer death. Identification of defined patient groups based on a prognostic index may improve the prediction of survival and selection of therapy. Many prognostic factors have been identified often based on retrospective, underpowered studies with...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2538756/ https://www.ncbi.nlm.nih.gov/pubmed/19238630 http://dx.doi.org/10.1038/sj.bjc.6604568 |
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author | Stocken, D D Hassan, A B Altman, D G Billingham, L J Bramhall, S R Johnson, P J Freemantle, N |
author_facet | Stocken, D D Hassan, A B Altman, D G Billingham, L J Bramhall, S R Johnson, P J Freemantle, N |
author_sort | Stocken, D D |
collection | PubMed |
description | Pancreatic cancer is the fifth most common cause of cancer death. Identification of defined patient groups based on a prognostic index may improve the prediction of survival and selection of therapy. Many prognostic factors have been identified often based on retrospective, underpowered studies with unclear analyses. Data from 653 patients were analysed. Continuous variables are often simplified assuming a linear relationship with log hazard or introducing a step function (dichotomising). Misspecification may lead to inappropriate conclusions but has not been previously investigated in pancreatic cancer studies. Models based on standard assumptions were compared with a novel approach using nonlinear fractional polynomial (FP) transformations. The model based on FP-transformed covariates was most appropriate and confirmed five previously reported prognostic factors: albumin, CA19-9, alkaline phosphatase, LDH and metastases, and identified three additional factors not previously reported: WBC, AST and BUN. The effects of CA19-9, alkaline phosphatase, AST and BUN may go unrecognised due to simplistic assumptions made in statistical modelling. We advocate a multivariable approach that uses information contained within continuous variables appropriately. The functional form of the relationship between continuous covariates and survival should always be assessed. Our model should aid individual patient risk stratification and the design and analysis of future trials in pancreatic cancer. |
format | Text |
id | pubmed-2538756 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-25387562009-09-16 Modelling prognostic factors in advanced pancreatic cancer Stocken, D D Hassan, A B Altman, D G Billingham, L J Bramhall, S R Johnson, P J Freemantle, N Br J Cancer Clinical Study Pancreatic cancer is the fifth most common cause of cancer death. Identification of defined patient groups based on a prognostic index may improve the prediction of survival and selection of therapy. Many prognostic factors have been identified often based on retrospective, underpowered studies with unclear analyses. Data from 653 patients were analysed. Continuous variables are often simplified assuming a linear relationship with log hazard or introducing a step function (dichotomising). Misspecification may lead to inappropriate conclusions but has not been previously investigated in pancreatic cancer studies. Models based on standard assumptions were compared with a novel approach using nonlinear fractional polynomial (FP) transformations. The model based on FP-transformed covariates was most appropriate and confirmed five previously reported prognostic factors: albumin, CA19-9, alkaline phosphatase, LDH and metastases, and identified three additional factors not previously reported: WBC, AST and BUN. The effects of CA19-9, alkaline phosphatase, AST and BUN may go unrecognised due to simplistic assumptions made in statistical modelling. We advocate a multivariable approach that uses information contained within continuous variables appropriately. The functional form of the relationship between continuous covariates and survival should always be assessed. Our model should aid individual patient risk stratification and the design and analysis of future trials in pancreatic cancer. Nature Publishing Group 2008-09-16 2008-08-26 /pmc/articles/PMC2538756/ /pubmed/19238630 http://dx.doi.org/10.1038/sj.bjc.6604568 Text en Copyright © 2008 Cancer Research UK https://creativecommons.org/licenses/by/4.0/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 https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Clinical Study Stocken, D D Hassan, A B Altman, D G Billingham, L J Bramhall, S R Johnson, P J Freemantle, N Modelling prognostic factors in advanced pancreatic cancer |
title | Modelling prognostic factors in advanced pancreatic cancer |
title_full | Modelling prognostic factors in advanced pancreatic cancer |
title_fullStr | Modelling prognostic factors in advanced pancreatic cancer |
title_full_unstemmed | Modelling prognostic factors in advanced pancreatic cancer |
title_short | Modelling prognostic factors in advanced pancreatic cancer |
title_sort | modelling prognostic factors in advanced pancreatic cancer |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2538756/ https://www.ncbi.nlm.nih.gov/pubmed/19238630 http://dx.doi.org/10.1038/sj.bjc.6604568 |
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