Bleeding control improves after switching to emicizumab: Real-world experience of 177 children in the PedNet registry

Despite the rapid uptake of emicizumab in the paediatric haemophilia A (HA) population, real-world data on the safety and efficacy is limited. To report on bleeding and safety in paediatric patients receiving emicizumab prophylaxis. Data were extracted from the multicentre prospective observational...

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Veröffentlicht in:Haemophilia : the official journal of the World Federation of Hemophilia 2024-05, Vol.30 (3), p.685-692
Hauptverfasser: van der Zwet, Konrad, de Kovel, Marloes, Motwani, Jayashree, van Geet, Chris, Nolan, Beatrice, Glosli, Heidi, Escuriola Ettingshausen, Carmen, Königs, Christoph, Kenet, Gili, Fischer, Kathelijn
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Sprache:eng
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Zusammenfassung:Despite the rapid uptake of emicizumab in the paediatric haemophilia A (HA) population, real-world data on the safety and efficacy is limited. To report on bleeding and safety in paediatric patients receiving emicizumab prophylaxis. Data were extracted from the multicentre prospective observational PedNet Registry (NCT02979119). Children with haemophilia A, and ≥50 FVIII exposures or inhibitors present receiving emicizumab maintenance therapy were analysed. Data were summarized as medians with interquartile range (IQR, P25-P75). Mean (95% confidence interval (CI)), annualized (joint) bleeding rate (A(J)BR) during emicizumab and ≤2 years before emicizumab prophylaxis were modelled and compared using negative binomial regression. Total of 177 patients started emicizumab at median 8.6 years (IQR 4.8-13.1), most had no FVIII inhibitors (64%). Follow up before emicizumab was median: 1.68 years (IQR: 1.24-1.90) and during emicizumab: 1.32 years (IQR: .94-2.11). In patients without inhibitors, mean ABR reduced after starting emicizumab from 2.41 (CI 1.98-2.95) to 1.11 (CI .90-1.36, p 
ISSN:1351-8216
1365-2516
DOI:10.1111/hae.15015