Low-dose Immune Tolerance Induction in Hemophilia: A Single-Center Experience

J Pediatr Hematol Oncol. 2019 Aug;41(6):e355-e358. doi: 10.1097/MPH.0000000000001391.

Abstract

Introduction: The development of inhibitors against factors VIII/IX is the most serious complication in hemophilia. The best treatment strategy for inhibitor eradication is immune tolerance induction (ITI). The aim of this study was to evaluate patients treated with low-dose ITI at a single center with limited resources.

Materials and methods: In total, 29 (8.05%) of 360 hemophilia A patients exhibited inhibitors. The data from hemophilia patients with inhibitors undergoing ITI between 1999 and 2017 were collected and analyzed.

Results: Seventeen ITIs administered to 15 hemophilia A patients with inhibitors were analyzed, and the data from 13 ITIs conducted in 12 patients were evaluated. The median age at ITI onset was 10 years (range: 1.25 to 52 y). The maximum inhibitor titer before ITI was 30 Bethesda Units (BU) (range: 4.48 to 135), and the median inhibitor titer was 1.25 BU (range: 0 to 5.6) at the onset of ITI. The median time interval between the inhibitor development and ITI onset was 60 months (range: 7 to 264 mo). The median inhibitor titer during ITI was 3.4 BU (range: 0 to 158.7). At the end of the treatment, 4 of the 12 patients (33.3%) exhibited a complete response, 4 (33.3%) had partial responses (with continuing ITI), and 4 (33.3%) exhibited ITI failure.

Conclusions: Treatment of hemophilia patients with inhibitors is challenging, and ITI is the best treatment method; however, a high-dose daily ITI regimen cannot be given to every patient in every country due to its high cost. Our results show that low-dose ITI may be a choice for selected patients with inhibitors.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Blood Coagulation Factor Inhibitors / administration & dosage*
  • Child
  • Factor VIII / antagonists & inhibitors*
  • Female
  • Follow-Up Studies
  • Hemophilia A / drug therapy*
  • Hemophilia A / immunology*
  • Hemophilia A / pathology
  • Humans
  • Immune Tolerance / drug effects*
  • Infant
  • Male
  • Middle Aged
  • Prognosis
  • Young Adult

Substances

  • Blood Coagulation Factor Inhibitors
  • F8 protein, human
  • Factor VIII