Preoperative portal vein or portal and hepatic vein embolization: DRAGON collaborative group analysis.


Journal

The British journal of surgery
ISSN: 1365-2168
Titre abrégé: Br J Surg
Pays: England
ID NLM: 0372553

Informations de publication

Date de publication:
23 07 2021
Historique:
received: 25 08 2020
revised: 20 10 2020
accepted: 30 11 2020
pubmed: 5 3 2021
medline: 6 10 2021
entrez: 4 3 2021
Statut: ppublish

Résumé

The extent of liver resection for tumours is limited by the expected functional reserve of the future liver remnant (FRL), so hypertrophy may be induced by portal vein embolization (PVE), taking 6 weeks or longer for growth. This study assessed the hypothesis that simultaneous embolization of portal and hepatic veins (PVE/HVE) accelerates hypertrophy and improves resectability. All centres of the international DRAGON trials study collaborative were asked to provide data on patients who had PVE/HVE or PVE on 2016-2019 (more than 5 PVE/HVE procedures was a requirement). Liver volumetry was performed using OsiriX MD software. Multivariable analysis was performed for the endpoints of resectability rate, FLR hypertrophy and major complications using receiver operating characteristic (ROC) statistics, regression, and Kaplan-Meier analysis. In total, 39 patients had undergone PVE/HVE and 160 had PVE alone. The PVE/HVE group had better hypertrophy than the PVE group (59 versus 48 per cent respectively; P = 0.020) and resectability (90 versus 68 per cent; P = 0.007). Major complications (26 versus 34 per cent; P = 0.550) and 90-day mortality (3 versus 16 per cent respectively, P = 0.065) were comparable. Multivariable analysis confirmed that these effects were independent of confounders. PVE/HVE achieved better FLR hypertrophy and resectability than PVE in this collaborative experience.

Sections du résumé

BACKGROUND
The extent of liver resection for tumours is limited by the expected functional reserve of the future liver remnant (FRL), so hypertrophy may be induced by portal vein embolization (PVE), taking 6 weeks or longer for growth. This study assessed the hypothesis that simultaneous embolization of portal and hepatic veins (PVE/HVE) accelerates hypertrophy and improves resectability.
METHODS
All centres of the international DRAGON trials study collaborative were asked to provide data on patients who had PVE/HVE or PVE on 2016-2019 (more than 5 PVE/HVE procedures was a requirement). Liver volumetry was performed using OsiriX MD software. Multivariable analysis was performed for the endpoints of resectability rate, FLR hypertrophy and major complications using receiver operating characteristic (ROC) statistics, regression, and Kaplan-Meier analysis.
RESULTS
In total, 39 patients had undergone PVE/HVE and 160 had PVE alone. The PVE/HVE group had better hypertrophy than the PVE group (59 versus 48 per cent respectively; P = 0.020) and resectability (90 versus 68 per cent; P = 0.007). Major complications (26 versus 34 per cent; P = 0.550) and 90-day mortality (3 versus 16 per cent respectively, P = 0.065) were comparable. Multivariable analysis confirmed that these effects were independent of confounders.
CONCLUSION
PVE/HVE achieved better FLR hypertrophy and resectability than PVE in this collaborative experience.

Identifiants

pubmed: 33661306
pii: 6154479
doi: 10.1093/bjs/znaa149
doi:

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

834-842

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press on behalf of BJS Society Ltd. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

J Heil (J)

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

R Korenblik (R)

GROW - School for Oncology and Developmental Biology, Maastricht University, Maastricht, the Netherlands.
Department of Surgery, Maastricht University Medical Centre, Maastricht, the Netherlands.

F Heid (F)

Institute of Physiology, University of Zurich, Zurich, Switzerland.
Department of General and Visceral Surgery, Cantonal Hospital Winterthur, Winterthur, Switzerland.

W O Bechstein (WO)

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

M Bemelmans (M)

Department of Surgery, Maastricht University Medical Centre, Maastricht, the Netherlands.

C Binkert (C)

Department of Radiology, Cantonal Hospital Winterthur, Winterthur, Switzerland.

B Björnsson (B)

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

S Breitenstein (S)

Department of General and Visceral Surgery, Cantonal Hospital Winterthur, Winterthur, Switzerland.

O Detry (O)

Department of Abdominal Surgery and Transplantation, University of Liege, Centre Hospitalier Universitaire de Liege, Liege, Belgium.

A Dili (A)

Department of Abdominal Surgery, Centre Hospitalier Universitaire Dinant Godinne Saint-Elisabeth - UCL-Namur, Yvoir, Belgium.

R F Dondelinger (RF)

Department of Imaging, University Hospital Liege, Liege, Belgium.

L Gerard (L)

Department of Imaging, University Hospital Liege, Liege, Belgium.

T Giménez-Maurel (T)

Department of Surgery, Miguel University Hospital and University of Zaragoza, Zaragoza, Spain.

B Guiu (B)

Department of Radiology, St Eloi University Hospital, Montpellier, France.

D Heise (D)

Department of General, Visceral and Transplant Surgery, University Hospital Aachen, Aachen, Germany.

M Hertl (M)

Department of Surgery, Rush University Medical Center, Chicago, Illinois, USA.

J A Kalil (JA)

Department of Surgery, Rush University Medical Center, Chicago, Illinois, USA.

J J Klein (JJ)

Department of Surgery, Rush University Medical Center, Chicago, Illinois, USA.

A Lakoma (A)

Department of Surgery, Section of Hepato-Pancreatico-Biliary Surgery, McGill University Health Center, Montreal, Quebec, Canada.

U P Neumann (UP)

Department of General, Visceral and Transplant Surgery, University Hospital Aachen, Aachen, Germany.

B Olij (B)

Department of Surgery, Maastricht University Medical Centre, Maastricht, the Netherlands.

S G Pappas (SG)

Department of Surgery, Rush University Medical Center, Chicago, Illinois, USA.

P Sandström (P)

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

A Schnitzbauer (A)

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

A Serrablo (A)

Department of Surgery, Miguel University Hospital and University of Zaragoza, Zaragoza, Spain.

J Tasse (J)

Department of Radiology, Rush University Medical Center, Chicago, USA.

C Van der Leij (C)

Department of Radiology, Maastricht University Medical Centre, Maastricht, the Netherlands.

P Metrakos (P)

Department of Surgery, Section of Hepato-Pancreatico-Biliary Surgery, McGill University Health Center, Montreal, Quebec, Canada.

R Van Dam (R)

GROW - School for Oncology and Developmental Biology, Maastricht University, Maastricht, the Netherlands.
Department of Surgery, Maastricht University Medical Centre, Maastricht, the Netherlands.
Department of General, Visceral and Transplant Surgery, University Hospital Aachen, Aachen, Germany.

E Schadde (E)

Institute of Physiology, University of Zurich, Zurich, Switzerland.
Department of General and Visceral Surgery, Cantonal Hospital Winterthur, Winterthur, Switzerland.
Department of Surgery, Rush University Medical Center, Chicago, Illinois, USA.

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