Literature DB >> 33396748

Epidemiological Challenges in Rare Bleeding Disorders: FVIII Inhibitor Incidence in Haemophilia A Patients-A Known Issue of Unknown Origin.

Christine Keipert1, Ursula Drechsel-Bäuerle2, Doris Oberle2, Mirco Müller-Olling3, Anneliese Hilger3.   

Abstract

There is a broad range of factor products approved in Germany for haemophilia A treatment. Since the introduction of recombinant coagulation factor VIII (FVIII) products in the 1990s, there has been substantial debate whether there is a difference in inhibitor incidence between single FVIII products or product classes. Neither haemophilia registries nor clinical studies, including a randomised controlled clinical trial, provided a consistent and definite answer. The reasons were mainly related to methodological challenges in conducting controlled studies in a rare disease. In this analysis, the most relevant epidemiological challenges and main problems were examined, including study bias, potential overlap of individual studies and advanced development of therapy and methods in the course of time. Meta-analyses on two levels showed that therapies using recombinant products resulted in different event rates when compared to plasma-derived products. These results are accompanied by substantial study heterogeneity evidenced by Cochran's Q tests. Only three studies have been identified that meet the standards of current clinical guidance. To finally resolve this ongoing and disputable safety issue of replacement therapy, collaboration among registry owners, academia and regulators must be fostered.

Entities:  

Keywords:  epidemiology; haemophilia A; inhibitor development; rare diseases

Mesh:

Year:  2020        PMID: 33396748      PMCID: PMC7795862          DOI: 10.3390/ijerph18010225

Source DB:  PubMed          Journal:  Int J Environ Res Public Health        ISSN: 1660-4601            Impact factor:   3.390


  48 in total

1.  Inhibitor development in haemophilia according to concentrate. Four-year results from the European HAemophilia Safety Surveillance (EUHASS) project.

Authors:  Kathelijn Fischer; Riita Lassila; Flora Peyvandi; Gabriele Calizzani; Alex Gatt; Thierry Lambert; Jerzy Windyga; Alfonso Iorio; Estelle Gilman; Michael Makris
Journal:  Thromb Haemost       Date:  2015-01-08       Impact factor: 5.249

2.  Absence of inhibitors in previously untreated patients with severe haemophilia A after exposure to a single intermediate purity factor VIII product.

Authors:  T T Yee; M D Williams; F G Hill; C A Lee; K J Pasi
Journal:  Thromb Haemost       Date:  1997-09       Impact factor: 5.249

Review 3.  Plasma-derived versus recombinant factor concentrates in PUPs: a never ending debate?

Authors:  Erik Berntorp
Journal:  Hamostaseologie       Date:  2016-11-23       Impact factor: 1.778

4.  Clinical trials and registries in haemophilia: Opponents or collaborators? Comparison of PUP data derived from different data sources.

Authors:  C Keipert; C J Jonker; H M van den Berg; A Hilger
Journal:  Haemophilia       Date:  2018-02-13       Impact factor: 4.287

5.  Factor VIII brand and the incidence of factor VIII inhibitors in previously untreated UK children with severe hemophilia A, 2000-2011.

Authors:  Peter W Collins; Benedict P Palmer; Elizabeth A Chalmers; Daniel P Hart; Ri Liesner; Savita Rangarajan; Katherine Talks; Michael Williams; Charles R M Hay
Journal:  Blood       Date:  2014-10-22       Impact factor: 22.113

6.  Incidence of low-titre factor VIII inhibitors in patients with haemophilia A: meta-analysis of observational studies.

Authors:  A Messori; F Peyvandi; D Mengato; P M Mannucci
Journal:  Haemophilia       Date:  2017-02-20       Impact factor: 4.287

7.  Human recombinant DNA-derived antihemophilic factor in the treatment of previously untreated patients with hemophilia A: final report on a hallmark clinical investigation.

Authors:  J Lusher; C Abildgaard; S Arkin; P M Mannucci; R Zimmermann; L Schwartz; D Hurst
Journal:  J Thromb Haemost       Date:  2004-04       Impact factor: 5.824

8.  Inhibitor development in previously untreated patients with hemophilia A: a prospective long-term follow-up comparing plasma-derived and recombinant products.

Authors:  Wolfhart Kreuz; Carmen Escuriola Ettingshausen; Alex Zyschka; Johannes Oldenburg; Inmaculada Martinez Saguer; Silke Ehrenforth; Thomas Klingebiel
Journal:  Semin Thromb Hemost       Date:  2002-06       Impact factor: 4.180

9.  Viral safety and inhibitor development associated with factor VIIIC ultra-purified from plasma in hemophiliacs previously unexposed to factor VIIIC concentrates. The Monoclate Study Group.

Authors:  J M Lusher; P M Salzman
Journal:  Semin Hematol       Date:  1990-04       Impact factor: 3.851

Review 10.  Many factor VIII products available in the treatment of hemophilia A: an embarrassment of riches?

Authors:  Kenneth Lieuw
Journal:  J Blood Med       Date:  2017-06-15
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  1 in total

1.  Predictors of the outcome of immune tolerance induction in patients with haemophilia A and inhibitors: The Brazilian Immune Tolerance (BrazIT) Study protocol.

Authors:  Ricardo Mesquita Camelo; Daniel Gonçalves Chaves; Luciana Werneck Zuccherato; Suely Meireles Rezende
Journal:  PLoS One       Date:  2021-08-26       Impact factor: 3.240

  1 in total

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