Literature DB >> 30783066

Inhibitors: A Need for Eradication?

Elena Santagostino1, Guy Young2, Carmen Escuriola Ettingshausen3, Victor Jimenez-Yuste4, Manuel Carcao5.   

Abstract

The development of inhibitors against factor VIII (FVIII) concentrates represents a significant treatment complication for hemophilia. Immune tolerance induction (ITI) therapy eradicates inhibitors in 60-80% of patients, resulting in a normal FVIII response. This article, based on presentations at the 6th International Coagulation Meeting, held in Barcelona, Spain, in September 2017, provides an overview of management approaches for patients with inhibitors and briefly tabulates four cases of ITI therapy (first-line or rescue ITI therapy in pediatric and adult patients) with successful outcomes. Switching FVIII product from recombinant FVIII to plasma-derived FVIII/VWF concentrate may be helpful in eradicating inhibitors. The rate of decline of inhibitor titer in the initial stages of ITI therapy is a good indicator of the success or failure of therapy, although prognostic biomarkers are needed. The development of the bispecific monoclonal antibody emicizumab, which was recently shown to reduce bleeding in inhibitor patients, offers a potential alternative therapeutic option. However, the benefits of inhibitor eradication, including a wider choice of cheaper therapeutic products for preventing and treating bleeds, suggest that at least one attempt of ITI therapy should be offered to patients who develop inhibitors.
© 2019 S. Karger AG, Basel.

Entities:  

Keywords:  Factor VIII concentrate; Hemophilia; Immune tolerance induction; Inhibitors; Von Willebrand factor

Mesh:

Substances:

Year:  2019        PMID: 30783066     DOI: 10.1159/000495454

Source DB:  PubMed          Journal:  Acta Haematol        ISSN: 0001-5792            Impact factor:   2.195


  4 in total

1.  Immune Tolerance Induction (ITI) with a pdFVIII/VWF Concentrate (octanate) in 100 Patients in the Observational ITI (ObsITI) Study.

Authors:  Carmen Escuriola Ettingshausen; Vladimír Vdovin; Nadezhda Zozulya; Pavel Svirin; Tatiana Andreeva; Majda Benedik-Dolničar; Victor Jiménez-Yuste; Lidija Kitanovski; Silva Zupancic-Šalek; Anna Pavlova; Angelika Bátorová; Cesar Montaño Mejía; Gulnara Abdilova; Sigurd Knaub; Martina Jansen; Shannely Lowndes; Larisa Belyanskaya; Olaf Walter; Johannes Oldenburg
Journal:  TH Open       Date:  2022-05-26

2.  Clinical Care of Bone Health in Patients on the Immune Tolerance Induction's Protocols With an Immunosuppressive Agent for Inhibitor Eradication in Hemophilia.

Authors:  Zahra Rezaieyazdi; Hassan Mansouritorghabeh
Journal:  Clin Appl Thromb Hemost       Date:  2020 Jan-Dec       Impact factor: 2.389

3.  Design of an international investigator-initiated study on MOdern Treatment of Inhibitor-positiVe pATiEnts with haemophilia A (MOTIVATE).

Authors:  Carmen Escuriola Ettingshausen; Robert F Sidonio
Journal:  Ther Adv Hematol       Date:  2021-09-23

4.  Simoctocog Alfa (Nuwiq) in Previously Untreated Patients with Severe Haemophilia A: Final Results of the NuProtect Study.

Authors:  Ri J Liesner; Aby Abraham; Carmen Altisent; Mark J Belletrutti; Manuel Carcao; Manuela Carvalho; Hervé Chambost; Anthony K C Chan; Leonid Dubey; Jonathan Ducore; Michael Gattens; Paolo Gresele; Yves Gruel; Benoit Guillet; Victor Jimenez-Yuste; Lidija Kitanovski; Anna Klukowska; Sunil Lohade; Maria Elisa Mancuso; Johannes Oldenburg; Anna Pavlova; Berardino Pollio; Marianne Sigaud; Vladimir Vdovin; Kateryna Vilchevska; John K M Wu; Martina Jansen; Larisa Belyanskaya; Olaf Walter; Sigurd Knaub; Ellis J Neufeld
Journal:  Thromb Haemost       Date:  2021-02-13       Impact factor: 5.249

  4 in total

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