Acute myeloid leukemia risk stratification in younger and older patients through transcriptomic machine learning models

Acute Myeloid Leukemia (AML) is a genetically and clinically heterogeneous disease that can develop at any age. While AML incidence increases with age and distinct genetic alterations are observed in younger versus older patients, current classification systems do not incorporate age as a defining factor. In this study, we analyzed RNA-seq data from 404 AML patients at initial diagnosis, leveraging a k-mer-based machine learning approach to uncover age-related transcriptomic differences in favorable and adverse risk groups. Our model achieved over 90% accuracy in risk prediction and identified key gene signatures distinguishing ELN2017 favorable and adverse groups. From these signatures, we selected prognostic biomarkers with significant impacts on survival. Additionally, we explored the biological context underlying transcriptomic complexity across age groups, revealing distinct tumor profiles and differences in immune and stromal cell populations, particularly in older patients. These findings underscore the importance of age-related molecular features in AML and provide new insights for risk stratification and therapeutic targeting.

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Publication Details

Journal
Scientific Reports
Published
2025-11-13
DOI
https://doi.org/10.1038/s41598-025-23468-z
Primary Topic
Acute Myeloid Leukemia Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Acute myeloid leukemia risk stratification in younger and older patients through transcriptomic machine learning models

Raíssa Silva, Thérèse Commes, Florence Rufflé, Nicolas Gilbert et al.
Scientific Reports
Acute Myeloid Leukemia Research
article

Acute myeloid leukemia risk stratification in younger and older patients through transcriptomic machine learning models

Raíssa Silva, Thérèse Commes, Florence Rufflé, Nicolas Gilbert, Maïlis Amico, Benoît Guibert, Jérôme Reboul, Chloé Bessière, Cédric Riedel, Anthony Boureux, Camelia Sennaoui
article en

Abstract

Acute Myeloid Leukemia (AML) is a genetically and clinically heterogeneous disease that can develop at any age. While AML incidence increases with age and distinct genetic alterations are observed in younger versus older patients, current classification systems do not incorporate age as a defining factor. In this study, we analyzed RNA-seq data from 404 AML patients at initial diagnosis, leveraging a k-mer-based machine learning approach to uncover age-related transcriptomic differences in favorable and adverse risk groups. Our model achieved over 90% accuracy in risk prediction and identified key gene signatures distinguishing ELN2017 favorable and adverse groups. From these signatures, we selected prognostic biomarkers with significant impacts on survival. Additionally, we explored the biological context underlying transcriptomic complexity across age groups, revealing distinct tumor profiles and differences in immune and stromal cell populations, particularly in older patients. These findings underscore the importance of age-related molecular features in AML and provide new insights for risk stratification and therapeutic targeting.

Scientific ReportsVol. 15(1)
Centre National de la Recherche Scientifique (FR), Université Toulouse III - Paul Sabatier (FR), Inserm (FR), Université de Montpellier (FR), Centre de Recherches en Cancérologie de Toulouse (FR)
Agence Nationale de la Recherche, Institut National de la Santé et de la Recherche Médicale, Ligue Contre le Cancer, Fondation de France
Openalex Percentile: Top 55%
Acute Myeloid Leukemia Research
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