Automated Assessment of Disease Progression in Acute Myeloid Leukemia by Probabilistic Analysis of Flow Cytometry Data

被引:24
作者
Rajwa, Bartek [1 ]
Wallace, Paul K. [2 ]
Griffiths, Elizabeth A. [3 ]
Dundar, Murat [4 ]
机构
[1] Purdue Univ, Bindley Biosci Ctr, W Lafayette, IN 47907 USA
[2] Roswell Pk Canc Inst, Dept Flow & Image Cytometry, Buffalo, NY 14263 USA
[3] Roswell Pk Canc Inst, Dept Med, Buffalo, NY 14263 USA
[4] Indiana Univ Purdue Univ, Dept Comp & Informat Sci, Indianapolis, IN 46202 USA
基金
美国国家科学基金会;
关键词
Acute myeloid leukemia (AML); Dirichlet process (DP); flow cytometry (FC); minimal residual disease (MRD); nonparametric Bayesian (NPB); IDENTIFICATION; DIAGNOSIS;
D O I
10.1109/TBME.2016.2590950
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Objective: Flow cytometry (FC) is a widely acknowledged technology in diagnosis of acute myeloid leukemia (AML) and has been indispensable in determining progression of the disease. Although FC plays a key role as a posttherapy prognosticator and evaluator of therapeutic efficacy, the manual analysis of cytometry data is a barrier to optimization of reproducibility and objectivity. This study investigates the utility of our recently introduced nonparametric Bayesian framework in accurately predicting the direction of change in disease progression in AML patients using FC data. Methods: The highly flexible nonparametric Bayesian model based on the infinite mixture of infinite Gaussian mixtures is used for jointly modeling data from multiple FC samples to automatically identify functionally distinct cell populations and their local realizations. Phenotype vectors are obtained by characterizing each sample by the proportions of recovered cell populations, which are, in turn, used to predict the direction of change in disease progression for each patient. Results: We used 200 diseased and nondiseased immunophenotypic panels for training and tested the system with 36 additional AML cases collected at multiple time points. The proposed framework identified the change in direction of disease progression with accuracies of 90% (nine out of ten) for relapsing cases and 100% (26 out of 26) for the remaining cases. Conclusions: We believe that these promising results are an important first step toward the development of automated predictive systems for disease monitoring and continuous response evaluation. Significance: Automated measurement and monitoring of therapeutic response is critical not only for objective evaluation of disease status prognosis but also for timely assessment of treatment strategies.
引用
收藏
页码:1089 / 1098
页数:10
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