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Current Hematologic Malignancy Reports

, Volume 12, Issue 6, pp 547–556 | Cite as

The Prognostic Significance of Measurable (“Minimal”) Residual Disease in Acute Myeloid Leukemia

  • Francesco BuccisanoEmail author
  • Christopher S. Hourigan
  • Roland B. Walter
Acute Myeloid Leukemias (H Erba, Section Editor)
Part of the following topical collections:
  1. Topical Collection on Acute Myeloid Leukemias

Abstract

Purpose of Review

The purpose of this review was to evaluate recent literature on detection methodologies for, and prognostic significance of, measurable (“minimal”) residual disease (MRD) in acute myeloid leukemia (AML).

Recent Findings

There is no “one-fits-all” approach to MRD testing in AML. Most exploited to date are methods relying on immunophenotypic aberrancies (identified via multiparameter flow cytometry) or genetic abnormalities (identified via PCR-based assays). Current methods have important shortcomings, including the lack of assay platform standardization/harmonization across laboratories. In parallel to refinements of existing technologies and data analysis/interpretation, new methodologies (e.g., next-generation sequencing-based assays) are emerging that eventually may complement or replace existing ones.

Summary

This dynamic evolution of MRD testing has complicated comparisons between individual studies. Nonetheless, an ever-growing body of data demonstrates that a positive MRD test at various time points throughout chemotherapy and hematopoietic cell transplantation identifies patients at particularly high risks of disease recurrence and short survival even after adjustment for other risk factors.

Keywords

Acute myeloid leukemia Flow cytometry Minimal residual disease Next-generation sequencing Polymerase chain reaction Prognostication 

Notes

Acknowledgements

R.B.W. is a Leukemia & Lymphoma Society Scholar in Clinical Research. This work was supported in part by the Intramural Research Program of the National Heart, Lung, and Blood Institute of the National Institutes of Health.

Compliance with Ethical Standards

Conflict of Interest

Francesco Buccisano and Roland B. Walter each report no conflict of interest.

Christopher S. Hourigan receives research funding from Merck Sharp & Dohme and SELLAS Life Sciences Group AG.

Human and Animal Rights and Informed Consent

This article does not contain any otherwise unpublished studies with human subjects or animals that were performed by the authors.

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Copyright information

© Springer Science+Business Media, LLC 2017

Authors and Affiliations

  • Francesco Buccisano
    • 1
    Email author
  • Christopher S. Hourigan
    • 2
  • Roland B. Walter
    • 3
    • 4
    • 5
  1. 1.Department of Biomedicine and Prevention, HematologyUniversity Tor VergataRomeItaly
  2. 2.Myeloid Malignancies Section, Hematology Branch, National Heart, Lung, and Blood InstituteNational Institutes of HealthBethesdaUSA
  3. 3.Clinical Research DivisionFred Hutchinson Cancer Research CenterSeattleUSA
  4. 4.Department of Medicine, Division of HematologyUniversity of WashingtonSeattleUSA
  5. 5.Department of EpidemiologyUniversity of WashingtonSeattleUSA

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