Post-Transplant Relapse in Acute Leukemia: Comparative Value of MRD and Chimerism
Sinem Başak Tan Öksüz1, Güldane Cengiz Seval2, Klara Dalva2
1Department of Internal Medicine, Ankara University Faculty of Medicine, Ankara, Türkiye.
Measurable residual disease (MRD) monitoring at three months post-allogeneic hematopoietic stem cell transplantation (AHSCT) is a superior predictor of relapse in acute myeloid leukemia (AML) compared to donor chimerism. For acute lymphoblastic leukemia (ALL), both methods may be complementary.
Area of Science:
- Hematology
- Oncology
- Transplantation Medicine
Background:
- Relapse is a primary cause of treatment failure following allogeneic hematopoietic stem cell transplantation (AHSCT) for acute leukemia.
- Current post-transplant surveillance relies on measurable residual disease (MRD) and donor chimerism, but their predictive value and optimal timing are unclear.
Purpose of the Study:
- To compare the prognostic performance of MRD and donor chimerism in predicting relapse after AHSCT in adult patients with acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL).
Main Methods:
- Retrospective cohort study of 264 adult patients (186 AML, 78 ALL) undergoing AHSCT.
- MRD assessed by multiparametric flow cytometry at day 28, and months 3 and 12.
- Chimerism assessed by short tandem repeat PCR.
- Cox regression analysis to identify independent relapse predictors.
Main Results:
- In AML, MRD positivity at month 3 (HR 3.69) and mixed total chimerism at month 3 (HR 2.47) independently predicted relapse and were associated with inferior survival.
- MRD detected relapse earlier and more sensitively than chimerism in AML.
- In ALL, mixed chimerism at month 3 predicted relapse in univariate analysis; MRD had limited power due to small sample size.
Conclusions:
- Post-transplant MRD monitoring at month 3 offers superior risk stratification for relapse in AML compared to chimerism.
- In ALL, MRD and chimerism may be complementary, but further research with larger cohorts is needed.
- Disease-specific, risk-adapted surveillance strategies post-AHSCT are warranted.
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