Evidence map›Paper›PMID 42699731›Full record

ArticleResearch and practice in thrombosis and haemostasis2026

Integrating pharmacovigilance and machine learning: bleeding signal detection and risk prediction for oral anticoagulants in cancer patients.

Meina Lv, Xiaochun Zheng, Hang Xie, Bijuan Lin

Abstract read
In one paragraph

Article in Research and practice in thrombosis and haemostasis, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Meina LvDepartment of Pharmacy, Fujian Medical University Union Hospital, Fuzhou, Fujian, China.
Xiaochun ZhengDepartment of Pharmacy, Wuping County Hospital, Longyan, China.
Hang XieDepartment of Interventional Radiology, Fujian Medical University Union Hospital, Fuzhou, Fujian, China.
Bijuan LinDepartment of Pharmacy, Fujian Medical University Union Hospital, Fuzhou, Fujian, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Oral anticoagulants (OACs) have been widely used for the prevention and treatment of thrombosis in cancer patients, but the bleeding signals associated with different OACs in this population have not been fully studied. Objectives: This study aimed to compare bleeding signals, identify risk factors, and establish a prediction model for OACs in cancer patients. Methods: This study was based on the Food and Drug Administration Adverse Event Reporting System database and used the reporting odds ratio to evaluate the bleeding event signals associated with OACs in cancer patients from Q1 2014 to Q1 2024. Additionally, this study used a retrospective cohort design to assess the impact of OACs on bleeding risk in cancer patients. Results: This study analyzed 29,897 adverse event reports of OACs in cancer patients, which included 4084 bleeding events. We found that bleeding events were mainly concentrated within the first 2 months of medication use. Compared with apixaban, the other 4 OACs (warfarin, edoxaban, rivaroxaban, and dabigatran) showed increased risks of bleeding, especially in the gastrointestinal system. Male, cardiovascular diseases, cerebral infarction, renal insufficiency, gastrointestinal cancer, and elevated international normalized ratio are linked to an increased risk of bleeding from OACs in cancer patients. The XGBoost model was the top-performing model among the 4 bleeding prediction models (training set area under the curve = 0.788; test set area under the curve = 0.783). Conclusion: Bleeding adverse events related to OACs primarily occur early in the treatment. Apixaban shows weaker bleeding signals. Male sex, cardiovascular diseases, cerebral infarction, renal insufficiency, gastrointestinal cancer, and an elevated international normalized ratio may be potential risk factors for bleeding events. The prediction model for OACs-related bleeding developed in this study demonstrated acceptable performance in internal validation.

Indexed as

AnticoagulantsHemorrhageMachine LearningNeoplasmsPharmacovigilanceAdministration, OralAdverse Drug Reaction Reporting SystemsAgedDatabases, FactualFemaleHumansMaleMiddle AgedPrediction AlgorithmsPredictive Learning ModelsRetrospective StudiesAnticoagulantsanticoagulantsbleedingneoplasmspredictive learning modelsrisk factors

Identifiers

PMID42699731
PMCPMC13544180

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.