# Effect of pretransplant spleen volume on the prognosis of acute myeloid leukemia treated with allogeneic hematopoietic stem cell transplantation

**Authors:** Weiwei Liu, Bingjie Liu, Lihou Pang, Lixia Zhou, Fuxu Wang, Xuejun Zhang, Ying Wang

PMC · DOI: 10.3389/fimmu.2025.1675328 · Frontiers in Immunology · 2026-02-17

## TL;DR

This study found that larger spleen volume before stem cell transplant is linked to worse survival in acute myeloid leukemia patients.

## Contribution

The study identifies pre-transplant spleen volume as an independent prognostic factor for survival in AML patients undergoing allogeneic stem cell transplantation.

## Key findings

- Patients with large spleen volume had lower overall survival and higher non-relapse mortality.
- Spleen volume was confirmed as a significant risk factor for survival in multivariable analysis.
- No significant differences were found in relapse rates or graft-versus-host disease incidence.

## Abstract

This study aimed to evaluate the influence of pre-transplant spleen volume on the prognosis of patients with acute myeloid leukemia (AML) undergoing allogeneic hematopoietic stem cell transplantation (allo-HSCT).

We evaluated 58 patients diagnosed with AML and who have undergone first allogeneic stem cell transplant at the Department of Hematology, Second Hospital of Hebei Medical University from 2017 to 2022. All patients were consecutively evaluated. Patients with AML evolving from myeloproliferative neoplasms (MPN) or secondary AML were excluded. Only de novo AML patients were included. The median follow-up time was 24 months, and the patients were categorized into non-enlarged spleen volume (NLSV) and large spleen volume (LSV) groups based on the spleen volume ranges of 120 normal individuals. A retrospective analysis was performed to evaluate the impact of spleen volume on post-allo-HSCT outcomes, including the incidence of infection, graft-versus-host disease (GVHD), relapse, overall survival (OS), and non-relapse mortality (NRM). Log-rank test was employed to compare survival curves, and a multivariable Cox regression model was utilized to assess spleen volume as a prognostic factor for long-term survival.

According to the survival curve, the LSV group exhibited lower OS compared to the NLSV group (P=0.034), along with higher cumulative NRM (P=0.049) and lower relapse-free survival (P=0.023). No significant differences were observed in disease relapse, granulocyte engraftment, CMV infection, or GVHD incidence. The multivariable regression model confirmed spleen volume as a significant risk factor for OS, with cytomegalovirus (CMV) infection also influencing OS and NRM.

Pre-transplant splenomegaly is independently associated with poor prognosis in AML patients.

## Linked entities

- **Diseases:** acute myeloid leukemia (MONDO:0015667), graft-versus-host disease (MONDO:0013730), myeloproliferative neoplasms (MONDO:0020076), cytomegalovirus infection (MONDO:0005132)

## Full-text entities

- **Genes:** FCGR3A (Fc gamma receptor IIIa) [NCBI Gene 2214] {aka CD16-II, CD16A, FCG3, FCGR3, FCRIIIA, FcGRIIIA}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, HLA-A (major histocompatibility complex, class I, A) [NCBI Gene 3105] {aka HLAA}, MLLT1 (MLLT1 super elongation complex subunit) [NCBI Gene 4298] {aka ENL, LTG19, YEATS1}, CD34 (CD34 molecule) [NCBI Gene 947], FLT3 (fms related receptor tyrosine kinase 3) [NCBI Gene 2322] {aka CD135, FLK-2, FLK2, STK1}, MAP2K7 (mitogen-activated protein kinase kinase 7) [NCBI Gene 5609] {aka JNKK2, MAPKK7, MEK, MEK 7, MKK7, PRKMK7}
- **Diseases:** infection (MESH:D007239), death (MESH:D003643), hematological disease (MESH:D006402), leukemia (MESH:D007938), viral infections (MESH:D014777), splenic vein thrombosis (MESH:D012170), CMML (MESH:D015477), GVHD (MESH:D006086), MPN (MESH:D009369), Dysbiosis (MESH:D064806), marrow failure (MESH:D000080983), AML (MESH:D015470), MF (MESH:D055728), bleeding (MESH:D006470), cGVHD (MESH:D000092122), Splenomegaly (MESH:D013163), CMV infection (MESH:D003586)
- **Chemicals:** Bu (MESH:D002066), CSA (MESH:D016572), BMSC (-), azacitidine (MESH:D001374), Cy (MESH:D003545), cytarabine (MESH:D003561), AZA (MESH:D001379), MMF (MESH:D009173), cyclophosphamide (MESH:D003520), fludarabine (MESH:C024352), MTX (MESH:D008727)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

45 references — full list in the complete paper: https://tomesphere.com/paper/PMC12953115/full.md

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Source: https://tomesphere.com/paper/PMC12953115