Emicizumab prophylaxis in pups and mtps with severe haemophilia: The pednet real world experience in 80 infants

Abstract Emicizumab (Hemlibra®, Roche) is a humanized bispecific antibody used for subcutaneous prophylaxis in children of any age and adults with haemophilia A (HA). While the HAVEN-7 trial provided primary data on 55 infants with severe HA without FVIII inhibitors, real-world data regarding this age group remains limited. To address this, we analysed prospectively collected data on inhibitor development and bleeding in emicizumab-treated previously untreated patients (PUPs) and minimally treated patients (MTPs; i.e. <6 exposure days (EDs) to FVIII) at PedNet Centres. Data were extracted from the PedNet Registry (a prospective, observational multicentre study collecting data from 34 haemophilia treatment centres in 19 countries), as of January 1, 2025, focusing on children with severe HA without inhibitors who started emicizumab as either PUPs or MTPs, and had received emicizumab prophylaxis for ≥12 weeks. Children included in the HAVEN-7 trial were excluded. Ethical approval was obtained from the parents/guardians of all participants. Key endpoints were inhibitor development, and bleeding rates, including the proportion of children with zero treated bleeds. We analysed 80 infants (39/80 were PUP) with a median follow-up of 84.5 weeks and a median age at emicizumab initiation of 8.6 months (P25-P75 6.7-11.3; range 0.2-26.4). During follow-up, 46/80 infants received FVIII for bleeding episodes (median 3 (P25-P75 1-6; range 1-108 lifetime EDs)) and/or concomitant prophylaxis (n=10). The model-based annualized bleeding rate was 0.6 (95%CI 0.4 – 1.1) with 56% experiencing zero treated bleeds, and no serious adverse events or thromboses were reported. Five infants (2 MTPs) developed FVIII inhibitors (3 high responders (>5.0 BU/mL)) after 4-18 exposure days to FVIII. These data support the safety and efficacy of early emicizumab prophylaxis. However, long-term effects on FVIII inhibitor development require further investigation.

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Journal
Blood
Published
2025-11-03
DOI
https://doi.org/10.1182/blood-2025-305
Primary Topic
Hemophilia Treatment and Research
Type
article
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article

Emicizumab prophylaxis in pups and mtps with severe haemophilia: The pednet real world experience in 80 infants

Giancarlo Castaman, Caroline Oudot, Martin Olivieri, Ester Zápotocká et al.
Blood
Hemophilia Treatment and Research
article

Emicizumab prophylaxis in pups and mtps with severe haemophilia: The pednet real world experience in 80 infants

Giancarlo Castaman, Caroline Oudot, Martin Olivieri, Ester Zápotocká, Nadine G. Andersson, Beatrice Nolan, Manuel Carção, Helen Pergantou, Christoph Male, Chris Königs, Marloes de Kovel, Susanna Ranta, Jayashree Motwani, Carmen Escuriola-Ettingshausen, Kathelijn Fischer, Gili Kenet, Jan Blanty
article en

Abstract

Abstract Emicizumab (Hemlibra®, Roche) is a humanized bispecific antibody used for subcutaneous prophylaxis in children of any age and adults with haemophilia A (HA). While the HAVEN-7 trial provided primary data on 55 infants with severe HA without FVIII inhibitors, real-world data regarding this age group remains limited. To address this, we analysed prospectively collected data on inhibitor development and bleeding in emicizumab-treated previously untreated patients (PUPs) and minimally treated patients (MTPs; i.e. <6 exposure days (EDs) to FVIII) at PedNet Centres. Data were extracted from the PedNet Registry (a prospective, observational multicentre study collecting data from 34 haemophilia treatment centres in 19 countries), as of January 1, 2025, focusing on children with severe HA without inhibitors who started emicizumab as either PUPs or MTPs, and had received emicizumab prophylaxis for ≥12 weeks. Children included in the HAVEN-7 trial were excluded. Ethical approval was obtained from the parents/guardians of all participants. Key endpoints were inhibitor development, and bleeding rates, including the proportion of children with zero treated bleeds. We analysed 80 infants (39/80 were PUP) with a median follow-up of 84.5 weeks and a median age at emicizumab initiation of 8.6 months (P25-P75 6.7-11.3; range 0.2-26.4). During follow-up, 46/80 infants received FVIII for bleeding episodes (median 3 (P25-P75 1-6; range 1-108 lifetime EDs)) and/or concomitant prophylaxis (n=10). The model-based annualized bleeding rate was 0.6 (95%CI 0.4 – 1.1) with 56% experiencing zero treated bleeds, and no serious adverse events or thromboses were reported. Five infants (2 MTPs) developed FVIII inhibitors (3 high responders (>5.0 BU/mL)) after 4-18 exposure days to FVIII. These data support the safety and efficacy of early emicizumab prophylaxis. However, long-term effects on FVIII inhibitor development require further investigation.

BloodVol. 146(Supplement 1)
Goethe University Frankfurt (DE), University of Vienna (AT), Karolinska University Hospital (SE), Malmö University (SE), Lund University (SE), Masaryk University (CZ), Sheba Medical Center (IL), Hospital for Sick Children (CA), Children's Health Ireland at Crumlin (IE), LMU Klinikum (DE), Apotheek Haagse Ziekenhuizen (NL), University Hospital in Motol (CZ), Haemophilia Foundation Australia (AU), Birmingham Children's Hospital (GB), Azienda Ospedaliero-Universitaria Careggi (IT), Children's Hospital Agia Sophia (GR), University Hospital Frankfurt (DE), Rheinmetall (Switzerland) (CH), Hôpital Purpan (FR), Medical University of Vienna (AT), Ludwig-Maximilians-Universität München (DE)
Openalex Percentile: Top 48%
Hemophilia Treatment and Research
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