Literature DB >> 36188439

Comparison of Real-World Dose and Consumption for Two Extended Half-Life Recombinant Factor VIII Products for the Treatment of Hemophilia A in the United States.

Yanyu Wu1, Shawn X Sun1, Tao Fan2.   

Abstract

Background: US patients with hemophilia A can receive prophylaxis with extended half-life recombinant factor VIII (rFVIII) products, including efmoroctocog alfa (fragment crystallizable fusion protein) and rurioctocog alfa pegol (antihemophilic factor [recombinant], PEGylated). Objective: To evaluate dosing patterns and weekly consumption of extended half-life rFVIII products in the United States.
Methods: We performed a retrospective analysis using the US Specialty Pharmacy Database (2015-2018). Included patients had a diagnosis of hemophilia A, ≥2 consecutive monthly claims for efmoroctocog alfa or rurioctocog alfa pegol for prophylaxis, and weight data. Outcome measures included weekly dosing frequency and dispensed weekly dose.
Results: The analysis included 774 patients (efmoroctocog alfa, 506; rurioctocog alfa pegol, 268). Mean (SD) age was 24.2 (15.8) and 26.3 (14.9) years for patients receiving efmoroctocog alfa and rurioctocog alfa pegol, respectively; mean (SD) weight was 68.4 (36.8) and 79.8 (37.7) kg, respectively. The most frequent efmoroctocog alfa regimen was twice weekly (45.7%), followed by every 4 days (20.6%), every 3 days (9.1%), and 3 times per week (7.5%). The most frequent rurioctocog alfa pegol regimen was twice weekly (72.4%), followed by 3 times per week (8.7%), every 4 days (7.6%), and every 3 days (5.5%). The proportion of efmoroctocog alfa twice-weekly dispensing records increased from 31.5% to 50.9%, and every 4 days dispensing records decreased from 31.3% to 14.5% (2015-2018). The proportion of rurioctocog alfa pegol dispensing records remained broadly stable (2016-2018). Overall, mean (SD; median) weekly prophylactic dose was 105.4 (77.9; 92.6) IU/kg with efmoroctocog alfa, and 96.8 (41.9; 90.9) IU/kg with rurioctocog alfa pegol.
Conclusion: In this database study, the most frequently observed dosing frequency was twice weekly for patients receiving efmoroctocog alfa or rurioctocog alfa pegol. The observed mean weekly consumption was slightly higher, and variation was greater, in patients receiving efmoroctocog alfa versus rurioctocog alfa pegol.
© 2022 Wu et al.

Entities:  

Keywords:  PEGylated; antihemophilic factor (recombinant); dosing patterns; efmoroctocog alfa; fragment crystallizable fusion protein; hemophilia A; rurioctocog alfa pegol

Year:  2022        PMID: 36188439      PMCID: PMC9518681          DOI: 10.2147/JBM.S359510

Source DB:  PubMed          Journal:  J Blood Med        ISSN: 1179-2736


  21 in total

1.  Guidelines for the management of hemophilia.

Authors:  A Srivastava; A K Brewer; E P Mauser-Bunschoten; N S Key; S Kitchen; A Llinas; C A Ludlam; J N Mahlangu; K Mulder; M C Poon; A Street
Journal:  Haemophilia       Date:  2012-07-06       Impact factor: 4.287

Review 2.  Optimal treatment strategies for hemophilia: achievements and limitations of current prophylactic regimens.

Authors:  Johannes Oldenburg
Journal:  Blood       Date:  2015-02-23       Impact factor: 22.113

3.  Patient and caregiver preferences for haemophilia A treatments: A discrete choice experiment.

Authors:  Jun Su; Nanxin Li; Namita Joshi; Xinyi Ng; Marc Botteman; Rachel Shah; Nisha Jain; Nicole Lyn; Ronald Preblick
Journal:  Haemophilia       Date:  2020-09-16       Impact factor: 4.287

4.  Rurioctocog alfa pegol PK-guided prophylaxis in hemophilia A: results from the phase 3 PROPEL study.

Authors:  Robert Klamroth; Jerzy Windyga; Vlad Radulescu; Peter W Collins; Oleksandra Stasyshyn; Hishamshah Mohd Ibrahim; Werner Engl; Srilatha D Tangada; William Savage; Bruce Ewenstein
Journal:  Blood       Date:  2021-04-01       Impact factor: 22.113

5.  Association of peak factor VIII levels and area under the curve with bleeding in patients with haemophilia A on every third day pharmacokinetic-guided prophylaxis.

Authors:  L A Valentino; S W Pipe; P W Collins; V S Blanchette; E Berntorp; K Fischer; B M Ewenstein; M Oh; G Spotts
Journal:  Haemophilia       Date:  2016-03-01       Impact factor: 4.287

6.  Establishing the Prevalence and Prevalence at Birth of Hemophilia in Males: A Meta-analytic Approach Using National Registries.

Authors:  Alfonso Iorio; Jeffrey S Stonebraker; Hervé Chambost; Michael Makris; Donna Coffin; Christine Herr; Federico Germini
Journal:  Ann Intern Med       Date:  2019-09-10       Impact factor: 25.391

7.  Real-world outcomes associated with standard half-life and extended half-life factor replacement products for treatment of haemophilia A and B.

Authors:  Amit Chhabra; Dean Spurden; Patrick F Fogarty; Bartholomew J Tortella; Emily Rubinstein; Simon Harris; Andreas M Pleil; Jennifer Mellor; Jonathan de Courcy; José Alvir
Journal:  Blood Coagul Fibrinolysis       Date:  2020-04       Impact factor: 1.061

8.  Extended half-life factor VIII concentrates in adults with hemophilia A: Comparative pharmacokinetics of two products.

Authors:  Jerome Teitel; Michelle Sholzberg; Alfonso Iorio
Journal:  Res Pract Thromb Haemost       Date:  2021-02-23

9.  A Retrospective Observational Study of Rurioctocog Alfa Pegol in Clinical Practice in the United States.

Authors:  Louis Aledort; Scott Milligan; Maureen Watt; Jason Booth
Journal:  J Manag Care Spec Pharm       Date:  2020-04

Review 10.  Hemophilia therapy: the future has begun.

Authors:  Pier Mannuccio Mannucci
Journal:  Haematologica       Date:  2020-02-14       Impact factor: 9.941

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