# Navigating the Latest Hepatitis B Virus Reactivation Guidelines

**Authors:** Zeyad Elharabi, Jowana Saba, Hakan Akin

PMC · DOI: 10.3390/diseases13110355 · Diseases · 2025-11-01

## TL;DR

This paper compares recent guidelines on managing hepatitis B virus reactivation during immunosuppressive therapies to help clinicians make informed decisions.

## Contribution

The paper provides a comparative analysis of the latest HBV reactivation guidelines from AGA, EASL, and APASL to clarify conflicting recommendations.

## Key findings

- All three guidelines categorize HBV reactivation risk into high, moderate, and low levels.
- Prophylaxis is most cost-effective for high-risk patients and less so for low-risk individuals.
- Entecavir, TDF, and TAF are effective and economically viable for high-risk patients.

## Abstract

Hepatitis B virus (HBV) infection is a global health concern with an estimated 254 million people with chronic HBV infection. The utilization of immunosuppressive therapies (ISTs) is increasing and expanding continuously with new agents being implemented across multiple medical disciplines. The occurrence of HBV reactivation (HBVr) during or after IST varies from 15% to 50% in HBsAg-positive individuals and can be higher than 75% after stem cell transplantation. HBVr is gaining increasing significance in contemporary clinical practice. The American Gastroenterological Association (AGA) in 2025, the European Association for the Study of the Liver (EASL) in 2025, and the Asian Pacific Association for the Study of the Liver (APASL) in 2021, published their most recent clinical guidelines as major societies in the area, which enables us to better predict and manage HBVr. This narrative review focuses on comparing these three current guidelines, highlighting key similarities and differences to provide valuable guidance for practitioners navigating the complex, sometimes conflicting recommendations, thereby aiding clinicians in their decision-making. The risk of HBVr during IST has been stratified into three categories in all three guidelines: high (>10%), moderate (1–10%), and low (<1%). The effectiveness of prophylaxis scales with baseline risk for HBV reactivation. Prophylaxis is clearly cost-effective for high-risk patients, potentially beneficial for those at moderate risk, and generally may not be justified for low-risk individuals. Entecavir (ETV), tenofovir disoproxil fumarate (TDF), and tenofovir alafenamide (TAF) are all highly effective in preventing HBV reactivation during immunosuppression and all are considered to be economically viable options for HBVr high risk patients. When selecting among these agents, safety considerations—particularly renal and bone toxicity—and insurance coverage remain the primary factors directing clinical decision-making.

## Linked entities

- **Chemicals:** Entecavir (PubChem CID 135398508), tenofovir disoproxil fumarate (PubChem CID 5486830), tenofovir alafenamide (PubChem CID 461543)

## Full-text entities

- **Diseases:** HBV infection (MESH:D006509), renal and bone toxicity (MESH:D007674)
- **Chemicals:** TDF (MESH:D000068698), ETV (MESH:C413685), TAF (MESH:C442442)
- **Species:** Homo sapiens (human, species) [taxon 9606], Hepatitis B virus (no rank) [taxon 10407]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12651630/full.md

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12651630/full.md

## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12651630/full.md

---
Source: https://tomesphere.com/paper/PMC12651630