Developing a machine learning model for bleeding prediction in patients with cancer-associated thrombosis receiving anticoagulation therapy.
anticoagulation
bleeding
cancer-associated thrombosis
machine learning
risk assessment model
Journal
Journal of thrombosis and haemostasis : JTH
ISSN: 1538-7836
Titre abrégé: J Thromb Haemost
Pays: England
ID NLM: 101170508
Informations de publication
Date de publication:
04 Jan 2024
04 Jan 2024
Historique:
received:
23
05
2023
revised:
07
12
2023
accepted:
12
12
2023
medline:
7
1
2024
pubmed:
7
1
2024
entrez:
6
1
2024
Statut:
aheadofprint
Résumé
Only one conventional score is available for assessing bleeding risk in patients with cancer-associated thrombosis (CAT): the CAT-BLEED score. Our aim was to develop a machine learning-based risk assessment model for predicting bleeding in CAT and to evaluate its predictive performance in comparison to the CAT-BLEED score. We collected 488 attributes (clinical data, biochemistry, and ICD-10 diagnosis) in 1080 unique patients with CAT. We compared CAT-BLEED score, Ridge and Lasso Logistic Regression, Random Forest, and XGBoost algorithms for predicting major bleeding or clinically relevant non-major bleeding (CRNMB) occurring 1-90 days, 1-365 days, and 90-455 days after venous thromboembolism (VTE). The predictive performances of Lasso Logistic Regression, Random Forest, and XGBoost were higher compared to the CAT-BLEED score in the prediction of bleeding occurring 1-90 days and 1-365 days. For predicting major bleeding or CRNMB 1-90 days after VTE, the CAT-BLEED score achieved a mean AUC of 0.48 ± 0.13, while Lasso Logistic Regression and XGBoost both achieved AUCs of 0.64 ± 0.12. For predicting bleeding 1-365 days after VTE, the CAT-BLEED score achieved a mean AUC of 0.47 ± 0.08, while Lasso Logistic Regression and XGBoost achieved AUCs of 0.64 ± 0.08 and 0.59 ± 0.08, respectively. This is the first machine learning risk model for bleeding prediction in patients with CAT receiving anticoagulation therapy. Its predictive performance was higher compared with the conventional CAT-BLEED score. With further development, this novel algorithm might enable clinicians to perform personalized anticoagulation strategies with improved clinical outcomes.
Sections du résumé
BACKGROUND
BACKGROUND
Only one conventional score is available for assessing bleeding risk in patients with cancer-associated thrombosis (CAT): the CAT-BLEED score.
OBJECTIVE
OBJECTIVE
Our aim was to develop a machine learning-based risk assessment model for predicting bleeding in CAT and to evaluate its predictive performance in comparison to the CAT-BLEED score.
PATIENTS/METHODS
METHODS
We collected 488 attributes (clinical data, biochemistry, and ICD-10 diagnosis) in 1080 unique patients with CAT. We compared CAT-BLEED score, Ridge and Lasso Logistic Regression, Random Forest, and XGBoost algorithms for predicting major bleeding or clinically relevant non-major bleeding (CRNMB) occurring 1-90 days, 1-365 days, and 90-455 days after venous thromboembolism (VTE).
RESULTS
RESULTS
The predictive performances of Lasso Logistic Regression, Random Forest, and XGBoost were higher compared to the CAT-BLEED score in the prediction of bleeding occurring 1-90 days and 1-365 days. For predicting major bleeding or CRNMB 1-90 days after VTE, the CAT-BLEED score achieved a mean AUC of 0.48 ± 0.13, while Lasso Logistic Regression and XGBoost both achieved AUCs of 0.64 ± 0.12. For predicting bleeding 1-365 days after VTE, the CAT-BLEED score achieved a mean AUC of 0.47 ± 0.08, while Lasso Logistic Regression and XGBoost achieved AUCs of 0.64 ± 0.08 and 0.59 ± 0.08, respectively.
CONCLUSION
CONCLUSIONS
This is the first machine learning risk model for bleeding prediction in patients with CAT receiving anticoagulation therapy. Its predictive performance was higher compared with the conventional CAT-BLEED score. With further development, this novel algorithm might enable clinicians to perform personalized anticoagulation strategies with improved clinical outcomes.
Identifiants
pubmed: 38184201
pii: S1538-7836(24)00005-9
doi: 10.1016/j.jtha.2023.12.034
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
Copyright © 2024. Published by Elsevier Inc.