» Articles » PMID: 22987078

Prognostic Significance of the European LeukemiaNet Standardized System for Reporting Cytogenetic and Molecular Alterations in Adults with Acute Myeloid Leukemia

Abstract

Purpose: To evaluate the prognostic significance of the international European LeukemiaNet (ELN) guidelines for reporting genetic alterations in acute myeloid leukemia (AML).

Patients And Methods: We analyzed 1,550 adults with primary AML, treated on Cancer and Leukemia Group B first-line trials, who had pretreatment cytogenetics and, for cytogenetically normal patients, mutational status of NPM1, CEBPA, and FLT3 available. We compared complete remission (CR) rates, disease-free survival (DFS), and overall survival (OS) among patients classified into the four ELN genetic groups (favorable, intermediate-I, intermediate-II, adverse) separately for 818 younger (age < 60 years) and 732 older (age ≥ 60 years) patients.

Results: The percentages of younger versus older patients in the favorable (41% v 20%; P < .001), intermediate-II (19% v 30%; P < .001), and adverse (22% v 31%; P < .001) genetic groups differed. The favorable group had the best and the adverse group the worst CR rates, DFS, and OS in both age groups. Both intermediate groups had significantly worse outcomes than the favorable but better than the adverse group. Intermediate-I and intermediate-II groups in older patients had similar outcomes, whereas the intermediate-II group in younger patients had better OS but not better CR rates or DFS than the intermediate-I group. The prognostic significance of ELN classification was confirmed by multivariable analyses. For each ELN group, older patients had worse outcomes than younger patients.

Conclusion: The ELN classification clearly separates the genetic groups by outcome, supporting its use for risk stratification in clinical trials. Because they have different proportions of genetic alterations and outcomes, younger and older patients should be reported separately when using the ELN classification.

Citing Articles

The Prognostic Impact of Additional Molecular and Cytogenetic Abnormalities on AML Patients with NPM1- and/or FLT3-ITD Mutations Receiving Intensive Chemotherapy: Real-World Data from the Greek Registry.

Lazana I, Papathanassiou M, Konstantellos I, Tzenou T, Kopsaftopoulou A, Liga M Cancers (Basel). 2025; 17(4).

PMID: 40002262 PMC: 11853380. DOI: 10.3390/cancers17040667.


Genetic abnormalities predict outcomes in patients with core binding factor acute myeloid leukemia.

Yu S, Yang S, Hu L, Duan W, Zhao T, Qin Y Ann Hematol. 2025; .

PMID: 39966122 DOI: 10.1007/s00277-024-06182-0.


DNMT1 inhibition improves the activity of memory-like natural killer cells by enhancing the level of autophagy.

Li Y, Guo C, Zhang F, Cheng S, Li Y, Luo S Mol Biol Rep. 2024; 52(1):68.

PMID: 39704855 PMC: 11662054. DOI: 10.1007/s11033-024-10181-9.


Improving risk stratification for 2022 European LeukemiaNet favorable-risk patients with acute myeloid leukemia.

Archer K, Fu H, Mrozek K, Nicolet D, Mims A, Uy G Innovation (Camb). 2024; 5(6):100719.

PMID: 39529956 PMC: 11551470. DOI: 10.1016/j.xinn.2024.100719.


Certainty in uncertainty: Determining the rate and reasons for reclassification of variants of uncertain significance in haematological malignancies.

Enjeti A, Walker N, Fahey O, Johnston E, Legge-Wilkinson H, Ramsurrun N EJHaem. 2024; 5(5):957-963.

PMID: 39415915 PMC: 11474286. DOI: 10.1002/jha2.1002.


References
1.
Baer M, George S, Sanford B, Mrozek K, Kolitz J, Moore J . Escalation of daunorubicin and addition of etoposide in the ADE regimen in acute myeloid leukemia patients aged 60 years and older: Cancer and Leukemia Group B Study 9720. Leukemia. 2011; 25(5):800-7. PMC: 3821040. DOI: 10.1038/leu.2011.9. View

2.
Kolitz J, George S, Marcucci G, Vij R, Powell B, Allen S . P-glycoprotein inhibition using valspodar (PSC-833) does not improve outcomes for patients younger than age 60 years with newly diagnosed acute myeloid leukemia: Cancer and Leukemia Group B study 19808. Blood. 2010; 116(9):1413-21. PMC: 2938834. DOI: 10.1182/blood-2009-07-229492. View

3.
Ley T, Ding L, Walter M, McLellan M, Lamprecht T, Larson D . DNMT3A mutations in acute myeloid leukemia. N Engl J Med. 2010; 363(25):2424-33. PMC: 3201818. DOI: 10.1056/NEJMoa1005143. View

4.
Smith M, Hills R, Grimwade D . Independent prognostic variables in acute myeloid leukaemia. Blood Rev. 2010; 25(1):39-51. DOI: 10.1016/j.blre.2010.10.002. View

5.
Byrd J, Mrozek K, Dodge R, Carroll A, Edwards C, Arthur D . Pretreatment cytogenetic abnormalities are predictive of induction success, cumulative incidence of relapse, and overall survival in adult patients with de novo acute myeloid leukemia: results from Cancer and Leukemia Group B (CALGB 8461). Blood. 2002; 100(13):4325-36. DOI: 10.1182/blood-2002-03-0772. View