Liver transplantation for hilar cholangiocarcinoma: A systematic review.

Published

Journal Article (Review)

Patients with hilar cholangiocarcinoma (hCCA) have advanced disease at presentation and therefore curative treatment options are limited. Liver transplantation (LT), in the case of unresectable disease, is theoretically an attractive option, as it offers the maximum resection margin and at the same time removes the underlying parenchymal liver disease. In the past years a number of studies have aimed to evaluate to potential beneficial role of neo adjuvant therapy followed by LT for treating patients with unresectable hCCA. The objective of our systematic review was to collect and evaluate long-term outcomes of patients with hCCA undergoing LT. A systematic search of 4 electronic databases (Medline, Scopus, Google Scholar and ClinicalTrails.gov databases) was performed for articles published between January 2000 and May 2019. A total of 13 studies with 698 patients were finally included in the present systematic review. A proportion of 74.4% of patients received combination of chemotherapy and radiation as a part of neoadjuvant therapy. One-, 3- and 5-year overall survival rates ranged greatly among the included studies from 58% to 92%, 31% to 80% and 20% to 74%, respectively. Recurrence rates ranged from 16% to 61%, whilst perioperative mortality ranged from 0% to 25.5%. LT could provide acceptable long-term outcomes in the setting of neoadjuvant chemoradiation and strict patient selection criteria. Taking into account organ shortage, combined with the lack of level I evidence, more prospective randomized trials are needed in order to establish certain indications, rigorous criteria and standardized protocols for LT in hCCA and provide the maximal potential benefits for these patients.

Full Text

Duke Authors

Cited Authors

  • Machairas, N; Kostakis, ID; Tsilimigras, DI; Prodromidou, A; Moris, D

Published Date

  • January 2020

Published In

Volume / Issue

  • 34 / 1

Start / End Page

  • 100516 -

PubMed ID

  • 31711828

Pubmed Central ID

  • 31711828

Electronic International Standard Serial Number (EISSN)

  • 1557-9816

International Standard Serial Number (ISSN)

  • 0955-470X

Digital Object Identifier (DOI)

  • 10.1016/j.trre.2019.100516

Language

  • eng