Original article

Blood Transfusion - 5 2020 (September-October)

Optimising prophylaxis outcomes and costs in haemophilia patients switching to recombinant FVIII-Fc: a single-centre real-world experience

Authors

Key words: extended half-life rFVIII, rFVIII-Fc, haemophilia, pharmacokinetics, prophylaxis
Publication Date: 2020-11-04

Abstract

Background. The recombinant factor VIII (rFVIII)-IgG1 Fc fusion protein (rFVIII-Fc) was the first available extended half-life rFVIII, shown to prolong dosing intervals of individualised prophylaxis in patients with severe haemophilia A, maintaining low bleeding rates and unchanged or lower FVIII dose versus standard half-life (SHL) rFVIII. Few data are available about real-world experience with rFVIII-Fc, including criteria for patient switching from SHL products, follow up and prophylaxis optimisation.
Materials and methods. A single-centre retrospective study was designed to review patients switched to rFVIII-Fc, based on individual needs, after pharmacokinetic (PK) assessment, according to routine clinical practice. In patients with adequate post-switch follow up, data about rFVIII-Fc prophylaxis were compared with those from the last 18-months SHL rFVIII prophylaxis.
Results. Of 25 candidates, 18 patients (15 severe, 3 moderate; aged 9-62 years; 3 with inhibitor history) started rFVIII-Fc regimens, with comparable FVIII weekly dose and reduced infusion frequency (mean −30%) in all 17 patients previously on SHL rFVIII prophylaxis thrice weekly or every other day. Over a mean 18-month follow up in 13 patients, compared with SHL products, further reduced infusion frequency (mean −40%; p<0.001; interval ≥4 days in 9 patients), improved treatment satisfaction (Hemo-sat questionnaires), significantly lower FVIII weekly dose and annual consumption (mean −12%; p=0.019), comparable bleeding rates and FVIII trough levels, and improved management of breakthrough bleeding were observed. von Willebrand Factor Antigen (VWF:Ag) correlated to PK variables and both had relationships with rFVIII-Fc weekly dose, increasing statistical significance over the follow-up period. No inhibitors or drug-related adverse events were recorded.
Discussion. In this real-world series of patients, a switch to rFVIII-Fc, based on careful assessment of clinical needs, PK testing and treatment monitoring, was able to optimise individual convenience, efficacy and costs of prophylaxis.

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Authors

Annarita Tagliaferri Regional Reference Centre for Inherited Bleeding Disorders

Annalisa Matichecchia Regional Reference Centre for Inherited Bleeding Disorders

Gianna F. Rivolta Regional Reference Centre for Inherited Bleeding Disorders

Federica Riccardi Regional Reference Centre for Inherited Bleeding Disorders

Gabriele Quintavalle Regional Reference Centre for Inherited Bleeding Disorders

Anna Benegiamo Laboratory of Coagulation, Department of Diagnostics, University Hospital of Parma, Parma, Italy

Antonio Coppola Laboratory of Coagulation, Department of Diagnostics, University Hospital of Parma, Parma, Italy

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