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Survival of children after liver transplantation for hepatocellular carcinoma

Authors :
Baumann, Ulrich
Adam, René
Duvoux, Christophe
Mikolajczyk, Rafael
Karam, Vincent
D'Antiga, Lorenzo
Chardot, Christophe
Coker, Ahmet
Colledan, Michele
Ericzon, Bo-Goran
Line, Pål Dag
Hadzic, Nedim
Isoniemi, Helena
Klempnauer, Jürgen L
Reding, Raymond
McKiernan, Patrick J
Mclin, Valérie Anne
Paul, Andreas
Salizzoni, Mauro
Furtado, Emanuel San Bento
Schneeberger, Stefan
Karch, André
European Liver and Intestine Transplant Association
Baumann, U
Adam, R
Duvoux, C
Mikolajczyk, R
Karam, V
D'Antiga, L
Chardot, C
Coker, A
Colledan, M
Ericzon, B
Line, P
Hadzic, N
Isoniemi, H
Klempnauer, J
Reding, R
Mckiernan, P
Mclin, V
Paul, A
Salizzoni, M
Furtado, E
Schneeberger, S
Karch, A
Helmholtz-Zentrum für Infektionsforschung GmbH, Inhoffenstr. 7, 38124 Braunschweig, Germany.
Source :
Liver Transplantation, Vol. 24, No 2 (2018) pp. 246-255, Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society
Publication Year :
2017

Abstract

Hepatocellular carcinoma (HCC) in childhood differs from adult HCC because it is often associated with inherited liver disease. It is, however, unclear whether liver transplantation (LT) for HCC in childhood with or without associated inherited disease has a comparable outcome to adult HCC. On the basis of data from the European Liver Transplant Registry (ELTR), we aimed to investigate if there are differences in patient and graft survival after LT for HCC between children and adults and between patients with underlying inherited versus noninherited liver disease, respectively. We included all 175 children who underwent LT for HCC and were enrolled in ELTR between 1985 and 2012. Of these, 38 had an associated inherited liver disease. Adult HCC patients with (n = 79) and without (n = 316, matched by age, sex, and LT date) inherited liver disease served as an adult comparison population. We used multivariable piecewise Cox regression models with shared frailty terms (for LT center) to compare patient and graft survival between the different HCC groups. Survival analyses demonstrated a superior longterm survival of children with inherited liver disease when compared with children with HCC without inherited liver disease (hazard ratio [HR], 0.29; 95% CI, 0.10-0.90; P = 0.03) and adults with HCC with inherited liver disease (HR, 0.27; 95% CI, 0.06-1.25; P = 0.09). There was no survival difference between adults with and without inherited disease (HR, 1.05; 95% CI, 0.66-1.66; P = 0.84). In conclusion, the potential survival advantage of children with an HCC based on inherited disease should be acknowledged when considering transplantation and prioritization for these patients. Further prospective studies accounting for tumor size and extension at LT are necessary to fully interpret our findings. Liver Transplantation 24 246-255 2018 AASLD.

Details

ISSN :
15276473 and 15276465
Volume :
24
Issue :
2
Database :
OpenAIRE
Journal :
Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society
Accession number :
edsair.doi.dedup.....733b40ee5dd36a4c89eee54d3543da1b