# Dalpiciclib induced hepatitis B virus reactivation leading to liver failure: a rare case report and review of the literature

**Authors:** Yuchen Peng, Yalin Xi, Aili Ding, Fanli Kong

PMC · DOI: 10.3389/fmed.2026.1769544 · Frontiers in Medicine · 2026-03-18

## TL;DR

A breast cancer patient with a history of hepatitis B experienced severe liver failure after treatment with dalpiciclib, highlighting the need for HBV screening and monitoring.

## Contribution

This is the first reported case of HBV reactivation-induced liver failure in an HBV carrier treated with dalpiciclib.

## Key findings

- HBV DNA increased significantly in a patient receiving dalpiciclib, confirming HBV reactivation.
- Failure to perform clinical risk stratification for HBV reactivation led to severe liver complications.
- Antiviral therapy with entecavir suppressed HBV replication and improved liver function.

## Abstract

Dalpiciclib is a cyclin-dependent kinase 4/6 (CDK4/6) inhibitor that plays a key role in hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER-2)-negative breast cancer. However, there have been no reports of acute liver failure in Hepatitis B virus (HBV) carriers caused by HBV reactivation induced by dalpiciclib. We present a 50-year-old female with recurrent breast cancer and a history of asymptomatic HBV carriage. After dalpiciclib initiation, she developed progressive liver impairment, with hepatitis B virus DNA (HBV DNA) escalating from 1.02 × 103 to 2.13 × 106 IU/ml and HBeAg seroconversion from negative to positive, confirming HBV reactivation. Notably, the patient received initial dalpiciclib-based therapy at an external hospital, where antiviral prophylaxis was not initiated despite the availability of baseline HBV serological and viral load data, due to the failure to conduct clinical risk stratification for HBV reactivation based on these results—a critical gap in pre-therapy assessment for HBV-related risk stratification. Entecavir antiviral therapy led to suppressed viral replication and improved liver function during follow-up. This case emphasizes the need for HBV screening and close monitoring of viral markers/liver function in asymptomatic HBV carriers receiving dalpiciclib, as early antiviral intervention prevents severe liver complications. It also highlights the importance of clinical pharmacist-led medication follow-up management for outpatients receiving targeted anticancer therapy to avoid oversight of comorbidities and associated prophylactic treatment.

## Linked entities

- **Chemicals:** dalpiciclib (PubChem CID 86279927), entecavir (PubChem CID 135398508)
- **Diseases:** breast cancer (MONDO:0004989), liver failure (MONDO:0100192)

## Full-text entities

- **Genes:** ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, NR4A1 (nuclear receptor subfamily 4 group A member 1) [NCBI Gene 3164] {aka GFRP1, HMR, N10, NAK-1, NGFIB, NP10}
- **Diseases:** liver complications (MESH:D008107), breast cancer (MESH:D001943), liver failure (MESH:D017093), acute liver failure (MESH:D017114)
- **Chemicals:** Entecavir (MESH:C413685), Dalpiciclib (MESH:C000720752)
- **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

33 references — full list in the complete paper: https://tomesphere.com/paper/PMC13038858/full.md

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Source: https://tomesphere.com/paper/PMC13038858