Key result
Factor XI/XIa inhibitors do not significantly increase bleeding vs. placebo in hemodialysis patients.
Why the study?
Preclinical evidence suggests FXI/XIa inhibition prevents thrombosis without impeding hemostasis, which is promising for patients with ESKD on hemodialysis who are at high risk for both thromboembolism and bleeding.
Do Factor XI/XIa inhibitors prevent thromboembolic events without increasing bleeding risk in patients with end-stage kidney disease on hemodialysis?
Meta-Analysis (n=1,270)
Do Factor XI/XIa inhibitors prevent thromboembolic events without increasing bleeding risk in patients with end-stage kidney disease on hemodialysis?
Odds Ratio: 0.8 (95% CI 0.47–1.35)
In patients with end-stage kidney disease on hemodialysis, factor XI/XIa inhibitors did not significantly increase bleeding risk compared to placebo, demonstrating a promising safety profile that warrants adequately powered phase 3 trials to evaluate efficacy.
Supports phase 3 efficacy trials in hemodialysis; extends safety data for FXI/XIa inhibitors.
Introduction: Factor XI/XIa (FXI/XIa) has emerged as a potential target for antithrombotic therapy, driven by preclinical evidence showing the role of FXI/XIa inhibition for preventing thrombosis without impeding hemostasis. This is particularly promising for patients at high risk of both thromboembolic events and bleeding, such as patients with end-stage kidney disease (ESKD) on hemodialysis (HD). Methods: We systematically searched Embase, MEDLINE, and ClinicalTrials.gov for randomized controlled trials evaluating FXI/XIa inhibitors in patients with ESKD on HD, without restricting inclusion to specific comparators or indications. Interventional treatment arms were pooled, and study results were synthesized by fitting random-effects models, calculating odds ratios (ORs) and 95% confidence intervals (CIs). Results: osocimab, or fesomersen in the general HD population and using placebo as a comparator. Four studies were fully published and included in the meta-analysis. Use of FXI/XIa inhibitors was associated with an OR of 0.80 (95% CI = 0.47-1.35) for clinically relevant bleeding, 0.51 (95% CI = 0.21-1.28) for major bleeding, and 0.90 (95% CI = 0.49-1.68) for clinically relevant nonmajor bleeding. The ORs for thromboembolic events and all-cause mortality were 0.66 (95% CI = 0.28-1.56) and 0.46 (95% CI = 0.15-1.40), respectively. Conclusion: Currently available evidence does not indicate a significantly increased bleeding risk of FXI/XIa inhibitors in patients with ESKD on HD compared to placebo. Their efficacy and their association with all-cause mortality need to be investigated in sufficiently powered, randomized controlled phase 3 trials.
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Steiner et al. (2024) conducted a meta-analysis in End-stage kidney disease (ESKD) on hemodialysis (n=1,270). Factor XI/XIa inhibitors vs. Placebo was evaluated on Clinically relevant bleeding (OR 0.80, 95% CI 0.47-1.35). Factor XI/XIa inhibitors did not significantly increase the risk of clinically relevant bleeding compared to placebo in patients with end-stage kidney disease on hemodialysis (OR 0.80).
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