Literature DB >> 25879247

Inhibitors in nonsevere haemophilia A: outcome and eradication strategies.

Alice S van Velzen, Corien L Eckhardt, Daniel P Hart, Marjolein Peters, Savita Rangarajan, Maria Elisa Mancuso, Frans J Smiers, Kate Khair, Pia Petrini, Victor Jiménez-Yuste, Charles R M Hay, Johanna G van der Bom, Thynn T Yee, Karin Fijnvandraat1.   

Abstract

In nonsevere haemophilia A (HA) patients the presence of an inhibitor may exacerbate the bleeding phenotype dramatically. There are very limited data on the optimal therapeutic approach to eradicate inhibitors in these patients. We aimed to describe inhibitor eradication treatment in a large cohort of unselected nonsevere HA patients with inhibitors. We included 101 inhibitor patients from a source population of 2,709 nonsevere HA patients (factor VIII 2-40 IU/dl), treated in Europe and Australia (median age 37 years, interquartile range (IQR) 15-60; median peak titre 7 BU/ml, IQR 2-30). In the majority of the patients (71 %; 72/101) the inhibitor disappeared; either spontaneously (70 %, 51/73) or after eradication treatment (75 %, 21/28). Eradication treatment strategies varied widely, including both immune tolerance induction and immunosuppression. Sustained success (no inhibitor after rechallenge with factor VIII concentrate after inhibitor disappearance) was achieved in 64 % (30/47) of those patients rechallenged with FVIII concentrate. In high-titre inhibitor patients sustained success was associated with eradication treatment (unadjusted relative risk 2.3, 95 % confidence interval 1.3-4.3), compared to no eradication treatment. In conclusion, in nonsevere HA patients most inhibitors disappear spontaneously. However, in 35 % (25/72) of these patients an anamnestic response still can occur when rechallenged, thus disappearance in these patients does not always equal sustained response. Treatment for those requiring eradication has to be decided case by case, as one single approach is unlikely to be appropriate for all.

Entities:  

Keywords:  Haemophilia A; eradication treatment; factor VIII inhibitors; immune tolerance induction

Mesh:

Substances:

Year:  2015        PMID: 25879247     DOI: 10.1160/TH14-11-0940

Source DB:  PubMed          Journal:  Thromb Haemost        ISSN: 0340-6245            Impact factor:   5.249


  11 in total

Review 1.  Diagnosis and care of patients with mild haemophilia: practical recommendations for clinical management.

Authors:  Gary Benson; Günter Auerswald; Gerry Dolan; Anne Duffy; Cedric Hermans; Rolf Ljung; Massimo Morfini; Silva Zupančić Šalek
Journal:  Blood Transfus       Date:  2017-11-14       Impact factor: 3.443

2.  Inhibitors and mortality in persons with nonsevere hemophilia A in the United States.

Authors:  Ming Y Lim; Dunlei Cheng; Michael Recht; Christine L Kempton; Nigel S Key
Journal:  Blood Adv       Date:  2020-10-13

3.  Expert opinion on the UK standard of care for haemophilia patients with inhibitors: a modified Delphi consensus study.

Authors:  Kate Khair; Elizabeth Chalmers; Thuvia Flannery; Annabel Griffiths; Felicity Rowley; Guillermo Tobaruela; Pratima Chowdary
Journal:  Ther Adv Hematol       Date:  2021-04-30

Review 4.  Treatment and Prevention of Bleeds in Haemophilia Patients with Inhibitors to Factor VIII/IX.

Authors:  Angiola Rocino; Massimo Franchini; Antonio Coppola
Journal:  J Clin Med       Date:  2017-04-17       Impact factor: 4.241

Review 5.  European principles of inhibitor management in patients with haemophilia.

Authors:  P L F Giangrande; C Hermans; B O'Mahony; P de Kleijn; M Bedford; A Batorova; J Blatný; K Jansone
Journal:  Orphanet J Rare Dis       Date:  2018-04-27       Impact factor: 4.123

6.  Navigating Speed Bumps on the Innovation Highway in Hemophilia Therapeutics.

Authors:  Donna M DiMichele
Journal:  Hemasphere       Date:  2018-10-02

7.  Factor VIII cross-matches to the human proteome reduce the predicted inhibitor risk in missense mutation hemophilia A.

Authors:  Daniel P Hart; Nazmiye Uzun; Stuart Skelton; Alison Kakoschke; Jacob Househam; David S Moss; Adrian J Shepherd
Journal:  Haematologica       Date:  2018-09-28       Impact factor: 9.941

Review 8.  Inhibitors in haemophilia A and B: Management of bleeds, inhibitor eradication and strategies for difficult-to-treat patients.

Authors:  Rolf Ljung; Guenter Auerswald; Gary Benson; Gerry Dolan; Anne Duffy; Cedric Hermans; Victor Jiménez-Yuste; Thierry Lambert; Massimo Morfini; Silva Zupančić-Šalek; Elena Santagostino
Journal:  Eur J Haematol       Date:  2018-12-06       Impact factor: 2.997

9.  Product type and the risk of inhibitor development in nonsevere haemophilia A patients: a case-control study.

Authors:  Alice S van Velzen; Corien L Eckhardt; Marjolein Peters; Johannes Oldenburg; Marjon Cnossen; Ri Liesner; Massimo Morfini; Giancarlo Castaman; Simon McRae; Johanna G van der Bom; Karin Fijnvandraat
Journal:  Br J Haematol       Date:  2020-03-22       Impact factor: 6.998

Review 10.  FVIII Immunogenicity-Bioinformatic Approaches to Evaluate Inhibitor Risk in Non-severe Hemophilia A.

Authors:  Daniel P Hart
Journal:  Front Immunol       Date:  2020-07-28       Impact factor: 7.561

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