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Published on: August 7, 2017
Emicizumab treatment and monitoring in a paediatric cohort: real-world data
Assaf A Barg1,2, Tami Livnat1,2, Ivan Budnik3
1National Hemophilia Center, Sheba Medical Center, Tel Hashomer, Israel.
Insights
Emicizumab prophylaxis is safe and effective for severe haemophilia A in children, with zero bleeds in half of patients. However, laboratory monitoring, including thrombin generation, cannot predict trauma-related bleeding risk.
Area of Science:
- Paediatric Haematology
- Pharmacology
- Clinical Trials
Background:
- Limited real-world data exists on emicizumab use in paediatric severe haemophilia A (HA).
- Evaluating safety, efficacy, and monitoring is crucial for this population, including infants and non-inhibitor patients.
Purpose of the Study:
- To assess the safety, efficacy, and laboratory monitoring parameters of emicizumab prophylaxis in children with severe HA.
- To investigate bleeding risk, adverse events, and surgical outcomes in this cohort.
Main Methods:
- A cohort of 40 children with severe HA received emicizumab prophylaxis.
- Data collected included bleeding events, trauma, adverse events, surgeries, emicizumab levels, aPTT, and thrombin generation.
- Median follow-up was 45 weeks.
Main Results:
- Twenty patients experienced zero bleeds; all bleeds were trauma-related.
- Sixteen surgical interventions in 12 patients showed no thrombotic complications.
- Prolonged aPTT normalized with emicizumab, correlating with its plasma levels. Thrombin generation increased, but was lower in younger infants.
Conclusions:
- Emicizumab prophylaxis is safe and well-tolerated in paediatric severe HA.
- Laboratory monitoring, including thrombin generation, did not predict bleeding risk in this study.
- Further research is needed for surgical procedures, but routine thrombin generation monitoring is not supported.
Abstract:
Real-world data on emicizumab use and monitoring in paediatric severe haemophilia A (HA) patients are scarce. We therefore sought to evaluate safety, efficacy, and laboratory monitoring of emicizumab prophylaxis in a cohort of 40 children with severe HA, including 22 non-inhibitor patients and nine infants younger than one year. Bleeding, trauma, adverse events, and surgeries were documented during a median follow-up of 45 weeks. Emicizumab levels, activated partial thromboplastin time (aPTT) values, and thrombin generation were measured before and during therapy. Twenty patients experienced zero bleeds. All bleeding was trauma-related, and bleeding risk was positively correlated with the length of emicizumab prophylaxis. Sixteen surgical interventions were performed in 12 patients, with no thrombotic complications or thrombotic microangiopathy. Prolonged aPTT values normalised after emicizumab initiation, correlating with an increase in emicizumab plasma levels. Elevation in the thrombin generation was observed following emicizumab prophylaxis, with lower values recorded in younger infants. Emicizumab prophylaxis was safe and well tolerated. As all bleedings were trauma-related, laboratory monitoring could not predict bleeding risk. Our results do not support routine thrombin generation monitoring in children treated by emicizumab, yet further studies are warranted in the context of surgical procedures.
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