학술논문
Minimal residual disease detection defined as the malignant fraction of the total primitive stem cell compartment offers additional prognostic information in acute myeloid leukaemia.
Document Type
Article
Author
Source
Subject
*ACUTE myeloid leukemia
*BONE marrow
*FLOW cytometry
*MULTIVARIATE analysis
*PROBABILITY theory
*PROGNOSIS
*RESEARCH funding
*STEM cells
*SURVIVAL analysis (Biometry)
*SURVIVAL
*RELATIVE medical risk
*PREDICTIVE tests
*PROPORTIONAL hazards models
*RETROSPECTIVE studies
*DATA analysis software
*KAPLAN-Meier estimator
BONE marrow examination
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Language
ISSN
1751-5521
Abstract
Introduction: Immunophenotypic detection of minimal residual disease (MRD) in bone marrow (BM) of acute myeloid leukaemia (AML) patients is of high prognostic relevance. Standard MRD percentage is assessed as a percentage of total white blood cells (WBCs) and is therefore highly dependent on WBC count. Peripheral blood (PB) contains more than five times lower MRD percentages. Therefore, PB in BM aspirates cause dilution of the MRD cells, possibly leading to false-negative results for BM MRD. The latter is avoided when relating the fraction of malignant primitive cells, identified by aberrant marker expression [aberrant primitive cells (aPC)], to the total population of primitive cells. Such a fraction may in addition reflect an important biological parameter. Methods: As this approach is thus independent of WBC count and the total size of the primitive compartment, we investigated the role of aPC fractions on overall and relapse-free survival (RFS) in 98 patients with AML under the age of 60. Results: We show that this approach identifies MRD-negative (as defined by % of WBC) but aPC-positive (as defined by % of primitive cells) patients with poor outcome after both first and second induction cycle of chemotherapy. Conclusion: As a result, in cases with a primitive marker present, RFS is best predicted when combining standard MRD percentage with aPC fractions. [ABSTRACT FROM AUTHOR]