A Crowdsourcing Approach to Developing and Assessing Prediction Algorithms for AML Prognosis
Author(s) -
David P. Noren,
Byron L. Long,
Raquel Norel,
Kahn Rrhissorrakrai,
Kenneth R. Hess,
Chenyue W. Hu,
Alex J. Bisberg,
André Schultz,
Erik Engquist,
Li Liu,
Xihui Lin,
Gregory M. Chen,
Honglei Xie,
Geoffrey A. M. Hunter,
Paul C. Boutros,
О. А. Степанов,
Thea Norman,
Stephen Friend,
Gustavo Stolovitzky,
Steven M. Kornblau,
Amina A. Qutub
Publication year - 2016
Publication title -
plos computational biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.628
H-Index - 182
eISSN - 1553-7358
pISSN - 1553-734X
DOI - 10.1371/journal.pcbi.1004890
Subject(s) - myeloid leukemia , medicine , crowdsourcing , oncology , machine learning , bioinformatics , computer science , biology , world wide web
Acute Myeloid Leukemia (AML) is a fatal hematological cancer. The genetic abnormalities underlying AML are extremely heterogeneous among patients, making prognosis and treatment selection very difficult. While clinical proteomics data has the potential to improve prognosis accuracy, thus far, the quantitative means to do so have yet to be developed. Here we report the results and insights gained from the DREAM 9 Acute Myeloid Prediction Outcome Prediction Challenge (AML-OPC), a crowdsourcing effort designed to promote the development of quantitative methods for AML prognosis prediction. We identify the most accurate and robust models in predicting patient response to therapy, remission duration, and overall survival. We further investigate patient response to therapy, a clinically actionable prediction, and find that patients that are classified as resistant to therapy are harder to predict than responsive patients across the 31 models submitted to the challenge. The top two performing models, which held a high sensitivity to these patients, substantially utilized the proteomics data to make predictions. Using these models, we also identify which signaling proteins were useful in predicting patient therapeutic response.
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