Computers in biology and medicine · 2025
A machine learning framework for cross-institute standardized analysis of flow cytometry in differentiating acute myeloid leukemia from non-neoplastic conditions.
СтатьяНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Wang Yu-Fen, Chu En-Ping, Lin Fong-Ci, Chen Huan-Yu, Chen Tsung-Chih, Hanson Joseph, Tario Joseph D, Fu Kai, Monaghan Sara A, Wallace Paul K, Lee Chi-Chun, Ko Bor-Sheng
Аннотация
Flow cytometry (FC) remains a cornerstone diagnostic tool for acute myeloid leukemia (AML), yet standardizing panels across laboratories presents persistent challenges. Our study introduces a validated machine learning framework enabling cross-panel AML classification by leveraging common parameters shared across diverse FC protocols. We employed FC data from 215 samples (110 AML, 105 non-neoplastic) collected in five institutions using different panel configurations as model training set, and another 196 similarly collected samples (90 AML and 106 non-neoplastic) for independent validation set. The framework employs GMM-SVM classification based on 16 common parameters (FSC-A, FSC-H, SSC-A, CD7, CD11b, CD13, CD14, CD16, CD19, CD33, CD34, CD45, CD56, CD64, CD117, and HLA-DR) that are consistently present across various panel designs. The framework demonstrated robust performance with 98.15 % accuracy, 99.82 % area under curve (AUC), 97.30 % sensitivity, and 99.05 % specificity. Independent validation on 196 additional samples further confirmed the framework's effectiveness, maintaining high performance with 93.88 % accuracy and 98.71 % AUC. This research establishes the viability of standardized FC analysis across diverse panel configurations and instruments through machine learning implementation. The framework's robust performance suggests promising applications for harmonized multi-center FC analysis, potentially resolving current standardization challenges in flow cytometry interpretation.