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Regression of Liver Fibrosis in Patients on Hepatitis B Therapy Is Associated With Decreased Liver-Related Events

医学 内科学 胃肠病学 肝纤维化 纤维化 慢性肝炎 乙型肝炎 丙型肝炎 病毒学 病毒
作者
Yameng Sun,Wei Chen,Shuyan Chen,Xiaoning Wu,Xinxin Zhang,Lingyi Zhang,Hong Zhao,Mingyi Xu,Yongpeng Chen,Hongxin Piao,Ping Li,Lei Li,Wei Jiang,Xiaodong Li,Huichun Xing,Xudong Liu,Yuxi Zhang,Bingqiong Wang,Jialing Zhou,Tongtong Meng
出处
期刊:Clinical Gastroenterology and Hepatology [Elsevier BV]
卷期号:22 (3): 591-601.e3 被引量:12
标识
DOI:10.1016/j.cgh.2023.11.017
摘要

Background & Aims

Liver fibrosis in patients with chronic hepatitis B can regress with successful antiviral therapy. However, the long-term clinical benefits of fibrosis regression have not been fully elucidated. This study investigated the association between biopsy-proven fibrosis regression by predominantly progressive, indeterminate, and predominantly regressive (P-I-R) score and liver-related events (LREs) in chronic hepatitis B patients.

Methods

Patients with on-treatment liver biopsy and significant fibrosis/cirrhosis (Ishak stage ≥3) were included in this analysis. Fibrosis regression was evaluated according to the P-I-R score of the Beijing Classification. LREs were defined as decompensations, hepatocellular carcinoma, liver transplantation, or death. The Cox proportional hazards model was used to determine associations of fibrosis regression with LREs.

Results

A total of 733 patients with Ishak stages 3/4 (n = 456; 62.2%) and cirrhosis (Ishak stages 5/6; n = 277; 37.8%) by on-treatment liver biopsy were enrolled. According to the P-I-R score, fibrosis regression, indeterminate, and progression were observed in 314 (42.8%), 230 (31.4%), and 189 (25.8%) patients, respectively. The 7-year cumulative incidence of LREs was 4.1%, 8.7%, and 18.1% in regression, indeterminate, and progression, respectively (log-rank, P < .001). Compared with patients with fibrosis progression, those with fibrosis regression had a lower risk of LREs (adjusted hazard ratio, 0.40; 95% CI, 0.16–0.99; P = .047), followed by the indeterminate group (adjusted hazard ratio, 0.86; 95% CI, 0.40–1.85; P = .691). Notably, this favorable association also was observed in patients with cirrhosis or low platelet counts (<150 × 109/L).

Conclusions

Antiviral therapy–induced liver fibrosis regression assessed by P-I-R score is associated with reduced LREs. This shows the utility of histologic fibrosis regression assessed by on-treatment P-I-R score as a surrogate endpoint for clinical events in patients with hepatitis B virus–related fibrosis or early cirrhosis.
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