Analysis of Complete Blood Count Data and Use in Classification Machine Learning Models to Predict Icans Incidence Following CAR-T Cell Therapy

• Published in: Transplantation and cellular therapy 2024-02, Vol.30 (2), p.S133-S134
• Main Authors: Olesnavich, Mary, Sandford, Erin, Ly, Andrew, Canbaz, Ata, Rozwadowski, Michelle, Valle, Bengie Ortiz-Del, Kumar, Rajnish, Tang, Shengpu, Bonifant, Challice L, Jain, Dr. Tania, Choi, Sung Won, Tewari, Muneesh
• Format: Article
• Language: English
• ISSN: 2666-6367; 2666-6367
• DOI: 10.1016/j.jtct.2024.01.027

CD19 directed CAR-T cell therapies are increasingly used for treatment of hematological malignancies, however immune cell-associated neurotoxicity syndrome (ICANS), remains a challenge to predict and treat. We retrieved demographic and complete blood count (CBC) data from electronic health records (EHR) to evaluate whether this simple, accessible, and routinely collected data could be used to train classification machine learning (ML) models for prediction of ICANS. Demographic and CBC measures from n=96 patients treated for B-cell malignancies at the University of Michigan (UM) were analyzed for univariate significance at baseline (prior to lymphodepletion) and through day (D) 3 post CAR-T infusion. Complete datasets were available for n=76 patients. These were then used for feature selection and ML model training. Features found significant were used as inputs in binary classification models to predict ICANS incidence within 20 days post-infusion. Models were validated using data from a test set of n=29 patients treated at Johns Hopkins Hospital (JHH). Data analysis was completed in RStudio-4.1.3, R Core Team 2022. Overall incidence of ICANS was 45% in the training set (UM) and 34% in the test set (JHH). While baseline data alone was not predictive, between D0 and D3, univariate analysis revealed lymphocyte count, monocyte count, red blood cell count, hemoglobin, hematocrit, C-reactive protein, ferritin, and white blood cell count as differentially associated with patients that developed Grade 3 ICANS versus those that developed Grade 1-2 or No ICANS. On D0 (after lymphodepletion and prior to CAR-T cell infusion), the combination of C-reactive protein, monocyte count, red blood cell count, and age used in ML models were able to predict incidence of any grade ICANS with an AU-ROC of 0.80-0.82, MCC=0.51-0.54, and F1=0.74-0.76. This model was robust to validation in the independent test set cohort (i.e., JHH patients), with an AU-ROC of 0.92-0.95, MCC=0.63-0.85, and F1=0.67-0.90. ML-based classification using CBC data and commonly measured clinical blood analytes holds promise for ICANS prediction. Future work may integrate additional blood- clinical-, and/or digital-based biomarkers from other predictive models of ICANS to develop further improved models. Our findings suggest that ML-based models may be able to risk-stratify patients receiving CAR-T therapy, to identify those who may benefit from close monitoring and/or early therapeutic intervention to pr