Cedric Hermans, Milad Karimi, Charlotte Camp, Steven W Pipe, Sandra Santos, Simon Harris, Matthew Reaney, David Hinds, Patrick Fogarty, Wolfgang Miesbach, Flora Peyvandi
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引用次数: 0
Abstract
Introduction: Haemophilia-free mind is an aspirational concept defined as a state in which affected individuals are liberated from physical, mental, and treatment burdens of haemophilia. A conceptual framework has been proposed for the haemophilia-free mind that comprises ten dimensions.
Aim: To evaluate changes in achievement towards a haemophilia-free mind in participants with haemophilia A who received valoctocogene roxaparvovec gene therapy in the GENEr8-1 trial (NCT03370913), by confirming relevant dimensions, with measures and thresholds for each.
Methods: An expert panel comprising four haemophilia clinicians and one patient expert identified dimensions of the haemophilia-free mind relevant to gene therapy. Measures and thresholds were defined for each dimension and used to analyse GENEr8-1 data to determine the proportion of participants achieving these thresholds at Baseline and Week 208.
Results: The expert panel confirmed 7/10 dimensions as appropriate for use in gene therapy trials and defined measurement thresholds for each dimension. Among GENEr8-1 trial participants, improvements were observed across all seven dimensions. The proportion of participants with zero treated bleeds increased from 33% (Baseline) to 54% (Week 208). Similarly, those reporting no exogenous factor VIII use rose from 0% to 33%. Improvements in perceived burden on family members, physical activity, and travel were 8%, 16%, and 18%, respectively.
Conclusion: This expert-led analysis demonstrates application of the haemophilia-free mind framework to clinical trial data using existing outcome measures. Mapping GENEr8-1 data to this framework demonstrated improvements of up to 33% in domains that contribute towards a haemophilia-free mind in participants after valoctocogene roxaparvovec treatment.
期刊介绍:
Haemophilia is an international journal dedicated to the exchange of information regarding the comprehensive care of haemophilia. The Journal contains review articles, original scientific papers and case reports related to haemophilia care, with frequent supplements. Subjects covered include:
clotting factor deficiencies, both inherited and acquired: haemophilia A, B, von Willebrand''s disease, deficiencies of factor V, VII, X and XI
replacement therapy for clotting factor deficiencies
component therapy in the developing world
transfusion transmitted disease
haemophilia care and paediatrics, orthopaedics, gynaecology and obstetrics
nursing
laboratory diagnosis
carrier detection
psycho-social concerns
economic issues
audit
inherited platelet disorders.