Evidence map›Paper›PMID 41992635›Full record

ArticleCancer medicine2026

Direct Oral Anticoagulants Versus Low-Molecular-Weight Heparin for Treating Venous Thromboembolism in Patients With Gastrointestinal Cancer.

Wei-Ting Chang, Mei-Chuan Lee, Hui-Wen Lin, Sheng-Hsiang Lin, Yi-Heng Li

Abstract readComparative Study
In one paragraph

Article in Cancer medicine, 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

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

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

5 authors.

Wei-Ting ChangSchool of Medicine and Doctoral Program of Clinical and Experimental Medicine, College of Medicine and Center of Excellence for Metabolic Associated Fatty Liver Disease, National Sun Yat-sen University, Kaohsiung, Taiwan.
Mei-Chuan LeeDepartment of Pharmacy, Chi Mei Medical Center, Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Hui-Wen LinDepartment of Internal Medicine, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Sheng-Hsiang LinDepartment of Public Health, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Yi-Heng LiDepartment of Internal Medicine, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.ORCID https://orcid.org/0000-0003-3160-1143

Funding

Chi Mei Medical CenterNational Cheng Kung University HospitalNational Science and Technology Council NSTC 113-2314-B-110-004-MY3
6 · The paper itself

Abstract

backgroundDirect oral anticoagulants (DOACs) have demonstrated non-inferiority to low-molecular-weight heparin (LMWH) for preventing recurrent venous thromboembolism (VTE) in cancer-associated thrombosis. However, patients with gastrointestinal (GI) cancer receiving DOACs have reported increased major bleeding events. Hereby, we aim to compare the risks of recurrent thromboembolism and bleeding between those treated with DOACs and LMWH.

methodsUsing Taiwan's National Health Insurance Research Database, we retrospectively identified GI cancer patients with newly diagnosed VTE from 2011 to 2020. Outcomes were recurrent VTE and major bleeding. Covariate balancing was performed using inverse probability weighting, and Cox proportional hazards models compared risks, with a competing risk model for death. Follow-up was 12 months.

resultsAmong 1895 patients (1038 on DOACs, 857 on enoxaparin), recurrent VTE occurred in 20.71% of DOAC and 19.25% of enoxaparin patients. Competing risk analysis showed relatively higher recurrent VTE risk with DOACs (subdistribution HR, 1.27; 95% CI, 1.09-1.48; p < 0.01). Regarding composite bleeding risk, DOACs were similar compared with LMWH (subdistribution HR, 0.99; 95% CI, 0.68-1.45; p = 0.97). However, DOACs presented with an increased GI bleeding risk (subdistribution HR, 2.59; 95% CI, 1.48-4.54; p < 0.01) but a reduced intracranial hemorrhage risk (subdistribution HR, 0.35; 95% CI, 0.16-0.78; p = 0.01).

conclusionsCompared with DOACs, LMWH expressed a lower risk of recurrent VTE in GI cancer patients. However, DOAC presented with a lower intracranial hemorrhage risk but a higher GI bleeding risk. Further research is needed to confirm these findings.

Indexed as

AnticoagulantsFactor Xa InhibitorsGastrointestinal NeoplasmsHeparin, Low-Molecular-WeightVenous ThromboembolismAdministration, OralAgedAged, 80 and overFemaleHemorrhageHumansMaleMiddle AgedRecurrenceRetrospective StudiesRisk FactorsAnticoagulantsFactor Xa InhibitorsHeparin, Low-Molecular-Weightgastrointestinal cancerlow molecular‐weight heparinoral anticoagulantsvenous thromboembolism

Identifiers

PMID41992635
PMCPMC13087435

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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.