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PAGE-B incorporating moderate HBV DNA levels predicts risk of HCC among patients entering into HBeAg-positive chronic hepatitis B.
Chun, Ho Soo; Papatheodoridis, George V; Lee, Minjong; Lee, Hye Ah; Kim, Yeong Hwa; Kim, Seo Hyun; Oh, Yun-Seo; Park, Su Jin; Kim, Jihye; Lee, Han Ah; Kim, Hwi Young; Kim, Tae Hun; Yoon, Eileen L; Jun, Dae Won; Ahn, Sang Hoon; Sypsa, Vana; Yurdaydin, Cihan; Lampertico, Pietro; Calleja, Jose Luis; Janssen, Harry LA; Dalekos, George N; Goulis, John; Berg, Thomas; Buti, Maria; Kim, Seung Up; Kim, Yoon Jun.
  • Chun HS; Department of Internal Medicine, Ewha Womans University College of Medicine, Seoul, Korea; Department of Internal Medicine, Ewha Womans University Medical Center, Seoul, Korea.
  • Papatheodoridis GV; Department of Gastroenterology, Medical School of National and Kapodistrian University of Athens, General Hospital of Athens "Laiko", Athens, Greece.
  • Lee M; Department of Internal Medicine, Ewha Womans University College of Medicine, Seoul, Korea; Department of Internal Medicine, Ewha Womans University Medical Center, Seoul, Korea. Electronic address: minjonglee2@naver.com.
  • Lee HA; Clinical Trial Center, Ewha Womans University Seoul Hospital, Seoul, Korea.
  • Kim YH; Department of Internal Medicine, Ewha Womans University College of Medicine, Seoul, Korea.
  • Kim SH; Department of Internal Medicine, Ewha Womans University College of Medicine, Seoul, Korea.
  • Oh YS; Department of Internal Medicine, Ewha Womans University College of Medicine, Seoul, Korea.
  • Park SJ; Department of Internal Medicine, Ewha Womans University College of Medicine, Seoul, Korea.
  • Kim J; Department of Internal Medicine and Liver Research Institute, Seoul National University College of Medicine, Seoul, Korea.
  • Lee HA; Department of Internal Medicine, Ewha Womans University College of Medicine, Seoul, Korea; Department of Internal Medicine, Ewha Womans University Medical Center, Seoul, Korea.
  • Kim HY; Department of Internal Medicine, Ewha Womans University College of Medicine, Seoul, Korea; Department of Internal Medicine, Ewha Womans University Medical Center, Seoul, Korea.
  • Kim TH; Department of Internal Medicine, Ewha Womans University College of Medicine, Seoul, Korea; Department of Internal Medicine, Ewha Womans University Medical Center, Seoul, Korea.
  • Yoon EL; Department of Internal Medicine, Hanyang University College of Medicine, Seoul, Korea.
  • Jun DW; Department of Internal Medicine, Hanyang University College of Medicine, Seoul, Korea.
  • Ahn SH; Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea; Yonsei Liver Center, Severance Hospital, Seoul, Korea.
  • Sypsa V; Department of Gastroenterology, Medical School of National and Kapodistrian University of Athens, General Hospital of Athens "Laiko", Athens, Greece.
  • Yurdaydin C; Department of Gastroenterology & Hepatology, Koc University Medical School, Istanbul, Turkey.
  • Lampertico P; Division of Gastroenterology and Hepatology, CRC "A. M. and A. Migliavacca" Center for Liver Disease, Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
  • Calleja JL; Hospital U Puerta de Hierro, IDIPHIM CIBERehd, Madrid, Spain.
  • Janssen H; Department of Gastroenterology & Hepatology, Erasmus MC University Medical Center, Rotterdam, Netherlands.
  • Dalekos GN; Department of Medicine and Research Laboratory of Internal Medicine, National Expertise Center of Greece in Autoimmune Liver Diseases, General University Hospital of Larissa, Larissa, Greece.
  • Goulis J; 4th Department of Internal Medicine, Αristotle University of Thessaloniki Medical School, Thessaloniki, Greece.
  • Berg T; Division of Hepatology, Department of Medicine II, Leipzig University Medical Center, Leipzig, Germany.
  • Buti M; Hospital General Universitario Vall Hebron and Ciberehd, Barcelona, Spain.
  • Kim SU; Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea; Yonsei Liver Center, Severance Hospital, Seoul, Korea. Electronic address: ksukorea@yuhs.ac.
  • Kim YJ; Department of Internal Medicine and Liver Research Institute, Seoul National University College of Medicine, Seoul, Korea. Electronic address: yoonjun@snu.ac.kr.
J Hepatol ; 80(1): 20-30, 2024 01.
Article en En | MEDLINE | ID: mdl-37734683
ABSTRACT
BACKGROUND &

AIMS:

Recent studies reported that moderate HBV DNA levels are significantly associated with hepatocellular carcinoma (HCC) risk in hepatitis B e antigen (HBeAg)-positive, non-cirrhotic patients with chronic hepatitis B (CHB). We aimed to develop and validate a new risk score to predict HCC development using baseline moderate HBV DNA levels in patients entering into HBeAg-positive CHB from chronic infection.

METHODS:

This multicenter cohort study recruited 3,585 HBeAg-positive, non-cirrhotic patients who started antiviral treatment with entecavir or tenofovir disoproxil fumarate at phase change into CHB from chronic infection in 23 tertiary university-affiliated hospitals of South Korea (2012-2020). A new HCC risk score (PAGED-B) was developed (training cohort, n = 2,367) based on multivariable Cox models. Internal validation using bootstrap sampling and external validation (validation cohort, n = 1,218) were performed.

RESULTS:

Sixty (1.7%) patients developed HCC (median follow-up, 5.4 years). In the training cohort, age, gender, platelets, diabetes and moderate HBV DNA levels (5.00-7.99 log10 IU/ml) were independently associated with HCC development; the PAGED-B score (based on these five predictors) showed a time-dependent AUROC of 0.81 for the prediction of HCC development at 5 years. In the validation cohort, the AUROC of PAGED-B was 0.85, significantly higher than for other risk scores (PAGE-B, mPAGE-B, CAMD, and REAL-B). When stratified by the PAGED-B score, the HCC risk was significantly higher in high-risk patients than in low-risk patients (sub-distribution hazard ratio = 8.43 in the training and 11.59 in the validation cohorts, all p <0.001).

CONCLUSIONS:

The newly established PAGED-B score may enable risk stratification for HCC at the time of transition into HBeAg-positive CHB. IMPACT AND IMPLICATIONS In this study, we developed and validated a new risk score to predict hepatocellular carcinoma (HCC) development in patients entering into hepatitis B e antigen (HBeAg)-positive chronic hepatitis B (CHB) from chronic infection. The newly established PAGED-B score, which included baseline moderate HBV DNA levels (5-8 log10 IU/ml), improved on the predictive performance of prior risk scores. Based on a patient's age, gender, diabetic status, platelet count, and moderate DNA levels (5-8 log10 IU/ml) at the phase change into CHB from chronic infection, the PAGED-B score represents a reliable and easily available risk score to predict HCC development during the first 5 years of antiviral treatment in HBeAg-positive patients entering into CHB. With a scoring range from 0 to 12 points, the PAGED-B score significantly differentiated the 5-year HCC risk low <7 points and high ≥7 points.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Carcinoma Hepatocelular / Hepatitis B Crónica / Neoplasias Hepáticas Tipo de estudio: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Child, preschool / Humans Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Carcinoma Hepatocelular / Hepatitis B Crónica / Neoplasias Hepáticas Tipo de estudio: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Child, preschool / Humans Idioma: En Año: 2024 Tipo del documento: Article