The LEukemia Artificial Intelligence Program (LEAP) in chronic myeloid leukemia in chronic phase: A model to improve patient outcomes

Extreme gradient boosting methods outperform conventional machine‐learning models. Here, we have developed the LEukemia Artificial intelligence Program (LEAP) with the extreme gradient boosting decision tree method for the optimal treatment recommendation of tyrosine kinase inhibitors (TKIs) in pati...

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Published inAmerican journal of hematology Vol. 96; no. 2; pp. 241 - 250
Main Authors Sasaki, Koji, Jabbour, Elias J., Ravandi, Farhad, Konopleva, Marina, Borthakur, Gautam, Wierda, William G., Daver, Naval, Takahashi, Koichi, Naqvi, Kiran, DiNardo, Courtney, Montalban‐Bravo, Guillermo, Kanagal‐Shamanna, Rashmi, Issa, Ghayas, Jain, Preetesh, Skinner, Jeffrey, Rios, Mary B., Pierce, Sherry, Soltysiak, Kelly A., Sato, Junya, Garcia‐Manero, Guillermo, Cortes, Jorge E.
Format Journal Article
LanguageEnglish
Published Hoboken, USA John Wiley & Sons, Inc 01.02.2021
Wiley Subscription Services, Inc
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Summary:Extreme gradient boosting methods outperform conventional machine‐learning models. Here, we have developed the LEukemia Artificial intelligence Program (LEAP) with the extreme gradient boosting decision tree method for the optimal treatment recommendation of tyrosine kinase inhibitors (TKIs) in patients with chronic myeloid leukemia in chronic phase (CML‐CP). A cohort of CML‐CP patients was randomly divided into training/validation (N = 504) and test cohorts (N = 126). The training/validation cohort was used for 3‐fold cross validation to develop the LEAP CML‐CP model using 101 variables at diagnosis. The test cohort was then applied to the LEAP CML‐CP model and an optimum TKI treatment was suggested for each patient. The area under the curve in the test cohort was 0.81899.Backward multivariate analysis identified age at diagnosis, the degree of comorbidities, and TKI recommended therapy by the LEAP CML‐CP model as independent prognostic factors for overall survival. The bootstrapping method internally validated the association of the LEAP CML‐CP recommendation with overall survival as an independent prognostic for overall survival. Selecting treatment according to the LEAP CML‐CP personalized recommendations, in this model, is associated with better survival probability compared to treatment with a LEAP CML‐CP non‐recommended therapy. This approach may pave a way of new era of personalized treatment recommendations for patients with cancer.
Bibliography:Funding information
This work is supported in part by the University of Texas MD Anderson Cancer Center Support Grant from the National Institutes of Health P30 CA016672, the National Institutes of Health/National Cancer Institute under award P01 CA049639, the University of Texas MD Anderson MDS/AML Moon Shot, and Leukemia Texas.
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AUTHOR CONTRIBUTIONS
Koji Sasaki: Concept and design; provision of study materials data collection; data analysis; interpretation; and manuscript writing and final approval. Elias J. Jabbour, Farhad Ravandi, Marina Konopleva, Gautam Borthakur, William G. Wierda, Naval Daver, Koichi Takahashi, Kiran Naqvi, Courtney DiNardo, Guillermo Montalban-Bravo, Rashmi Kanagal-Shamanna, Ghayas Issa, Preetesh Jain, Jeffrey Skinner, Mary B. Rios, Sherry Pierce: Collection and assembly of data; data analysis and interpretation; manuscript writing; and final approval of manuscript. Jeffrey Skinner: Data analysis, and interpretation; and manuscript writing and final approval. Kelly A. Soltysiak: Administrative support; data analysis and interpretation; and manuscript writing and final approval. Guillermo Garcia-Manero and Jorge E. Cortes: Concept and design; administrative support; provision of study materials and patients; data collection, analysis, interpretation; and manuscript writing and final approval.
ISSN:0361-8609
1096-8652
DOI:10.1002/ajh.26047