DIFFERENTIAL IMPACT OF CD34+ CELL DOSE FOR DIFFERENT AGE GROUPS IN ALLOGENEIC HEMATOPOIETIC CELL TRANSPLANTATION FOR ACUTE LEUKEMIA: A MACHINE LEARNING-BASED DISCOVERY.
Yiyang Qu, Hamed Shourabizadeh, Aravind Subramanian, Dionne M Aleman, Louis-Martin Rousseau, Arjun D Law, Auro Viswabandya, Fotios V Michelis
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引用次数: 0
Abstract
Allogeneic hematopoietic cell transplantation (allo-HCT) presents a potentially curative treatment for hematologic malignancies, yet carries associated risks and complications. Continuous research focuses on predicting outcomes and identifying risk factors. Notably, the influence of CD34+ cell dose on overall survival (OS) has been the subject of numerous studies yielding contradictory results. We developed machine learning (ML) models to predict allo-HCT outcomes and through the application of SHAP (SHapley Additive exPlanations), an explainable artificial intelligence (XAI) technique, enabled the identification of new and clinically relevant feature-outcome relationships. In particular, we identified clear interaction between CD34+ cell dose of peripheral blood stem cell (PBSC) grafts and patient age at allo-HCT for acute leukemia patients. Results of multivariable analysis validated the interaction effect: On young acute leukemia patients (≤45-year-old), low dose of CD34+ cells (<4.3 × 106 CD34+/kg) was associated with better OS against high dose (≥7 × 106 CD34+/kg) (hazard ratio [HR] 0.38, p=0.019), while for older acute leukemia patients (>45-year-old), low CD34+ cell dose (<3.8 × 106 CD34+/kg) was associated with worse OS against high dose (≥6.1 × 106 CD34+/kg) (HR 1.58, P = 0.033). In conclusion, our findings suggest that tailoring CD34+ cell dose by patient age may benefit acute leukemia patients undergoing allo-HCT, while XAI showcases excellent proficiency in revealing such interactions.
期刊介绍:
Experimental Hematology publishes new findings, methodologies, reviews and perspectives in all areas of hematology and immune cell formation on a monthly basis that may include Special Issues on particular topics of current interest. The overall goal is to report new insights into how normal blood cells are produced, how their production is normally regulated, mechanisms that contribute to hematological diseases and new approaches to their treatment. Specific topics may include relevant developmental and aging processes, stem cell biology, analyses of intrinsic and extrinsic regulatory mechanisms, in vitro behavior of primary cells, clonal tracking, molecular and omics analyses, metabolism, epigenetics, bioengineering approaches, studies in model organisms, novel clinical observations, transplantation biology and new therapeutic avenues.