Liver stiffness measurement for risk assessment of hepatocellular carcinoma. Issue 5 (20th October 2014)

• Record Type: Journal Article
• Authors: Tatsumi, Akihisa; Maekawa, Shinya; Sato, Mitsuaki; Komatsu, Nobutoshi; Miura, Mika; Amemiya, Fumitake; Nakayama, Yasuhiro; Inoue, Taisuke; Sakamoto, Minoru; Enomoto, Nobuyuki
• Is Part Of: Hepatology research. Volume 45:Issue 5(2015:May)
• Page Start: 523
• Page End: 532
• Publication Date: 2014-10-20
• Subjects: FibroScan -- hepatocellular carcinoma -- liver fibrosis; Liver -- Diseases -- Periodicals; Liver Diseases -- Periodicals; Foie -- Maladies -- Périodiques; 616.362
• DOI: 10.1111/hepr.12377
• Languages: English
• ISSNs: 1386-6346

Abstract

Abstract : Aim: Liver fibrosis is a risk factor for hepatocellular carcinoma (HCC), but at what fibrotic stage the risk for HCC is increased has been poorly investigated quantitatively. This study aimed to determine the appropriate cut‐off value of liver stiffness for HCC concurrence by FibroScan, and its clinical significance in hepatitis B virus (HBV), hepatitis C virus (HCV) and non‐B, non‐C (NBNC) liver disease. Methods: Subjects comprised 1002 cases (246 with HCC and 756 without HCC) with chronic liver disease (HBV, 104; HCV, 722; and NBNC, 176). Results: Liver stiffness was significantly greater in all groups with HCC, and the determined cut‐off value for HCC concurrence was more than 12.0 kPa in those with HCV, more than 8.5 kPa in those with HBV and more than 12.0 kPa in those with NBNC. Liver stiffness of more than 12.0 kPa was an independent risk factor for new HCC development in HCV. For HCV, risk factors for HCC concurrence were old age, male sex, low albumin, low platelets and liver stiffness, while for HBV they were old age, low platelets and liver stiffness, and for NBNC they were old age, elevated α‐fetoprotein and liver stiffness. Conclusion: Liver stiffness cut‐off values and their association with HCC concurrence were different depending on the etiology. In HCV, liver stiffness of more than 12.0 kPa was an independent risk factor for new HCC development. Collectively, determining the fibrotic cut‐off values for HCC concurrence would be important in evaluating HCC risks.