The Use of Flow Cytometric DNA Ploidy Analysis of Liver Biopsies in Liver Cirrhosis and Hepatocellular Carcinoma

Hepatocellular carcinoma (HCC) is the fifth most common human cancer world-wide but the third most common cause of mortality and evidence has been accumulating in various countries that HCC is increasing (Andrisani et al., 2011; Parkin et al., 2000; Perkin, 2004). Major etiologic agents in HCC pathogenesis are chronic infection with hepatitis B virus or hepatitis C virus (Bruix et al., 2004; Poynard et al., 2003). Advanced liver fibrosis and HCC have been indicated to develop in about 30% of patients with chronic hepatitis B or C. Other causal factors of lower incidence include alcohol abuse, metabolic disorders, and environmental agents, e.g., exposure to aflatoxin B1 (Llovet et al., 2003). HCC typically develops in the cirrhotic liver in about 80% of cases and develops only in the non-cirrhotic liver in less than 20% of cases (Alkofer, 2011). When diagnosed at early stage, HCC remains eligible for potential curative options such as surgical resection, orthotopic liver transplantation or percutaneous destructions. The absence of advanced fibrosis or cirrhosis makes resection feasible more often. However, most of HCCs have widespread dissemination within the liver at diagnosis (intermediary stage) or show extrahepatic dissemination within the portal tract, lymph nodes or distant visceral metastasis (Llovet et al., 2008). As recommended by Llovet and Bruix (2008), new and efficacious therapies are needed, along with new diagnostic biomarkers for early detection of liver cancer. Liver biopsy, since its initial introduction by Klatskin as a clinical tool 100 years ago, soon became the major diagnostic test for liver disease (Afdhal & Manning, 2008). Many studies have been performed to evaluate the use of readily available laboratory biomarkers to predict significant fibrosis or cirrhosis or HCC to substantially reduce the number of performed biopsies (Attallah et al., 2007; 2009a, Ismail, 2010; Pinzani, 2010). However, biomarkers alone are not sufficient to allow definitive decisions to be made for a given patient (Halfon et al., 2008). Reproducibility studies of noninvasive markers should be performed according to professional recommendations and respecting standards previously