Development of a Dynamic Counterfactual Risk Stratification Strategy for Newly Diagnosed Patients With AML Treated With Venetoclax and Azacitidine.
[PURPOSE] The objective of this study was to develop a flexible risk stratification strategy for AML that is specific for venetoclax plus azacitidine (ven/aza), addresses real-world data (RWD) issues,
APA
Islam N, Dale JL, et al. (2025). Development of a Dynamic Counterfactual Risk Stratification Strategy for Newly Diagnosed Patients With AML Treated With Venetoclax and Azacitidine.. JCO clinical cancer informatics, 9, e2400308. https://doi.org/10.1200/CCI-24-00308
MLA
Islam N, et al.. "Development of a Dynamic Counterfactual Risk Stratification Strategy for Newly Diagnosed Patients With AML Treated With Venetoclax and Azacitidine.." JCO clinical cancer informatics, vol. 9, 2025, pp. e2400308.
PMID
41329902
Abstract
[PURPOSE] The objective of this study was to develop a flexible risk stratification strategy for AML that is specific for venetoclax plus azacitidine (ven/aza), addresses real-world data (RWD) issues, and is also adaptable to different use cases.
[METHODS] A series of tunable risk models (RMs) were generated from a dynamic counterfactual machine learning (ML) strategy. These used a range of features from diagnostic AML samples and were tested using objective metrics on a single-institution cohort of 316 newly diagnosed patients treated with ven/aza. RM performance was tested using various model assumptions, data elements, and end points and with applications to an external AML real-world cohort (RWC).
[RESULTS] Favorable, intermediate, and adverse risk groups were identified in a series of ML-based RMs using different assumptions, for genetic-only or genetic-plus-phenotypic data elements and with overall survival and event-free survival as end points. Most RMs demonstrated equitable patient distribution (approximately 20%-40% in each risk group), significant separation between risk strata (log-rank-based values <0.001), and predictability computed by time-dependent survival AUC values of 0.60-0.70. Similar performance was observed when the proposed RM strategy was adapted and compared with the European Leukemia Net 2022 using the external RWC.
[CONCLUSION] The proposed ML strategy addresses a variety of RWD considerations and is readily tunable through coding and parameter updates for different contexts and use case needs. This strategy represents a novel approach to developing more effective RMs for AML and possibly other diseases.
[METHODS] A series of tunable risk models (RMs) were generated from a dynamic counterfactual machine learning (ML) strategy. These used a range of features from diagnostic AML samples and were tested using objective metrics on a single-institution cohort of 316 newly diagnosed patients treated with ven/aza. RM performance was tested using various model assumptions, data elements, and end points and with applications to an external AML real-world cohort (RWC).
[RESULTS] Favorable, intermediate, and adverse risk groups were identified in a series of ML-based RMs using different assumptions, for genetic-only or genetic-plus-phenotypic data elements and with overall survival and event-free survival as end points. Most RMs demonstrated equitable patient distribution (approximately 20%-40% in each risk group), significant separation between risk strata (log-rank-based values <0.001), and predictability computed by time-dependent survival AUC values of 0.60-0.70. Similar performance was observed when the proposed RM strategy was adapted and compared with the European Leukemia Net 2022 using the external RWC.
[CONCLUSION] The proposed ML strategy addresses a variety of RWD considerations and is readily tunable through coding and parameter updates for different contexts and use case needs. This strategy represents a novel approach to developing more effective RMs for AML and possibly other diseases.
MeSH Terms
Humans; Leukemia, Myeloid, Acute; Sulfonamides; Bridged Bicyclo Compounds, Heterocyclic; Azacitidine; Male; Female; Risk Assessment; Antineoplastic Combined Chemotherapy Protocols; Aged; Middle Aged; Machine Learning; Adult; Aged, 80 and over; Prognosis