Emicizumab prophylaxis among infants and toddlers with severe hemophilia A and inhibitors-a single-center cohort
- PMID: 31348595
- DOI: 10.1002/pbc.27886
Emicizumab prophylaxis among infants and toddlers with severe hemophilia A and inhibitors-a single-center cohort
Abstract
Background: Emicizumab is a bispecific antibody that bridges factor IXa and factor X to restore hemostasis in patients with hemophilia A (HA). Its efficacy and safety have been proven in multicenter trials. However, real world data regarding its use in very young children are currently lacking. Ancillary test results for monitoring emicizumab's hemostatic effect and their clinical correlations are scarce.
Methods: Children with HA and inhibitors treated by emicizumab were prospectively followed at our center. Laboratory follow-up included rotational thromboelastometry (ROTEM) and thrombin generation (TG), prior to and during treatment.
Results: Eleven children whose median age was 26 months were treated by emicizumab and followed for a median of 36 weeks. During follow-up, none experienced hemarthrosis or any other spontaneous bleeds. For 7/11 patients, emicizumab prophylaxis was sufficient to maintain hemostasis without additional supplemental therapy. Only 4/11 patients were occasionally treated with recombinant activated FVII for trauma. Two minor surgeries were safely performed without supplemental therapy while another procedure was complicated by major bleeding. TG parameters improved for all patients, correlating with their clinical status. Interestingly, the lowest TG values were obtained for patients experiencing bleeding episodes, while ROTEM parameters in all patients were close to the normal range.
Conclusions: This study confirms the safety and efficacy of emicizumab in reducing bleeds in young children with HA with inhibitors, including infants. However, surgeries warrant caution as emicizumab prophylaxis may not be sufficient for some procedures. TG may more accurately reflect the hemostasis state than ROTEM in pediatric patients treated with emicizumab.
Keywords: ROTEM; emicizumab; hemophilia A; inhibitors; thrombin generation.
© 2019 Wiley Periodicals, Inc.
Similar articles
-
Emicizumab prophylaxis: Prospective longitudinal real-world follow-up and monitoring.Haemophilia. 2021 May;27(3):383-391. doi: 10.1111/hae.14318. Epub 2021 Apr 23. Haemophilia. 2021. PMID: 33892524
-
Global coagulation function assessed by rotational thromboelastometry predicts coagulation-steady state in individual hemophilia A patients receiving emicizumab prophylaxis.Int J Hematol. 2019 Oct;110(4):419-430. doi: 10.1007/s12185-019-02698-8. Epub 2019 Jun 28. Int J Hematol. 2019. PMID: 31254165
-
A modified thrombin generation assay to evaluate the plasma coagulation potential in the presence of emicizumab, the bispecific antibody to factors IXa/X.Int J Hematol. 2020 Nov;112(5):621-630. doi: 10.1007/s12185-020-02959-x. Epub 2020 Aug 3. Int J Hematol. 2020. PMID: 32748217
-
Real-world case series and summary of current literature of infants and toddlers with severe hemophilia A with inhibitor on prophylaxis with emicizumab.Pediatr Blood Cancer. 2021 May;68(5):e28942. doi: 10.1002/pbc.28942. Epub 2021 Feb 8. Pediatr Blood Cancer. 2021. PMID: 33559300 Review.
-
Bispecific Antibody Emicizumab for Haemophilia A: A Breakthrough for Patients with Inhibitors.BioDrugs. 2018 Dec;32(6):561-570. doi: 10.1007/s40259-018-0315-0. BioDrugs. 2018. PMID: 30430367 Review.
Cited by
-
Two pediatric cases of severe hemophilia A in which emicizumab prophylaxis failed to prevent traumatic extra-articular hemorrhage.Int J Hematol. 2023 Apr;117(4):607-612. doi: 10.1007/s12185-022-03490-x. Epub 2022 Nov 12. Int J Hematol. 2023. PMID: 36370317 Free PMC article.
-
Emicizumab state-of-the-art update.Haemophilia. 2022 May;28 Suppl 4(Suppl 4):103-110. doi: 10.1111/hae.14524. Haemophilia. 2022. PMID: 35521723 Free PMC article.
-
Emergency management in patients with haemophilia A and inhibitors on prophylaxis with emicizumab: AICE practical guidance in collaboration with SIBioC, SIMEU, SIMEUP, SIPMeL and SISET.Blood Transfus. 2020 Mar;18(2):143-151. doi: 10.2450/2019.0186-19. Epub 2019 Oct 18. Blood Transfus. 2020. PMID: 31657709 Free PMC article.
-
Advances in the management of haemophilia: emerging treatments and their mechanisms.J Biomed Sci. 2021 Sep 14;28(1):64. doi: 10.1186/s12929-021-00760-4. J Biomed Sci. 2021. PMID: 34521404 Free PMC article. Review.
-
Non-clotting factor therapies for preventing bleeds in people with congenital hemophilia A or B.Cochrane Database Syst Rev. 2024 Feb 27;2(2):CD014544. doi: 10.1002/14651858.CD014544.pub2. Cochrane Database Syst Rev. 2024. PMID: 38411279 Free PMC article.
References
REFERENCES
-
- Pipe SW, Valentino LA. Optimizing outcomes for patients with severe haemophilia A. Haemophilia. 2007;4(13Suppl):1-16.
-
- Manco-Johnson MJ, Soucie JM, Gill JC. Joint Outcomes Committee of the Universal Data Collection, US Hemophilia Treatment Center Network. Prophylaxis usage, bleeding rates, and joint outcomes of hemophilia, 1999 to 2010: a surveillance project. Blood. 2017;129:2368-2374.
-
- Kempton CL, Meeks SL. Toward optimal therapy for inhibitors in hemophilia. Blood. 2014;124:3365-3372.
-
- Abbonizio F, Giampaolo A, Coppola A; Italian Association of Haemophilia Centres, Arcieri R, Hassan HJ. Therapeutic management and costs of severe haemophilia A patients with inhibitors in Italy. Haemophilia. 2014;20:e243-e250.
-
- Leissinger CA, Singleton T, Kruse-Jarres R. How I use bypassing therapy for prophylaxis in patients with hemophilia A and inhibitors. Blood. 2015;126:153-159.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous