Key result
API-CAT tests if reduced-dose apixaban is noninferior to full-dose for recurrent VTE in active cancer.
Why the study?
Extended anticoagulation for cancer-associated thrombosis carries a risk of bleeding, leaving an open question whether a reduced-dose regimen can maintain efficacy while lowering bleeding risk.
Does a reduced-dose regimen of apixaban (2.5 mg twice daily) prevent recurrent VTE non-inferiorly to a full-dose regimen (5 mg twice daily) in patients with active cancer who have completed ≥6 months of anticoagulant therapy?
RCT (n=1,722)
Double-blind
1:1
Yes
Does a reduced-dose regimen of apixaban (2.5 mg twice daily) prevent recurrent VTE non-inferiorly to a full-dose regimen (5 mg twice daily) in patients with active cancer who have completed ≥6 months of anticoagulant therapy?
The API-CAT trial is designed to evaluate whether a reduced dose of apixaban is noninferior to a full dose for the extended treatment of cancer-associated venous thromboembolism, potentially reducing bleeding risk.
API-CAT will test reduced-dose apixaban noninferiority for extended cancer VTE prevention; extends evidence on balancing recurrence and bleeding risk.
Cancer-associated thrombosis (CT) is associated with a high risk of recurrent venous thromboembolic (VTE) events that require extended anticoagulation in patients with active cancer, putting them at risk of bleeding. The aim of the API-CAT study (NCT03692065) is to assess whether a reduced-dose regimen of apixaban (2.5 mg twice daily [bid]) is noninferior to a full-dose regimen of apixaban (5 mg bid) for the prevention of recurrent VTE in patients with active cancer who have completed ≥6 months of anticoagulant therapy for a documented index event of proximal deep-vein thrombosis and/or pulmonary embolism. API-CAT is an international, randomized, parallel-group, double-blind, noninferiority trial with blinded adjudication of outcome events. Consecutive patients are randomized to receive apixaban 2.5 or 5 mg bid for 12 months. The primary efficacy outcome is a composite of recurrent symptomatic or incidental VTE during the treatment period. The principal safety endpoint is clinically relevant bleeding, defined as a composite of major bleeding or nonmajor clinically relevant bleeding. Assuming a 12-month incidence of the primary outcome of 4% with apixaban and an upper limit of the two-sided 95% confidence interval of the hazard ratio <2.0, 1,722 patients will be randomized, assuming an up to 10% loss in total patient-years (β = 80%; α one-sided = 0.025). This trial has the potential to demonstrate that a regimen of extended treatment for patients with CT beyond an initial 6 months, with a reduced apixaban dose, has an acceptable risk of recurrent VTE recurrence and decreases the risk of bleeding.
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Mahé et al. (2021) conducted an RCT in Cancer-Associated Venous Thromboembolism (n=1,722). Apixaban vs. Apixaban 5 mg twice daily was evaluated on Composite of adjudicated recurrent symptomatic VTE or incidental VTE, or death due to PE. The API-CAT study is designed to evaluate whether reduced-dose apixaban (2.5 mg twice daily) is noninferior to full-dose apixaban (5 mg twice daily) for preventing recurrent VTE in patients with active cancer.
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