Host phenotype is associated with reduced survival independent of tumour biology in patients with colorectal liver metastases.


Journal

Journal of cachexia, sarcopenia and muscle
ISSN: 2190-6009
Titre abrégé: J Cachexia Sarcopenia Muscle
Pays: Germany
ID NLM: 101552883

Informations de publication

Date de publication:
02 2019
Historique:
received: 16 05 2018
revised: 24 08 2018
accepted: 13 09 2018
pubmed: 1 11 2018
medline: 9 4 2020
entrez: 1 11 2018
Statut: ppublish

Résumé

Most prognostic scoring systems for colorectal liver metastases (CRLMs) account for factors related to tumour biology. Little is known about the effects of the host phenotype to the tumour. Our objective was to delineate the relationship of systemic inflammation and body composition features [i.e. low skeletal muscle mass (sarcopenia) and low visceral adipose tissue (VAT)], two well-described host phenotypes in cancer. Clinical data and pre-operative blood samples were collected from 99 patients who underwent resection of CRLM. Pre-operative computed tomography scans were available for 97 patients; body composition was analysed at the L3 level, stratified for sex and age. Clinicopathological variables, serum C-reactive protein (CRP), and various body composition variables were evaluated. Overall survival was evaluated as a function of these same variables in multivariate Cox regression analysis. Skeletal muscle was significantly correlated with VAT (r = 0.46, P < 0.001). Of patients with sarcopenia, 35 (65%) also had low VAT. C-reactive protein was elevated (≥5 mg/mL) in 42 patients (43.3%). Elevated CRP was more common in patients with sarcopenia (73.8% vs. 51.1%, P = 0.029). The most significant prognostic factors were the coincidence of elevated CRP and adverse body composition features (sarcopenia and/or low VAT; hazard ratio 4.3, 95% confidence interval 1.5-13.0, P = 0.008), as well as Fong clinical prognostic score (hazard ratio 2.9, 95% confidence interval 1.5-5.5, P = 0.002). Body composition in patients with CRLM is not directly linked to the presence of systemic inflammation. However, when systemic inflammation coincides with sarcopenia and/or low VAT, prognosis is adversely affected, independent of the Fong clinical prognostic score.

Sections du résumé

BACKGROUND
Most prognostic scoring systems for colorectal liver metastases (CRLMs) account for factors related to tumour biology. Little is known about the effects of the host phenotype to the tumour. Our objective was to delineate the relationship of systemic inflammation and body composition features [i.e. low skeletal muscle mass (sarcopenia) and low visceral adipose tissue (VAT)], two well-described host phenotypes in cancer.
METHODS
Clinical data and pre-operative blood samples were collected from 99 patients who underwent resection of CRLM. Pre-operative computed tomography scans were available for 97 patients; body composition was analysed at the L3 level, stratified for sex and age. Clinicopathological variables, serum C-reactive protein (CRP), and various body composition variables were evaluated. Overall survival was evaluated as a function of these same variables in multivariate Cox regression analysis.
RESULTS
Skeletal muscle was significantly correlated with VAT (r = 0.46, P < 0.001). Of patients with sarcopenia, 35 (65%) also had low VAT. C-reactive protein was elevated (≥5 mg/mL) in 42 patients (43.3%). Elevated CRP was more common in patients with sarcopenia (73.8% vs. 51.1%, P = 0.029). The most significant prognostic factors were the coincidence of elevated CRP and adverse body composition features (sarcopenia and/or low VAT; hazard ratio 4.3, 95% confidence interval 1.5-13.0, P = 0.008), as well as Fong clinical prognostic score (hazard ratio 2.9, 95% confidence interval 1.5-5.5, P = 0.002).
CONCLUSIONS
Body composition in patients with CRLM is not directly linked to the presence of systemic inflammation. However, when systemic inflammation coincides with sarcopenia and/or low VAT, prognosis is adversely affected, independent of the Fong clinical prognostic score.

Identifiants

pubmed: 30378742
doi: 10.1002/jcsm.12358
pmc: PMC6438330
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

123-130

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2018 The Authors. Journal of Cachexia, Sarcopenia and Muscle published by John Wiley & Sons Ltd on behalf of the Society on Sarcopenia, Cachexia and Wasting Disorders.

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Auteurs

David P J van Dijk (DPJ)

Department of Surgery, Maastricht University Medical Centre, Maastricht, The Netherlands.
NUTRIM School of Nutrition and Translational Research in Metabolism, Maastricht University, Maastricht, The Netherlands.

Matthew Krill (M)

Department of Surgery and Oncology, Tom Baker Cancer Centre, University of Calgary, Calgary, Canada.

Farshad Farshidfar (F)

Arnie Charbonneau Cancer Institute, Calgary, Canada.

Ting Li (T)

Department of Surgery and Oncology, Tom Baker Cancer Centre, University of Calgary, Calgary, Canada.

Sander S Rensen (SS)

Department of Surgery, Maastricht University Medical Centre, Maastricht, The Netherlands.
NUTRIM School of Nutrition and Translational Research in Metabolism, Maastricht University, Maastricht, The Netherlands.

Steven W M Olde Damink (SWM)

Department of Surgery, Maastricht University Medical Centre, Maastricht, The Netherlands.
NUTRIM School of Nutrition and Translational Research in Metabolism, Maastricht University, Maastricht, The Netherlands.
Department of General, Visceral and Transplantation Surgery, RWTH University Hospital Aachen, Aachen, Germany.
Institute for Liver and Digestive Health, University College London, London, UK.

Elijah Dixon (E)

Department of Surgery and Oncology, Tom Baker Cancer Centre, University of Calgary, Calgary, Canada.

Francis R Sutherland (FR)

Department of Surgery and Oncology, Tom Baker Cancer Centre, University of Calgary, Calgary, Canada.

Chad G Ball (CG)

Department of Surgery and Oncology, Tom Baker Cancer Centre, University of Calgary, Calgary, Canada.

Vera C Mazurak (VC)

Division of Human Nutrition, Department of Agricultural, Food and Nutritional Science, University of Alberta, Edmonton, Canada.

Vickie E Baracos (VE)

Department of Oncology, University of Alberta, Edmonton, Canada.

Oliver F Bathe (OF)

Department of Surgery and Oncology, Tom Baker Cancer Centre, University of Calgary, Calgary, Canada.
Arnie Charbonneau Cancer Institute, Calgary, Canada.

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