Longitudinal clinical data improve survival prediction after hematopoietic cell transplantation using machine learning

Author:

Zhou Yiwang1,Smith Jesse1ORCID,Keerthi Dinesh2,Li Cai1ORCID,Sun Yilun1,Mothi Suraj Sarvode1,Shyr David C.3,Spitzer Barbara4,Harris Andrew4ORCID,Chatterjee Avijit5,Chatterjee Subrata5ORCID,Shouval Roni67,Naik Swati2,Bertaina Alice3ORCID,Boelens Jaap Jan4ORCID,Triplett Brandon M.2ORCID,Tang Li1ORCID,Sharma Akshay2ORCID

Affiliation:

1. 1Department of Biostatistics, St. Jude Children’s Research Hospital, Memphis, TN

2. 2Department of Bone Marrow Transplantation and Cellular Therapy, St. Jude Children’s Research Hospital, Memphis, TN

3. 3Division of Hematology, Oncology, Stem Cell Transplantation and Regenerative Medicine, Department of Pediatrics, Stanford University School of Medicine, Palo Alto, CA

4. 4Department of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, NY

5. 5Digital, Informatics and Technology Solutions, Memorial Sloan Kettering Cancer Center, New York, NY

6. 6Adult Bone Marrow Transplantation Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY

7. 7Department of Medicine, Weill Cornell Medical College, New York, NY

Abstract

Abstract Serial prognostic evaluation after allogeneic hematopoietic cell transplantation (allo-HCT) might help identify patients at high risk of lethal organ dysfunction. Current prediction algorithms based on models that do not incorporate changes to patients’ clinical condition after allo-HCT have limited predictive ability. We developed and validated a robust risk-prediction algorithm to predict short- and long-term survival after allo-HCT in pediatric patients that includes baseline biological variables and changes in the patients’ clinical status after allo-HCT. The model was developed using clinical data from children and young adults treated at a single academic quaternary-care referral center. The model was created using a randomly split training data set (70% of the cohort), internally validated (remaining 30% of the cohort) and then externally validated on patient data from another tertiary-care referral center. Repeated clinical measurements performed from 30 days before allo-HCT to 30 days afterwards were extracted from the electronic medical record and incorporated into the model to predict survival at 100 days, 1 year, and 2 years after allo-HCT. Naïve-Bayes machine learning models incorporating longitudinal data were significantly better than models constructed from baseline variables alone at predicting whether patients would be alive or deceased at the given time points. This proof-of-concept study demonstrates that unlike traditional prognostic tools that use fixed variables for risk assessment, incorporating dynamic variability using clinical and laboratory data improves the prediction of mortality in patients undergoing allo-HCT.

Publisher

American Society of Hematology

Subject

Hematology

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