Abstract

Simple SummaryChronic kidney disease is a major public health issue globally and the risk of hepatocellular cancer appears greater in patients with chronic kidney disease compared with the general population. Non-alcoholic fatty liver disease is a liver disorder ranging from simple fatty infiltration to advanced fibrosis plus inflammation; it plays a role in developing liver-related and extra liver-related diseases including HCC and CKD, respectively. Approximately 90% of HCCs are associated with a known underlying etiology; viral hepatitis is a well-known cause of HCC, particularly in CKD population. Antiviral therapy of HBV and HCV is important in the management of HCC in CKD patients. Therapy of HCC in CKD patients includes liver transplant (in selected patients), local approach (surgery or interventional radiology), and tyrosine kinase inhibitors (advanced HCC).Chronic kidney disease is a major public health issue globally and the risk of cancer (including HCC) is greater in patients on long-term dialysis and kidney transplant compared with the general population. According to an international study on 831,804 patients on long-term dialysis, the standardized incidence ratio for liver cancer was 1.2 (95% CI, 1.0–1.4) and 1.5 (95% CI, 1.3–1.7) in European and USA cohorts, respectively. It appears that important predictors of HCC in dialysis population are hepatotropic viruses (HBV and HCV) and cirrhosis. 1-, 3-, and 5-year survival rates are lower in HCC patients on long-term dialysis than those with HCC and intact kidneys. NAFLD is a metabolic disease with increasing prevalence worldwide and recent evidence shows that it is an important cause of liver-related and extra liver-related diseases (including HCC and CKD, respectively). Some longitudinal studies have shown that patients with chronic hepatitis B are aging and the frequency of comorbidities (such as HCC and CKD) is increasing over time in these patients; it has been suggested to connect these patients to an appropriate care earlier. Antiviral therapy of HBV and HCV plays a pivotal role in the management of HCC in CKD and some combinations of DAAs (elbasvir/grazoprevir, glecaprevir/pibrentasvir, sofosbuvir-based regimens) are now available for HCV positive patients and advanced chronic kidney disease. The interventional management of HCC includes liver resection. Some ablative techniques have been suggested for HCC in CKD patients who are not appropriate candidates to surgery. Transcatheter arterial chemoembolization has been proposed for HCC in patients who are not candidates to liver surgery due to comorbidities. The gold standard for early-stage HCC in patients with chronic liver disease and/or cirrhosis is still liver transplant.

Highlights

  • Solid evidence suggests an increased risk of cancer after kidney transplant; on the contrary, the risk of cancer in patients receiving dialysis is more controversial

  • Based on the C-SURFER trial data, daily fixed-dose elbasvir/grazoprevir is recommended for the treatment of HCV genotype 1 and 4 in patients with chronic kidney disease stage 4/5

  • Patients with chronic kidney disease such as patients on maintenance dialysis and kidney transplant recipients are at risk for development of cancer including hepatocellular carcinoma

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Summary

Introduction

Solid evidence suggests an increased risk of cancer after kidney transplant; on the contrary, the risk of cancer in patients receiving dialysis is more controversial. A collaborative study which assembled a cohort of 831,804 patients who underwent regular dialysis (1980–1994) for end stage kidney disease in Europe, USA, Australia, and New Zealand [4] has been published. The SIR for liver cancer was 1.5 (0.5–4.6) in the cohort from Australia and New Zealand Another piece of evidence on this topic has been offered by a survey on 92,348 chronic dialysis patients retrieved from the National Health Insurance Research Database (NHIRD). The cancer risk associated with dialysis has been addressed in a population-based cohort study of 28,855 patients (Australia and New Zealand Dialysis and Transplant Registry, ANZDATA) with end-stage kidney disease; 24,926 patients (14,144 men) underwent dialysis with a mean follow-up of 2.7 ± 2.5 years. The conclusion of the investigators was that, after matching for hepatitis and liver cirrhosis, there is no greater incidence of HCC in patients with end-stage renal disease

Risk Factors for HCC in Dialysis Population
Survival of HCC
HCC and CKD in Chronic HB Patients
Findings
13. Conclusions
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