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Peer-reviewedCC BY-NC-ND 4.0Blood Research

Post-transplant monitoring of NGS-based measurable residual disease and donor chimerism as a prognostic tool in older patients with AML/MDS

  1. 1Division of Hemato-Oncology, Department of Internal Medicine, Soonchunhyang University Bucheon Hospital, 170 Jomaru-Ro, Wonmi-Gu, Bucheon, 14584 Republic of Korea
  2. 2Division of Hematology-Oncology, Department of Internal Medicine, Soonchunhyang University Seoul Hospital, 59, Daesagwan-ro, Yongsan-gu, Seoul, 04401 Korea

Abstract

Purpose: To evaluate the prognostic value of integrated post-transplant monitoring of NGS-based measurable residual disease (MRD) and donor chimerism in older patients with acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS), undergoing reduced-intensity conditioning (RIC) allogeneic stem cell transplantation (allo-SCT).

Materials and methods: This retrospective study analyzed the clinical outcomes of 113 patients with AML or MDS, aged ≥ 60 years or ≥ 55 years if deemed unfit for standard-intensity conditioning, who underwent RIC allo-SCT. NGS-based MRD testing and donor chimerism were assessed at 3 months post-transplant.

Results: A total of 113 patients participated in the study (median age 63 years; 69.9% with AML); among the 105 patients evaluable at 3 months post-transplantation, MRD positivity occurred in 28 patients (26.7%) and predicted inferior overall survival (hazard ratio [HR] 6.373, 95% confidence interval [CI] 3.005–13.517; P < 0.001), while complete donor chimerism (CDC), achieved in 82 patients (78.1%), predicted improved survival (HR 0.356, 95% CI 0.195–0.916; P = 0.028). MRD positivity remained an independent predictor of survival on multivariate analysis (HR 3.315, 95% CI 1.423–7.230, P = 0.005), while CDC showed a trend toward improved survival that did not reach statistical significance (HR 0.494, 95% CI 0.306–1.009, P = 0.051). Two-year overall survival differed markedly across the four MRD/CDC subgroups, ranging from 85.6% [MRD(–)/CDC( +)] to 13.6% [MRD( +)/CDC(–)] (P < 0.001), with the MRD( +)/CDC(–) group showing the highest 2-year relapse incidence (69.7%).

Conclusion: The combination of NGS-based MRD and chimerism monitoring is a critical prognostic strategy for older patients with AML/MDS undergoing RIC allo-SCT. Early identification of MRD positivity or mixed chimerism allows timely, risk-adapted interventions, including donor lymphocyte infusion, hypomethylating agents, and targeted therapies to reduce relapse and improve survival.

Supplementary Information: The online version contains supplementary material available at https://doi.org/10.1007/s44313-026-00187-6.

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BibTeX
@article{kim2026posttransplant,
  title = {{Post-transplant monitoring of NGS-based measurable residual disease and donor chimerism as a prognostic tool in older patients with AML/MDS}},
  author = {Se Hyung Kim and Jina Yun and Kyoung Ha Kim and Seug Yun Yoon and Chan Kyu Kim and Seong Kyu Park},
  journal = {Blood Research},
  year = {2026},
  month = oct,
  doi = {10.1007/s44313-026-00187-6},
  url = {https://doi.org/10.1007/s44313-026-00187-6},
  note = {CC BY-NC-ND 4.0},
}
RIS
TY  - JOUR
TI  - Post-transplant monitoring of NGS-based measurable residual disease and donor chimerism as a prognostic tool in older patients with AML/MDS
AU  - Se Hyung Kim
AU  - Jina Yun
AU  - Kyoung Ha Kim
AU  - Seug Yun Yoon
AU  - Chan Kyu Kim
AU  - Seong Kyu Park
PY  - 2026
DA  - 2026/10/26
JO  - Blood Research
DO  - 10.1007/s44313-026-00187-6
UR  - https://doi.org/10.1007/s44313-026-00187-6
AB  - Purpose: To evaluate the prognostic value of integrated post-transplant monitoring of NGS-based measurable residual disease (MRD) and donor chimerism in older patients with acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS), undergoing reduced-intensity conditioning (RIC) allogeneic stem cell transplantation (allo-SCT).  Materials and methods: This retrospective study analyzed the clinical outcomes of 113 patients with AML or MDS, aged ≥ 60 years or ≥ 55 years if deemed unfit for standard-intensity conditioning, who underwent RIC allo-SCT. NGS-based MRD testing and donor chimerism were assessed at 3 months post-transplant.  Results: A total of 113 patients participated in the study (median age 63 years; 69.9% with AML); among the 105 patients evaluable at 3 months post-transplantation, MRD positivity occurred in 28 patients (26.7%) and predicted inferior overall survival (hazard ratio [HR] 6.373, 95% confidence interval [CI] 3.005–13.517; P < 0.001), while complete donor chimerism (CDC), achieved in 82 patients (78.1%), predicted improved survival (HR 0.356, 95% CI 0.195–0.916; P = 0.028). MRD positivity remained an independent predictor of survival on multivariate analysis (HR 3.315, 95% CI 1.423–7.230, P = 0.005), while CDC showed a trend toward improved survival that did not reach statistical significance (HR 0.494, 95% CI 0.306–1.009, P = 0.051). Two-year overall survival differed markedly across the four MRD/CDC subgroups, ranging from 85.6% [MRD(–)/CDC( +)] to 13.6% [MRD( +)/CDC(–)] (P < 0.001), with the MRD( +)/CDC(–) group showing the highest 2-year relapse incidence (69.7%).  Conclusion: The combination of NGS-based MRD and chimerism monitoring is a critical prognostic strategy for older patients with AML/MDS undergoing RIC allo-SCT. Early identification of MRD positivity or mixed chimerism allows timely, risk-adapted interventions, including donor lymphocyte infusion, hypomethylating agents, and targeted therapies to reduce relapse and improve survival.  Supplementary Information: The online version contains supplementary material available at https://doi.org/10.1007/s44313-026-00187-6.
SN  - 2287-979X
SN  - 2288-0011
ER  -