Full-dose or reduced-dose DOACs in high-risk VTE on extended therapy?

For VTE patients who needed extended anticoagulation, a reduced DOAC dose did not meet non-inferiority criteria for efficacy, compared to full DOACs.

Clinically-relevant major bleeding more common in the full-dose arm

The phase 3 RENOVE trial (NCT03285438) investigated whether a reduced dose of DOACs is a valid option in patients with VTE who need extended anticoagulant therapy1. Patients with VTE at high risk of recurrence (n=2,768) received standard anticoagulation therapy for 6–24 months. Hereafter, they were randomised to receive a reduced dose of DOACs (2.5 mg apixaban twice daily or 10 mg rivaroxaban once daily) or a full dose of DOACs (5.0 mg apixaban twice daily or 20 mg rivaroxaban once daily). The primary outcome was adjudicated symptomatic recurrent VTE.

The 5-year cumulative incidence of symptomatic recurrent VTE was 2.2% in the reduced-dose arm and 1.8% in the full-dose arm (adjusted HR 1.32; 95% CI 0.67–2.60; Pnon-inferiority=0.23). “With these rates, the reduced-dose arm did not meet the trial’s non-inferiority criteria,” explained Prof. Francis Couturaud (Brest University Hospital, France).

The corresponding annual incidence rates were 0.50% and 0.40%, respectively. Clinically relevant major bleeding was more common in the full-dose arm than in the reduced-dose arm (15.2% vs 9.9%; adjusted HR 0.61; 95% CI 0.48–0.79). Furthermore, looking at a composite of recurrent VTE or clinically relevant bleeding, the reduced-dose arm appeared to perform better than the full-dose arm (11.8% vs 16.5%; adjusted HR 0.67; 95% CI 0.53–0.86).

“These findings will be useful to strengthen future guidelines and enrich shared decision-making processes for patients with VTE who need extended anticoagulation,” concluded Prof. Couturaud.

Medical writing support was provided by Robert van den Heuvel.

Source
  1. Couturaud F, et al. Extended treatment of venous thromboembolism with reduced- vs full-dose direct oral anticoagulants in patients at high risk of recurrence. Late-breaking Abstract 3, 66th ASH Annual Meeting, 7–10 December 2024, San Diego, CA, USA.