The relationship between computed tomography‐derived body composition, systemic inflammatory response, and survival in patients undergoing surgery for colorectal cancer

Abstract Introduction Colorectal cancer is the fourth leading cause of cancer mortality in developed countries. There is evidence supporting a disproportionate loss of skeletal muscle as an independent prognostic factor. The importance of the systemic inflammatory response as a unifying mechanism fo...

Full description

Bibliographic Details
Main Authors: Ross D. Dolan, Arwa S. Almasaudi, Ly B. Dieu, Paul G. Horgan, Stephen T. McSorley, Donald C. McMillan
Format: Article
Language:English
Published: Wiley 2019-02-01
Series:Journal of Cachexia, Sarcopenia and Muscle
Subjects:
Online Access:https://doi.org/10.1002/jcsm.12357
_version_ 1797204510572019712
author Ross D. Dolan
Arwa S. Almasaudi
Ly B. Dieu
Paul G. Horgan
Stephen T. McSorley
Donald C. McMillan
author_facet Ross D. Dolan
Arwa S. Almasaudi
Ly B. Dieu
Paul G. Horgan
Stephen T. McSorley
Donald C. McMillan
author_sort Ross D. Dolan
collection DOAJ
description Abstract Introduction Colorectal cancer is the fourth leading cause of cancer mortality in developed countries. There is evidence supporting a disproportionate loss of skeletal muscle as an independent prognostic factor. The importance of the systemic inflammatory response as a unifying mechanism for specific loss of skeletal muscle mass in patients with cancer is increasingly recognized. The aim of the present study was to delineate the relationship between the systemic inflammatory response, skeletal muscle index (SMI), skeletal muscle density (SMD), and overall survival in patients with colorectal cancer. Materials and methods The study included 650 patients with primary operable colorectal cancer. Computed tomography scans were used to define the presence of visceral obesity, sarcopenia (low SMI), and myosteatosis (low SMD). Tumour and patient characteristics were recorded. Survival analysis was carried out using univariate and multivariate Cox regression. Results A total of 650 patients (354 men and 296 women) were included. The majority of patients were over 65 years of age (64%) and overweight or obese (68%). On univariate survival analysis, age, ASA, TNM stage, modified Glasgow Prognostic Score (mGPS), body mass index, subcutaneous fat index, visceral obesity, SMI, and SMD were significantly associated with overall survival (all P < 0.05). A low SMI and SMD were significantly associated with an elevated mGPS (<0.05). On multivariate analysis, SMI (Martin) [hazard ratio (HR) 1.50, 95% confidence interval (CI) 1.04–2.18, P = 0.031], SMD (Xiao) (HR 1.42, 95% CI 0.98–2.05, P = 0.061), and mGPS (HR 1.44, 95% CI 1.15–1.79, P = 0.001) were independently associated with overall survival. SMD but not SMI was significantly associated with ASA (P < 0.001). Conclusions This study delineates the relationship between the loss of quantity and quality of skeletal muscle mass, the systemic inflammatory response, and survival in patients with operable colorectal cancer.
first_indexed 2024-04-24T08:36:23Z
format Article
id doaj.art-064ad3b67fa44fb09182fa158178241f
institution Directory Open Access Journal
issn 2190-5991
2190-6009
language English
last_indexed 2024-04-24T08:36:23Z
publishDate 2019-02-01
publisher Wiley
record_format Article
series Journal of Cachexia, Sarcopenia and Muscle
spelling doaj.art-064ad3b67fa44fb09182fa158178241f2024-04-16T16:43:25ZengWileyJournal of Cachexia, Sarcopenia and Muscle2190-59912190-60092019-02-0110111112210.1002/jcsm.12357The relationship between computed tomography‐derived body composition, systemic inflammatory response, and survival in patients undergoing surgery for colorectal cancerRoss D. Dolan0Arwa S. Almasaudi1Ly B. Dieu2Paul G. Horgan3Stephen T. McSorley4Donald C. McMillan5Academic Unit of Surgery University of Glasgow Glasgow United KingdomAcademic Unit of Surgery University of Glasgow Glasgow United KingdomAcademic Unit of Surgery University of Glasgow Glasgow United KingdomAcademic Unit of Surgery University of Glasgow Glasgow United KingdomAcademic Unit of Surgery University of Glasgow Glasgow United KingdomAcademic Unit of Surgery University of Glasgow Glasgow United KingdomAbstract Introduction Colorectal cancer is the fourth leading cause of cancer mortality in developed countries. There is evidence supporting a disproportionate loss of skeletal muscle as an independent prognostic factor. The importance of the systemic inflammatory response as a unifying mechanism for specific loss of skeletal muscle mass in patients with cancer is increasingly recognized. The aim of the present study was to delineate the relationship between the systemic inflammatory response, skeletal muscle index (SMI), skeletal muscle density (SMD), and overall survival in patients with colorectal cancer. Materials and methods The study included 650 patients with primary operable colorectal cancer. Computed tomography scans were used to define the presence of visceral obesity, sarcopenia (low SMI), and myosteatosis (low SMD). Tumour and patient characteristics were recorded. Survival analysis was carried out using univariate and multivariate Cox regression. Results A total of 650 patients (354 men and 296 women) were included. The majority of patients were over 65 years of age (64%) and overweight or obese (68%). On univariate survival analysis, age, ASA, TNM stage, modified Glasgow Prognostic Score (mGPS), body mass index, subcutaneous fat index, visceral obesity, SMI, and SMD were significantly associated with overall survival (all P < 0.05). A low SMI and SMD were significantly associated with an elevated mGPS (<0.05). On multivariate analysis, SMI (Martin) [hazard ratio (HR) 1.50, 95% confidence interval (CI) 1.04–2.18, P = 0.031], SMD (Xiao) (HR 1.42, 95% CI 0.98–2.05, P = 0.061), and mGPS (HR 1.44, 95% CI 1.15–1.79, P = 0.001) were independently associated with overall survival. SMD but not SMI was significantly associated with ASA (P < 0.001). Conclusions This study delineates the relationship between the loss of quantity and quality of skeletal muscle mass, the systemic inflammatory response, and survival in patients with operable colorectal cancer.https://doi.org/10.1002/jcsm.12357Colorectal cancerTNM stageSystemic inflammationGlasgow prognostic scoreBody compositionComputed tomography
spellingShingle Ross D. Dolan
Arwa S. Almasaudi
Ly B. Dieu
Paul G. Horgan
Stephen T. McSorley
Donald C. McMillan
The relationship between computed tomography‐derived body composition, systemic inflammatory response, and survival in patients undergoing surgery for colorectal cancer
Journal of Cachexia, Sarcopenia and Muscle
Colorectal cancer
TNM stage
Systemic inflammation
Glasgow prognostic score
Body composition
Computed tomography
title The relationship between computed tomography‐derived body composition, systemic inflammatory response, and survival in patients undergoing surgery for colorectal cancer
title_full The relationship between computed tomography‐derived body composition, systemic inflammatory response, and survival in patients undergoing surgery for colorectal cancer
title_fullStr The relationship between computed tomography‐derived body composition, systemic inflammatory response, and survival in patients undergoing surgery for colorectal cancer
title_full_unstemmed The relationship between computed tomography‐derived body composition, systemic inflammatory response, and survival in patients undergoing surgery for colorectal cancer
title_short The relationship between computed tomography‐derived body composition, systemic inflammatory response, and survival in patients undergoing surgery for colorectal cancer
title_sort relationship between computed tomography derived body composition systemic inflammatory response and survival in patients undergoing surgery for colorectal cancer
topic Colorectal cancer
TNM stage
Systemic inflammation
Glasgow prognostic score
Body composition
Computed tomography
url https://doi.org/10.1002/jcsm.12357
work_keys_str_mv AT rossddolan therelationshipbetweencomputedtomographyderivedbodycompositionsystemicinflammatoryresponseandsurvivalinpatientsundergoingsurgeryforcolorectalcancer
AT arwasalmasaudi therelationshipbetweencomputedtomographyderivedbodycompositionsystemicinflammatoryresponseandsurvivalinpatientsundergoingsurgeryforcolorectalcancer
AT lybdieu therelationshipbetweencomputedtomographyderivedbodycompositionsystemicinflammatoryresponseandsurvivalinpatientsundergoingsurgeryforcolorectalcancer
AT paulghorgan therelationshipbetweencomputedtomographyderivedbodycompositionsystemicinflammatoryresponseandsurvivalinpatientsundergoingsurgeryforcolorectalcancer
AT stephentmcsorley therelationshipbetweencomputedtomographyderivedbodycompositionsystemicinflammatoryresponseandsurvivalinpatientsundergoingsurgeryforcolorectalcancer
AT donaldcmcmillan therelationshipbetweencomputedtomographyderivedbodycompositionsystemicinflammatoryresponseandsurvivalinpatientsundergoingsurgeryforcolorectalcancer
AT rossddolan relationshipbetweencomputedtomographyderivedbodycompositionsystemicinflammatoryresponseandsurvivalinpatientsundergoingsurgeryforcolorectalcancer
AT arwasalmasaudi relationshipbetweencomputedtomographyderivedbodycompositionsystemicinflammatoryresponseandsurvivalinpatientsundergoingsurgeryforcolorectalcancer
AT lybdieu relationshipbetweencomputedtomographyderivedbodycompositionsystemicinflammatoryresponseandsurvivalinpatientsundergoingsurgeryforcolorectalcancer
AT paulghorgan relationshipbetweencomputedtomographyderivedbodycompositionsystemicinflammatoryresponseandsurvivalinpatientsundergoingsurgeryforcolorectalcancer
AT stephentmcsorley relationshipbetweencomputedtomographyderivedbodycompositionsystemicinflammatoryresponseandsurvivalinpatientsundergoingsurgeryforcolorectalcancer
AT donaldcmcmillan relationshipbetweencomputedtomographyderivedbodycompositionsystemicinflammatoryresponseandsurvivalinpatientsundergoingsurgeryforcolorectalcancer