A field study evaluating the activity of N8-GP in spiked plasma samples at clinical haemostasis laboratories.

Abstract

AimN8‐GP (turoctocog alfa pegol) is a glycoPEGylated, extended half‐life human recombinant factor VIII (FVIII) shown to be an efficacious treatment for patients with haemophilia A. Accurate monitoring of replacement therapy helps ensure proper dosing, leading to better patient care. The objective of this field study was to evaluate the accuracy and intra‐ and inter‐laboratory variabilities of N8‐GP and rAHF (Advate®) FVIII activity (FVIII:C) measurements in clinical laboratories using their routine methods and reagents.MethodsLaboratories measured plasma samples spiked with 0.03, 0.2, 0.6 and 0.9 IU/mL N8‐GP or rAHF. Samples were blinded, and laboratories were instructed to perform evaluations using their routine FVIII activity assays and calibrators.ResultsOf the 67 participating laboratories from 25 countries, 60 used a one‐stage assay, 36 used a chromogenic assay, and 29 used both one‐stage and chromogenic assays. Participating laboratories used nine different activated partial thromboplastin time (aPTT) reagents, the most common being SynthASil® and Actin® FS. Most aPTT reagents recovered N8‐GP close to target. Three silica‐based aPTT reagents (APTT‐SP, TriniCLOT™ and STA® PTT‐Automate) underestimated N8‐GP, recovering 40%‐83% of target concentration. For chromogenic assays, N8‐GP and rAHF recoveries were comparable at all concentrations, with overall mean recoveries for both products close to 130%. Assay variability was similar for both assay types and both products; inter‐laboratory variability was greater than intra‐laboratory variability and highest at 0.03 IU/mL.ConclusionsMost clinical laboratories accurately measured N8‐GP and rAHF when using their in‐house one‐stage or chromogenic FVIII:C assays. However, three silica‐based aPTT reagents underestimated N8‐GP recovery.