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- Title
First prospective report on immune tolerance in poor risk haemophilia A inhibitor patients with a single factor VIII/von Willebrand factor concentrate in an observational immune tolerance induction study.
- Authors
Kreuz, W.; Escuriola Ettingshausen, C.; Vdovin, V.; Zozulya, N.; Plyushch, O.; Svirin, P.; Andreeva, T.; Bubanská, E.; Campos, M.; Benedik‐Dolničar, M.; Jiménez‐Yuste, V.; Kitanovski, L.; Klukowska, A.; Momot, A.; Osmulskaya, N.; Prieto, M.; Šalek, S. Z.; Velasco, F.; Pavlova, A.; Oldenburg, J.
- Abstract
Introduction/background Development of neutralizing inhibitors against factor VIII (FVIII) is a major complication of haemophilia A treatment. Aim The ongoing, international, open-label, uncontrolled, observational immune tolerance induction (ObsITI) study evaluates ITI, the standard of care in patients with inhibitors. Patients/methods Forty-eight prospective patients in this interim analysis received a single plasma-derived, von Willebrand factor-stabilized, FVIII concentrate (pdFVIII/VWF) for ITI. According to recommended Bonn protocol, 'low responders' at ITI start (<5 BU) received 50-100 IU FVIII kg−1 daily, or every other day; 'high responders' (≥5 BU) received 100 IU FVIII kg−1 every 12 h. Results Forty of 48 patients (83.3%), had at least one risk factor for poor ITI-prognosis at ITI start (i.e. age ≥7 years, >2 years since inhibitor diagnosis, inhibitor titre ≥10 BU at the start of ITI, or prior ITI failure). Nonetheless, 34 patients (70.8%) achieved complete success, 3 (6.3%) partial success, 1 (2.1%) partial response; ITI failed in 10 patients (20.8%), all with poor prognosis factors. All six low responders achieved complete success. ITI outcome was significantly associated with inhibitor titre level at ITI start ( P = 0.0068), number of poor prognosis factors for ITI success ( P = 0.0187), monthly bleeding rate during ITI ( P = 0.0005) and peak inhibitor titre during ITI ( P = 0.0007). Twenty-two of 35 high responder patients (62.9%) with ≥1 poor prognosis factor achieved complete success. Conclusion Treatment with a single pdFVIII/VWF concentrate, mainly according to the Bonn protocol, resulted in a high ITI success rate in haemophilia A patients with inhibitors and poor prognosis for ITI success.
- Subjects
HEMOPHILIA; BLOOD coagulation factor VIII; IMMUNOLOGICAL tolerance; VON Willebrand factor; BLOOD coagulation factors; PROGNOSIS
- Publication
Haemophilia, 2016, Vol 22, Issue 1, p87
- ISSN
1351-8216
- Publication type
Article
- DOI
10.1111/hae.12774