Literature DB >> 31975419

Validation of hepatocellular carcinoma risk scores in Japanese chronic hepatitis B cohort receiving nucleot(s)ide analog.

Sakura Kirino1, Nobuharu Tamaki1, Shun Kaneko1, Masayuki Kurosaki1, Kento Inada1, Koji Yamashita1, Leona Osawa1, Yuka Hayakawa1, Shuhei Sekiguchi1, Keiya Watakabe1, Mao Okada1, Wan Wang1, Takao Shimizu1, Mayu Higuchi1, Kenta Takaura1, Chiaki Maeyashiki1, Yutaka Yasui1, Hiroyuki Nakanishi1, Kaoru Tsuchiya1, Jun Itakura1, Yuka Takahashi1, Namiki Izumi1.   

Abstract

BACKGROUND AND AIM: The prediction of hepatocellular carcinoma (HCC) development during nucleotide/nucleoside analog (NA) therapy is clinically important in patients with chronic hepatitis B. Although several useful models for HCC prediction have been previously reported, their usefulness in the Japanese population is unclear. Therefore, this study examines the applicability of these models in Japanese patients.
METHODS: Four hundred forty-three patients with no history of HCC who were treated with entecavir, tenofovir alafenamide, or tenofovir disoproxil fumarate were enrolled. PAGE-B, modified-PAGE-B, and REACH-B scores were calculated, and subsequent HCC development was investigated.
RESULTS: The mean follow-up duration was 5.1 years, and a total of 33 patients (7.4%) developed HCC during the follow-up period. Multivariate analysis revealed that old age (hazard ratio [HR] 1.05, 95% confidence interval [CI] 1.01-1.09, P = 0.011), male gender (HR 2.62, 95% CI 1.06-6.49, P = 0.037), and low platelet count (HR 0.83, 95% CI 0.77-0.91, P < 0.001) were independent predictors of HCC development. These factors are the same as the factors identified in the PAGE-B model. Time-dependent area under the receiver operating characteristic (AUROC) curve revealed that the AUROCs for 3 and 7 years of PAGE-B (AUROC: 0.786 and 0.744 at 3 and 7 years, respectively) were continuously higher than those of REACH-B (0.658 and 0.543) and modified PAGE-B AUROC (0.772 and 0.731).
CONCLUSIONS: PAGE-B, which can easily identify high-risk cases, can be useful for predicting HCC development in Japanese patients treated with NA therapy.
© 2020 Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd.

Entities:  

Keywords:  chronic hepatitis B; hepatocellular carcinoma; nucleotide/nucleoside analog

Mesh:

Substances:

Year:  2020        PMID: 31975419     DOI: 10.1111/jgh.14990

Source DB:  PubMed          Journal:  J Gastroenterol Hepatol        ISSN: 0815-9319            Impact factor:   4.029


  4 in total

1.  Assessing efficacy of hepatocellular carcinoma prediction scores to prioritise hepatitis B surveillance in the COVID-19 era.

Authors:  Ricky Sinharay; Andrew J Grant; Lucy Rivett; Rebecca Blackwell; George Mells; William Gelson
Journal:  GastroHep       Date:  2021-02-24

2.  Validation of Hepatocellular Carcinoma Risk Prediction Models in Patients with Hepatitis B-Related Cirrhosis.

Authors:  Ran Cheng; Xiaoyuan Xu
Journal:  J Hepatocell Carcinoma       Date:  2022-09-12

3.  Evaluation of the Hepatocellular Carcinoma Predictive Scores PAGE-B and mPAGE-B among Brazilian Patients with Chronic Hepatitis B Virus Infection.

Authors:  Ana Caroline Ferreira da Silva; Marlone Cunha-Silva; Tiago Sevá-Pereira; Daniel F Mazo
Journal:  Viruses       Date:  2022-09-05       Impact factor: 5.818

Review 4.  Screening for Hepatocellular Carcinoma in Patients with Hepatitis B.

Authors:  Yashasavi Sachar; Mayur Brahmania; Renumathy Dhanasekaran; Stephen E Congly
Journal:  Viruses       Date:  2021-07-08       Impact factor: 5.048

  4 in total

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