Long-term survival of patients with hepatocellular carcinoma (HCC) after liver transplantation is affected mainly by recurrence of HCC. There is the opinion that the chance of recurrence after 2 years post-transplantation is remote, and therefore lifelong surveillance is not justified because of limited resources. The aims of the present study were to determine the rate of late HCC recurrence (≥2 years after transplantation) and to compare the long-term patient survival outcomes between cases of early recurrence (<2 years after transplantation) and late recurrence.
Patients
A total of 139 adult HCC patients having liver transplantation during the period from July 1994 to December 2007 were included in the analysis. The median follow-up period was 55 months. Thirty-two patients received deceased-donor grafts and 107 received living-donor grafts.
Results
Hepatocellular carcinoma recurrence occurred in 24 (17.3%) patients, among them 22 (86%) had living-donor grafts and 7 (5%) developed late recurrence. Patients in the early recurrence group and patients in the late recurrence group had comparable demographics and disease pathology. The former group, when compared with the latter, had significantly worse overall survival at 3 years (13.3 versus 100%) and 5 years (6.67 versus 71.4%) (log-rank test; p < 0.001).
Conclusions
Both early recurrence and late recurrence of HCC after liver transplantation were not uncommon, mostly detected at a subclinical stage. Regular and long-term surveillance with imaging and blood tests is essential for early detection.
Introduction
Hepatocellular carcinoma (HCC) is the leading cause of death in patients with hepatitis B or C, and its incidence has increased considerably over the past decade [1]. Among various modalities for treating HCC and underlying cirrhosis, liver transplantation (LT) is the ultimate solution. Unfortunately, HCC recurs in 10–60% of patients after LT [2‐6]. The average time for recurrence ranges between 1 and 2 years after LT [2‐6]. However, there have been limited studies on late recurrence ≥2 years after LT) of HCC, and its occurrence is poorly understood. The present study was designed to determine the rate of late HCC recurrence and to compare the long-term patient survival outcomes between cases of early recurrence (<2 years after LT) and late recurrence.
Patients and methods
Data of all adult HCC patients who underwent LT, with deceased donor or living donor, at Department of Surgery, Queen Mary Hospital, Hong Kong, China, in the period from July 1994 to December 2007 were reviewed. The strategies adopted for selection and management of patients with known HCC for LT have been described elsewhere [7]. In brief, only patients aged 65 years or below with disease not amenable to partial hepatectomy and local ablation were considered for LT. Before 2002, the radiological Milan criteria [2] (solitary tumor up to 5 cm in size, or a maximum of 3 tumor nodules with each no larger than 3 cm) were observed in selection of patients. Since 2002, the tumor number and size limits have been expanded to match the criteria of University of California, San Francisco (UCSF criteria) [8] (solitary tumor not exceeding 6.5 cm, or a maximum of three tumor nodules totaling up to 8 cm in diameter with each nodule no bigger than 4.5 cm). Tumor evaluation was done with computed tomography of the abdomen and thorax, in addition to radionuclide bone scan at initial diagnosis. In recent years dual-tracer [11C-acetate and 18F-fluorodeoxyglucose (FDG)] positron emission tomography was occasionally performed on selected patients to exclude extrahepatic metastasis. Imaging was repeated every 3–6 months for patients with prolonged waiting time, and transarterial lipiodol chemoembolization was given to patients with adequate liver reserve to contain tumor growth. Patients whose tumors progressed to beyond the acceptance criteria as shown by serial imaging were excluded from transplantation. Also excluded were patients who had major vascular invasion or extrahepatic diseases.
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All living liver graft donors must have compatible ABO blood group, serology negative of hepatitis B surface antigen and hepatitis C antibody, and no evidence of any acute or chronic illness that would increase operation risk. Computed tomography with volumetry was performed to determine the size of the donor liver, and left-lobe graft or right-lobe graft was decided with the principle that the graft must be larger than 40% of the recipient’s standard liver weight [9] as estimated according to the Urata formula [10].
Hospital mortality was defined as death occurring during the hospital admission for the primary operation. Patients were followed up at the outpatient clinic weekly within the first 3 months after operation, and afterwards every 1–3 months, depending on clinical status and results of liver function tests. Routine blood tests, including hepatic and renal function tests, were carried out in every follow-up visit. Serum α-fetoprotein check, chest X-ray, and computed tomography (or magnetic resonance imaging for patients with impaired renal function) were performed every 3–6 months during the first 5 years after operation. After 5 years, imaging was done every 6 months–1 year or when deemed indicated (e.g., serum α-fetoprotein level showing a rising trend).
Statistical analysis
Comparison of categorical variables was performed using a chi-square test or Fisher’s exact test where appropriate. Nonparametric continuous variables were compared with the Mann–Whitney U-test and presented as medians with range. Parametric continuous variables were compared with Student’s t-test and presented as means with standard deviation. Survival was analyzed with the Kaplan–Meier method, and comparison of variables was performed using the log-rank test. All p values less than 0.05 were regarded as statistically significant, and all p values were two-tailed.
Results
A total of 139 patients, 119 male and 20 female, were included for analysis. Among them, 115 patients had no recurrence of HCC, 17 patients had early recurrence, and 7 patients had late recurrence. The early recurrence group and the late recurrence group had comparable demographics and disease pathology (Table 1). Two patients developed very late recurrence (>5 years after LT). One of them had recurrence in the left adrenal gland 5.2 years after LT, and was treated with laparoscopic adrenalectomy. She remained free of disease for 1 year until a recent computed tomography scan revealed a 1 cm intrahepatic recurrence, which was treated with percutaneous radiofrequency ablation. She has been free of disease since then. The other patient had recurrence in the retrocaval lymph node 6.5 years after LT. The recurrence was deemed unresectable because there was tumor thrombus inside the inferior vena cava. Treatments for other patients’ recurrence are listed in Table 2. All surgical specimens were sent for histopathologic examination and were confirmed to be metastatic HCC. The early recurrence group, when compared with the late recurrence group, had significantly poorer overall survival (Fig. 1). The former had overall survival at 1, 3, and 5 years at 100, 13.3, and 6.67%, respectively, and the latter had 100, 100, and 71.4%, respectively (Table 3). Similarly, survival after recurrence was also poorer in the early recurrence group, although it did not reach statistical significance (Fig. 2).
Table 1
Demographic and pathologic data of the two groups
Early recurrence (n = 17)
Late recurrence (n = 7)
p value
Sex (male:female)
17:0
6:1
0.292
Median age, years (range)
47 (40–61)
52 (41–56)
0.292
Deceased-donor LT:living-donor LT
1:16
1:6
0.507
HBV carrier
17
7
HCV carrier
0
0
HBV and HCV co-infection
0
0
Median preoperative α-fetoprotein, ng/ml (range)
84 (4–117,850)
411 (3–975)
0.391
Pretransplant treatment
No treatment
4
3
Transarterial chemoembolization
6
2
Ethanol injection
0
0
Hepatectomy
5
2
Chemotherapy
1
0
Radiofrequency ablation
5
1
Pretransplant anti-HBV therapy
Lamivudine
13
5
Lamivudine + adefovir
1
2
Entecavir
2
0
Lamivudine + Tenofovir
0
0
Lamivudine + Adefovir + Entecavir
1
0
HBV-DNA positivity at study end point (%)
8 (47.1)
1 (14.3)
0.002
HBV mutant detected at study end point (%)
4 (23.5)
2 (28.6)
0.900
Salvage transplantation (%)
9 (52.9)
3 (42.9)
1.000
Explant pathology (no. of tumors)a
0.998
1
7
3
2
2
1
3
2
1
≥4
5
2
Median largest tumor size, cm (range)
3.6 (1.5–19.5)
2.5 (1.0–7.5)
0.482
Presence of microvascular permeation (%)
11 (64.7)
3 (42.9)
0.393
TNM staging 2003
0.133
I (%)
3 (17.6)
3 (42.9)
II (%)
10 (58.8)
1 (14.3)
IIIA (%)
4 (23.5)
3 (42.9)
IIIB (%)
0 (0)
0 (0)
Within Milan criteria
7
4
0.659
Beyond Milan criteria
10
3
Within UCSF criteria
9
4
1.000
Beyond UCSF criteria
8
3
LT liver transplant, HBV hepatitis B virus, HCV hepatitis C virus, UCSF University of California San Francisco
aOne patient in the early recurrence group had no viable tumor on histopathology after transarterial chemoembolization
Table 2
Treatments of recurrences in the two groups
Treatmenta
Early recurrence (n = 17)
Late recurrence (n = 7)
Intrahepatic recurrence
Hepatectomy
2
0
Transarterial chemoembolization
4
1
Radiofrequency ablation
3
1
Extrahepatic recurrence
Adrenalectomy
1
1
Lung resection
6
0
Excision of solitary peritoneal metastasis
0
1
Excision of retrocaval lymph node
0
1
Excision of inferior vena cava tumor thrombus
0
1
Excision of common hepatic artery lymph node
0
1
Chemotherapy
4
1
Radiotherapy
6
3
Interferon
3
0
Tamoxifen
0
1
Sorafenib
5
0
Xeloda
1
1
Nailing and plating of bone metastasis
2
1
aA patient might receive more than one treatment modality
Fig. 1
Overall survival of patients after liver transplantation
Table 3
Postoperative outcomes in the two groups
Early recurrence (n = 17)
Late recurrence (n = 7)
p value
Latest HBsAg in HBV patients
0.393
Negative
11
3
Positive
6
4
History of rejection
3 (17.6%)
0
0.611
Latest immunosuppression
0.665
FK 506
8
5
Sirolimus
7
2
FK 506 + prednisolone
1
0
FK 506 + sirolimus
1
0
Hospital mortality (%)
0 (0)
0 (0)
a
Patient overall survival
0.001
1 year (%)
100
100
3 years (%)
13.3
100
5 years (%)
6.67
71.4
HBsAg hepatitis B surface antigen
aNo HBV serology checked before death
Fig. 2
Survival rates after recurrence
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×
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Discussion
The tumor recurrence rate in this study was 17.3% (24/139), which is not uncommon. Late recurrence occurred in 5% (7/139) of patients; 2 patients even developed recurrence after 5 years of LT. All recurrences were found at a subclinical stage, and this demonstrates the importance of regular surveillance as early intervention may prolong survival. Patients with early recurrence had much worse overall survival than those with late recurrence. More intrahepatic recurrences were found in the early recurrence group, whereas more extrahepatic recurrences were found in the late recurrence group (Table 2), which is consistent with findings of previous studies [11, 12]. This also reflects the difference in tumor biology, but the mechanism is still poorly understood.
Late recurrence of HCC after LT was quite common in this study. As noted by Poon [13], a strict surveillance program monitoring recurrence should be adopted before any recommendation can be made with a large cohort. After all, current evidence is suboptimal. It was showed that viral load of hepatitis B may be an important risk factor for late recurrence after resection [14]. However, all the patients in this study were on some sort of antiviral therapy before LT surgery, and hepatitis B surface antigen positivity was similar in the two recurrence groups. So, at least in this study, the role of viral load might not have been too significant in recurrence.
In Western countries, HCC is mainly caused by HCV infection, but in our locality, HBV infection is the main cause. Although effective treatments for HBV infection are available, recurrence of HCC is still common. To decrease the rate of HCC recurrence, further adjuvant treatments for high-risk patients have to be developed.
Notoriously, HCC recurrence after LT carries very poor prognosis in the presence of the effects of immunosuppression. An early report suggested that recurrent HCC after transplantation has a more aggressive course than recurrent HCC after resection, presumably because of immunosuppression [15]. Nonetheless, our center adopts an aggressive approach in managing patients with recurrence after LT, and treatments include resection and ablation. In addition, decreasing dosage of immunosuppressants may help to hinder the progression of disease. Recently, medications have been used on high-risk patients. Sirolimus is an inhibitor of mTOR and is used as an immunosuppressive medication on patients who are at high risk of tumor recurrence after LT. Sorafenib (Nexavar, Bayer HealthCare, Wayne, NJ) is a multi-kinase inhibitor approved for the treatment of advanced HCC. A recent study reported that the combination use of sirolimus and sorafenib appeared to have a synergistic effect in treating recurrent HCC after LT [16]. For the time-being, there is no well-established protocol on the use of sorafenib at our center. In general, it is prescribed mainly to patients with widespread extrahepatic diseases. For patients with solitary extrahepatic metastasis or intrahepatic recurrence, resection or ablation is the treatment of choice. Further research on the efficacy of these medications, used solely or in combination, will certainly contribute to the management of recurrent HCC after LT.
In conclusion, early and late recurrences of HCC after LT are not uncommon and can be detected at a subclinical stage with regular monitoring. Long-term surveillance with imaging and blood tests is essential for early detection.
Open Access
This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
Open AccessThis is an open access article distributed under the terms of the Creative Commons Attribution Noncommercial License (https://creativecommons.org/licenses/by-nc/2.0), which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
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