4.4 Article

Evaluation of direct oral anticoagulants versus low molecular weight heparins for venous thromboembolism treatment in patients with gastrointestinal malignancies

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JOURNAL OF THROMBOSIS AND THROMBOLYSIS
卷 56, 期 3, 页码 439-446

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SPRINGER
DOI: 10.1007/s11239-023-02858-y

关键词

Direct oral anticoagulant; DOAC; Low-molecular-weight heparin; LMWH; Venous thromboembolism; VTE; Gastrointestinal malignancies

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This study compared the safety and effectiveness of DOACs and LMWHs in the treatment of CA-VTE in patients with GI malignancies. The results showed that there was a difference in bleeding events between DOAC and LMWH, but DOAC did not increase the risk of bleeding. Careful selection of DOAC therapy is still needed for bleeding risk.
BackgroundDirect oral anticoagulant (DOAC) use in cancer-associated venous thromboembolism (CA-VTE) has increased due to updates in recent guidelines and literature. However, select guidelines caution against DOAC use in patients with gastrointestinal (GI) malignancies due to reported increased bleeding events. The objective of this study was to compare the safety and effectiveness of DOACs versus low-molecular-weight heparins (LMWHs) for CA-VTE treatment in patients with GI malignancies.Patients and methodsThis multicenter, retrospective cohort study included patients with primary GI malignancies who received therapeutic anticoagulation with a DOAC or LMWH for CA-VTE between January 1, 2018, and December 31, 2019. The primary outcome was the incidence rate of bleeding events (major, clinically relevant non-major, or minor bleeding events) within a 12-month period following the initiation of therapeutic anticoagulation. The secondary endpoint was the incidence rate of recurrent VTE events within a 12-month period following the start of therapeutic anticoagulation.ResultsAfter screening, 141 patients met inclusion criteria. The incidence rate of all bleeding events significantly differed between DOAC (4.98 events/100 person-months) and LWMH (10.2 events/100 person-months) recipients. The corresponding incidence rate ratio (IRR) with the DOAC group serving as the reference was 2.05 (p = 0.01), with the majority of bleeds in both groups presenting as minor bleeds. No difference was found between the incidence rate of recurrent VTE within a 12-month period of starting therapeutic anticoagulation between groups (IRR 3.08, p = 0.06).ConclusionOur results suggest that DOACs do not pose an additional bleeding risk compared to LMWH in patients with certain GI malignancies. Careful selection of DOAC therapy with respect to bleeding risk is still warranted.

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