Abstract

BackgroundThe heterogeneous nature of human hepatocellular carcinoma (HCC) impedes both treatment strategies and prognostic predictions. Several markers have been proposed for the diagnosis of HCC. Cytoskeleton-associated proteins have been known as cellular integrators in neoplasm formation. Hepatic progenitor cells are thought to express alpha-fetoprotein (AFP) and hematopoietic as well as biliary markers such as cytokeratin 19 (CK 19) and cytokeratin 7. The aim of this study was to verify the role of serum CK 19 alone or in combination with AFP as a diagnostic marker of HCC and to assess the changes in its levels after ablation of HCV-related HCC to evaluate its role as a predictor marker for recurrence of HCC after ablation. The study was conducted on 102 HCV-related cirrhotic patients categorized into three different groups according to the clinical, laboratory, and radiological evaluation: group I—62 patients with early or intermediate HCC who underwent locoregional intervention, group II—20 patients with advanced HCC not fit for any intervention apart from best supportive treatment, and group III—20 cirrhotic patients with no evidence of HCC as proved by two imaging techniques.ResultsThe mean serum levels of CK 19 were 6.5 ± 5.7, 10.5 ± 12.5, and 6.8 ± 2.8 ng/ml in groups I, II, and III, respectively, with no significant difference between groups. Sensitivity, specificity, positive, and negative predictive values of combined AFP and human CK 19 at cutoff levels of 25.5 ng/ml and 6.25 ng/ml were 93.9%, 45%, 87.5%, and 64.3%, respectively. In group I patients, CK 19 levels were comparable in patients with ablated focal lesion and those who did not at baseline; then, it was significantly higher in ablated patients than in patients with residual tumor 1 and 6 months after the intervention.ConclusionsCombination of both AFP and CK 19 levels could increase the diagnostic accuracy of suspected HCCs. CK 19 levels are good predictors of ablation/recurrence in patients who underwent interventional procedures minimizing the need for follow-up imaging modalities.

Highlights

  • The heterogeneous nature of human hepatocellular carcinoma (HCC) impedes both treatment strategies and prognostic predictions

  • Clinical and abdominal ultrasonography data showed that jaundice, pallor, ascites, and lower limb edema were present in 25%, 30%, 50%, and 30%, respectively, of the HCC group not fit for intervention but not present in other groups

  • There was no significant difference between all groups regarding the mean value of alanine transaminase (ALT), aspartate transaminase (AST), and platelet count

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Summary

Introduction

The heterogeneous nature of human hepatocellular carcinoma (HCC) impedes both treatment strategies and prognostic predictions. The heterogeneous nature of human hepatocellular carcinoma (HCC), which represents a serious health problem being the fifth most common malignancy worldwide, and a common cause of death in patients with chronic liver disease [1], impedes both treatment strategies and prognostic predictions [2]. It has been proposed that a subset of HCC originates from hepatic progenitor cells (HPCs) [5]. This subset of HCC results enriched for genes expressed earlier in fetal hepatoblasts, including some progenitor cell markers. HPC activation was demonstrated to be the most relevant liver carcinogenic condition in chronic viral hepatitis, alcoholic, and non-alcoholic fatty liver disease [8]

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