Machine learning applications for prediction of relapse in childhood acute lymphoblastic leukemia

The prediction of relapse in childhood acute lymphoblastic leukemia (ALL) is a critical factor for successful treatment and follow-up planning. Our goal was to construct an ALL relapse prediction model based on machine learning algorithms. Monte Carlo cross-validation nested by 10-fold cross-validat...

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Published inScientific reports Vol. 7; no. 1; pp. 7402 - 9
Main Authors Pan, Liyan, Liu, Guangjian, Lin, Fangqin, Zhong, Shuling, Xia, Huimin, Sun, Xin, Liang, Huiying
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 07.08.2017
Nature Publishing Group
Nature Portfolio
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Summary:The prediction of relapse in childhood acute lymphoblastic leukemia (ALL) is a critical factor for successful treatment and follow-up planning. Our goal was to construct an ALL relapse prediction model based on machine learning algorithms. Monte Carlo cross-validation nested by 10-fold cross-validation was used to rank clinical variables on the randomly split training sets of 336 newly diagnosed ALL children, and a forward feature selection algorithm was employed to find the shortest list of most discriminatory variables. To enable an unbiased estimation of the prediction model to new patients, besides the split test sets of 150 patients, we introduced another independent data set of 84 patients to evaluate the model. The Random Forest model with 14 features achieved a cross-validation accuracy of 0.827 ± 0.031 on one set and an accuracy of 0.798 on the other, with the area under the curve of 0.902 ± 0.027 and 0.904, respectively. The model performed well across different risk-level groups, with the best accuracy of 0.829 in the standard-risk group. To our knowledge, this is the first study to use machine learning models to predict childhood ALL relapse based on medical data from Electronic Medical Record, which will further facilitate stratification treatments.
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ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-017-07408-0