Literature DB >> 26382916

Inhibitor recurrence after immune tolerance induction: a multicenter retrospective cohort study.

A Antun1, P E Monahan2, M J Manco-Johnson3, M U Callaghan4, M Kanin5, C Knoll6, S L Carpenter7, J A Davis8, M F Guerrera9, R Kruse-Jarres10, M V Ragni11, C Witmer12, C E McCracken13, C L Kempton1.   

Abstract

BACKGROUND: Immune tolerance induction (ITI) in patients with congenital hemophilia A is successful in up to 70%. Although there is growing understanding of predictors of response to ITI, the probability and predictors of inhibitor recurrence after successful ITI are not well understood.
OBJECTIVES: To determine the association of clinical characteristics, particularly adherence to factor VIII (FVIII) prophylaxis after ITI, with inhibitor recurrence in patients with hemophilia A who were considered tolerant after ITI.
METHODS: In this multicenter retrospective cohort study, 64 subjects with FVIII level < 2% who were considered successfully tolerant after ITI were analyzed to estimate the cumulative probability of inhibitor recurrence using the Kaplan-Meier method. The association of clinical characteristics with inhibitor recurrence was assessed using logistic regression.
RESULTS: A recurrent inhibitor titer ≥ 0.6 BU mL(-1) occurred at least once in 19 (29.7%) and more than once in 12 (18.8%). The probability of any recurrent inhibitor at 1 and 5 years was 12.8% and 32.5%, respectively. Having a recurrent inhibitor was associated with having received immune modulation during ITI (odds ratio [OR] 3.8, 95% confidence interval [CI] 1.2-22.4) and FVIII recovery of < 85% at the end of ITI (OR 2.6, 95% CI 1.3-5.9) but was not associated with adherence to post-ITI prophylactic FVIII infusion (OR 0.5, 95% CI 0.06-4.3).
CONCLUSIONS: The use of immune modulation therapy during ITI and lower FVIII recovery at the end of ITI appear to be associated with an increased risk of inhibitor recurrence after successful ITI. Adherence to post-ITI prophylactic FVIII infusions is not a major determinant of recurrence.
© 2015 International Society on Thrombosis and Haemostasis.

Entities:  

Keywords:  hemophilia; immune tolerance; incidence; prophylaxis; recurrence

Mesh:

Substances:

Year:  2015        PMID: 26382916      PMCID: PMC4639409          DOI: 10.1111/jth.13143

Source DB:  PubMed          Journal:  J Thromb Haemost        ISSN: 1538-7836            Impact factor:   5.824


  9 in total

1.  The principal results of the International Immune Tolerance Study: a randomized dose comparison.

Authors:  Charles R M Hay; Donna M DiMichele
Journal:  Blood       Date:  2011-11-18       Impact factor: 22.113

Review 2.  Adherence to medication.

Authors:  Lars Osterberg; Terrence Blaschke
Journal:  N Engl J Med       Date:  2005-08-04       Impact factor: 91.245

3.  The North American Immune Tolerance Registry: practices, outcomes, outcome predictors.

Authors:  D M DiMichele; B L Kroner
Journal:  Thromb Haemost       Date:  2002-01       Impact factor: 5.249

4.  F8 and F9 mutations in US haemophilia patients: correlation with history of inhibitor and race/ethnicity.

Authors:  C H Miller; J Benson; D Ellingsen; J Driggers; A Payne; F M Kelly; J M Soucie; W Craig Hooper
Journal:  Haemophilia       Date:  2011-11-21       Impact factor: 4.287

5.  Characterization of the human factor VIII gene.

Authors:  J Gitschier; W I Wood; T M Goralka; K L Wion; E Y Chen; D H Eaton; G A Vehar; D J Capon; R M Lawn
Journal:  Nature       Date:  1984 Nov 22-28       Impact factor: 49.962

6.  Immune tolerance in hemophilia with factor VIII inhibitors: predictors of success.

Authors:  G Mariani; B Kroner
Journal:  Haematologica       Date:  2001-11       Impact factor: 9.941

7.  Population pharmacokinetics of recombinant factor VIII: the relationships of pharmacokinetics to age and body weight.

Authors:  Sven Björkman; MyungShin Oh; Gerald Spotts; Phillip Schroth; Sandor Fritsch; Bruce M Ewenstein; Kathleen Casey; Kathelijn Fischer; Victor S Blanchette; Peter W Collins
Journal:  Blood       Date:  2011-10-31       Impact factor: 22.113

8.  Rituximab and immune tolerance in severe hemophilia A: a consecutive national cohort.

Authors:  P W Collins; M Mathias; J Hanley; D Keeling; R Keenan; M Laffan; D Perry; R Liesner
Journal:  J Thromb Haemost       Date:  2009-03-05       Impact factor: 5.824

9.  Factor VIII gene (F8) mutations as predictors of outcome in immune tolerance induction of hemophilia A patients with high-responding inhibitors.

Authors:  A Coppola; M Margaglione; E Santagostino; A Rocino; E Grandone; P M Mannucci; G Di Minno
Journal:  J Thromb Haemost       Date:  2009-09-09       Impact factor: 5.824

  9 in total
  14 in total

Review 1.  Factor-mimetic and rebalancing therapies in hemophilia A and B: the end of factor concentrates?

Authors:  Patrick Ellsworth; Alice Ma
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2021-12-10

Review 2.  Gene therapy for immune tolerance induction in hemophilia with inhibitors.

Authors:  V R Arruda; B J Samelson-Jones
Journal:  J Thromb Haemost       Date:  2016-05-14       Impact factor: 5.824

3.  Combination therapy for inhibitor reversal in haemophilia A using monoclonal anti-CD20 and rapamycin.

Authors:  Moanaro Biswas; Geoffrey L Rogers; Alexandra Sherman; Barry J Byrne; David M Markusic; Haiyan Jiang; Roland W Herzog
Journal:  Thromb Haemost       Date:  2016-09-29       Impact factor: 5.249

Review 4.  The impact of the immune system on the safety and efficiency of enzyme replacement therapy in lysosomal storage disorders.

Authors:  A Broomfield; S A Jones; S M Hughes; B W Bigger
Journal:  J Inherit Metab Dis       Date:  2016-02-16       Impact factor: 4.982

5.  B cell-activating factor modulates the factor VIII immune response in hemophilia A.

Authors:  Bhavya S Doshi; Jyoti Rana; Giancarlo Castaman; Mostafa A Shaheen; Radoslaw Kaczmarek; John Ss Butterfield; Shannon L Meeks; Cindy Leissinger; Moanaro Biswas; Valder R Arruda
Journal:  J Clin Invest       Date:  2021-04-15       Impact factor: 14.808

6.  Overexpression of Mutant FKRP Restores Functional Glycosylation and Improves Dystrophic Phenotype in FKRP Mutant Mice.

Authors:  Jason D Tucker; Pei J Lu; Xiao Xiao; Qi L Lu
Journal:  Mol Ther Nucleic Acids       Date:  2018-03-06       Impact factor: 8.886

7.  Clinical Care of Bone Health in Patients on the Immune Tolerance Induction's Protocols With an Immunosuppressive Agent for Inhibitor Eradication in Hemophilia.

Authors:  Zahra Rezaieyazdi; Hassan Mansouritorghabeh
Journal:  Clin Appl Thromb Hemost       Date:  2020 Jan-Dec       Impact factor: 2.389

Review 8.  Emerging therapies for hemophilia: controversies and unanswered questions.

Authors:  Valder R Arruda; Bhavya S Doshi; Benjamin J Samelson-Jones
Journal:  F1000Res       Date:  2018-04-24

Review 9.  Bispecific Antibodies and Advances in Non-Gene Therapy Options in Hemophilia.

Authors:  Midori Shima
Journal:  Res Pract Thromb Haemost       Date:  2020-04-28

10.  Low-dose immune tolerance induction for children with hemophilia A with poor-risk high-titer inhibitors: A pilot study in China.

Authors:  Zekun Li; Zhenping Chen; Xiaoling Cheng; Xinyi Wu; Gang Li; Yingzi Zhen; Siyu Cai; Man-Chiu Poon; Runhui Wu
Journal:  Res Pract Thromb Haemost       Date:  2019-08-09
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