# Risk of HBV reactivation in HBV/HCV-co-infected HCV-treated patients: A single-center study

**Authors:** Young Joo Park, Ki Youn Yi, Hyun Young Woo, Jeong Heo, Geun Am Song, Riccardo Nevola, Riccardo Nevola, Riccardo Nevola, Riccardo Nevola

PMC · DOI: 10.1371/journal.pone.0324019 · PLOS One · 2025-05-30

## TL;DR

This study finds that HBV reactivation is more common and occurs sooner in patients treated with DAA after failed IFN-based therapy for HCV, highlighting the need for HBV screening and monitoring.

## Contribution

The study identifies DAA treatment after IFN-based therapy failure as a significant risk factor for HBV reactivation, offering new clinical insights for managing co-infected patients.

## Key findings

- HBV reactivation occurred in 31.9% of patients, most frequently after DAA treatment following IFN-based therapy failure.
- HBV reactivation happened significantly earlier in DAA-treated patients compared to IFN-based therapy patients.
- SVR rates for HCV were high across all treatment groups but did not differ significantly.

## Abstract

Hepatitis B virus (HBV) reactivation in patients with HBV/hepatitis C virus (HCV) co-infection due to direct-acting antiviral agent (DAA) therapy is a growing concern. This study focused on 47 patients with chronic hepatitis C (CHC) and positivity for HBV surface antigen (HBsAg) who were treated with interferon (IFN)-based therapy, DAA, or DAA after IFN-based therapy failure and followed for a median of 53 months. Here, we aimed to determine HBV reactivation rates and associated factors, the incidence of HBV and liver-related events, and the rate of sustained virologic response (SVR) for HCV. Fifteen (15/47, 31.9%) patients experienced HBV reactivation during or after HCV treatment. This reactivation occurred significantly more frequently in patients who received DAA treatment after IFN-based treatment failure than in those who received IFN-based treatment (IFN-based vs. DAA vs. DAA treatment after IFN-based treatment failure 11.8% vs. 35.3% vs. 53.8%, respectively; p = 0.046). The interval from HCV treatment initiation to HBV reactivation was shortest in the DAA group (4.2 months), followed by the DAA after IFN-based treatment failure group (6.4 months) and the IFN-based treatment group (44.5 months) (p < 0.001). One case of HBV-related hepatitis spontaneously resolved after 4 weeks. The rate of SVR for the entire cohort was 87.2%, with no significant difference in this regard among the IFN-based treated, DAA-treated, and DAA-treated after IFN-based treatment failure arms at 82.4%, 88.2%, and 92.3%, respectively. HBV reactivation in HBsAg-positive CHC patients is more common and occurs earlier in those who receive DAA treatment after IFN-based treatment failure than in those with IFN-based treatment. Therefore, all patients with CHC should be tested for HBV exposure prior to DAA treatment. In addition, HBsAg positive patients, especially those among whom have previously experienced IFN-based treatment failure, should be closely monitored for HBV reactivation during DAA therapy.

## Linked entities

- **Diseases:** chronic hepatitis C (MONDO:0005231)

## Full-text entities

- **Diseases:** hepatitis (MESH:D056486), HBV/HCV-co-infected (MESH:D006509), CHC (MESH:D019698), HBV/hepatitis C virus (HCV) co-infection (MESH:D006525)
- **Chemicals:** DAA (-)
- **Species:** Homo sapiens (human, species) [taxon 9606], Hepatitis B virus (no rank) [taxon 10407]

## Full text

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## Figures

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## References

44 references — full list in the complete paper: https://tomesphere.com/paper/PMC12124557/full.md

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Source: https://tomesphere.com/paper/PMC12124557