Journal of thrombosis and haemostasis : JTH · 2025
Reduced vs full-dose direct oral anticoagulants for extended treatment of cancer-associated venous thromboembolism: a systematic review and meta-analysis of randomized trials.
СтатьяСистематический обзорМетаанализНазвание и аннотация: Перевод в очереди
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de Lucena Larissa A, Duarte Amanda G, Hespanhol Larissa C, Muniz Juliana, Félix Nicole, Medeiros Kleyton, Gibson C Michael
Аннотация
BACKGROUND: Patients with cancer-associated venous thromboembolism (VTE) are at high risk of recurrent thrombosis and bleeding during prolonged anticoagulation. While full-dose direct oral anticoagulants (DOACs) are widely used, the safety and efficacy of reduced-dose regimens for extended treatment remain uncertain.
OBJECTIVES: This study compared the safety and efficacy of reduced-dose vs full-dose DOACs in the extended treatment of cancer-associated VTE.
METHODS: We conducted a systematic review and meta-analysis of randomized controlled trials comparing reduced- and full-dose DOACs in adults with active cancer and VTE. Searches were performed in PubMed, Embase, and the Cochrane Library. The primary outcomes were a composite of VTE recurrence, major bleeding, or clinically relevant nonmajor bleeding, and the combined risk of major or clinically relevant nonmajor bleeding.
RESULTS: Three randomized controlled trials comprising 2361 patients were included. Two trials evaluated apixaban 2.5 mg vs 5 mg twice daily, and 1 evaluated rivaroxaban 10 mg vs 20 mg once daily. Reduced-dose DOACs were associated with a lower risk of the composite outcome (relative risk, 0.77; 95% CI, 0.64-0.93; P = .006) and reduced bleeding (relative risk, 0.76; 95% CI, 0.62-0.93; P = .008) than full-dose DOACs. No significant differences were observed in major bleeding, clinically relevant nonmajor bleeding, VTE recurrence, or all-cause mortality when analyzed individually.
CONCLUSIONS: Reduced-dose DOACs appear as effective as full-dose regimens for extended treatment of cancer-associated VTE, with a lower risk of bleeding. These findings support their use as a safer long-term anticoagulation strategy in selected patients.
OBJECTIVES: This study compared the safety and efficacy of reduced-dose vs full-dose DOACs in the extended treatment of cancer-associated VTE.
METHODS: We conducted a systematic review and meta-analysis of randomized controlled trials comparing reduced- and full-dose DOACs in adults with active cancer and VTE. Searches were performed in PubMed, Embase, and the Cochrane Library. The primary outcomes were a composite of VTE recurrence, major bleeding, or clinically relevant nonmajor bleeding, and the combined risk of major or clinically relevant nonmajor bleeding.
RESULTS: Three randomized controlled trials comprising 2361 patients were included. Two trials evaluated apixaban 2.5 mg vs 5 mg twice daily, and 1 evaluated rivaroxaban 10 mg vs 20 mg once daily. Reduced-dose DOACs were associated with a lower risk of the composite outcome (relative risk, 0.77; 95% CI, 0.64-0.93; P = .006) and reduced bleeding (relative risk, 0.76; 95% CI, 0.62-0.93; P = .008) than full-dose DOACs. No significant differences were observed in major bleeding, clinically relevant nonmajor bleeding, VTE recurrence, or all-cause mortality when analyzed individually.
CONCLUSIONS: Reduced-dose DOACs appear as effective as full-dose regimens for extended treatment of cancer-associated VTE, with a lower risk of bleeding. These findings support their use as a safer long-term anticoagulation strategy in selected patients.