Dilemmas on emicizumab in children with haemophilia A: A survey of strategies from PedNet centres

Author:

Ranta Susanna1ORCID,Motwani Jayashree2,Blatny Jan3,Bührlen Martina4,Carcao Manuel5ORCID,Chambost Hervé6,Escuriola Carmen7,Fischer Kathelijn8ORCID,Kartal‐Kaess Mutlu9,de Kovel Marloes10,Kenet Gili11ORCID,Male Christoph12,Nolan Beatrice13ORCID,d'Oiron Roseline14ORCID,Olivieri Martin15ORCID,Zapotocka Ester16,Andersson Nadine G.17ORCID,Königs Christoph18

Affiliation:

1. Childhood Cancer Research Unit Department of Women's and Children's Health Karolinska Institutet Sweden and Astrid Lindgren Children's Hospital Karolinska University Hospital Stockholm Sweden

2. Birmingham Children's Hospital Birmingham UK

3. Department of Paediatric Haematology and Biochemistry University Hospital and Masaryk University Brno Czech Republic

4. Department of Pediatrics Klinikum Bremen Mitte Bremen Germany

5. Haemophilia Clinic and Haemostasis Program Division of Haematology/Oncology Department of Paediatrics Hospital for Sick Children University of Toronto Toronto Ontario Canada

6. AP‐HM Department of Pediatric Hematology Oncology Children Hospital La Timone & Aix Marseille University INSERM INRA C2VN Marseille France

7. Haemophilie‐Zentrum Rhein Main HZRM Mörfelden‐Walldorf Germany

8. Center for Benign Hematology Thrombosis and Hemostasis Van Creveldkliniek University Medical Center Utrecht University Utrecht the Netherlands

9. Division of Pediatric Hematology & Oncology Department of Pediatrics Inselspital University Hospital Bern Bern Switzerland

10. PedNet Haemophilia Research Foundation Baarn The Netherlands

11. The National Hemophilia Center& Institute of Thrombosis & Hemostasis Sheba Medical Center Tel Hashomer Israel and The Amalia Biron Research Institute of Thrombosis & Hemostasis Tel Aviv University Tel Aviv Israel

12. Department of Paediatrics Medical University of Vienna Vienna Austria

13. Children's Coagulation Centre Children's Health Ireland at Crumlin Dublin Ireland

14. Centre de Référence de l'Hémophilie et des Maladies Hémorragiques Constitutionnelles rares Hôpital Bicêtre AP‐HP et INSERM Hémostase inflammation thrombose HITH U1176 Université Paris‐Saclay Le Kremlin‐Bicêtre France

15. Pediatric thrombosis and Hemostasis Unit Pediatric Hemophilia Centre Dr. von Hauner Children´s Hospital LMU Munich Munich Germany

16. Department of Pediatric Hematology and Oncology University Hospital Motol Prague and 2nd Faculty of Medicine Charles University Prague Czech Republic

17. Center for Thrombosis and Hemostasis Department of Clinical Sciences and Pediatrics Skåne University Hospital, Malmö Lund University Lund Sweden

18. Department of Paediatrics and Adolescent Medicine Goethe University Frankfurt Frankfurt Germany

Abstract

AbstractIntroductionHaemophilia A care has changed with the introduction of emicizumab. Experience on the youngest children is still scarce and clinical practice varies between haemophilia treatment centres.AimWe aimed to assess the current clinical practice on emicizumab prophylaxis within PedNet, a collaborative research platform for paediatricians treating children with haemophilia.MethodsAn electronic survey was sent to all PedNet members (n = 32) between October 2022 and February 2023. The survey included questions on the availability of emicizumab, on the practice of initiating prophylaxis in previously untreated or minimally treated patients (PUPs or MTPs) and emicizumab use in patients with or without inhibitors.ResultsAll but four centres (28/32; 88%) responded. Emicizumab was available in clinical practice in 25/28 centres (89%), and in 3/28 for selected patients only (e.g. with inhibitors). Emicizumab was the preferred choice for prophylaxis in PUPs or MTPs in 20/25 centres; most (85%) started emicizumab prophylaxis before 1 year of age (30% before 6 months of age) and without concomitant FVIII (16/20; 80%). After the loading dose, 13/28 centres administered the recommended dosing, while the others adjusted the interval of injections to give whole vials. In inhibitor patients, the use of emicizumab during ITI was common, with low‐dose ITI being the preferred protocol.ConclusionMost centres choose to initiate prophylaxis with emicizumab before 12 months of age and without concomitant FVIII. In inhibitor patients, ITI is mostly given in addition to emicizumab, but there was no common practice on how to proceed after successful ITI.

Publisher

Wiley

Subject

Genetics (clinical),Hematology,General Medicine

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