A Crowdsourcing Approach to Developing and Assessing Prediction Algorithms for AML Prognosis.
David P NorenByron L LongRaquel NorelKahn RrhissorrakraiKenneth HessChenyue Wendy HuAlex J BisbergAndre SchultzErik EngquistLi LiuXihui LinGregory M ChenHonglei XieGeoffrey A M HunterPaul C BoutrosOleg A Stepanovnull nullThea NormanStephen H FriendGustavo StolovitzkySteven KornblauAmina A QutubPublished in: PLoS computational biology (2016)
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.
Keyphrases
- acute myeloid leukemia
- end stage renal disease
- ejection fraction
- newly diagnosed
- chronic kidney disease
- peritoneal dialysis
- high resolution
- prognostic factors
- allogeneic hematopoietic stem cell transplantation
- case report
- immune response
- systemic lupus erythematosus
- mass spectrometry
- machine learning
- patient reported outcomes
- stem cells
- dna methylation
- bone marrow
- drug delivery
- gene expression
- patient reported
- cell therapy
- climate change
- genome wide
- extracorporeal membrane oxygenation
- squamous cell