Sarcopenia predicts reduced liver growth and reduced resectability in patients undergoing portal vein embolization before liver resection - A DRAGON collaborative analysis of 306 patients.


Journal

HPB : the official journal of the International Hepato Pancreato Biliary Association
ISSN: 1477-2574
Titre abrégé: HPB (Oxford)
Pays: England
ID NLM: 100900921

Informations de publication

Date de publication:
03 2022
Historique:
received: 01 02 2021
revised: 06 07 2021
accepted: 05 08 2021
pubmed: 17 9 2021
medline: 6 4 2022
entrez: 16 9 2021
Statut: ppublish

Résumé

After portal vein embolization (PVE) 30% fail to achieve liver resection. Malnutrition is a modifiable risk factor and can be assessed by radiological indices. This study investigates, if sarcopenia affects resectability and kinetic growth rate (KGR) after PVE. A retrospective study was performed of the outcome of PVE at 8 centres of the DRAGON collaborative from 2010 to 2019. All malignant tumour types were included. Sarcopenia was defined using gender, body mass and skeletal muscle index. First imaging after PVE was used for liver volumetry. Primary and secondary endpoints were resectability and KGR. Risk factors impacting liver growth were assessed in a multivariable analysis. Eight centres identified 368 patients undergoing PVE. 62 patients (17%) had to be excluded due to unavailability of data. Among the 306 included patients, 112 (37%) were non-sarcopenic and 194 (63%) were sarcopenic. Sarcopenic patients had a 21% lower resectability rate (87% vs. 66%, p < 0.001) and a 23% reduced KGR (p = 0.02) after PVE. In a multivariable model dichotomized for KGR ≥2.3% standardized FLR (sFLR)/week, only sarcopenia and sFLR before embolization correlated with KGR. In this largest study of risk factors, sarcopenia was associated with reduced resectability and KGR in patients undergoing PVE.

Sections du résumé

BACKGROUND
After portal vein embolization (PVE) 30% fail to achieve liver resection. Malnutrition is a modifiable risk factor and can be assessed by radiological indices. This study investigates, if sarcopenia affects resectability and kinetic growth rate (KGR) after PVE.
METHODS
A retrospective study was performed of the outcome of PVE at 8 centres of the DRAGON collaborative from 2010 to 2019. All malignant tumour types were included. Sarcopenia was defined using gender, body mass and skeletal muscle index. First imaging after PVE was used for liver volumetry. Primary and secondary endpoints were resectability and KGR. Risk factors impacting liver growth were assessed in a multivariable analysis.
RESULTS
Eight centres identified 368 patients undergoing PVE. 62 patients (17%) had to be excluded due to unavailability of data. Among the 306 included patients, 112 (37%) were non-sarcopenic and 194 (63%) were sarcopenic. Sarcopenic patients had a 21% lower resectability rate (87% vs. 66%, p < 0.001) and a 23% reduced KGR (p = 0.02) after PVE. In a multivariable model dichotomized for KGR ≥2.3% standardized FLR (sFLR)/week, only sarcopenia and sFLR before embolization correlated with KGR.
CONCLUSION
In this largest study of risk factors, sarcopenia was associated with reduced resectability and KGR in patients undergoing PVE.

Identifiants

pubmed: 34526229
pii: S1365-182X(21)01458-1
doi: 10.1016/j.hpb.2021.08.818
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

413-421

Informations de copyright

Crown Copyright © 2021. Published by Elsevier Ltd. All rights reserved.

Auteurs

Jan Heil (J)

Institute of Physiology, University of Zurich, Zurich, Switzerland; Department of General, Visceral and Transplant Surgery, University Hospital Frankfurt, Goethe-University Frankfurt, Frankfurt, Main, Germany.

Franziska Heid (F)

Institute of Physiology, University of Zurich, Zurich, Switzerland; Department of Surgery, Cantonal Hospital Winterthur, Zurich, Switzerland.

Wolf O Bechstein (WO)

Department of General, Visceral and Transplant Surgery, University Hospital Frankfurt, Goethe-University Frankfurt, Frankfurt, Main, Germany.

Bergthor Björnsson (B)

Department of Surgery in Linköping and Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden.

Torkel B Brismar (TB)

Department of Clinical Science and Technology (CLINTEC), Radiology Unit, Karolinska Institutet, Stockholm, Sweden.

Ulrik Carling (U)

Department of Radiology Rikshospitalet, Oslo University Hospital, Oslo, Norway.

Joris Erdmann (J)

Department of Surgery, Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands.

Åsmund A Fretland (ÅA)

Department of Hepato-Pancreatic-Biliary Surgery, Oslo University Hospital, Oslo, Norway; The Intervention Centre, Oslo University Hospital, Oslo, Norway.

Dirk Grunhagen (D)

Department of Surgery, Erasmus MC Cancer Institute, Erasmus University, Rotterdam, the Netherlands.

Renato A Hana (RA)

Department of Diagnostic Radiology, McGill General Hospital, Montreal, Canada.

Joachim Hohmann (J)

Department of Radiology and Nuclear Medicine, Cantonal Hospital Winterthur, Winterthur, Switzerland; Medical Faculty, University of Basel, Basel, Switzerland.

Richard Linke (R)

Department of General, Visceral and Transplant Surgery, University Hospital Frankfurt, Goethe-University Frankfurt, Frankfurt, Main, Germany.

Yannick Meyer (Y)

Department of Surgery, Erasmus MC Cancer Institute, Erasmus University, Rotterdam, the Netherlands.

Abrar Nawawi (A)

Department of Surgery, McGill Health Center Research Institute, Cancer Program, Montreal, Canada.

Pim B Olthof (PB)

Department of Surgery, Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands; Department of Surgery, Erasmus MC Cancer Institute, Erasmus University, Rotterdam, the Netherlands.

Per Sandström (P)

Department of Surgery in Linköping and Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden.

Andreas A Schnitzbauer (AA)

Department of General, Visceral and Transplant Surgery, University Hospital Frankfurt, Goethe-University Frankfurt, Frankfurt, Main, Germany.

Ernesto Sparrelid (E)

Department of Clinical Science, Intervention and Technology, Division of Surgery, Karolinska Institutet, Karolinska Hospital, Stockholm, Sweden.

Cornelis Verhoef (C)

Department of Surgery, Erasmus MC Cancer Institute, Erasmus University, Rotterdam, the Netherlands.

Peter Metrakos (P)

Department of Surgery, McGill Health Center Research Institute, Cancer Program, Montreal, Canada.

Erik Schadde (E)

Institute of Physiology, University of Zurich, Zurich, Switzerland; Department of Surgery, Cantonal Hospital Winterthur, Zurich, Switzerland; Department of Surgery, Division of Transplant Surgery, Rush University Medical Center, Chicago, IL, USA. Electronic address: erik.schadde@icloud.com.

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