Disease and treatment burden of patients with haemophilia entering the explorer6 non‐interventional study

Author:

Windyga Jerzy1ORCID,Apte Shashikant2,Frei‐Jones Melissa3,Fujii Teruhisa4,Lyu Chuhl Joo5,Villarreal Martinez Laura6,Sathar Jameela7,Stasyshyn Oleksandra8,Tran Huyen9,Zozulya Nadezhda10,Brown Frandsen Renée11,Neergaard Jesper Skov11,Thaung Zaw Jay Jay11,Mahlangu Johnny12ORCID

Affiliation:

1. Department of Hemostasis Disorders and Internal Medicine Laboratory of Hemostasis and Metabolic Diseases, Institute of Hematology and Transfusion Medicine Warsaw Poland

2. Sahyadri Speciality Hospital Pune India

3. Pediatric Hematology‐Oncology Joe R. and Teresa Lozano Long School of Medicine, University of Texas Health Science Center at San Antonio San Antonio Texas USA

4. Hiroshima University Hospital Hiroshima Japan

5. Yonsei University Severance Hospital Seoul Korea

6. Hospital Universitario Dr. José Eleuterio González Monterrey Mexico

7. Hospital Ampang Ampang Selangor Darul Ehsan Malaysia

8. Institute of Blood Pathology and Transfusion Medicine Lviv Ukraine

9. The Alfred Hospital Melbourne Victoria Australia

10. National Medical Center for Hematology Moscow Russia

11. Novo Nordisk A/S Søborg Denmark

12. University of the Witwatersrand and NHLS, Charlotte Maxeke Johannesburg Academic Hospital Johannesburg South Africa

Abstract

AbstractObjectivesWe aimed to characterise baseline disease and treatment burden in a large population with haemophilia A/B, both with (HAwI/HBwI) and without (HA/HB) inhibitors.MethodsThe prospective, non‐interventional explorer6 study included patients ≥12 years old with severe HA, severe/moderate HB or HAwI/HBwI of any severity, treated according to local standard of care (excluding previous/current exposure to concizumab or emicizumab). Baseline characteristics and historical clinical data were collected and patient‐reported outcomes, including treatment burden, were assessed.ResultsThe explorer6 study enrolled 231 patients with haemophilia (84 HAwI/HBwI) from 33 countries. At baseline, patients with HA/HB treated with prophylaxis had the lowest median annualised bleeding rates (ABRs; 2.0), irrespective of haemophilia type; of these patients, 27.5% (HA) and 31.4% (HB) had target joints. Patients with HAwI/HBwI treated episodically reported the highest treatment burden. Of these patients, 28.5% (HAwI) and 25.1% (HBwI) performed sports activities in the month before screening.ConclusionDespite receiving routine clinical care, historical and baseline information from patients enrolled in explorer6 showed that patients with HA/HB treated episodically and patients with HAwI/HBwI had higher ABRs, higher treatment burden and participated in sports less than those with HA/HB treated with prophylaxis. Emerging treatments could be beneficial in addressing these unmet medical needs.

Publisher

Wiley

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