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A prospective study examining cachexia predictors in patients with incurable cancer

BACKGROUND: Early intervention against cachexia necessitates a predictive model. The aims of this study were to identify predictors of cachexia development and to create and evaluate accuracy of a predictive model based on these predictors. METHODS: A secondary analysis of a prospective, observation...

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Autores principales: Vagnildhaug, Ola Magne, Brunelli, Cinzia, Hjermstad, Marianne J., Strasser, Florian, Baracos, Vickie, Wilcock, Andrew, Nabal, Maria, Kaasa, Stein, Laird, Barry, Solheim, Tora S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6549342/
https://www.ncbi.nlm.nih.gov/pubmed/31164115
http://dx.doi.org/10.1186/s12904-019-0429-2
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author Vagnildhaug, Ola Magne
Brunelli, Cinzia
Hjermstad, Marianne J.
Strasser, Florian
Baracos, Vickie
Wilcock, Andrew
Nabal, Maria
Kaasa, Stein
Laird, Barry
Solheim, Tora S.
author_facet Vagnildhaug, Ola Magne
Brunelli, Cinzia
Hjermstad, Marianne J.
Strasser, Florian
Baracos, Vickie
Wilcock, Andrew
Nabal, Maria
Kaasa, Stein
Laird, Barry
Solheim, Tora S.
author_sort Vagnildhaug, Ola Magne
collection PubMed
description BACKGROUND: Early intervention against cachexia necessitates a predictive model. The aims of this study were to identify predictors of cachexia development and to create and evaluate accuracy of a predictive model based on these predictors. METHODS: A secondary analysis of a prospective, observational, multicentre study was conducted. Patients, who attended a palliative care programme, had incurable cancer and did not have cachexia at baseline, were amenable to the analysis. Cachexia was defined as weight loss (WL) > 5% (6 months) or WL > 2% and body mass index< 20 kg/m(2). Clinical and demographic markers were evaluated as possible predictors with Cox analysis. A classification and regression tree analysis was used to create a model based on optimal combinations and cut-offs of significant predictors for cachexia development, and accuracy was evaluated with a calibration plot, Harrell’s c-statistic and receiver operating characteristic curve analysis. RESULTS: Six-hundred-twenty-eight patients were included in the analysis. Median age was 65 years (IQR 17), 359(57%) were female and median Karnofsky performance status was 70(IQR 10). Median follow-up was 109 days (IQR 108), and 159 (25%) patients developed cachexia. Initial WL, cancer type, appetite and chronic obstructive pulmonary disease were significant predictors (p ≤ 0.04). A five-level model was created with each level carrying an increasing risk of cachexia development. For Risk-level 1-patients (WL < 3%, breast or hematologic cancer and no or little appetite loss), median time to cachexia development was not reached, while Risk-level 5-patients (WL 3–5%) had a median time to cachexia development of 51 days. Accuracy of cachexia predictions at 3 months was 76%. CONCLUSION: Important predictors of cachexia have been identified and used to construct a predictive model of cancer cachexia. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT01362816.
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spelling pubmed-65493422019-06-06 A prospective study examining cachexia predictors in patients with incurable cancer Vagnildhaug, Ola Magne Brunelli, Cinzia Hjermstad, Marianne J. Strasser, Florian Baracos, Vickie Wilcock, Andrew Nabal, Maria Kaasa, Stein Laird, Barry Solheim, Tora S. BMC Palliat Care Research Article BACKGROUND: Early intervention against cachexia necessitates a predictive model. The aims of this study were to identify predictors of cachexia development and to create and evaluate accuracy of a predictive model based on these predictors. METHODS: A secondary analysis of a prospective, observational, multicentre study was conducted. Patients, who attended a palliative care programme, had incurable cancer and did not have cachexia at baseline, were amenable to the analysis. Cachexia was defined as weight loss (WL) > 5% (6 months) or WL > 2% and body mass index< 20 kg/m(2). Clinical and demographic markers were evaluated as possible predictors with Cox analysis. A classification and regression tree analysis was used to create a model based on optimal combinations and cut-offs of significant predictors for cachexia development, and accuracy was evaluated with a calibration plot, Harrell’s c-statistic and receiver operating characteristic curve analysis. RESULTS: Six-hundred-twenty-eight patients were included in the analysis. Median age was 65 years (IQR 17), 359(57%) were female and median Karnofsky performance status was 70(IQR 10). Median follow-up was 109 days (IQR 108), and 159 (25%) patients developed cachexia. Initial WL, cancer type, appetite and chronic obstructive pulmonary disease were significant predictors (p ≤ 0.04). A five-level model was created with each level carrying an increasing risk of cachexia development. For Risk-level 1-patients (WL < 3%, breast or hematologic cancer and no or little appetite loss), median time to cachexia development was not reached, while Risk-level 5-patients (WL 3–5%) had a median time to cachexia development of 51 days. Accuracy of cachexia predictions at 3 months was 76%. CONCLUSION: Important predictors of cachexia have been identified and used to construct a predictive model of cancer cachexia. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT01362816. BioMed Central 2019-06-04 /pmc/articles/PMC6549342/ /pubmed/31164115 http://dx.doi.org/10.1186/s12904-019-0429-2 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Vagnildhaug, Ola Magne
Brunelli, Cinzia
Hjermstad, Marianne J.
Strasser, Florian
Baracos, Vickie
Wilcock, Andrew
Nabal, Maria
Kaasa, Stein
Laird, Barry
Solheim, Tora S.
A prospective study examining cachexia predictors in patients with incurable cancer
title A prospective study examining cachexia predictors in patients with incurable cancer
title_full A prospective study examining cachexia predictors in patients with incurable cancer
title_fullStr A prospective study examining cachexia predictors in patients with incurable cancer
title_full_unstemmed A prospective study examining cachexia predictors in patients with incurable cancer
title_short A prospective study examining cachexia predictors in patients with incurable cancer
title_sort prospective study examining cachexia predictors in patients with incurable cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6549342/
https://www.ncbi.nlm.nih.gov/pubmed/31164115
http://dx.doi.org/10.1186/s12904-019-0429-2
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