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Support for the use of objective comorbidity indices in the assessment of noncancer death risk in prostate cancer patients
BACKGROUND: Prostate cancer management involves a balance between the risks of cancer death against those from other causes. To evaluate the performance of several comorbidity indices in predicting comorbid death in a prostate cancer radiotherapy cohort. METHODS: 2,131 men with localised prostate ca...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Asian Pacific Prostate Society
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5357856/ https://www.ncbi.nlm.nih.gov/pubmed/28352617 http://dx.doi.org/10.1016/j.prnil.2016.12.001 |
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author | Ng, Sweet Ping Duchesne, Gillian Tai, Keen-Hun Foroudi, Farshad Kothari, Gargi Williams, Scott |
author_facet | Ng, Sweet Ping Duchesne, Gillian Tai, Keen-Hun Foroudi, Farshad Kothari, Gargi Williams, Scott |
author_sort | Ng, Sweet Ping |
collection | PubMed |
description | BACKGROUND: Prostate cancer management involves a balance between the risks of cancer death against those from other causes. To evaluate the performance of several comorbidity indices in predicting comorbid death in a prostate cancer radiotherapy cohort. METHODS: 2,131 men with localised prostate cancer treated with radical radiotherapy between 1999 and 2007 were studied. Tumour features, androgen deprivation usage, age, number of prescription medications (PMN) and Adult Comorbidity Evaluation-27 Index (ACE-27) were recorded. Death from prostate cancer (DPC) and death from other causes (DOC) were analysed as competing causes of death using a competing risks model, with discrimination assessed using the concordance index. RESULTS: ACE-27 scores correlated with patient’s PMN (median PMN = 2). Tumour features were independent of ACE-27 scores. Estimated cumulative incidences of DOC and DPC at 10 years were 16.4% and 7.7% respectively. In the low/intermediate risk group (n = 1026) there was a 3.4-fold predominance of DOC inside 10 years (cumulative incidence: 15.8% DOC vs 3.4% DPC). High-risk men had approximately equal rates of DPC and DOC at 10 years. Multivariable analysis showed age, ACE-27 score ≥ 1 and PMN to have significant associations with DOC (P < 0.002 for all). A multivariable model incorporating all 3 variables resulted in C-Index = 0.646. CONCLUSION: Age, ACE-27 score and PMN act as independent prognostic factors for DOC in prostate cancer patients and can improve patient’s life expectancy prediction. |
format | Online Article Text |
id | pubmed-5357856 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Asian Pacific Prostate Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-53578562017-03-28 Support for the use of objective comorbidity indices in the assessment of noncancer death risk in prostate cancer patients Ng, Sweet Ping Duchesne, Gillian Tai, Keen-Hun Foroudi, Farshad Kothari, Gargi Williams, Scott Prostate Int Original Article BACKGROUND: Prostate cancer management involves a balance between the risks of cancer death against those from other causes. To evaluate the performance of several comorbidity indices in predicting comorbid death in a prostate cancer radiotherapy cohort. METHODS: 2,131 men with localised prostate cancer treated with radical radiotherapy between 1999 and 2007 were studied. Tumour features, androgen deprivation usage, age, number of prescription medications (PMN) and Adult Comorbidity Evaluation-27 Index (ACE-27) were recorded. Death from prostate cancer (DPC) and death from other causes (DOC) were analysed as competing causes of death using a competing risks model, with discrimination assessed using the concordance index. RESULTS: ACE-27 scores correlated with patient’s PMN (median PMN = 2). Tumour features were independent of ACE-27 scores. Estimated cumulative incidences of DOC and DPC at 10 years were 16.4% and 7.7% respectively. In the low/intermediate risk group (n = 1026) there was a 3.4-fold predominance of DOC inside 10 years (cumulative incidence: 15.8% DOC vs 3.4% DPC). High-risk men had approximately equal rates of DPC and DOC at 10 years. Multivariable analysis showed age, ACE-27 score ≥ 1 and PMN to have significant associations with DOC (P < 0.002 for all). A multivariable model incorporating all 3 variables resulted in C-Index = 0.646. CONCLUSION: Age, ACE-27 score and PMN act as independent prognostic factors for DOC in prostate cancer patients and can improve patient’s life expectancy prediction. Asian Pacific Prostate Society 2017-03 2016-12-18 /pmc/articles/PMC5357856/ /pubmed/28352617 http://dx.doi.org/10.1016/j.prnil.2016.12.001 Text en © 2017 Asian Pacific Prostate Society, Published by Elsevier Korea LLC. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Ng, Sweet Ping Duchesne, Gillian Tai, Keen-Hun Foroudi, Farshad Kothari, Gargi Williams, Scott Support for the use of objective comorbidity indices in the assessment of noncancer death risk in prostate cancer patients |
title | Support for the use of objective comorbidity indices in the assessment of noncancer death risk in prostate cancer patients |
title_full | Support for the use of objective comorbidity indices in the assessment of noncancer death risk in prostate cancer patients |
title_fullStr | Support for the use of objective comorbidity indices in the assessment of noncancer death risk in prostate cancer patients |
title_full_unstemmed | Support for the use of objective comorbidity indices in the assessment of noncancer death risk in prostate cancer patients |
title_short | Support for the use of objective comorbidity indices in the assessment of noncancer death risk in prostate cancer patients |
title_sort | support for the use of objective comorbidity indices in the assessment of noncancer death risk in prostate cancer patients |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5357856/ https://www.ncbi.nlm.nih.gov/pubmed/28352617 http://dx.doi.org/10.1016/j.prnil.2016.12.001 |
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