A Randomized Trial of Factor VIII and Neutralizing Antibodies in Hemophilia A

Flora Peyvandi(University of Milan), Pier Mannuccio Mannucci(University of Milan), Isabella Garagiola(University of Milan), Amal El‐Beshlawy(Cairo University), Mohsen Saleh Elalfy(Ain Shams University), Vijay Ramanan(Jehangir Hospital), Peyman Eshghi(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Suresh Hanagavadi(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Ramabadran Varadarajan(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Mehran Karimi(Shiraz University of Medical Sciences), Mamta Manglani(Lokmanya Tilak Municipal General Hospital and Lokmanya Tilak Municipal Medical College), Cecil Ross(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Guy Young(Children's Hospital of Los Angeles), Tulika Seth(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Shashikant Apte(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Dinesh Nayak(Manipal Academy of Higher Education), Elena Santagostino(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Maria Elisa Mancuso(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), A.C. Sandoval Gonzalez(Mexican Social Security Institute), Johnny Mahlangu(National Health Laboratory Service), Santiago Bonanad Boix(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), M. Cerqueira(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Nadia P. Ewing(City Of Hope National Medical Center), Christoph Male(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Tarek Owaidah(King Faisal Specialist Hospital & Research Centre), V. Soto Arellano(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Nathan L. Kobrinsky(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Suvankar Majumdar(Jackson Memorial Hospital), Rosario Garrido(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Anupam Sachdeva(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Mindy Simpson(Rush University Medical Center), Mathew Thomas(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Ezio Zanon(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Bülent Antmen(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Kaan Kavaklı(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Marilyn J. Manco‐Johnson(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Mònica Martínez(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), E. Marzouka(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Maria Gabriella Mazzucconi(Policlinico Umberto I), Daniela Neme(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Ángeles Palomo Bravo(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Rogelio Paredes Aguilera(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), A. Prezotti(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Klaus Schmitt(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Brian M. Wicklund(Children's Mercy Hospital), Bülent Zülfikar(Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico), Frits R. Rosendaal(Leiden University Medical Center)
New England Journal of Medicine
May 25, 2016
Cited by 488Open Access
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Abstract

BACKGROUND: The development of neutralizing anti-factor VIII alloantibodies (inhibitors) in patients with severe hemophilia A may depend on the concentrate used for replacement therapy. METHODS: We conducted a randomized trial to assess the incidence of factor VIII inhibitors among patients treated with plasma-derived factor VIII containing von Willebrand factor or recombinant factor VIII. Patients who met the eligibility criteria (male sex, age <6 years, severe hemophilia A, and no previous treatment with any factor VIII concentrate or only minimal treatment with blood components) were included from 42 sites. RESULTS: Of 303 patients screened, 264 underwent randomization and 251 were analyzed. Inhibitors developed in 76 patients, 50 of whom had high-titer inhibitors (≥5 Bethesda units). Inhibitors developed in 29 of the 125 patients treated with plasma-derived factor VIII (20 patients had high-titer inhibitors) and in 47 of the 126 patients treated with recombinant factor VIII (30 patients had high-titer inhibitors). The cumulative incidence of all inhibitors was 26.8% (95% confidence interval [CI], 18.4 to 35.2) with plasma-derived factor VIII and 44.5% (95% CI, 34.7 to 54.3) with recombinant factor VIII; the cumulative incidence of high-titer inhibitors was 18.6% (95% CI, 11.2 to 26.0) and 28.4% (95% CI, 19.6 to 37.2), respectively. In Cox regression models for the primary end point of all inhibitors, recombinant factor VIII was associated with an 87% higher incidence than plasma-derived factor VIII (hazard ratio, 1.87; 95% CI, 1.17 to 2.96). This association did not change in multivariable analysis. For high-titer inhibitors, the hazard ratio was 1.69 (95% CI, 0.96 to 2.98). When the analysis was restricted to recombinant factor VIII products other than second-generation full-length recombinant factor VIII, effect estimates remained similar for all inhibitors (hazard ratio, 1.98; 95% CI, 0.99 to 3.97) and high-titer inhibitors (hazard ratio, 2.59; 95% CI, 1.11 to 6.00). CONCLUSIONS: Patients treated with plasma-derived factor VIII containing von Willebrand factor had a lower incidence of inhibitors than those treated with recombinant factor VIII. (Funded by the Angelo Bianchi Bonomi Foundation and others; ClinicalTrials.gov number, NCT01064284; EudraCT number, 2009-011186-88.).


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