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
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.

Auteurs

Aleksandra G Grdinic (AG)

Department of Cardiology, Østfold Hospital, Sarpsborg, Norway; Department of Research, Østfold Hospital, Sarpsborg, Norway. Electronic address: aleksandragg@outlook.com.

Sandro Radovanovic (S)

University of Belgrade, Faculty of Organizational Sciences.

Jostein Gleditsch (J)

Department of Radiology, Østfold Hospital, Sarpsborg, Norway; Institute of Clinical Medicine, University of Oslo, Oslo, Norway.

Camilla Tøvik Jørgensen (CT)

Institute of Clinical Medicine, University of Oslo, Oslo, Norway; Department of Emergency medicine, Østfold Hospital, Sarpsborg, Norway.

Elia Asady (E)

Department of Research, Østfold Hospital, Sarpsborg, Norway; Institute of Clinical Medicine, University of Oslo, Oslo, Norway.

Heidi Hassel Pettersen (HH)

Department of Research, Østfold Hospital, Sarpsborg, Norway.

Boris Delibasic (B)

University of Belgrade, Faculty of Organizational Sciences.

Waleed Ghanima (W)

Department of Research, Østfold Hospital, Sarpsborg, Norway; Institute of Clinical Medicine, University of Oslo, Oslo, Norway; Department of hematology, Oslo University Hospital, Norway.

Classifications MeSH