Incidence and risk factors for inhibitor development in previously untreated severe haemophilia A patients born between 2005 and 2010

Haemophilia. 2014 Nov;20(6):771-6. doi: 10.1111/hae.12479. Epub 2014 Jul 17.

Abstract

The objective of this study was to evaluate the inhibitor development (ID) in previously untreated patients (PUPs) with severe haemophilia A (FVIII ≤ 0.01 IU mL(-1) ). All Canadian Haemophilia Treatment Centres completed a questionnaire on patients born between September 2005 and August 2010 and followed for up to 7 years. Eligible patients had at least 20 exposure days (ED) or had developed an inhibitor. The odds ratio (OR) and 95% confidence intervals (95% CI) for risk factors to develop an inhibitor were estimated using unconditional logistic regression. A total of 99 haemophilia A PUPs were studied. Thirty-four (34%) developed an inhibitor (24/34 of high titre). Inhibitors developed in 25/63 (40%) patients with a high-risk mutation. ID was most frequent in Aboriginals (86%). Dose intensity (IU kg(-1) day(-1) X number of ED) at first exposure to factor VIII (FVIII) was associated with a crude OR increase of 1.10 (95% CI: 0.99-1.23) with each increase of 100 dose-intensity units. Haemarthrosis and intracranial bleeding as the indication for first exposure to FVIII concentrate were associated with a crude OR for ID of 7.63 (95% CI: 2.14-27.17) and 5.08 (95% CI: 1.11-23.31) respectively. ID according to FVIII concentrate used was: Advate (®) 18/50 (36%), Kogenate FS(®) or Helixate FS(®) 15/36 (42%), Wilate(®) 0/11 and Xyntha(®) 1/2. In multivariate analysis, Aboriginal ethnicity (OR = 11.69; 95% CI: 1.11-122.86) and haemarthrosis (OR = 4.49; 95% CI: 1.08-18.61) were statistically significant. The cumulative incidence of ID in severe haemophilia A PUPs was 34% and varied according to ethnicity, type of bleeding at first ED, type of FVIII product and dose intensity at first exposure.

Keywords: PUP; anti-FVIII; danger signal; environment; haemophilia A; inhibitor.

Publication types

  • Multicenter Study

MeSH terms

  • Blood Coagulation Factor Inhibitors / blood
  • Blood Coagulation Factor Inhibitors / immunology*
  • Canada / epidemiology
  • Child, Preschool
  • Factor VIII / genetics
  • Factor VIII / therapeutic use
  • Follow-Up Studies
  • Health Care Surveys
  • Hemophilia A / diagnosis
  • Hemophilia A / drug therapy
  • Hemophilia A / epidemiology*
  • Hemophilia A / immunology*
  • Humans
  • Incidence
  • Infant
  • Infant, Newborn
  • Isoantibodies / blood
  • Isoantibodies / immunology
  • Male
  • Mutation
  • Odds Ratio
  • Retrospective Studies
  • Risk Factors
  • Treatment Outcome

Substances

  • Blood Coagulation Factor Inhibitors
  • Isoantibodies
  • Factor VIII