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Prediction of liver-related events in patients with compensated HBV-induced cirrhosis receiving antiviral therapy.
Wu, Xiaoning; Zhou, Jialing; Sun, Yameng; Ding, Huiguo; Chen, Guofeng; Xie, Wen; Piao, Hongxin; Xu, Xiaoyuan; Jiang, Wei; Ma, Hui; Ma, Anlin; Chen, Yongpeng; Xu, Mingyi; Cheng, Jilin; Xu, Youqing; Meng, Tongtong; Wang, Bingqiong; Chen, Shuyan; Shi, Yiwen; Kong, Yuanyuan; Ou, Xiaojuan; You, Hong; Jia, Jidong.
Afiliación
  • Wu X; Liver Research Center, Beijing Friendship Hospital, Capital Medical University, 95 Yong-an Road, Xi-Cheng District, Beijing, 100050, China.
  • Zhou J; Beijing Key Laboratory of Translational Medicine in Liver Cirrhosis, Beijing, China.
  • Sun Y; National Clinical Research Center of Digestive Disease, Beijing, China.
  • Ding H; Liver Research Center, Beijing Friendship Hospital, Capital Medical University, 95 Yong-an Road, Xi-Cheng District, Beijing, 100050, China.
  • Chen G; Beijing Key Laboratory of Translational Medicine in Liver Cirrhosis, Beijing, China.
  • Xie W; National Clinical Research Center of Digestive Disease, Beijing, China.
  • Piao H; Liver Research Center, Beijing Friendship Hospital, Capital Medical University, 95 Yong-an Road, Xi-Cheng District, Beijing, 100050, China.
  • Xu X; Beijing Key Laboratory of Translational Medicine in Liver Cirrhosis, Beijing, China.
  • Jiang W; National Clinical Research Center of Digestive Disease, Beijing, China.
  • Ma H; Department of Gastroenterology, Beijing Youan Hospital, Capital Medical University, Beijing, China.
  • Ma A; Division of Liver Fibrosis, The Fifth Medical Center, General Hospital of the People's Liberation Army, Beijing, China.
  • Chen Y; Liver Research Center, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
  • Xu M; Office of Clinical Trials, Affiliated Hospital of Yanbian University, Yanji, Jilin, China.
  • Cheng J; Division of Infectious Diseases, Peking University First Hospital, Beijing, China.
  • Xu Y; Department of Gastroenterology, Zhongshan Hospital, Fudan University, Shanghai, China.
  • Meng T; Liver Research Center, Peking University People's Hospital, Beijing, China.
  • Wang B; Division of Infectious Diseases, China-Japan Friendship Hospital, Beijing, China.
  • Chen S; Department of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China.
  • Shi Y; Department of Gastroenterology and Hepatology, Shanghai General Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
  • Kong Y; Department of Gastroenterology, Shanghai Public Health Clinical Center, Shanghai, China.
  • Ou X; Department of Gastroenterology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
  • You H; Liver Research Center, Beijing Friendship Hospital, Capital Medical University, 95 Yong-an Road, Xi-Cheng District, Beijing, 100050, China.
  • Jia J; Beijing Key Laboratory of Translational Medicine in Liver Cirrhosis, Beijing, China.
Hepatol Int ; 15(1): 82-92, 2021 Feb.
Article en En | MEDLINE | ID: mdl-33460002
ABSTRACT
BACKGROUND AND

AIMS:

Many models have been developed to predict liver-related events (LRE) in chronic hepatitis B, few focused on compensated HBV-induced cirrhosis. We aimed to describe the incidence of LRE and to determine independent risk predictors of LRE in compensated HBV-induced cirrhosis patients receiving antiviral therapy using routinely available parameters.

METHODS:

Prospective cohorts of treatment-naïve adults with compensated HBV-induced cirrhosis were enrolled. Patients were treated with entecavir (ETV) or ETV + thymosin-alpha1 (Thy-α1) or lamivudine (LAM) + adefovir (ADV). Data were collected at baseline and every 6 months. LRE was defined as development of decompensation, HCC or death.

RESULTS:

Totally 937 patients were included, 608 patients treated with ETV, 252 with ETV + Thy-α1, and 77 with LAM + ADV. After a median follow-up of 4.5 years, 88 patients developed LRE including 48 with HCC. The cumulative incidence of LRE at year 1, 3, and 5 was 2.1%, 7.0%, and 12.7%, respectively, and was similar for three treatment groups. All models using variables at month 6 or 12 had better fit than models using baseline values. The best model for prediction of LRE used PLT, GGT, and AFP at month 6 [AUC 0.762 (0.678-0.814)], for hepatic decompensation-PLT, LSM and GGT at month 12 (AUC 0.834 (0.675-0.919)), and for HCC-AFP and GGT at month 6 [AUC 0.763 (0.691-0.828)]. All models had negative predictive values of 94.0-98.8%.

CONCLUSION:

Models using on-treatment variables are more accurate than models using baseline variables in predicting LRE in patient with compensated HBV-induced cirrhosis receiving antiviral therapy. ClincialTrials.gov number NCT01943617, NCT01720238, NCT03366571, NCT02849132.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Carcinoma Hepatocelular / Hepatitis B Crónica / Cirrosis Hepática Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies Límite: Adult / Humans Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Carcinoma Hepatocelular / Hepatitis B Crónica / Cirrosis Hepática Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies Límite: Adult / Humans Idioma: En Año: 2021 Tipo del documento: Article