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Serum C-reactive protein is an important and powerful prognostic biomarker in most adult solid tumors

INTRODUCTION: Prognostication in cancer is challenging and inaccurate. C-Reactive Protein (CRP), a cheap and sensitive marker of inflammation may help. This study investigated the relationship between CRP and prognosis in a large cohort of solid tumors with mixed cancer diagnoses and stages. METHODS...

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Autores principales: Shrotriya, Shiva, Walsh, Declan, Nowacki, Amy S., Lorton, Cliona, Aktas, Aynur, Hullihen, Barbara, Benanni-Baiti, Nabila, Hauser, Katherine, Ayvaz, Serkan, Estfan, Bassam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107177/
https://www.ncbi.nlm.nih.gov/pubmed/30138391
http://dx.doi.org/10.1371/journal.pone.0202555
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author Shrotriya, Shiva
Walsh, Declan
Nowacki, Amy S.
Lorton, Cliona
Aktas, Aynur
Hullihen, Barbara
Benanni-Baiti, Nabila
Hauser, Katherine
Ayvaz, Serkan
Estfan, Bassam
author_facet Shrotriya, Shiva
Walsh, Declan
Nowacki, Amy S.
Lorton, Cliona
Aktas, Aynur
Hullihen, Barbara
Benanni-Baiti, Nabila
Hauser, Katherine
Ayvaz, Serkan
Estfan, Bassam
author_sort Shrotriya, Shiva
collection PubMed
description INTRODUCTION: Prognostication in cancer is challenging and inaccurate. C-Reactive Protein (CRP), a cheap and sensitive marker of inflammation may help. This study investigated the relationship between CRP and prognosis in a large cohort of solid tumors with mixed cancer diagnoses and stages. METHODS: Electronic medical records of 4931 adults with solid tumors who attended the Taussig Cancer Institute from 2006–2012 were reviewed. Demographic and clinical characteristics were recorded. Maximum CRP (mCRP) was identified for each individual. CRP was analysed as a time-dependent, continuous and categorical variable for association with survival. RESULTS: Two thirds of patients had a high mCRP. This was consistently associated with shorter survival, even after correction for time from diagnosis, and when analysed as a continuous or a categorical variable. When mCRP values above 10 mg/L were subcategorized, a higher mCRP was always worse. Even among those with normal values, statistically and clinically significant shorter survival was noted at mCRP levels >5 mg/L. CONCLUSIONS: In a large representative cohort of consecutive solid tumor patients the risk of death was clinically and statistically significantly greater with a high mCRP. This was independent of other variables and regardless of statistical method from both dates of diagnosis and test. CRP appeared to be underutilized. Our results support the routine use of CRP as a universal cost-effective independent prognostic indicator in most solid tumors.
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spelling pubmed-61071772018-08-30 Serum C-reactive protein is an important and powerful prognostic biomarker in most adult solid tumors Shrotriya, Shiva Walsh, Declan Nowacki, Amy S. Lorton, Cliona Aktas, Aynur Hullihen, Barbara Benanni-Baiti, Nabila Hauser, Katherine Ayvaz, Serkan Estfan, Bassam PLoS One Research Article INTRODUCTION: Prognostication in cancer is challenging and inaccurate. C-Reactive Protein (CRP), a cheap and sensitive marker of inflammation may help. This study investigated the relationship between CRP and prognosis in a large cohort of solid tumors with mixed cancer diagnoses and stages. METHODS: Electronic medical records of 4931 adults with solid tumors who attended the Taussig Cancer Institute from 2006–2012 were reviewed. Demographic and clinical characteristics were recorded. Maximum CRP (mCRP) was identified for each individual. CRP was analysed as a time-dependent, continuous and categorical variable for association with survival. RESULTS: Two thirds of patients had a high mCRP. This was consistently associated with shorter survival, even after correction for time from diagnosis, and when analysed as a continuous or a categorical variable. When mCRP values above 10 mg/L were subcategorized, a higher mCRP was always worse. Even among those with normal values, statistically and clinically significant shorter survival was noted at mCRP levels >5 mg/L. CONCLUSIONS: In a large representative cohort of consecutive solid tumor patients the risk of death was clinically and statistically significantly greater with a high mCRP. This was independent of other variables and regardless of statistical method from both dates of diagnosis and test. CRP appeared to be underutilized. Our results support the routine use of CRP as a universal cost-effective independent prognostic indicator in most solid tumors. Public Library of Science 2018-08-23 /pmc/articles/PMC6107177/ /pubmed/30138391 http://dx.doi.org/10.1371/journal.pone.0202555 Text en © 2018 Shrotriya et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Shrotriya, Shiva
Walsh, Declan
Nowacki, Amy S.
Lorton, Cliona
Aktas, Aynur
Hullihen, Barbara
Benanni-Baiti, Nabila
Hauser, Katherine
Ayvaz, Serkan
Estfan, Bassam
Serum C-reactive protein is an important and powerful prognostic biomarker in most adult solid tumors
title Serum C-reactive protein is an important and powerful prognostic biomarker in most adult solid tumors
title_full Serum C-reactive protein is an important and powerful prognostic biomarker in most adult solid tumors
title_fullStr Serum C-reactive protein is an important and powerful prognostic biomarker in most adult solid tumors
title_full_unstemmed Serum C-reactive protein is an important and powerful prognostic biomarker in most adult solid tumors
title_short Serum C-reactive protein is an important and powerful prognostic biomarker in most adult solid tumors
title_sort serum c-reactive protein is an important and powerful prognostic biomarker in most adult solid tumors
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107177/
https://www.ncbi.nlm.nih.gov/pubmed/30138391
http://dx.doi.org/10.1371/journal.pone.0202555
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