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 Jun 23;12(13):1703.
doi: 10.3390/cells12131703.

Prognosis in Chronic Myeloid Leukemia: Baseline Factors, Dynamic Risk Assessment and Novel Insights

Affiliations
Review

Prognosis in Chronic Myeloid Leukemia: Baseline Factors, Dynamic Risk Assessment and Novel Insights

Miriam Iezza et al. Cells. .

Abstract

The introduction of tyrosine kinase inhibitors (TKIs) has changed the treatment paradigm of chronic myeloid leukemia (CML), leading to a dramatic improvement of the outcome of CML patients, who now have a nearly normal life expectancy and, in some selected cases, the possibility of aiming for the more ambitious goal of treatment-free remission (TFR). However, the minority of patients who fail treatment and progress from chronic phase (CP) to accelerated phase (AP) and blast phase (BP) still have a relatively poor prognosis. The identification of predictive elements enabling a prompt recognition of patients at higher risk of progression still remains among the priorities in the field of CML management. Currently, the baseline risk is assessed using simple clinical and hematologic parameters, other than evaluating the presence of additional chromosomal abnormalities (ACAs), especially those at "high-risk". Beyond the onset, a re-evaluation of the risk status is mandatory, monitoring the response to TKI treatment. Moreover, novel critical insights are emerging into the role of genomic factors, present at diagnosis or evolving on therapy. This review presents the current knowledge regarding prognostic factors in CML and their potential role for an improved risk classification and a subsequent enhancement of therapeutic decisions and disease management.

Keywords: chronic myeloid leukemia; genomic factors; prognosis; risk assessment.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

References

    1. Rowley J. A New Consistent Chromosomal Abnormality in Chronic Myelogenous Leukaemia Identified by Quinacrine Fluorescence and Giemsa Staining. Nature. 1973;243:290–293. - PubMed
    1. Bartram C.R., De Klein A., Hagemeijer A., Van Agthoven T., Van Kessel A.G., Bootsma D., Grosveld G., Ferguson-smith M.A., Davies T., Stone M., et al. Translocation of C-Abl Oncogene Correlates with the Presence of a Philadelphia Chromosome In chronic myelocytic Leukaemia. Nature. 1983;306:277–280. doi: 10.1038/306277a0. - DOI - PubMed
    1. Deininger M.W.N., Goldman J.M., Melo J.V. The Molecular Biology of Chronic Myeloid Leukemia. Blood. 2000;96:3343–3356. doi: 10.1182/blood.v96.10.3343. - DOI - PubMed
    1. Koschmieder S., Göttgens B., Zhang P., Iwasaki-Arai J., Akashi K., Kutok J.L., Dayaram T., Geary K., Green A.R., Tenen D.G., et al. Inducible Chronic Phase of Myeloid Leukemia with Expansion of Hematopoietic Stem Cells in a Transgenic Model of BCR-ABL Leukemogenesis. Blood. 2005;105:324–334. doi: 10.1182/blood-2003-12-4369. - DOI - PubMed
    1. Savona M., Talpaz M. Getting to the Stem of Chronic Myeloid Leukaemia. Nat. Rev. Cancer. 2008;8:341–350. doi: 10.1038/nrc2368. - DOI - PubMed

MeSH terms