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

被引:22
|
作者
Dargaud, Y. [1 ]
Negrier, C. [1 ]
Rusen, L. [2 ]
Windyga, J. [3 ]
Georgiev, P. [4 ,5 ]
Bichler, J. [6 ]
Solomon, C. [6 ,7 ]
Knaub, S. [6 ]
Lissitchkov, T. [8 ]
Klamroth, R. [9 ]
机构
[1] Univ Lyon, Hop Cardiol Louis Pradel, Lyon, France
[2] Sanador SRL, Bucharest, Romania
[3] Inst Haematol & Transfus Med, Dept Disorders Haemostasis & Internal Med, Warsaw, Poland
[4] Univ Multiprofile Hosp Act Treatment Sveti Georgi, Clin Haematol, Plovdiv, Bulgaria
[5] Med Univ, Plovdiv, Bulgaria
[6] Octapharma AG, Lachen, Switzerland
[7] Paracelsus Med Univ, Salzburg Univ Hosp, Dept Anesthesiol Perioperat Care & Gen Intens Car, Salzburg, Austria
[8] Specialized Hosp Act Treatment Joan Pavel, Dept Clin Haematol Haemorrhag Diathesis & Anaemia, Sofia, Bulgaria
[9] Vivantes Klinikum Friedrichshain, Berlin, Germany
关键词
bleeding; endogenous thrombin potential; factor VIII; haemophilia A; prophylaxis; thrombin generation; FACTOR-VIII LEVELS; COMMUNICATION; MANAGEMENT; ASSAYS; FVIII; SSC;
D O I
10.1111/hae.13493
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IntroductionFor individuals with haemophilia A, prophylaxis with factor VIII (FVIII) is typically directed towards trough activity >1IU/dL; however, some patients still experience spontaneous bleeding events (sBEs). AimAims were to evaluate relationships of endogenous thrombin potential (ETP) and FVIII:C with occurrence of clinical bleeding. MethodsGENA-21 was a prospective, open-label, phase IIIb study investigating the safety and efficacy of Nuwiq((R)) (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. ResultsBaseline 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. ConclusionsIn 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.
引用
收藏
页码:619 / 627
页数:9
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