Progression Rates by Age, Sex, Treatment, and Disease Activity by AASLD and EASL Criteria: Data for Precision Medicine.


Journal

Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association
ISSN: 1542-7714
Titre abrégé: Clin Gastroenterol Hepatol
Pays: United States
ID NLM: 101160775

Informations de publication

Date de publication:
04 2022
Historique:
received: 30 01 2021
revised: 05 05 2021
accepted: 25 05 2021
pubmed: 6 6 2021
medline: 17 3 2022
entrez: 5 6 2021
Statut: ppublish

Résumé

Antiviral treatment criteria are based on disease progression risk, and hepatocellular carcinoma (HCC) surveillance recommendations for patients with chronic hepatitis B (CHB) without cirrhosis is based on an annual incidence threshold of 0.2%. However, accurate and precise disease progression estimate data are limited. Thus, we aimed to determine rates of cirrhosis and HCC development stratified by age, sex, treatment status, and disease activity based on the 2018 American Association for the Study of Liver Diseases and 2017 European Association for the Study of the Liver guidelines. We analyzed 18,338 patients (8914 treated, 9424 untreated) from 6 centers from the United States and 27 centers from Asia-Pacific countries. The Kaplan-Meier method was used to estimate annual progression rates to cirrhosis or HCC in person-years. The cohort was 63% male, with a mean age of 46.19 years, with baseline cirrhosis of 14.3% and median follow up of 9.60 years. By American Association for the Study of Liver Diseases criteria, depending on age, sex, and disease activity, annual incidence rates ranged from 0.07% to 3.94% for cirrhosis, from 0.04% to 2.19% for HCC in patients without cirrhosis, and from 0.40% to 8.83% for HCC in patients with cirrhosis. Several subgroups of patients without cirrhosis including males younger than 40 years of age and females younger than 50 years of age had annual HCC risk near or exceeding 0.2%. Similar results were found using European Association for the Study of the Liver criteria. There is great variability in CHB disease progression rates even among "lower-risk" populations. Future CHB modeling studies, public health planning, and HCC surveillance recommendation should be based on more precise disease progression rates based on sex, age, and disease activity, plus treatment status.

Sections du résumé

BACKGROUND & AIMS
Antiviral treatment criteria are based on disease progression risk, and hepatocellular carcinoma (HCC) surveillance recommendations for patients with chronic hepatitis B (CHB) without cirrhosis is based on an annual incidence threshold of 0.2%. However, accurate and precise disease progression estimate data are limited. Thus, we aimed to determine rates of cirrhosis and HCC development stratified by age, sex, treatment status, and disease activity based on the 2018 American Association for the Study of Liver Diseases and 2017 European Association for the Study of the Liver guidelines.
METHODS
We analyzed 18,338 patients (8914 treated, 9424 untreated) from 6 centers from the United States and 27 centers from Asia-Pacific countries. The Kaplan-Meier method was used to estimate annual progression rates to cirrhosis or HCC in person-years.
RESULTS
The cohort was 63% male, with a mean age of 46.19 years, with baseline cirrhosis of 14.3% and median follow up of 9.60 years. By American Association for the Study of Liver Diseases criteria, depending on age, sex, and disease activity, annual incidence rates ranged from 0.07% to 3.94% for cirrhosis, from 0.04% to 2.19% for HCC in patients without cirrhosis, and from 0.40% to 8.83% for HCC in patients with cirrhosis. Several subgroups of patients without cirrhosis including males younger than 40 years of age and females younger than 50 years of age had annual HCC risk near or exceeding 0.2%. Similar results were found using European Association for the Study of the Liver criteria.
CONCLUSION
There is great variability in CHB disease progression rates even among "lower-risk" populations. Future CHB modeling studies, public health planning, and HCC surveillance recommendation should be based on more precise disease progression rates based on sex, age, and disease activity, plus treatment status.

Identifiants

pubmed: 34089852
pii: S1542-3565(21)00601-7
doi: 10.1016/j.cgh.2021.05.062
pii:
doi:

Substances chimiques

Antiviral Agents 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

874-885.e4

Informations de copyright

Copyright © 2022 AGA Institute. Published by Elsevier Inc. All rights reserved.

Auteurs

Jiyoon Park (J)

Department of Medicine, Santa Clara Valley Medical Center, Santa Clara, California; Division of Gastroenterology and Hepatology, Stanford University Medical Center, California.

An K Le (AK)

Division of Gastroenterology and Hepatology, Stanford University Medical Center, California.

Tai-Chung Tseng (TC)

Division of Gastroenterology and Hepatology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.

Ming-Lun Yeh (ML)

Hepatobiliary Division, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan; Hepatitis Research Center, College of Medicine and Center for Liquid Biopsy and Cohort Research, Kaohsiung Medical University, Kaohsiung, Taiwan.

Dae Won Jun (DW)

Department of Gastroenterology, Hanyang University College of Medicine, Seoul, Republic of Korea.

Huy Trinh (H)

San Jose Gastroenterology, San Jose, California.

Grace L H Wong (GLH)

Department of Medicine and Therapeutics, the Chinese University of Hong Kong, Hong Kong SAR, China.

Chien-Hung Chen (CH)

Department of Internal Medicine, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan.

Cheng-Yuan Peng (CY)

Department of Gastroenterology, China Medical University Hospital, Taichung, Taiwan.

Sung Eun Kim (SE)

Department of Internal Medicine, Hallym University Sacred Heart Hospital, Hallym University College of Medicine, Anyang, Republic of Korea.

Hyunwoo Oh (H)

Department of Internal Medicine and Liver Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea.

Min-Sun Kwak (MS)

Department of Internal Medicine and Liver Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea.

Ka Shing Cheung (KS)

Department of Medicine, the University of Hong Kong, Hong Kong SAR, China.

Hidenori Toyoda (H)

Department of Gastroenterology, Ogaki Municipal Hospital, Ogaki, Japan.

Yao-Chun Hsu (YC)

Division of Gastroenterology and Hepatology, Department of Internal Medicine, E-Da Hospital/I-Shou University, Kaohsiung, Taiwan.

Jae Yoon Jeong (JY)

Department of Internal Medicine, National Medical Center, Seoul, Republic of Korea.

Eileen L Yoon (EL)

Department of Gastroenterology, Hanyang University College of Medicine, Seoul, Republic of Korea.

Teerapat Ungtrakul (T)

Faculty of Medicine and Public Health, HRH Princess Chulabhorn College of Medical Science, Chulabhorn Royal Academy, Bangkok, Thailand.

Jian Zhang (J)

Chinese Hospital, San Francisco, California.

Qing Xie (Q)

Department of Infectious Diseases, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Sang Bong Ahn (SB)

Department of Internal Medicine, Nowon Eulji Medical Center, Eulji University College of Medicine, Seoul, Republic of Korea.

Masaru Enomoto (M)

Department of Hepatology, Graduate School of Medicine, Osaka City University, Osaka, Japan.

Jae-Jun Shim (JJ)

Department of Internal Medicine, Kyung Hee University Hospital, Kyung Hee University School of Medicine, Seoul, Republic of Korea.

Chris Cunningham (C)

Research Centre for Maori Health and Development, Massey University, Wellington, New Zealand.

Soung Won Jeong (SW)

Department of Internal Medicine, Soonchunhyang University Hospital, Soonchunhyang University College of Medicine, Seoul, Republic of Korea.

Yong Kyun Cho (YK)

Department of Internal Medicine, Sungkyunkwan University, Seoul, Republic of Korea.

Eiichi Ogawa (E)

Department of General Internal Medicine, Kyushu University Hospital, Fukuoka, Japan.

Rui Huang (R)

Department of Infectious Diseases, Nanjing Drum Tower Hospital, Nanjing University Medical School, Nanjing, Jiangsu, China.

Dong-Hyun Lee (DH)

Department of Gastroenterology, Good Gang-An Hospital, Busan, Republic of Korea.

Hirokazu Takahashi (H)

Department of Internal Medicine, Saga University Hospital, Saga, Japan.

Pei-Chien Tsai (PC)

Hepatobiliary Division, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan; Hepatitis Research Center, College of Medicine and Center for Liquid Biopsy and Cohort Research, Kaohsiung Medical University, Kaohsiung, Taiwan.

Chung-Feng Huang (CF)

Hepatobiliary Division, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan; Hepatitis Research Center, College of Medicine and Center for Liquid Biopsy and Cohort Research, Kaohsiung Medical University, Kaohsiung, Taiwan.

Chia-Yen Dai (CY)

Hepatobiliary Division, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan; Hepatitis Research Center, College of Medicine and Center for Liquid Biopsy and Cohort Research, Kaohsiung Medical University, Kaohsiung, Taiwan.

Cheng-Hao Tseng (CH)

Division of Gastroenterology and Hepatology, Department of Internal Medicine, E-Da Hospital/I-Shou University, Kaohsiung, Taiwan.

Satoshi Yasuda (S)

Department of Gastroenterology, Ogaki Municipal Hospital, Ogaki, Japan.

Ritsuzo Kozuka (R)

Department of Hepatology, Graduate School of Medicine, Osaka City University, Osaka, Japan.

Jiayi Li (J)

Palo Alto Medical Foundation, Mountain View Division, Mountain View, California.

Christopher Wong (C)

Wong Clinics, San Francisco, California.

Clifford C Wong (CC)

Wong Clinics, San Francisco, California; Department of Cirrhosis, Institute of Liver Disease, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, China.

Changqing Zhao (C)

Department of Cirrhosis, Institute of Liver Disease, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, China.

Joseph Hoang (J)

Division of Gastroenterology and Hepatology, Stanford University Medical Center, California.

Yuichiro Eguchi (Y)

Department of Internal Medicine, Saga University Hospital, Saga, Japan.

Chao Wu (C)

Department of Infectious Diseases, Nanjing Drum Tower Hospital, Nanjing University Medical School, Nanjing, Jiangsu, China.

Yasuhito Tanaka (Y)

Department of Gastroenterology and Hepatology, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan.

Ed Gane (E)

New Zealand Liver Transplant Unit, Auckland City Hospital, Auckland, New Zealand.

Tawesak Tanwandee (T)

Department of Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.

Ramsey Cheung (R)

Division of Gastroenterology and Hepatology, Stanford University Medical Center, California.

Man-Fung Yuen (MF)

Department of Medicine, the University of Hong Kong, Hong Kong SAR, China.

Hyo-Suk Lee (HS)

Department of Internal Medicine and Liver Research Institute, Seoul National University College of Medicine, Seoul, Republic of Korea.

Ming-Lung Yu (ML)

Hepatobiliary Division, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan; Hepatitis Research Center, College of Medicine and Center for Liquid Biopsy and Cohort Research, Kaohsiung Medical University, Kaohsiung, Taiwan.

Jia-Horng Kao (JH)

Division of Gastroenterology and Hepatology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.

Hwai-I Yang (HI)

Genomics Research Center, Academia Sinica, Taipei, Taiwan.

Mindie H Nguyen (MH)

Division of Gastroenterology and Hepatology, Stanford University Medical Center, California; Department of Epidemiology and Population Health, Stanford University, Stanford, California. Electronic address: mindiehn@stanford.edu.

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