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HCC influence on patient survival after liver transplantation for HDV cirrhosis
Georgios Imvrios1, Dionisios Vrochides, Vasilios Papanikolaou
1Aristotle University, Thessaloniki, Greece.
Insights
Liver transplant recipients with hepatocellular cancer (HCC) for hepatitis B/D virus (HB/DV) cirrhosis showed superior long-term survival. This unexpected finding may be linked to lower infection rates in HCC patients post-transplant.
Area of Science:
- Hepatology
- Transplantation immunology
- Viral hepatitis research
Background:
- Hepatocellular cancer (HCC) impact on liver transplant outcomes for hepatitis B/D virus (HB/DV) cirrhosis is understudied.
- HB/DV cirrhosis is a significant indication for liver transplantation worldwide.
- Understanding HCC's role is crucial for optimizing post-transplant management.
Purpose of the Study:
- To investigate long-term survival in liver transplant recipients with HB/DV cirrhosis, comparing those with and without HCC.
- To analyze the influence of HCC on post-transplant outcomes and complications.
- To identify factors affecting survival in this specific patient cohort.
Main Methods:
- Retrospective analysis of 231 adult liver transplants (1990-2007).
- Focus on 27 patients with HB/DV cirrhosis (excluding early post-operative deaths).
- Median follow-up of 1515 days, comparing outcomes between HCC and non-HCC groups.
Main Results:
- Mean survival was 3760 days; HCC patients survived longer (4036 days) than non-HCC patients (3011 days).
- HCC recurrence was not observed in any of the six HCC cases.
- Microbial infection incidence was lower in HCC patients (33.3%) versus non-HCC patients (61.9%).
Conclusions:
- Liver transplantation for HB/DV cirrhosis with HCC demonstrates excellent long-term survival exceeding 11 years.
- The superior survival in HCC patients warrants further investigation.
- Reduced microbial infections in HCC recipients may contribute to better outcomes.
Background/Aims:
The effect of hepatocellular cancer (HCC) in patients transplanted for hepatitis B and D virus (HB/DV) cirrhosis is not well studied. Our aim was to study the long-term survival outcomes of patients who underwent liver transplantation for HB/DV cirrhosis with and without HCC.
Methodology:
A total of 231 primary, adult, single- organ liver transplants were performed from 1990 to 2007. HB/DV was the cause of cirrhosis in 36 patients. Nine patients died during the first 3 postoperative months from surgical complications. The study group comprised the remaining 27 patients. The median follow-up was 1515 days.
Results:
The mean patient survival was 3760 days (95% CI: 3013-4507). Six patients were diagnosed with HCC. The mean patient survival was 3011 days (95% CI: 2344-3679) and 4036 days (95% CI: 3002-5070) for recipients without and with HCC, respectively. For the same groups, the incidence of microbial infections was 61.9% and 33.3%, respectively (p=0.219). HCC has not recurred in any of the six patients.
Conclusions:
The mean long-term survival after liver transplantation for HB/DV and HCC surpassed 11 years. The superior survival of HCC patients is difficult to explain. The increased number (almost double) of microbial infections in the non- HCC population might be held accountable.
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