Prognostic value of adipose tissue and muscle mass in advanced colorectal cancer: a post hoc analysis of two non-randomized phase II trials.


Journal

BMC cancer
ISSN: 1471-2407
Titre abrégé: BMC Cancer
Pays: England
ID NLM: 100967800

Informations de publication

Date de publication:
12 Feb 2019
Historique:
received: 26 07 2018
accepted: 24 01 2019
entrez: 13 2 2019
pubmed: 13 2 2019
medline: 30 5 2019
Statut: epublish

Résumé

The prognostic value of body composition in cancer patients has been widely studied during the last decade. The main finding of these studies is that sarcopenia, or skeletal muscle depletion, assessed by CT imaging correlates with a reduced overall survival (OS). By contrast, the prognostic value of fat mass remains ill-defined. This study aims to analyze the influence of body composition including both muscle mass and adipose tissue on OS in a homogeneous population of advanced colorectal cancer (CRC) patients. Among 235 patients with chemorefractory advanced CRC included in the SoMore and RegARd-C trials, body composition was assessed in 217 patients on baseline CT images. The relationship between body composition (sarcopenia, muscle density, subcutaneous and visceral fat index and density), body mass index (BMI) and OS were evaluated. Patients with a higher BMI had a better OS (≥30 versus < 30, HR: 0.50; 0.33-0.76). Those with low muscle index and muscle density had an increased mortality (HR: 2.06; 1.45-2.93 and HR: 1.54; 1.09-2.18, respectively). Likewise, low subcutaneous and visceral fat index were associated with an increased risk of dying (HR: 1.63; 1.23-2.17 and 1.48; 1.09-2.02 respectively), as were a high subcutaneous and visceral adipose tissue density (HR: 1.93; 1.44-2.57 and 2.40; 1.79-3.20 respectively). In multivariate analysis, a high visceral fat density was the main predictor of poor survival. Our results confirm the protective role of obesity in CRC patients at an advanced stage, as well as the negative prognostic impact of muscle depletion on survival. More importantly, our data show for the first time that visceral adipose tissue density is an important prognostic factor in metastatic CRC. NCT01290926 , 07/02/2011 and NCT01929616 , 28/08/2013.

Sections du résumé

BACKGROUND BACKGROUND
The prognostic value of body composition in cancer patients has been widely studied during the last decade. The main finding of these studies is that sarcopenia, or skeletal muscle depletion, assessed by CT imaging correlates with a reduced overall survival (OS). By contrast, the prognostic value of fat mass remains ill-defined. This study aims to analyze the influence of body composition including both muscle mass and adipose tissue on OS in a homogeneous population of advanced colorectal cancer (CRC) patients.
METHODS METHODS
Among 235 patients with chemorefractory advanced CRC included in the SoMore and RegARd-C trials, body composition was assessed in 217 patients on baseline CT images. The relationship between body composition (sarcopenia, muscle density, subcutaneous and visceral fat index and density), body mass index (BMI) and OS were evaluated.
RESULTS RESULTS
Patients with a higher BMI had a better OS (≥30 versus < 30, HR: 0.50; 0.33-0.76). Those with low muscle index and muscle density had an increased mortality (HR: 2.06; 1.45-2.93 and HR: 1.54; 1.09-2.18, respectively). Likewise, low subcutaneous and visceral fat index were associated with an increased risk of dying (HR: 1.63; 1.23-2.17 and 1.48; 1.09-2.02 respectively), as were a high subcutaneous and visceral adipose tissue density (HR: 1.93; 1.44-2.57 and 2.40; 1.79-3.20 respectively). In multivariate analysis, a high visceral fat density was the main predictor of poor survival.
CONCLUSIONS CONCLUSIONS
Our results confirm the protective role of obesity in CRC patients at an advanced stage, as well as the negative prognostic impact of muscle depletion on survival. More importantly, our data show for the first time that visceral adipose tissue density is an important prognostic factor in metastatic CRC.
TRIAL REGISTRATION BACKGROUND
NCT01290926 , 07/02/2011 and NCT01929616 , 28/08/2013.

Identifiants

pubmed: 30744591
doi: 10.1186/s12885-019-5319-8
pii: 10.1186/s12885-019-5319-8
pmc: PMC6371452
doi:

Substances chimiques

Biomarkers 0

Banques de données

ClinicalTrials.gov
['NCT01290926', 'NCT01929616']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

134

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Auteurs

Nicolas Charette (N)

Gastroenterology Department, Hôpital Civil Marie Curie, Charleroi, Belgium. nicolas.charette@chu-charleroi.be.
Department of Gastroenterology, CHU de Charleroi, Hôpital Civil Marie Curie, Chaussée de Bruxelles, 140, 6042, Lodelinsart, Belgium. nicolas.charette@chu-charleroi.be.

Caroline Vandeputte (C)

Gastro-Oncology translational laboratory, Institut Jules Bordet - Université Libre de Bruxelles (ULB), Brussels, Belgium.

Lieveke Ameye (L)

Data centre, Institut Jules Bordet, Université Libre de Bruxelles (ULB), Brussels, Belgium.

Camille Van Bogaert (CV)

Medical Oncology Department, Institut Jules Bordet, Université Libre de Bruxelles (ULB), Brussels, Belgium.

Jonathan Krygier (J)

Medical Oncology Department, Institut Jules Bordet, Université Libre de Bruxelles (ULB), Brussels, Belgium.

Thomas Guiot (T)

Nuclear Medicine Department, Institut Jules Bordet, Université Libre de Bruxelles (ULB), Brussels, Belgium.

Amélie Deleporte (A)

Medical Oncology Department, Institut Jules Bordet, Université Libre de Bruxelles (ULB), Brussels, Belgium.

Thierry Delaunoit (T)

Oncology department, Hôpital de Jolimont, La Louvière, Belgium.

Karen Geboes (K)

Service of digestive oncology, Universitair Ziekenhuis Gent, Ghent, Belgium.

Jean-Luc Van Laethem (JL)

Gastroenterology Medico-Surgical Department, Erasme University Hospital, Université Libre de Bruxelles (ULB), Brussels, Belgium.

Marc Peeters (M)

Oncology department, Universitair Ziekenhuis Antwerpen, Antwerpen, Belgium.

Gauthier Demolin (G)

Gastroenterology Department, Centre Hospitalier Chrétien St-Joseph, Liège, Belgium.

Stéphane Holbrechts (S)

Oncology Department, CHU Ambroise Paré, Mons, Belgium.

Patrick Flamen (P)

Nuclear Medicine Department, Institut Jules Bordet, Université Libre de Bruxelles (ULB), Brussels, Belgium.

Marianne Paesmans (M)

Data centre, Institut Jules Bordet - Université Libre de Bruxelles (ULB), Brussels, Belgium.

Alain Hendlisz (A)

Medical Oncology Department, Institut Jules Bordet, Université Libre de Bruxelles (ULB), Brussels, Belgium.

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