Abstract
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.
Original language | English |
---|---|
Pages (from-to) | 874-885.e4 |
Journal | Clinical Gastroenterology and Hepatology |
Volume | 20 |
Issue number | 4 |
DOIs | |
Publication status | Published - Apr 2022 |
All Science Journal Classification (ASJC) codes
- Hepatology
- Gastroenterology
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Progression Rates by Age, Sex, Treatment, and Disease Activity by AASLD and EASL Criteria : Data for Precision Medicine. / Park, Jiyoon; Le, An K.; Tseng, Tai Chung et al.
In: Clinical Gastroenterology and Hepatology, Vol. 20, No. 4, 04.2022, p. 874-885.e4.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Progression Rates by Age, Sex, Treatment, and Disease Activity by AASLD and EASL Criteria
T2 - Data for Precision Medicine
AU - Park, Jiyoon
AU - Le, An K.
AU - Tseng, Tai Chung
AU - Yeh, Ming Lun
AU - Jun, Dae Won
AU - Trinh, Huy
AU - Wong, Grace L.H.
AU - Chen, Chien Hung
AU - Peng, Cheng Yuan
AU - Kim, Sung Eun
AU - Oh, Hyunwoo
AU - Kwak, Min Sun
AU - Cheung, Ka Shing
AU - Toyoda, Hidenori
AU - Hsu, Yao Chun
AU - Jeong, Jae Yoon
AU - Yoon, Eileen L.
AU - Ungtrakul, Teerapat
AU - Zhang, Jian
AU - Xie, Qing
AU - Ahn, Sang Bong
AU - Enomoto, Masaru
AU - Shim, Jae Jun
AU - Cunningham, Chris
AU - Jeong, Soung Won
AU - Cho, Yong Kyun
AU - Ogawa, Eiichi
AU - Huang, Rui
AU - Lee, Dong Hyun
AU - Takahashi, Hirokazu
AU - Tsai, Pei Chien
AU - Huang, Chung Feng
AU - Dai, Chia Yen
AU - Tseng, Cheng Hao
AU - Yasuda, Satoshi
AU - Kozuka, Ritsuzo
AU - Li, Jiayi
AU - Wong, Christopher
AU - Wong, Clifford C.
AU - Zhao, Changqing
AU - Hoang, Joseph
AU - Eguchi, Yuichiro
AU - Wu, Chao
AU - Tanaka, Yasuhito
AU - Gane, Ed
AU - Tanwandee, Tawesak
AU - Cheung, Ramsey
AU - Yuen, Man Fung
AU - Lee, Hyo Suk
AU - Yu, Ming Lung
AU - Kao, Jia Horng
AU - Yang, Hwai I.
AU - Nguyen, Mindie H.
N1 - Funding Information: Funding This study was supported partially by Kaohsiung Medical University (KMU) Research Center Grants (KMU investigators): Center for Liquid Biopsy ( KMU TC108B06 ), Cohort Research Center ( KMU-TC108B07 and KMU-DK109002 ), and Center for Liquid Biopsy and Cohort Research ( KMU-TC109B05 ). Funding Information: Conflicts of interest These authors disclose the following: Hwai-I Yang has received research funding from Gilead Sciences, Inc. Ming-Lung Yu has received research support from Abbott, BMS, Gilead, and Merck; served as a consultant or on the advisory board for AbbVie, Abbott, Ascletis, BMS, Gilead, and Merck; and served as a speaker for AbbVie, Abbott, BMS, Gilead, Merck, and IPSEN. Hideonori Toyoda has served as a speaker for AbbVie and Gilead. Dong-Hyun Lee has received research funding from Gilead Sciences and Korea Pharma. Sung-Eun Kim has received research funding from Daewoong, served as consultant for Chonggwendang, and served as a speaker for Daewoong. Huy Trinh has received research funding from, served as a consultant and speaker for, and owns stock in Gilead. Cheng-Yuan Peng has served as a consultant or the advisory board for AbbVie, Bristol-Myers Squibb, Gilead, Merck Sharp & Dohme, and Roche. Tai-Chung Tseng has served on speaker’s bureau for AbbVie, Bristol-Myers Squibb, and Gilead Sciences; and received research funding from and served as a consulant for Gilead Sciences. Ramsey Cheung has received a research grant from Gilead. Mindie H. Nguyen has received research support from Gilead, Pfizer, Enanta, B.K. Kee Foundation, National Cancer Institute, Glycotest, and Vir; and served as a consultant or on the advisory board for Novartis, Bayer, Eisai, Gilead, Janssen, Laboratory of Advanced Medicine, Spring Bank, Exact Sciences, Helio, and Intercept. Teerapat Ungtrakul has received research funding from AstraZeneca and Roche. Tawesak Tanwandee has received Research grants from Roche, Janssen, and Merck. Chia-Yen Dai has served as a consultant for AbbVie and as a speaker for AbbVie, Merck, BMS, and Gilead. Man-Fung Yuen has served as a consultant for AbbVie, Arbutus Biopharma, Assembly Biosciences, Bristol Myers Squibb, Dicerna Pharmaceuticals, GlaxoSmithKline, Gilead Sciences, Janssen Pharmaceutical, Merck Sharp and Dohme, Clear B Therapeutics, and Springbank Pharmaceutical. Chao Wu has received research funding from Gilead Sciences. Jia-Horng Kao has received research funding from Gilead Sciences and BMS; served as a consultant for Gilead Sciences, Roche, AbbVie, and Arbutus; and served as a speaker for BMS, Gilead Sciences, MSD, AbbVie, and Fujirebio. Yasuhito Tanaka has received research funding from Janssen Pharmaceutical KK, Gilead Sciences, and GlaxoSmithKline PLC; and served as a speaker for Gilead Sciences and FUJIREBIO Inc. Grace Wong has received research funding from and served as a consultant for Gilead Sciences; and served as a speaker for Abbott, AbbVie, Bristol-Myers Squibb, Echosense, Furui, Gilead Sciences, Janssen Pharmaceutical, and Roche. Yao-Chun Hsu has received research funding from and served as a consultant for Gilead Sciences; and served as a speaker for AbbVie, Bristol-Myers Squibb, and Gilead Sciences. Eiichi Ogawa has served as a speaker for Gilead Sciences. The remaining authors disclose no conflicts. Funding Information: Funding This study was supported partially by Kaohsiung Medical University (KMU) Research Center Grants (KMU investigators): Center for Liquid Biopsy (KMU TC108B06), Cohort Research Center (KMU-TC108B07 and KMU-DK109002), and Center for Liquid Biopsy and Cohort Research (KMU-TC109B05). Conflicts of interest These authors disclose the following: Hwai-I Yang has received research funding from Gilead Sciences, Inc. Ming-Lung Yu has received research support from Abbott, BMS, Gilead, and Merck; served as a consultant or on the advisory board for AbbVie, Abbott, Ascletis, BMS, Gilead, and Merck; and served as a speaker for AbbVie, Abbott, BMS, Gilead, Merck, and IPSEN. Hideonori Toyoda has served as a speaker for AbbVie and Gilead. Dong-Hyun Lee has received research funding from Gilead Sciences and Korea Pharma. Sung-Eun Kim has received research funding from Daewoong, served as consultant for Chonggwendang, and served as a speaker for Daewoong. Huy Trinh has received research funding from, served as a consultant and speaker for, and owns stock in Gilead. Cheng-Yuan Peng has served as a consultant or the advisory board for AbbVie, Bristol-Myers Squibb, Gilead, Merck Sharp & Dohme, and Roche. Tai-Chung Tseng has served on speaker's bureau for AbbVie, Bristol-Myers Squibb, and Gilead Sciences; and received research funding from and served as a consulant for Gilead Sciences. Ramsey Cheung has received a research grant from Gilead. Mindie H. Nguyen has received research support from Gilead, Pfizer, Enanta, B.K. Kee Foundation, National Cancer Institute, Glycotest, and Vir; and served as a consultant or on the advisory board for Novartis, Bayer, Eisai, Gilead, Janssen, Laboratory of Advanced Medicine, Spring Bank, Exact Sciences, Helio, and Intercept. Teerapat Ungtrakul has received research funding from AstraZeneca and Roche. Tawesak Tanwandee has received Research grants from Roche, Janssen, and Merck. Chia-Yen Dai has served as a consultant for AbbVie and as a speaker for AbbVie, Merck, BMS, and Gilead. Man-Fung Yuen has served as a consultant for AbbVie, Arbutus Biopharma, Assembly Biosciences, Bristol Myers Squibb, Dicerna Pharmaceuticals, GlaxoSmithKline, Gilead Sciences, Janssen Pharmaceutical, Merck Sharp and Dohme, Clear B Therapeutics, and Springbank Pharmaceutical. Chao Wu has received research funding from Gilead Sciences. Jia-Horng Kao has received research funding from Gilead Sciences and BMS; served as a consultant for Gilead Sciences, Roche, AbbVie, and Arbutus; and served as a speaker for BMS, Gilead Sciences, MSD, AbbVie, and Fujirebio. Yasuhito Tanaka has received research funding from Janssen Pharmaceutical KK, Gilead Sciences, and GlaxoSmithKline PLC; and served as a speaker for Gilead Sciences and FUJIREBIO Inc. Grace Wong has received research funding from and served as a consultant for Gilead Sciences; and served as a speaker for Abbott, AbbVie, Bristol-Myers Squibb, Echosense, Furui, Gilead Sciences, Janssen Pharmaceutical, and Roche. Yao-Chun Hsu has received research funding from and served as a consultant for Gilead Sciences; and served as a speaker for AbbVie, Bristol-Myers Squibb, and Gilead Sciences. Eiichi Ogawa has served as a speaker for Gilead Sciences. The remaining authors disclose no conflicts. Publisher Copyright: © 2022 AGA Institute
PY - 2022/4
Y1 - 2022/4
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85110522121&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85110522121&partnerID=8YFLogxK
U2 - 10.1016/j.cgh.2021.05.062
DO - 10.1016/j.cgh.2021.05.062
M3 - Article
C2 - 34089852
AN - SCOPUS:85110522121
VL - 20
SP - 874-885.e4
JO - Clinical Gastroenterology and Hepatology
JF - Clinical Gastroenterology and Hepatology
SN - 1542-3565
IS - 4
ER -