# Impact of prior solid tumor on outcomes of hematopoietic stem cell transplantation for hematologic malignancies: a propensity score-matched study

**Authors:** Jieya Luo, Mingyang Wang, Yunxia Zhou, Wenhao Wang, Wenbin Cao, Rongli Zhang, Xin Chen, Qiaoling Ma, Jialin Wei, Weihua Zhai, Yi He, Donglin Yang, Aiming Pang, Sizhou Feng, Mingzhe Han, Erlie Jiang

PMC · DOI: 10.3389/fimmu.2026.1727469 · Frontiers in Immunology · 2026-02-05

## TL;DR

This study finds that prior solid tumors do not significantly increase transplant risk but may affect long-term survival after hematopoietic stem cell transplantation.

## Contribution

The study uses propensity score matching to assess the impact of prior solid tumors on HSCT outcomes, revealing nuanced long-term survival differences.

## Key findings

- Patients with prior solid tumors had similar 3-year survival rates compared to controls.
- Long-term survival was lower in the solid tumor group beyond 2 years post-transplant.
- Age and low platelet counts were significant predictors of worse outcomes in solid tumor patients.

## Abstract

The Hematopoietic Cell Transplantation-Specific Comorbidity Index (HCT-CI) assigns a high-risk score to patients who develop secondary hematologic malignancies following solid tumors, indicating an increased risk of non-relapse mortality (NRM). This study aimed to evaluate the impact of prior solid tumors on outcomes after hematopoietic stem cell transplantation (HSCT).

From a cohort of 2,382 patients who underwent HSCT for acute lymphoblastic leukemia (ALL), acute myeloid leukemia (AML), or myelodysplastic syndrome (MDS) between January 2014 and July 2024, we included 43 (1.8%) with a history of prior solid tumors and 82 matched controls for analysis by 1:2 propensity score matching.

The solid tumor cohort predominantly comprised breast cancer (48.8%). With a median follow-up of 31.0 months, only one patient exhibited post-transplant relapse or metastasis of the solid tumor. Compared to the control group, patients with solid tumors exhibited higher ECOG scores (≥ 2: 23.1% vs. 9.5%, P = 0.049), lower platelet counts (35.5 vs. 72×109/L, P = 0.010), a higher incidence of complex karyotypes (16.3% vs. 3.7%, P = 0.031). No significant differences were noted in 3-year overall survival (OS) (64.3% vs. 71.9%, P = 0.468), leukemia-free survival (LFS) (57.6% vs. 70.8%, P = 0.218), graft-versus-host disease/relapse-free survival (GRFS) (43.3% vs. 53.0%, P = 0.359) and NRM (23.9% vs. 11.7%, P = 0.246). In an exploratory landmark analysis, the solid tumor cohort appeared to have significantly lower OS (P = 0.030), LFS (P = 0.009), and GRFS (P = 0.038) from 2 years after transplantation. Multivariable analysis identified age greater than 55 years, baseline platelet counts less than 50×109/L as significant predictors of inferior OS and LFS in solid tumor patients.

Patients with hematologic diseases secondary to solid tumors showed no significant increase in overall transplantation risk. However, their adverse clinical characteristics and reduced long-term survival rates beyond 2 years post-transplantation, underscore the need to refine HCT-CI scoring and improve management strategies.

## Linked entities

- **Diseases:** acute lymphoblastic leukemia (MONDO:0004967), acute myeloid leukemia (MONDO:0015667), myelodysplastic syndrome (MONDO:0018881), breast cancer (MONDO:0004989)

## Full-text entities

- **Genes:** FLT3 (fms related receptor tyrosine kinase 3) [NCBI Gene 2322] {aka CD135, FLK-2, FLK2, STK1}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, KMT2A (lysine methyltransferase 2A) [NCBI Gene 4297] {aka ALL-1, ALL1, CXXC7, GAS7, HRX, HTRX}, NPM1 (nucleophosmin 1) [NCBI Gene 4869] {aka B23, NPM}
- **Diseases:** lung cancer (MESH:D008175), chromosomal abnormalities (MESH:D002869), Cancer (MESH:D009369), t-HMs (OMIM:613700), Acute Graft-versus-Host Disease (MESH:D006086), inflammation (MESH:D007249), prostate cancer (MESH:D011471), AML (MESH:D015470), MDS (MESH:D009190), hematologic malignancies (MESH:D019337), myelodysplastic syndrome/acute myeloid leukemia (MESH:D000077428), Chronic Graft-versus-Host Disease (MESH:D000092122), primary disease (MESH:D009202), infection (MESH:D007239), t-HNs (MESH:D016609), gynecologic tumors (MESH:D005833), ALL (MESH:D054198), cytotoxic (MESH:D064420), metastasis (MESH:D009362), lung, brain, and urinary tract tumors (MESH:D014571), NRM (MESH:D003643), myelodysplastic/myeloproliferative neoplasms (MESH:D054437), Blood Diseases (MESH:D006402), thyroid cancer (MESH:D013964), OS (MESH:D011475), LFS (MESH:D007938), chronic myelomonocytic leukemia (MESH:D015477), solid (MESH:D018250), chronic (MESH:D002908), Breast cancer (MESH:D001943), heart failure (MESH:D006333), gastrointestinal tumors (MESH:D005770), cervical and ovarian (MESH:D010051)
- **Chemicals:** Sabatolimab (MESH:C000723550), Magrolimab (MESH:C000629291), mycophenolate mofetil (MESH:D009173), thiotepa (MESH:D013852), methotrexate (MESH:D008727), busulfan (MESH:D002066), MAC (-), melphalan (MESH:D008558), tacrolimus (MESH:D016559), cyclosporine (MESH:D016572)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

51 references — full list in the complete paper: https://tomesphere.com/paper/PMC12916414/full.md

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Source: https://tomesphere.com/paper/PMC12916414