# Discussion on the duration of response following HBsAg clearance in patients with chronic hepatitis B treated with PegIFNα-2b

**Authors:** Tao Wang, Fei Tang, Fenghui Li, Jing Chen, Fei Yan, Qin Du, Weili Yin, Jing Liang, Lei Liu, Fang Wang, Baiguo Xu, Qing Ye, Huiling Xiang

PMC · DOI: 10.3389/fimmu.2025.1518048 · Frontiers in Immunology · 2025-04-08

## TL;DR

This study examines how long patients with chronic hepatitis B maintain HBsAg clearance after treatment with PegIFNα-2b and finds that most relapses occur within 48 weeks.

## Contribution

The study identifies key follow-up time points for sustained HBsAg clearance after interferon-based treatment in chronic hepatitis B.

## Key findings

- HBsAg reversion occurred in 15.03% of patients, predominantly within 48 weeks post-treatment.
- HBsAg sustained response at 48 weeks is critical, with 95.45% of patients maintaining clearance at this point.
- No serious adverse events were observed during the follow-up period.

## Abstract

Functional cure strategies based on interferon therapy for chronic hepatitis B (CHB) are gaining increasing attention among clinicians. However, studies investigating the duration of response after achieving HBsAg clearance with interferon treatment are limited. This study aims to explore the patterns of sustained response following HBsAg clearance in patients treated with pegylated interferon alpha-2b (PegIFNα-2b) through long-term follow-up, providing guidance for clinical practice.

We collected data from CHB patients who achieved HBsAg clearance and were treated with either PegIFNα-2b monotherapy or in combination with nucleos(t)ide analogs (NAs) at Tianjin Third Central Hospital from January 2018 to May 2024. Regular follow-up assessments were conducted to observe the dynamic changes in HBsAg, HBV DNA, and liver function during the follow-up period. We recorded the time to HBsAg reversion (defined as HBsAg ≥ 0.05 IU/mL), analyzed the patterns of HBsAg reversion, and investigated the optimal time points for evaluating sustained HBsAg clearance.

A total of 173 patients with CHB or compensated hepatitis B cirrhosis were included. The mean age was 41.5 ± 9.0 years, with 16.19% of patients having compensated cirrhosis. The median follow-up duration was 89.3 weeks (range: 18.6 to 289.1 weeks). HBsAg reversion occurred in 26 patients, yielding a reversion rate of 15.03% (26/173). Among these 26 patients, 50% (13/26) experienced reversion within 24 weeks, and 80.77% within 48 weeks; thereafter, the number of reversions gradually decreased. At 48 weeks post-treatment cessation, the HBsAg sustained response rate was 95.45%, stabilizing at 100% after 120 weeks. Among patients with regular follow-ups, virtually none experienced reversion beyond 72 weeks. At the time of HBsAg reversion, all 26 patients exhibited normal alanine aminotransferase (ALT), aspartate aminotransferase (AST), and total bilirubin (TBIL) levels, with a median HBsAg level of 0.70 IU/mL (range: 0.05 to 8.13 IU/mL), and only one patient showing low-level positive HBV DNA (117 IU/mL). No adverse events, including liver failure, decompensation, or hepatocellular carcinoma, occurred during the follow-up period.

Patients with chronic hepatitis B treated with PegIFNα-2b demonstrated favorable long-term persistence of HBsAg clearance. However, there remains a risk of HBsAg reversion after treatment cessation, predominantly within the first 48 weeks. HBsAg sustained response (HSR) at 48 weeks post-treatment is a critical follow-up time point for CHB patients post-HBsAg clearance, with HSR at 72 weeks potentially representing an ideal follow-up timeframe, while HSR at 120 weeks may serve as a marker for extended follow-up.

## Linked entities

- **Diseases:** chronic hepatitis B (MONDO:0005344), liver failure (MONDO:0100192), hepatocellular carcinoma (MONDO:0007256)

## Full-text entities

- **Genes:** GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}
- **Diseases:** CHB (MESH:D019694), liver failure (MESH:D017093), cirrhosis (MESH:D005355), hepatocellular carcinoma (MESH:D006528), hepatitis B cirrhosis (MESH:D006509)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12011802/full.md

## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC12011802/full.md

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Source: https://tomesphere.com/paper/PMC12011802