TRANSLATE

The aml Hub website uses a third-party service provided by Google that dynamically translates web content. Translations are machine generated, so may not be an exact or complete translation, and the aml Hub cannot guarantee the accuracy of translated content. The aml and its employees will not be liable for any direct, indirect, or consequential damages (even if foreseeable) resulting from use of the Google Translate feature. For further support with Google Translate, visit Google Translate Help.

The AML Hub is an independent medical education platform, sponsored by Astellas, Daiichi Sankyo, Johnson & Johnson, Kura Oncology and Syndax, and has been supported through educational grants from Bristol Myers Squibb and the Hippocrate Conference Institute, an association of the Servier Group. The funders are allowed no direct influence on our content. The levels of sponsorship listed are reflective of the amount of funding given. View funders.

Now you can support HCPs in making informed decisions for their patients

Your contribution helps us continuously deliver expertly curated content to HCPs worldwide. You will also have the opportunity to make a content suggestion for consideration and receive updates on the impact contributions are making to our content.

Find out more

ELN-refined 2024 Beat-AML risk stratification for older patients with newly diagnosed AML

By Haimanti Mandal

Share:

Nov 11, 2024

Learning objective: After reading this article, learners will be able to cite a new clinical development in acute myeloid leukemia.


Prognostic impact of the 2022 ELN risk classification and development of a refined BEAT-AML 2024 risk stratification for older patients (aged ≥60 years) with ND AML receiving LIT were published by Hoff et al.1 in Blood Advances. A total of 595 patients with ND AML from the Beat AML trial (NCT03013998) were included; the median age was 73 years, and 42% were female. 

Key learnings
According to the 2022 ELN risk stratification, 78% of patients were classified as adverse risk, 11% as favorable risk, and 11% as intermediate risk. Among 579 patients with OS data, ELN criteria did not distinguish between favorable- and intermediate-risk groups (p = 0.71) but predicted poor OS in those with adverse risk (p<0.001; C-index: 0.55), with 2-year OS of 47% vs 50% vs 23%, respectively. 
Multivariable analysis of the training set (n=316) identified IDH2 mutation as an independent favorable prognostic factor, while KRAS, MLL2, and TP53 mutations were independent unfavorable (p<0.05). 
A refined Beat-AML 2024 risk stratification resulted in a “mutation score” that classified patients into two risk groups: −1 to 0 points (Beat-AML intermediate; 41%) vs 1+ points (Beat-AML adverse; 37%). The 2022 ELN favorable- and intermediate-risk patients were reclassified as Beat-AML favorable-risk (22%). 
The refined risk model showed stronger prognostication for OS, with 2-year OS rates of 48% vs 33% vs 11% in Beat-AML favorable-, intermediate-, and adverse-risk groups, respectively; (p < 0.001; C-index: 0.60). 
The Beat-AML 2024 model redefines risk for older patients with ND AML undergoing LIT and informs treatment decisions. Further validation of the model is warranted.  

Abbreviations: AML, acute myeloid leukemia; ELN, European LeukemiaNet; LIT, lower-intensity treatment; ND, newly diagnosed; OS, overall survival. 

References

Please indicate your level of agreement with the following statements:

The content was clear and easy to understand

The content addressed the learning objectives

The content was relevant to my practice

I will change my clinical practice as a result of this content