The relationship between tumour necrosis, systemic inflammation, body composition and survival in patients with colon cancer

Abstract Background In cancer cachexia the relationship between the tumour, its environment and the systemic inflammatory response is not clear. This study aims to examine this relationship in greater detail. Methods Host characteristics included the presence of a Systemic Inflammatory Response (SIR...

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Main Authors: Ross D. Dolan, Kathryn Pennel, Joshua Thompson, Molly McKenzie, Peter Alexander, Colin Richards, Douglas Black, Tanvir Abbass, Noori Maka, Josh McGovern, Antonia Roseweir, Stephen T. McSorley, Paul G. Horgan, Campbell Roxburgh, Donald C. McMillan, Joanne Edwards
Format: Article
Language:English
Published: Nature Portfolio 2025-02-01
Series:BJC Reports
Online Access:https://doi.org/10.1038/s44276-024-00119-w
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author Ross D. Dolan
Kathryn Pennel
Joshua Thompson
Molly McKenzie
Peter Alexander
Colin Richards
Douglas Black
Tanvir Abbass
Noori Maka
Josh McGovern
Antonia Roseweir
Stephen T. McSorley
Paul G. Horgan
Campbell Roxburgh
Donald C. McMillan
Joanne Edwards
author_facet Ross D. Dolan
Kathryn Pennel
Joshua Thompson
Molly McKenzie
Peter Alexander
Colin Richards
Douglas Black
Tanvir Abbass
Noori Maka
Josh McGovern
Antonia Roseweir
Stephen T. McSorley
Paul G. Horgan
Campbell Roxburgh
Donald C. McMillan
Joanne Edwards
author_sort Ross D. Dolan
collection DOAJ
description Abstract Background In cancer cachexia the relationship between the tumour, its environment and the systemic inflammatory response is not clear. This study aims to examine this relationship in greater detail. Methods Host characteristics included the presence of a Systemic Inflammatory Response (SIR) as measured by Systemic Inflammatory Grade (SIG), sarcopenia (SMI) and myosteatosis (SMD) were measured. Categorical variables were analysed using χ2 test for linear-by-linear association, or χ2 test for 2 by 2 tables. Survival analysis was carried out using univariate and multivariate Cox regression. Results A total of 473 patients were included. Of these, 70.4% were over 65 years of age, 54.8% were male and 49.8% had an ASA grade of 1 or 2. Pathological examination showed that the majority of patients had a T3 (53.7%) or a T4 (34.0%) cancer and 73.0% had evidence of necrosis. A SIG score of 0 or 1 was present in 57.7% of patients. Tumour necrosis was associated with age (p < 0.01), tumour location (p < 0.01), T-stage (p < 0.001), margin involvement (p < 0.05), SIG (p < 0.001), SMI (p < 0.01), SMD (p < 0.05) and 5-year survival (p < 0.001). On multivariate survival analysis in patients with T3 cancers age (HR: 1.45 95% CI 1.13–1.86 p < 0.01), ASA grade (HR: 1.50 95% CI 1.15–1.95 p < 0.01) and SIG (HR: 1.28 95% CI 1.11–1.48 p < 0.001) remained independently associated with survival. Conclusion These results suggest that tumour necrosis and the subsequent SIR could result in profound changes in body composition and survival. Further pre-clinical and clinical work is required to prove causation.
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spelling doaj-art-329975dc235b4852b6397564ea36d3fb2025-02-09T12:15:56ZengNature PortfolioBJC Reports2731-93772025-02-013111010.1038/s44276-024-00119-wThe relationship between tumour necrosis, systemic inflammation, body composition and survival in patients with colon cancerRoss D. Dolan0Kathryn Pennel1Joshua Thompson2Molly McKenzie3Peter Alexander4Colin Richards5Douglas Black6Tanvir Abbass7Noori Maka8Josh McGovern9Antonia Roseweir10Stephen T. McSorley11Paul G. Horgan12Campbell Roxburgh13Donald C. McMillan14Joanne Edwards15Academic Unit of Surgery, School of Medicine, University of Glasgow, Glasgow Royal InfirmarySchool of Cancer Sciences, University of GlasgowAcademic Unit of Surgery, School of Medicine, University of Glasgow, Glasgow Royal InfirmarySchool of Cancer Sciences, University of GlasgowAcademic Unit of Surgery, School of Medicine, University of Glasgow, Glasgow Royal InfirmaryAcademic Unit of Surgery, School of Medicine, University of Glasgow, Glasgow Royal InfirmaryAcademic Unit of Surgery, School of Medicine, University of Glasgow, Glasgow Royal InfirmaryAcademic Unit of Surgery, School of Medicine, University of Glasgow, Glasgow Royal InfirmarySchool of Cancer Sciences, University of GlasgowAcademic Unit of Surgery, School of Medicine, University of Glasgow, Glasgow Royal InfirmarySchool of Cancer Sciences, University of GlasgowAcademic Unit of Surgery, School of Medicine, University of Glasgow, Glasgow Royal InfirmaryAcademic Unit of Surgery, School of Medicine, University of Glasgow, Glasgow Royal InfirmaryAcademic Unit of Surgery, School of Medicine, University of Glasgow, Glasgow Royal InfirmaryAcademic Unit of Surgery, School of Medicine, University of Glasgow, Glasgow Royal InfirmarySchool of Cancer Sciences, University of GlasgowAbstract Background In cancer cachexia the relationship between the tumour, its environment and the systemic inflammatory response is not clear. This study aims to examine this relationship in greater detail. Methods Host characteristics included the presence of a Systemic Inflammatory Response (SIR) as measured by Systemic Inflammatory Grade (SIG), sarcopenia (SMI) and myosteatosis (SMD) were measured. Categorical variables were analysed using χ2 test for linear-by-linear association, or χ2 test for 2 by 2 tables. Survival analysis was carried out using univariate and multivariate Cox regression. Results A total of 473 patients were included. Of these, 70.4% were over 65 years of age, 54.8% were male and 49.8% had an ASA grade of 1 or 2. Pathological examination showed that the majority of patients had a T3 (53.7%) or a T4 (34.0%) cancer and 73.0% had evidence of necrosis. A SIG score of 0 or 1 was present in 57.7% of patients. Tumour necrosis was associated with age (p < 0.01), tumour location (p < 0.01), T-stage (p < 0.001), margin involvement (p < 0.05), SIG (p < 0.001), SMI (p < 0.01), SMD (p < 0.05) and 5-year survival (p < 0.001). On multivariate survival analysis in patients with T3 cancers age (HR: 1.45 95% CI 1.13–1.86 p < 0.01), ASA grade (HR: 1.50 95% CI 1.15–1.95 p < 0.01) and SIG (HR: 1.28 95% CI 1.11–1.48 p < 0.001) remained independently associated with survival. Conclusion These results suggest that tumour necrosis and the subsequent SIR could result in profound changes in body composition and survival. Further pre-clinical and clinical work is required to prove causation.https://doi.org/10.1038/s44276-024-00119-w
spellingShingle Ross D. Dolan
Kathryn Pennel
Joshua Thompson
Molly McKenzie
Peter Alexander
Colin Richards
Douglas Black
Tanvir Abbass
Noori Maka
Josh McGovern
Antonia Roseweir
Stephen T. McSorley
Paul G. Horgan
Campbell Roxburgh
Donald C. McMillan
Joanne Edwards
The relationship between tumour necrosis, systemic inflammation, body composition and survival in patients with colon cancer
BJC Reports
title The relationship between tumour necrosis, systemic inflammation, body composition and survival in patients with colon cancer
title_full The relationship between tumour necrosis, systemic inflammation, body composition and survival in patients with colon cancer
title_fullStr The relationship between tumour necrosis, systemic inflammation, body composition and survival in patients with colon cancer
title_full_unstemmed The relationship between tumour necrosis, systemic inflammation, body composition and survival in patients with colon cancer
title_short The relationship between tumour necrosis, systemic inflammation, body composition and survival in patients with colon cancer
title_sort relationship between tumour necrosis systemic inflammation body composition and survival in patients with colon cancer
url https://doi.org/10.1038/s44276-024-00119-w
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