Literature DB >> 20536987

Inhibitors in previously treated patients: a review of the literature.

C L Kempton1.   

Abstract

Previously treated patients are the first patients to receive novel factor VIII products during clinical investigations under the rationale that a product with increased antigenicity is more likely to be detected in this population because of a low baseline risk of inhibitor formation compared with previously untreated patients. As clinical investigations of factor products are not typically randomized comparisons, the rate of new inhibitor formation in a clinical trial is compared with the expected rates based on prior reports. The published experience of inhibitors in previously treated patients (PTPs) informs the number of new inhibitors per cohort that are acceptable in a clinical trial. However, a single acceptable limit of new inhibitors fails to recognize the heterogeneity of inhibitors and their variable impact on clinical care. This review will discuss the published literature on epidemiology and clinical characteristics of inhibitors and possible risk factors for formation in PTPs.

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Year:  2010        PMID: 20536987      PMCID: PMC4277611          DOI: 10.1111/j.1365-2516.2010.02235.x

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


  20 in total

1.  Utilization of previously treated patients (PTPs), noninfected patients (NIPs), and previously untreated patients (PUPs) in the evaluation of new factor VIII and factor IX concentrates. Recommendation of the Scientific Subcommittee on Factor VIII and Factor IX of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis.

Authors:  G C White; D DiMichele; K Mertens; C Negrier; I R Peake; C Prowse; R Schwaab; A Yoshioka; J Ingerslev
Journal:  Thromb Haemost       Date:  1999-03       Impact factor: 5.249

2.  A multicenter study of recombinant factor VIII (Recombinate) in previously treated patients with hemophilia A. The Recombinate Previously Treated Patient Study Group.

Authors:  G C White; S Courter; G L Bray; M Lee; E D Gomperts
Journal:  Thromb Haemost       Date:  1997-04       Impact factor: 5.249

3.  Factor VIII inhibitors in previously treated haemophilia A patients with a double virus-inactivated plasma derived factor VIII concentrate.

Authors:  K Peerlinck; J Arnout; M Di Giambattista; J G Gilles; R Laub; M Jacquemin; J M Saint-Remy; J Vermylen
Journal:  Thromb Haemost       Date:  1997-01       Impact factor: 5.249

4.  A multicenter pharmacosurveillance study for the evaluation of the efficacy and safety of recombinant factor VIII in the treatment of patients with hemophilia A. German Kogenate Study Group.

Authors:  E Aygören-Pürsün; I Scharrer
Journal:  Thromb Haemost       Date:  1997-11       Impact factor: 5.249

5.  Surveillance for factor VIII inhibitor development in the Canadian Hemophilia A population following the widespread introduction of recombinant factor VIII replacement therapy.

Authors:  A R Giles; G E Rivard; J Teitel; I Walker
Journal:  Transfus Sci       Date:  1998-06

6.  Sucrose formulated recombinant human antihemophilic factor VIII is safe and efficacious for treatment of hemophilia A in home therapy--International Kogenate-FS Study Group.

Authors:  T C Abshire; H H Brackmann; I Scharrer; K Hoots; C Gazengel; J S Powell; E Gorina; E Kellermann; E Vosburgh
Journal:  Thromb Haemost       Date:  2000-06       Impact factor: 5.249

7.  Incidence of inhibitors in a cohort of 838 males with hemophilia A previously treated with factor VIII concentrates.

Authors:  C L Kempton; J M Soucie; T C Abshire
Journal:  J Thromb Haemost       Date:  2006-09-26       Impact factor: 5.824

8.  A higher than expected incidence of factor VIII inhibitors in multitransfused haemophilia A patients treated with an intermediate purity pasteurized factor VIII concentrate.

Authors:  K Peerlinck; J Arnout; J G Gilles; J M Saint-Remy; J Vermylen
Journal:  Thromb Haemost       Date:  1993-02-01       Impact factor: 5.249

9.  The incidence of factor VIII and factor IX inhibitors in the hemophilia population of the UK and their effect on subsequent mortality, 1977-99.

Authors:  S C Darby; D M Keeling; R J D Spooner; S Wan Kan; P L F Giangrande; P W Collins; F G H Hill; C R M Hay
Journal:  J Thromb Haemost       Date:  2004-07       Impact factor: 5.824

10.  The natural history of factor VIII:C inhibitors in patients with hemophilia A: a national cooperative study. II. Observations on the initial development of factor VIII:C inhibitors.

Authors:  C W McMillan; S S Shapiro; D Whitehurst; L W Hoyer; A V Rao; J Lazerson
Journal:  Blood       Date:  1988-02       Impact factor: 22.113

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  3 in total

Review 1.  Alloantibodies to therapeutic factor VIII in hemophilia A: the role of von Willebrand factor in regulating factor VIII immunogenicity.

Authors:  Johannes Oldenburg; Sébastien Lacroix-Desmazes; David Lillicrap
Journal:  Haematologica       Date:  2015-02       Impact factor: 9.941

2.  Economic analysis of not running tenders for recombinant Factor VIII procurement: a simplified analysis to estimate an otherwise unknown pharmacoeconomic index.

Authors:  Dario Maratea; Valeria Fadda; Sabrina Trippoli; Andrea Messori
Journal:  Eur J Hosp Pharm       Date:  2015-12-23

3.  Long-Term Outcomes of Previously Treated Adult and Adolescent Patients with Severe Hemophilia A Receiving Prophylaxis with Extended Half-Life FVIII Treatments: An Economic Analysis from a United Kingdom Perspective.

Authors:  Gary Benson; Tim Morton; Huw Thomas; Xin Ying Lee
Journal:  Clinicoecon Outcomes Res       Date:  2021-01-18
  3 in total

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