Prediction of liver stiffness hepatocellular carcinoma in chronic hepatitis C patients on interferon‐based anti‐viral therapy. Issue 1 (January 2014)

• Record Type: Journal Article
• Authors: Narita, Yutaka; Genda, Takuya; Tsuzura, Hironori; Sato, Shunsuke; Kanemitsu, Yoshio; Ishikawa, Sachiko; Kikuchi, Tetsu; Hirano, Katsuharu; Iijima, Katsuyori; Wada, Ryo; Ichida, Takafumi
• Is Part Of: Journal of gastroenterology and hepatology. Volume 29:Issue 1(2014:Jan.)
• Page Start: 137
• Page End: 143
• Publication Date: 2014-01
• Subjects: Gastroenterology -- Periodicals; Digestive organs -- Diseases -- Periodicals; Liver -- Diseases -- Periodicals; Gastroenterology -- Periodicals; Liver Diseases -- Periodicals; 616.33
• DOI: 10.1111/jgh.12401
• Languages: English
• ISSNs: 0815-9319

Abstract

<abstract abstract-type="main"> <title>Abstract</title> <sec id="jgh12401-sec-0001" sec-type="section"> <title>Background and Aim</title> <p>The purpose of this study was to evaluate the usefulness of liver stiffness measurement (LSM) for assessing the risk of hepatocellular carcinoma (HCC) in chronic hepatitis C (CHC) patients receiving interferon (IFN) therapy.</p> </sec> <sec id="jgh12401-sec-0002" sec-type="section"> <title>Methods</title> <p>One hundred fifty‐one CHC patients who underwent LSM and received IFN therapy were included in the estimation cohort, and 56 were included in the validation study. The cumulative HCC incidences were evaluated using Kaplan–Meier plot analysis and the log‐rank test. Multivariate Cox proportional hazard analyses were used to estimate the hazard ratios (HRs) of variables for HCC.</p> </sec> <sec id="jgh12401-sec-0003" sec-type="section"> <title>Results</title> <p>In the estimation cohort, 9 of 151 patients developed HCC during the median follow‐up time of 722 days. Multivariate analysis identified three independent risk factors for HCC: LSM (≥ 14.0 kPa, HR 5.58, <italic>P</italic> = 0.020), platelet count (< 14.1 × 10<sup>4</sup>/μL, HR 5.59, <italic>P</italic> = 0.034), and non‐sustained virological response (HR 8.28, <italic>P</italic> = 0.049). The cumulative incidence of HCC development at 3 years was 59.6%, 8.2%, and 0.0% in patients with all three risk factors, one to two risk factors, and none of these risk factors, respectively. The incidence of HCC was significantly different between these groups (<italic>P</italic> < 0.001). In the validation cohort, HCC incidence was also significantly different with respect to these risk factors (<italic>P</italic> = 0.037).</p> </sec> <sec id="jgh12401-sec-0004" sec-type="section"> <title>Conclusion</title> <p>LSM, platelet count, and IFN‐therapeutic effect could be used to successfully stratify the risk of HCC in patients receiving IFN therapy and demonstrate the usefulness of LSM before IFN therapy for the management of CHC patients.</p> </sec> </abstract>