Comparison of one‐stage and chromogenic factor VIII assays to tailor the dose of recombinant factor VIII‐Fc fusion protein (rFVIIIFc, efmoroctocog alfa) in adult patients with haemophilia A: Single‐centre, real‐world experience of surgery

Abstract

AbstractBackgroundEfmoroctocog alfa (rFVIIIFc) is an extended half‐life FVIII used notably in surgery for patients with haemophilia A. More information is needed of its usage in real‐life.MethodsAdult patients with HA followed at the Lyon Comprehensive Hemophilia Care Center who underwent a surgery with rFVIIIFc were included in this retrospective analysis. The pharmacokinetics of rFVIIIFc was assessed by plasma factor VIII clotting activity (FVIII:C) using both one‐stage (OSA) and chromogenic substrate (CSA) assays.ResultsA total of 39 major and 31 minor surgeries were performed in 49 patients treated with rFVIIIFc. The median dose of rFVIIIFc infused before major and minor surgeries respectively was 67.5 ((interquartile range [IQR] 52.6‐76.9) and 48.0 (38.5‐51.8) IU/kg. For major surgeries, during the first postoperative week, the median residual FVIII:C was 78 (64.5‐101.5) IU/dL with OSA and 99 (71‐118) IU/dL with CSA (p < .0001).After surgery, rFVIIIFc doses were adjusted according to CSA results. This led to a significant decrease of rFVIIIFc consumption compared to what would have been proposed according to the OSA assay, without unusual bleeding or appearance of inhibitor. Considering the high price of the molecule, this was also associated with a significant cost reduction.ConclusionDose adjustment of rFVIIIFc according to FVIII: C measured by CSA is effective, safe and well tolerated in patients with haemophilia A undergoing invasive surgery.