Literature DB >> 29855112

Individual thrombin generation and spontaneous bleeding rate during personalized prophylaxis with Nuwiq® (human-cl rhFVIII) in previously treated patients with severe haemophilia A.

Y Dargaud1, C Negrier1, L Rusen2, J Windyga3, P Georgiev4, J Bichler5, C Solomon5,6, S Knaub5, T Lissitchkov7, R Klamroth8.   

Abstract

INTRODUCTION: For individuals with haemophilia A, prophylaxis with factor VIII (FVIII) is typically directed towards trough activity >1 IU/dL; however, some patients still experience spontaneous bleeding events (sBEs). AIM: Aims were to evaluate relationships of endogenous thrombin potential (ETP) and FVIII:C with occurrence of clinical bleeding.
METHODS: GENA-21 was a prospective, open-label, phase IIIb study investigating the safety and efficacy of Nuwiq® (human-cl rhFVIII) in previously treated adults with severe haemophilia A. The study included a 72-hour pharmacokinetic (PK) evaluation phase and a 6-month personalized prophylaxis phase in which treatment was guided by PK parameters. This subanalysis assessed FVIII:C by one-stage assay and ETP by thrombin generation assay in blood samples.
RESULTS: Baseline mean ETP was lower in the 7 patients who experienced sBEs during personalized prophylaxis versus 25 who did not (n = 32 with data from PK phase and prophylaxis phase; P = .0002). During personalized prophylaxis (n = 49), only patients with lower median trough ETP experienced sBEs (8/49 patients; ROC AUC = 0.9421; P < .0001); there was no significant relationship for FVIII:C in predicting sBEs (ROC AUC = 0.5838; P = .4750). Directly following infusion of human-cl rhFVIII, ETP was lower in patients who experienced sBEs versus those who did not (P = .0002), whereas FVIII:C did not differ significantly between these groups.
CONCLUSIONS: In adults with severe haemophilia A and reduced thrombin generation, increased frequency of spontaneous bleeding was observed irrespective of trough FVIII levels. Thus, personalized prophylaxis should take into account variables other than FVIII:C. Large prospective trials are needed to verify ETP as a marker for spontaneous bleeding.
© 2018 John Wiley & Sons Ltd.

Entities:  

Keywords:  bleeding; endogenous thrombin potential; factor VIII; haemophilia A; prophylaxis; thrombin generation

Mesh:

Substances:

Year:  2018        PMID: 29855112     DOI: 10.1111/hae.13493

Source DB:  PubMed          Journal:  Haemophilia        ISSN: 1351-8216            Impact factor:   4.287


  5 in total

1.  Applicability of the Thrombin Generation Test to Evaluate the Hemostatic Status of Hemophilia A Patients in Daily Clinical Practice.

Authors:  Ángel Bernardo; Alberto Caro; Daniel Martínez-Carballeira; José Ramón Corte; Sonia Vázquez; Carmen Palomo-Antequera; Alfredo Andreu; Álvaro Fernández-Pardo; Julia Oto; Laura Gutiérrez; Inmaculada Soto; Pilar Medina
Journal:  J Clin Med       Date:  2022-06-10       Impact factor: 4.964

2.  Monitoring standard and extended half-life products in hemophilia: Assay discrepancies for factor VIII and IX in pre- and postinfusion samples.

Authors:  Cecilia Augustsson; Eva Norström; Nadine Gretenkort Andersson; Eva Zetterberg; Jan Astermark; Karin Strandberg
Journal:  Res Pract Thromb Haemost       Date:  2020-08-11

Review 3.  Thrombin generation for monitoring hemostatic therapy in hemophilia A: A narrative review.

Authors:  Marieke J A Verhagen; Lars L F G Valke; Saskia E M Schols
Journal:  J Thromb Haemost       Date:  2022-01-28       Impact factor: 16.036

4.  Combining factor VIII levels and thrombin/plasmin generation: A population pharmacokinetic-pharmacodynamic model for patients with haemophilia A.

Authors:  Laura H Bukkems; Lars L F G Valke; Wideke Barteling; Britta A P Laros-van Gorkom; Nicole M A Blijlevens; Marjon H Cnossen; Waander L van Heerde; Saskia E M Schols; Ron A A Mathôt
Journal:  Br J Clin Pharmacol       Date:  2022-01-15       Impact factor: 3.716

5.  Pharmacodynamic monitoring of factor VIII replacement therapy in hemophilia A: Combining thrombin and plasmin generation.

Authors:  Lars L F G Valke; Laura H Bukkems; Wideke Barteling; Britta A P Laros-van Gorkom; Nicole M A Blijlevens; Ron A A Mathôt; Waander L van Heerde; Saskia E M Schols
Journal:  J Thromb Haemost       Date:  2020-10-21       Impact factor: 16.036

  5 in total

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