Recurrence of hepatocellular carcinoma following deceased donor liver transplantation: case series

Cem Simsek, Amy Kim, Michelle Ma, Nilay Danis, Merve Gurakar, Andrew M. Cameron, Benjamin Philosophe, Jacqueline Garonzik-Wang, Shane Ottmann, Ahmet Gurakar, Behnam Saberi

1Johns Hopkins University School of Medicine, Division of Gastroenterology and Hepatology-Transplant Hepatology, Baltimore, MD 21205, USA.

2Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD 21205, USA.

3Johns Hopkins University School of Medicine, Division of Transplant Surgery, Baltimore, MD 21205, USA.

Abstract

Keywords: Hepatocellular carcinoma, liver transplant, liver resection, locoregional therapy

INTRODUCTION

Liver transplant (LT) has become the treatment of choice in patients with hepatocellular carcinoma (HCC) and cirrhosis who meet the Milan criteria (MC)[1]. Although additional extended criteria models have been proposed, HCC recurrence following LT remains an unfortunate incident associated with poor survival[2,3]. Tumor biology and alpha fetoprotein (AFP), as well as tumor size and number, have been proposed by various groups as other potentially relevant factors of tumor recurrence[4-6].

Overall, two thirds (2/3) of patients, who develop recurrent HCC post-LT, present with extrahepatic recurrence[7,8]. The treatment of choice in post LT HCC recurrence is determined based on the site and the extent of the recurrence[8]. However, treatments are not standardized and mostly based on expert opinion and retrospective studies[9]. Surgical treatment options have been proposed with promising outcomes in selected patients[10,11]. Locoregional therapy options, transarterial chemoembolization, radiofrequency ablation, and stereotactic radiation are considered in selected cases[9].

In a recent report, we published our experience in LT recipients with HCC at the Johns Hopkins University Comprehensive Liver Transplant Center[12]. As a follow-up study, we aimed to study the clinicopathological features and outcomes of 26 cases with HCC recurrence following LT. In addition, we evaluated the details on the outcomes and the application of different treatment modalities in this group.

METHODS

The study was approved by the institutional review board at the Johns Hopkins Hospital. HCC-related deceased donor LT recipients between January 2005 and December 2015 were evaluated. In total, 26 patients with post-LT HCC recurrence were identified among 165 recipients who were included in the study. All recipients were listed following a standard work up and discussion at the weekly selection meeting. They were within Milan criteria or downstaged into Milan criteria. The transplant was performed by piggyback technique. Postoperative HCC surveillance consisted of contrasted cross-sectional imaging with computerized tomography or magnetic resonance imaging with AFP every three months for the first year and every six months for the second and third years. There was no set therapeutic protocol for recurrence; treatment options were discussed in a multidisciplinary fashion. The Pre-LT AFP was obtained within the past three months prior to deceased donor liver transplantation (DDLT) and immediate post-LT AFP was obtained within three months post DDLT.

Data on clinical, radiologic, pathology, HCC recurrence, and survival were collected from the records, reviewed, and analyzed. Explant pathologies were reviewed retrospectively, and the following tumor parameters were collected: size, number of lesions, microvascular invasion status, and differentiation. It was determined whether patients met the Milan or University of California San Francisco (UCSF) criteria based on the number and size of HCC lesions on explant pathology. The data collected for categorical variables were reported as percentages. Data for continuous variables were reported by the mean and standard deviation. Patient survivals were analyzed using Kaplan-Meier statistics. STATA V.13 (StataCorp college station, TX) was used to perform the statistical analyses.

RESULTS

Patient characteristics

Among the deceased donor LT recipients, HCC was the primary indication for transplantation varying from 21% to 53% of patients [Figure 1] according to the year. Clinical information on the 26 LT recipients with recurrent HCC is summarized in Table 1. Patients were predominantly male (88.5%) with a mean age of 59 years (range 47-72 years). The majority of recipients were white (n= 17, 65.4%), followed by African American (n= 7, 27.0%) and Asian (n= 2, 7.6%) ethnicities. Primary etiology of liver disease was chronic hepatitis C (positive hepatitis C antibody and/or hepatitis C RNA) in 13 patients (50%) and hepatitis C and alcoholic liver disease in 6 (23%) patients. Chronic hepatitis B (positive hepatitis B surface antigen and/or hepatitis B DNA) was seen in three patients (11.5%), followed by alcoholic liver disease (n= 2, 7.7%), and non-alcoholic fatty liver disease (n= 1, 3.9%).

Figure 1. Overall, rate of deceased donor liver transplant for hepatocellular carcinoma indication at the Johns Hopkins Hospital from 2005 to 2015. HCC: hepatocellular carcinoma

Laboratory results

The average model for end-stage liver disease (MELD) score was 13, ranging from 6 to 35. Mean AFP was 27.6 ng/mL for pre-LTvs.23.6 ng/mL for post-LT time periods [Tables 1 and 2]. Four patients had pre-LT AFP levels of ＞ 1000 ng/mL. The other available laboratory results are summarized in Table 1.

Immunosuppression

Overall, nine (34.6%) patients were treated with mammalian target of rapamycin (mTOR) treatment with sirolimus in eight and everolimus in one patient. Seventeen patients received Tacrolimus-based therapy.

Explant-pathology findings

In the explant pathologies of LT recipients, 9 (34.6%) patients had only one lesion and 11 (42.4%) had 4 or more lesions. The average for the largest lesion size was 4.3 cm. In total, 12 patients (46.1%) had multilobar tumors and 13 (50%) had tumors that were located in the right lobe. Overall, 10 patients (38.4%) were within MC criteria and 11 patients (42.3%) were within UCSF criteria. Four patients (15.4%) were downstaged to MC with locoregional treatment. Seventeen (65.4%) patients underwent locoregional therapy before transplant. None of the tumors were well-differentiated. Overall, 14 (53.8%) patients had moderately differentiated HCC. Eleven (42.3%) patients had HCC with poor differentiation. Microvascular invasion was detected in 19 of the 26 cases (73.1%) while one patient had bile duct invasion only.

Recurrence and survival

The overall rate of HCC recurrence following LT in our series was 15%. The rate of HCC recurrence has improved over the years with a recurrence rate of 10% in 2015 [Figure 2]. Mean time for diagnosis of

HCC recurrence after LT was 427 days, ranging from 34 to 1502 days. The site of HCC recurrence was intrahepatic in 8 (31%), extrahepatic in 14 (54%), and both intra- and extrahepatic in 4 (15%) patients. Overall, 31% of recipients had intrahepatic HCC recurrence following LT when compared to 69% with extrahepatic recurrence. Twenty-two percent of the patients who had extrahepatic involvement had concomitant liver involvement. The most common sites of extrahepatic involvement were the lungs (44.4%) and bones (44.4%) (spine, rib, pelvis, and humerus), followed by mediastinum (27.8%), brain (22.2%), portal lymph nodes (11.1%), gastro-hepatic ligament (5.6%), adrenal gland (5.6%), pleura (5.6%), and peritoneum (5.6%).

Table 1. Characteristics of the study population

Table 2. Alpha fetoprotein levels pre and post-liver transplant

Figure 2. Overall, per year rate of hepatocellular carcinoma recurrence in deceased donor liver transplant recipients at the Johns Hopkins Hospital from 2005 to 2015. HCC: hepatocellular carcinoma

A range of different treatment modalities was used for recurrences [Table 3]. Six (21.4%) of the 26 patients were managed with supportive care. The remaining 20 cases received various treatment modalities including locoregional therapy (transarterial chemoembolization in 3, Y 90 in 1, and radiofrequency ablation in 1), external radiation in 10, and surgical resections in 8 (brain 4, spine 2, bone 1, and Whipple surgery in 1). Nine (32%) patients received combination therapies of the above-mentioned modalities. Seven patients (27%) received sorafenib. An additional two patients received chemotherapy regimens other than sorafenib [Table 3]. Recurrence-free survival and overall survival are shown in Figure 3. Patients who developed HCC recurrence following LT had an extremely poor overall survival (7.7%). In total, 19% of patients died within one year following LT. Overall, 24 out of 26 (92.3%) patients died throughout the fouryear follow-up period. Timing of death relevant to the time of LT is shown in Table 3.

DISCUSSION

In this series, we report a rate of 15% HCC recurrence following deceased donor LT at our transplant program. This rate is consistent with the literature report of 15%-20% post-LT HCC recurrence[13]. It is well known that the patients who are outside of MC prior to LT have higher rates of tumor recurrence following LT, compared to those within the MC[1]. Although all of the patients within our series were thought to be within MC radiographically prior to LT, according to radiology findings, only 34% were within the criteria by reviewing the explant. When including an additional four (15%) patients who were downstaged, in total 49% were within MC based on pathology. This discrepancy between radiology and pathology has been previously described by other groups in the literature[13].

Our sites of recurrence findings are very similar to the recent reports[8]. In a systematic review of post-LT HCC recurrence, extrahepatic site was the most common site of recurrence in 67% of cases, compared to intrahepatic in 33%[8]. The extrahepatic sites of involvement included: bone, pulmonary, adrenal, lymph nodes, and brain[8].

Within our series, 54% of the HCC recurrences were diagnosed within 1 year post-OLT, while 81% and 96% of recurrences occurred within 2 and 3 years following OLT, respectively. The average time to HCC recurrence within our series was 427 days (range 34-1502 days). It is shown by others that early versus late recurrence is a predictor of post-LT survival[14]. The patients with early HCC recurrence, defined as recurrence within 24 months post-LT, have a worse prognosis[14]. There are a few potential theories for early HCC recurrence post-LT: (1) biologically rapid growing, aggressive tumors; (2) lack of high-quality pre-LT imaging or overlooking intra- or extrahepatic imaging[8]; (3) extrahepatic microscopic viable HCC cells that could not be detected by conventional imaging prior to LT; and (4) presence of circulating tumor cells that seed to other sites. The mechanism by which the late recurrence occurs is unclear[15]. Presence of pre-LT HCCs that are biologically slow growing, or development ofde novoHCC recurrence in the liver allograft could be the cause. Within our series, we did not have any cases who had HCC recurrence that occurred or were diagnosed beyond five years following LT.

The selection of an ideal treatment for post LT HCC recurrence is a matter of debate, and the evidence is mainly based on expert opinion and non-randomized cohort studies[9]. The treatment modality will varybased on the type of recurrence (intrahepatic versus extrahepatic), organ of involvement, and extent of involvement. This includes a wide range of surgical (intra- or extrahepatic resection and re-transplantation) and non-surgical treatments (locoregional therapies, sorafenib, other systemic chemotherapy, mTOR inhibitors, and best supportive care)[16].

Table 3. Specific characteristics of the tumors, treatment, and outcomes

Figure 3. Survival analysis for 26 liver transplant recipients with hepatocellular carcinoma recurrence: A: Kaplan-Meier curve for recurrence-free survival; B: Kaplan-Meier curve for overall survival

Surgical options including extrahepatic resection, liver graft resection, and liver re- transplant have also been considered for patients presenting with HCC recurrence. In 2004, the Mount Sinai group reported resection of the liver allograft in five out of 18 recipients with HCC recurrence[11]. The authors concluded that, in selected cases with recurrent intrahepatic-HCC, liver resection improved survival[11]Similarly, Kornberget al.[10]reported that HCC recurrence should be treated surgically in eligible patients with good long-term outcomes. In multivariate analysis of post-LT HCC recurrence, late tumor recurrence (＞ 24 months) and surgical resection were the two independent predictors of survival[10]. A systematic review in 2015 reported that the surgical approach to localized intra- or extra-hepatic recurrences are uneventful and not associated with higher mortality[8]. Retransplantation for recurrent HCC is not a practical option[17]due to the higher risk of recurrence with a limited organ availability.

Sorafenib, a multikinase inhibitor, has been approved as first-line treatment for the management of advanced-stage HCC following two clinical trials in 2008 and 2009[18,19]. In a multicenter phase 2, blinded placebo-controlled, clinical trial, the efficacy of sorafenib for preventing HCC recurrence post-LT in highrisk recipients is being actively investigated [ClinicalTrials.gov identifier (NCT number): NCT01624285]. There are currently no systemic therapies that have been shown to improve survival in HCC recurrence post-LT. Recently, other tyrosine kinase inhibitors were approved as first- or second-line treatment in HCC in the non-transplant setting[20]. The role of these agents as adjuvant therapy or post-LT HCC recurrence is unclear and deserves further investigation in the near future. Nivolumab, an anti-PD1 inhibitor, was recently approved for the treatment of HCC, as second line, in the non-transplant setting, with the objective response rate of 20%[21]. The role of immunotherapy among post-LT recipients with HCC has not been yet established. It is possible that the immunotherapy will affect the liver allograft leading to acute cellular rejection[22].

Mammalian target of rapamycin (mTOR), a serine/threonine protein kinase, has been shown to be upregulated in 40%-50% of HCCs. mTOR is involved in the regulation of cell metabolism and growth[23]. Therefore, various studies have suggested that mTOR inhibitors may have antineoplastic properties in HCC patients and mTOR inhibitors should be used after LT. In a meta-analysis of 2950 patients from five studies, sirolimus-based immunosuppression reduced the rate of tumor recurrence and improved overall survival[24].

HCC recurrence following LT is an unfortunate event and associated with poor outcomes. In a recent meta-analysis, the median overall survival was 13 months following the diagnosis of HCC recurrence post-LT[8]. Herein, supportive care was associated with the lowest survival rate of 3.3 months[8]. There is no standardized protocol regarding the type and frequency of post-LT cross-sectional imaging in surveillance of HCC LT recipients. It is important to note that more than 50% of patients develop tumor recurrences that are outside of liver (extrahepatic), therefore imaging limited to the liver may not be sufficient for the diagnosis of majority of HCC recurrences. We also note that AFP is a useful marker in post-LT HCC surveillance only for high-AFP-secreting tumors. Four patients in our study had pre-AFP levels of ＞ 1000 ng/mL. It is well known that patients with high AFP producing tumors have worse tumor biology and have worse outcomes[12,25]. HCC candidates need to have AFP of ≤ 1000 ng/mL to receive extra points to shorten the waiting period for liver transplantation[25]. The overall prognosis of HCC recurrence following LT is poor in the majority of cases and there are no available studies evaluating cost-effectiveness of surveillance protocols specific to this group of patients.

In conclusion, HCC recurrence post liver transplant is an unfortunate event associated with extremely poor survival. The majority of the cases are early recurrence occurring 1-2 years following liver transplantation. More than 50% of HCC recurrences are extrahepatic. Therefore, post-liver transplant imaging confined to the liver may not be enough to detect all of the recurrences. In patients with AFP producing tumors, this marker may also be helpful to diagnose the HCC recurrence. There is no general consensus on the treatment for post liver transplant hepatocellular carcinoma recurrence. The current reports are mainly based on single-center retrospective experience.

DECLARATIONS

Authors’ contributions

Acquisition of data, analysis and interpretation of data, drafting of the manuscript: Simsek C

Interpretation of the data, Final Editing and Critical Review of the manuscript for important intellectual content: Kim A

Acquisition of data, analysis and interpretation of data, drafting of the manuscript: Ma M

Review of the data, drafting of the manuscript and editing: Danis N

Analysis and interpretation of data, statistical analysis: Gurakar M

Study concept and design, interpretation of data, critical revision manuscript for important intellectual content: Cameron AM

Study concept and design, interpretation of data, critical revision of the manuscript for important intellectual content: Philosophe B

Study concept and design, interpretation of data, statistical analysis, critical revision of the manuscript for important intellectual content: Garonzik-Wang J

Study concept and design, critical revision of the manuscript for important intellectual content: Ottmann S

Study concept and design, acquisition of data, drafting of the manuscript, analysis and interpretation of data, revision of the manuscript for important intellectual content study supervision: Gurakar A

Study concept and design, acquisition of data, drafting of the manuscript, analysis and interpretation of data, critical revision of the manuscript for important intellectual content, study supervision: Saberi B

Availability of data and materials

Data source has been the Electronic Medical System. Please contact the corresponding author for unidentified data availability.

Financial support and sponsorship

This Research is partially supported by NIH Grants: R44 CA165312 - Development of a urine test for the early detection of liver cancer. U01 CA230690 - Pathway Specific Functional Biomarkers for the Early Detection of Liver Cancer.

Conflicts of interest

All authors declared that there are no conflicts of interest.

Ethical approval and consent to participate

This retrospective study was approved by Johns Hopkins IRB NA_00028034.

Consent for publication

Not applicable.

Copyright

© The Author(s) 2020.