Extended anticoagulation is recommended in subjects with cancer-associated thrombosis (CAT). The API-CAT trial showed that reduced-dose apixaban is noninferior to full-dose for preventing recurrent venous thromboembolism (VTE), but the generalizability of these findings to real-world populations remains to be determined. We conducted a multicenter retrospective cohort study including patients with CAT receiving extended direct oral anticoagulants (DOACs) at full or reduced dose, after at least 6 months of anticoagulation. The primary efficacy outcome was recurrent VTE. The primary safety outcome was major bleeding (MB) and clinically relevant non-major bleeding (CRNMB). A total of 603 patients were included, of whom 381 (63.2%) received reduced-dose and 222 (36.8%) full-dose DOACs. During a median follow-up of 335 days, recurrent VTE occurred in 3.9% of patients in the reduced-dose and 2.7% in the full-dose group (p=0.4). MB occurred in 1.0% and 0.9% (p=0.9), and CRNMB in 4.7% and 5.4% (p=0.7), respectively. In adjusted analyses, reduced-dose DOACs were associated with a non-significant increase in VTE recurrence (hazard ratio 1.4, 95% CI 0.5-3.7), with no differences in bleeding outcomes. In this multicenter real-world cohort, reduced-dose DOACs were associated with low rates of recurrent VTE and bleeding, comparable to those observed with full-dose regimens. These findings suggest that reduced-dose anticoagulation may be a feasible option in selected patients with CAT requiring extended treatment, supporting individualized decision-making. Further studies are needed to better define optimal dose selection in this setting.
https://www.thieme-connect.de/products/ejournals/abstract/10.1055/a-2904-5824
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