The B-Natural study-The outcome of immune tolerance induction therapy in patients with severe haemophilia B

被引:12
|
作者
Astermark, Jan [1 ,2 ]
Holstein, Katharina [3 ]
Abajas, Yasmina L. [4 ]
Kearney, Susan [5 ]
Croteau, Stacy E. [6 ]
Liesner, Riana [7 ]
Funding, Eva [8 ]
Kempton, Christine L. [9 ]
Acharya, Suchitra [10 ]
Lethagen, Stefan [11 ]
LeBeau, Petra [12 ]
Bowen, Joel [13 ]
Berntorp, Erik [14 ]
Shapiro, Amy D. [13 ]
机构
[1] Lund Univ, Dept Translat Med, Malmo, Sweden
[2] Skane Univ Hosp, Dept Haematol Oncol & Radiat Phys, Malmo, Sweden
[3] Univ Med Ctr Hamburg Eppendorf, Dept Med, Hemophilia Ctr, Hamburg, Germany
[4] Univ N Carolina, Hemophilia & Thrombosis Ctr, Chapel Hill, NC 27515 USA
[5] Childrens Minnesota Ctr Bleeding & Clotting Disor, Minneapolis, MN USA
[6] Boston Childrens Hosp, Boston Haemophilia Ctr, Boston, MA USA
[7] BRC, GreatOrmond St Hosp Children, NHS Trust Supported NIHR, GOSH, London, England
[8] Univ Copenhagen, Rigshosp, Dept Haematol, Inst Clin Med,Univ Hosp, Copenhagen, Denmark
[9] Emory Univ, Sch Med, Atlanta, GA USA
[10] Northwell Haemostasis & Thrombosis Ctr, New York, NY USA
[11] Sobi, Stockholm, Sweden
[12] Rho Inc, Durham, NC USA
[13] Indiana Haemophilia & Thrombosis Ctr, Indianapolis, IN USA
[14] Lund Univ, Dept Translat Med, Clin Coagulat Res, Malmo, Sweden
关键词
allergy; factor IX deficiency; haemophilia B; immune tolerance induction; inhibitors; nephrotic syndrome; FACTOR-IX DEFICIENCY; REPLACEMENT THERAPY; NEPHROTIC SYNDROME; INHIBITORS; REGISTRY; EXPERIENCE; CHILDREN; ITI;
D O I
10.1111/hae.14357
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Inhibitors develop less frequently in haemophilia B (HB) than haemophilia A (HA). However, when present, the success of tolerization by immune tolerance induction (ITI) therapy is lower and the risk of complications higher. Aim To evaluate the use and outcome of ITI in patients with HB and inhibitors. Methods Subjects include singletons or siblings with a current/history of inhibitors enrolled in B-Natural-an observational study designed to increase understanding of clinical management of patients with HB. Patients were followed for 6 months and information on demographics, medical and social history, and treatment were recorded. Results Twenty-nine patients with severe HB and inhibitors were enrolled in 24 centres. Twenty-two underwent one or more courses of ITI with or without immune suppression. Eight patients (36.4%) were successfully tolerized after the first course of ITI. One of these successes (12.5%) experienced allergic manifestations, whereas the corresponding number for the 10 treatment failures was five (50%). One of seven (14.2%) patients with large deletions and three of eight (37.5%) with nonsense mutations were tolerized at the first attempt, and all patients experiencing nephrosis either failed or were on-going. At study end, 11 (50%) were considered successfully tolerized after one or more ITI courses, three were unsuccessful, and eight were still undergoing treatment. Conclusion Our data underscore the possibilities and difficulties of achieving tolerization in patients with HB with inhibitors. The type of mutation and complications appear to correlate with ITI outcome, but more accurate definitions of successful ITI are warranted.
引用
收藏
页码:802 / 813
页数:12
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