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Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2026

Peginterferon α-2b Enhances Hepatitis B Surface Antigen Loss in Nucleos(t)ide Analogue-Suppressed Low Hepatitis B Surface Antigen Chronic Hepatitis B Patients: Everest Study in China.

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Xie Chan, Lin Bingliang, Mo Zhishuo, Fu Lei, Chen Xinyue, Yang Jiahong, Li Guojun, Li Jiabin, Zeng Yilan, Gong Guozhong, Zhang Wenhua, Tang Hong, Guo Ying, Wei Jia, Jiang Jiaji, Wu Xiaoping, Lv Riying, Lin Minghua, Yu Zujiang, Shang Jia, Guan Yujuan, Li Junyi, Zhang Lingyi, Guo Qian, Ye Qing, Mao Qing, Li Yi, Xue Xiulan, Geng Jiawei, Mao Xiaorong, Lian Jianqi, Lu Xiaobo, Hu Guoxin, Bai Honglian, Cai Dachuan, Liu Youde, Zhang Liting, Mao Qianguo, Li Jia, Chen Hui, Chang Jiabao, Li Qiang, Xie Dongying, Deng Hong, Xu Qihuan, Peng Liang, Yang Xizhong, Zhuang Hui, Gao Zhiliang

Аннотация

BACKGROUND & AIMS: Patients with chronic hepatitis B (CHB) with low hepatitis B surface antigen (HBsAg) levels and suppressed hepatitis B virus (HBV) DNA on nucleos(t)ide analogues (NAs) may achieve functional cure with peginterferon α (PegIFNα)-based therapy. This real-world multicenter study (Everest Project) in China aimed to evaluate the effectiveness and safety of PegIFNα-2b and determine the predictors of HBsAg loss.

METHODS: Patients with NA-suppressed CHB who were hepatitis B e antigen (HBeAg)-negative, had HBsAg ≤1500 IU/mL, and undetectable HBV DNA, were administered PegIFNα-2b for 48 weeks, either as a switch-to or add-on therapy. The primary endpoint was HBsAg loss at week 48.

RESULTS: Among 15,896 patients in the full analysis set (FAS) and 12,260 in the per-protocol set (PPS), HBsAg loss rate at week 48 was 26.4% and 33.8%, respectively, after propensity score weighting, with no significant difference between switch-to and add-on groups. Key predictors of HBsAg loss included lower baseline HBsAg and HBsAg decline >63.3% at week 12 and >95.3% at week 24. Among patients who underwent >24 weeks of post-treatment follow-up, HBsAg loss rates at week 24 were 28.7% and 35.6% in the FAS and PPS, respectively. Of those who received consolidation therapy, 85.9% maintained HBsAg loss at week 72. Adverse event-related discontinuation occurred in 5.6% and 4.4% of those in the FAS and PPS, respectively.

CONCLUSIONS: PegIFNα-2b enhances HBsAg loss in patients with NA-suppressed, HBeAg-negative CHB with low HBsAg levels. Baseline and on-treatment predictors support the achievement of a functional cure.

CLINICALTRIALS: gov, Number: NCT04035837.

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

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