Literature DB >> 19943875

Factor VIII requirement to maintain a target plasma level in the prophylactic treatment of severe hemophilia A: influences of variance in pharmacokinetics and treatment regimens.

P W Collins1, S Björkman, K Fischer, V Blanchette, M Oh, P Schroth, S Fritsch, K Casey, G Spotts, B M Ewenstein.   

Abstract

BACKGROUND: Prophylactic factor (F)VIII has been shown to reduce bleeds and arthropathy in patients with severe hemophilia A.
OBJECTIVES: Assuming that the trough FVIII level is an important determinant of the efficacy of prophylaxis, this paper addresses the effect of the inter-patient variability in pharmacokinetics and different dosing regimens on trough levels.
METHODS: Simulations used FVIII half-lives and in vivo recoveries (IVR), observed during clinical trials with Advate [Antihemophilic Factor (Recombinant), Plasma/Albumin-Free Method], and commonly used prophylactic regimens to calculate their effect on FVIII levels during prophylaxis. RESULTS AND
CONCLUSIONS: Half-life and dose frequency had a larger effect on trough FVIII and time per week with FVIII<1 IU dL(-1) than IVR and infused dose per kg. The combined effect of these parameters resulted in substantial inter-patient variability in the amount of FVIII required to sustain a desired trough level. Prophylactic regimens based on Monday, Wednesday, Friday dosing were less cost effective in maintaining a desired trough level throughout the week. Dose escalation on Friday to cover the weekend would require potentially harmful doses of FVIII in many patients, especially in young children where more than 50% would require a Friday dose of over 100 IU kg(-1) and some would require more than 400 IU kg(-1). Knowledge of individual patients' half-lives and alteration of frequency of infusions may allow the more cost-effective use of FVIII and potentially expand access to prophylaxis to a greater number of patients, especially in regions where healthcare resources are scarce.

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Year:  2009        PMID: 19943875     DOI: 10.1111/j.1538-7836.2009.03703.x

Source DB:  PubMed          Journal:  J Thromb Haemost        ISSN: 1538-7836            Impact factor:   5.824


  38 in total

1.  Rationale for a randomized controlled trial comparing two prophylaxis regimens in adults with severe hemophilia A: the Hemophilia Adult Prophylaxis Trial.

Authors:  Margaret V Ragni
Journal:  Expert Rev Hematol       Date:  2011-10       Impact factor: 2.929

2.  Population pharmacokinetics of plasma-derived factor IX in adult patients with haemophilia B: implications for dosing in prophylaxis.

Authors:  Sven Björkman; Victor Ahlén
Journal:  Eur J Clin Pharmacol       Date:  2012-01-27       Impact factor: 2.953

Review 3.  Clinical use of factor VIII and factor IX concentrates.

Authors:  Massimo Morfini; Antonio Coppola; Massimo Franchini; Giovanni Di Minno
Journal:  Blood Transfus       Date:  2013-09       Impact factor: 3.443

4.  Target of prophylaxis in severe haemophilia: more than factor levels.

Authors:  Antonio Coppola; Massimo Franchini
Journal:  Blood Transfus       Date:  2012-12-21       Impact factor: 3.443

5.  Etranacogene dezaparvovec (AMT-061 phase 2b): normal/near normal FIX activity and bleed cessation in hemophilia B.

Authors:  Annette Von Drygalski; Adam Giermasz; Giancarlo Castaman; Nigel S Key; Susan Lattimore; Frank W G Leebeek; Wolfgang Miesbach; Michael Recht; Alison Long; Robert Gut; Eileen K Sawyer; Steven W Pipe
Journal:  Blood Adv       Date:  2019-11-12

6.  Rurioctocog alfa pegol PK-guided prophylaxis in hemophilia A: results from the phase 3 PROPEL study.

Authors:  Robert Klamroth; Jerzy Windyga; Vlad Radulescu; Peter W Collins; Oleksandra Stasyshyn; Hishamshah Mohd Ibrahim; Werner Engl; Srilatha D Tangada; William Savage; Bruce Ewenstein
Journal:  Blood       Date:  2021-04-01       Impact factor: 22.113

7.  [Treatment of haemophilia in Austria].

Authors:  Ingrid Pabinger; Max Heistinger; Wolfgang Muntean; Sylvia-Elisabeth Reitter-Pfoertner; Sabine Rosenlechner; Thomas Schindl; Gerhard Schuster; Werner Streif; Katharina Thom; Christoph Male
Journal:  Wien Klin Wochenschr       Date:  2015-11-02       Impact factor: 1.704

8.  Gene therapy in hemophilia A: a cost-effectiveness analysis.

Authors:  Nicoletta Machin; Margaret V Ragni; Kenneth J Smith
Journal:  Blood Adv       Date:  2018-07-24

Review 9.  Octocog alfa, antihaemophilic factor (recombinant), plasma/albumin free method (Advate®): a review of its use in the management of patients with haemophilia A.

Authors:  Sohita Dhillon
Journal:  Drugs       Date:  2012-05-07       Impact factor: 9.546

Review 10.  Pharmacokinetic-based prediction of real-life dosing of extended half-life clotting factor concentrates on hemophilia.

Authors:  Massimo Morfini; Stefano Gherardini
Journal:  Ther Adv Hematol       Date:  2018-06-05
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