Literature DB >> 26017627

Evaluation of safety and effectiveness of factor VIII treatment in haemophilia A patients with low titre inhibitors or a personal history of inhibitor. Patient Data Meta-analysis of rAFH-PFM Post-Authorization Safety Studies.

Vadim Romanov, Maura Marcucci, Ji Cheng, Lehana Thabane, Alfonso Iorio1.   

Abstract

There is no prospective evidence on inhibitor recurrence among haemophilia A patients with low titre inhibitors or history of inhibitors, and whether or how therapeutic choices affect the risk of recurrence. The aims of this study were to synthesise safety data in patients with moderate-severe haemophilia A and with low titre inhibitors or inhibitor history enrolled in the rAHF PFM (ADVATE) - Post-Authorization Safety Studies (ADVATE-PASS) international programme. The study was conducted in clinics participating to the ADVATE PASS programme. The patient population consisted of patients entering the studies with low titre (≤ 5 BU) inhibitors or a positive personal history of inhibitors. Patients on Immune Tolerance Induction at study entry were excluded. Primary outcome was new or recurrent inhibitor titre > 5 BU. Secondary outcomes were any increase of inhibitor titre not reaching 5 BU; any unexplained change in treatment regimen. Primary analysis was done by two-stage random effects meta-analysis. Secondary analysis was done by a hierarchical Bayesian random effects logistic model. A total of 219 patients from seven studies were included. Of these 214 (97.7 %) patients had been previously treated for more than 50 exposure days. Two hundred ten patients had positive history for inhibitors, nine a baseline measurable titre. No patient presented a primary outcome event (95 % confidence interval [CI] 0-1.6 %). Six patients with previous history developed a low titre recurrence (overall rate 2.2, 95 %CI 0-4.8 %). When any increase of inhibitor titre or any treatment change was accounted for, overall 3.7 % (95 % CI 0 %-8.0 %) of patients experienced the outcome. In conclusion, the observed rate of events does not support the definition of this population as at high risk for inhibitor development.

Entities:  

Keywords:  ADVATE; Haemophilia A; PASS; low titre inhibitors; switching

Mesh:

Substances:

Year:  2015        PMID: 26017627     DOI: 10.1160/TH14-10-0882

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


  2 in total

1.  Bayesian approach to the assessment of the population-specific risk of inhibitors in hemophilia A patients: a case study.

Authors:  Ji Cheng; Alfonso Iorio; Maura Marcucci; Vadim Romanov; Eleanor M Pullenayegum; John K Marshall; Lehana Thabane
Journal:  J Blood Med       Date:  2016-10-25

2.  Final Results of the Prospective ADVATE® Immune Tolerance Induction Registry (PAIR) Study with Plasma- and Albumin-Free Recombinant Factor VIII.

Authors:  Amy D Shapiro; Alejandro Fernandez; Jerome Teitel; Jaco Botha; Kate Khair
Journal:  J Blood Med       Date:  2021-11-20
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.