Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2023 May 23;30(6):5201-5213.
doi: 10.3390/curroncol30060395.

Novel Tools for Diagnosis and Monitoring of AML

Affiliations
Review

Novel Tools for Diagnosis and Monitoring of AML

Francesca Guijarro et al. Curr Oncol. .

Abstract

In recent years, major advances in the understanding of acute myeloid leukemia (AML) pathogenesis, together with technological progress, have led us into a new era in the diagnosis and follow-up of patients with AML. A combination of immunophenotyping, cytogenetic and molecular studies are required for AML diagnosis, including the use of next-generation sequencing (NGS) gene panels to screen all genetic alterations with diagnostic, prognostic and/or therapeutic value. Regarding AML monitoring, multiparametric flow cytometry and quantitative PCR/RT-PCR are currently the most implemented methodologies for measurable residual disease (MRD) evaluation. Given the limitations of these techniques, there is an urgent need to incorporate new tools for MRD monitoring, such as NGS and digital PCR. This review aims to provide an overview of the different technologies used for AML diagnosis and MRD monitoring and to highlight the limitations and challenges of current versus emerging tools.

Keywords: AML; MRD monitoring; NGS; diagnosis; digital PCR; flow cytometry.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Tools for diagnosis and monitoring of AML. A combination of immunophenotyping and molecular studies is required for AML diagnosis and MRD monitoring. MRD: Measurable residual disease; LAIP: Leukemia-associated immunophenotype; DfN: Different from normal; qPCR: quantitative PCR; ddPCR: Droplet digital PCR.

References

    1. Khoury J.D., Solary E., Abla O., Akkari Y., Alaggio R., Apperley J.F., Bejar R., Berti E., Busque L., Chan J.K.C., et al. The 5th edition of the World Health Organization Classification of Haematolymphoid Tumours: Myeloid and Histiocytic/Dendritic Neoplasms. Leukemia. 2022;36:1703–1719. doi: 10.1038/s41375-022-01613-1. - DOI - PMC - PubMed
    1. Arber D.A., Orazi A., Hasserjian R.P., Borowitz M.J., Calvo K.R., Kvasnicka H.-M., Wang S.A., Bagg A., Barbui T., Branford S., et al. International Consensus Classification of Myeloid Neoplasms and Acute Leukemias: Integrating morphologic, clinical, and genomic data. Blood. 2022;140:1200–1228. doi: 10.1182/blood.2022015850. - DOI - PMC - PubMed
    1. Döhner H., Wei A.H., Appelbaum F.R., Craddock C., DiNardo C.D., Dombret H., Ebert B.L., Fenaux P., Godley L.A., Hasserjian R.P., et al. Diagnosis and management of AML in adults: 2022 recommendations from an international expert panel on behalf of the ELN. Blood. 2022;140:1345–1377. doi: 10.1182/blood.2022016867. - DOI - PubMed
    1. Angelini D.F., Ottone T., Guerrera G., Lavorgna S., Cittadini M., Buccisano F., De Bardi M., Gargano F., Maurillo L., Divona M., et al. A leukemia-associated CD34/CD123/CD25/CD99+ immunophenotype identifies FLT3-mutated clones in acute myeloid Leukemia. Clinical Cancer Research. Clin. Cancer Res. 2015;21:3977–3985. doi: 10.1158/1078-0432.CCR-14-3186. - DOI - PubMed
    1. Kalina T., Flores-Montero J., van der Velden V.H.J., Martin-Ayuso M., Böttcher S., Ritgen M., Almeida J., Lhermitte L., Asnafi V., Mendonça A., et al. EuroFlow standardization of flow cytometer instrument settings and immunophenotyping protocols. Leukemia. 2012;26:1986–2010. doi: 10.1038/leu.2012.122. - DOI - PMC - PubMed

Publication types

MeSH terms