# Combining immunosuppressive therapy with low dosage eltrombopag in Chinese patients with severe aplastic anemia: mild aggravation of hepatic injury

**Authors:** Xiaoyu Chen, Qingling Yu, ChengTao Qin, Yawen Zhang, Jingnan Sun, Jinsong Jia, Baodong Ye, Yuemin Gong, Guangsheng He, Lei Fan

PMC · DOI: 10.1007/s00277-025-06210-7 · Annals of Hematology · 2025-02-05

## TL;DR

This study examines mild liver injury in Chinese patients with severe aplastic anemia treated with eltrombopag and immunosuppressive therapy.

## Contribution

The study evaluates the risk of hepatic injury when combining eltrombopag with standard immunosuppressive therapy in a Chinese patient population.

## Key findings

- The incidence of acute drug-induced liver injury was slightly higher but not significantly different in the IST + EPAG group.
- Serum ferritin levels were associated with severe liver injury events.
- There was a slight increase in severe hepatic injury events with EPAG, but it was not statistically significant.

## Abstract

Eltrombopag (EPAG) is an oral thrombopoietin receptor agonist analog with the potential risk to induce liver injury. This prospective registry study evaluated the prevalence and severity of hepatic injury in Chinese patients with severe aplastic anemia undergoing low-dose EPAG treatment (75 mg/day) in the context of standard immunosuppressive therapy (IST). The incidence of acute drug-induced liver injury was slightly higher in the IST + EPAG group than in the IST group at the 1st and 2nd month, but no statistically significant difference was observed: 10% vs 5% (p = 0.400), 9% vs 8% (p = 1.000). At the 1st month, the incidences of alanine aminotransferase, aspartate aminotransferase, and total bilirubin increased of grade 3 or higher in the IST + EPAG and the IST groups, were 5% vs 3% (p = 0.228), 2% vs 1% (p = 1.000), 2% vs 1% (p = 1.000), respectively. The logistic analysis indicated that serum ferritin level was associated with severe liver injury events. There was a slight increase in the incidence of severe hepatic injury events in the patients with SAA treated by EPAG, but it was insignificant.

## Linked entities

- **Chemicals:** Eltrombopag (PubChem CID 135449332), alanine aminotransferase (PubChem CID 251717)
- **Diseases:** drug-induced liver injury (MONDO:0005359)

## Full-text entities

- **Genes:** SAA [NCBI Gene 6287], MPL (MPL proto-oncogene, thrombopoietin receptor) [NCBI Gene 4352] {aka C-MPL, CD110, MPLV, THCYT2, THPOR, TPOR}
- **Diseases:** acute drug-induced liver injury (MESH:D056486), aplastic anemia (MESH:D000741), liver injury (MESH:D017093)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11868208/full.md

## References

2 references — full list in the complete paper: https://tomesphere.com/paper/PMC11868208/full.md

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Source: https://tomesphere.com/paper/PMC11868208