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Zhang et al. Hepatoma Res 2017;3:58-66                               Hepatoma Research
           DOI: 10.20517/2394-5079.2017.05
                                                                                                  www.hrjournal.net
            Original Article                                                                    Open Access

           Late recurrence of hepatocellular

           carcinoma after liver transplantation



           Julia A. Zhang , Sandi A. Kwee , Linda L. Wong
                                                    1
                                      2
                        1
           1 Department of Surgery, University of Hawaii School of Medicine, Honolulu, HI 96813, USA.
           2 The Queens Medical Center, Honolulu, HI 96813, USA.
           Correspondence to: Prof. Linda L. Wong, Department of Surgery, University of Hawaii School of Medicine, 550 S. Beretania Street, Suite 403, Honolulu,
           HI 96813, USA. E-mail: Hepatoma@aol.com

           How to cite this article: Zhang JA, Kwee SA, Wong LL. Late recurrence of hepatocellular carcinoma after liver transplantation Hepatoma Res
           2017;3:58-66.
                                         ABSTRACT

            Article history:              Aim: Hepatocellular carcinoma (HCC) is the third leading cause of cancer deaths worldwide
            Received: 29-01-2017          and liver transplant (LT) prolongs survival. However, 15-20% will experience recurrent HCC,
            Accepted: 24-03-2017          most occurring within 2 years of LT. HCC patients with late recurrences (> 5 years after
            Published: 10-04-2017         LT) may have distinctive clinical/biological characteristics. Methods: A retrospective review
                                          was conducted of 88 patients who underwent LT for HCC during 1993-2015, analyzing
            Key words:                    demographics, clinical factors, explant pathology, and outcome. Results: Median follow-up
            Hepatocellular carcinoma,     was 6.4 years. HCC recurred in 15 (17.0%) patients with mean time to recurrence of 3.96 ±
            liver transplantation,        3.99 years. Five patients reoccurred > 5 years post-LT. All late recurrences involved males in
            recurrence                    their 50s, recurring at 8.5 years on average. Recurrences occurred in chest wall (2), liver (2),
                                          lung (2), bone (1) and pelvis (1), with multifocal involvement in 2 patients. Four patients died
                                          within 18 months of late recurrence. The fifth patient is alive after ablation of liver recurrence
                                          and treatment with sorafenib and everolimus. Conclusion: One-third of post-LT patients with
                                          recurrent HCC experienced late recurrence. Although the sample size makes it difficult to
                                          identify significant risk factors, this study highlights the importance of long-term follow-up
                                          and need for biomarkers to identify patients at risk for late recurrences.

                                                                                                    [2]
           INTRODUCTION                                       compared to 10% in untreated HCC.  Despite
                                                              receiving optimal therapy with transplantation, up to
           Hepatocellular carcinoma (HCC) is the most common   20% of patients may experience recurrent HCC. Most
           primary liver cancer with 782,000 new cases and    of these recurrences occur within 2 years following
                                                [1]
           745,000 deaths annually worldwide.  The  best      transplantation. Although there are no clear guidelines
           treatments for HCC include liver resection and liver   on how to treat these recurrences, surgical resection
           transplantation (LT). However, most patients present   is the preferred treatment option. Other locoregional
           at advanced stage and are not candidates for these   therapies such as radiofrequency ablation (RFA)
           potentially curative therapies. LT, although limited by   and transarterial chemoembolization (TACE) may be
           the shortage of donor livers, has superior disease-  options, and sorafenib can be considered for more
           free survival, with improved 5-year survival of 70%   diffuse, unresectable disease. [3,4]

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