Literature DB >> 27385432

Changes in health-related quality of life with treatment of longer-acting clotting factors: results in the A-LONG and B-LONG clinical studies.

K W Wyrwich1, S Krishnan2, P Auguste1, J-L Poon1, R von Maltzahn1, R Yu1, G F Pierce2, B Mei2, J Mahlangu3, S von Mackensen4.   

Abstract

INTRODUCTION: In haemophilia, prophylactic infusion of replacement factor can result in improvements in health-related quality of life (HRQoL) when compared with episodic treatment. The Haemophilia-specific Quality of Life (Haem-A-QoL) questionnaire assessed HRQoL in adults with severe haemophilia A or B who received prophylactic or episodic treatment with recombinant factor VIII or IX Fc fusion protein (rFVIIIFc or rFIXFc) in the A-LONG or B-LONG clinical studies. AIMS: Understand changes in HRQoL during the A-LONG and B-LONG trials.
METHODS: Group-level and individual-level changes over time for the Haem-A-QoL key domains of 'Physical Health' and 'Sports & Leisure,' and 'Total Score' were evaluated in adults through baseline and 6-month HRQoL assessments. Previously determined responder definitions (RDs) were used for evaluating meaningful subject-level HRQoL improvements.
RESULTS: The analysis included 67 A-LONG and 51 B-LONG subjects who completed the Haem-A-QoL (baseline and 6 months). While HRQoL improvements were observed among all treatment groups, greater improvements in HRQoL were observed among subjects who received episodic treatment pre-study (and prophylaxis on-study) compared to those who received hyphenate prophylaxis. Applying the RDs for interpreting 6-month changes, 47.4%/33.3% ('Physical Health'), 35.9%/50.0% ('Sports & Leisure') and 23.9%/33.3% ('Total Score') of A-LONG subjects who received individualized or weekly prophylaxis were classified as HRQoL responders. In B-LONG, 69.2%/57.9% ('Physical Health'), 44.4%/56.7% ('Sports & Leisure') and 41.7%/44.1% ('Total Score') of subjects who received individualized or weekly prophylaxis were classified as HRQoL responders.
CONCLUSION: Changes in Haem-A-QoL key domains and 'Total Score' suggest that prophylaxis with long-acting rFVIIIFc or rFIXFc resulted in meaningful HRQoL improvements.
© 2016 John Wiley & Sons Ltd.

Entities:  

Keywords:  haemophilia; prophylactic treatment; quality of life; recombinant factor IX replacement; recombinant factor VIII replacement; responder definition

Mesh:

Substances:

Year:  2016        PMID: 27385432     DOI: 10.1111/hae.12987

Source DB:  PubMed          Journal:  Haemophilia        ISSN: 1351-8216            Impact factor:   4.287


  15 in total

1.  Optimising prophylaxis outcomes and costs in haemophilia patients switching to recombinant FVIII-Fc: a single-centre real-world experience.

Authors:  Annarita Tagliaferri; Annalisa Matichecchia; Gianna F Rivolta; Federica Riccardi; Gabriele Quintavalle; Anna Benegiamo; Rossana Rossi; Antonio Coppola
Journal:  Blood Transfus       Date:  2019-11-04       Impact factor: 3.443

2.  Eftrenonacog Alfa: A Review in Haemophilia B.

Authors:  Sheridan M Hoy
Journal:  Drugs       Date:  2017-07       Impact factor: 9.546

Review 3.  Clotting factor concentrates for preventing bleeding and bleeding-related complications in previously treated individuals with haemophilia A or B.

Authors:  Omotola O Olasupo; Megan S Lowe; Ashma Krishan; Peter Collins; Alfonso Iorio; Davide Matino
Journal:  Cochrane Database Syst Rev       Date:  2021-08-18

Review 4.  Current and emerging factor VIII replacement products for hemophilia A.

Authors:  Lorraine A Cafuir; Christine L Kempton
Journal:  Ther Adv Hematol       Date:  2017-08-26

5.  Predictive Modeling Identifies Total Bleeds at 12-Weeks Postswitch to N8-GP Prophylaxis as a Predictor of Treatment Response.

Authors:  Pratima Chowdary; Kingsley Hampton; Victor Jiménez-Yuste; Guy Young; Soraya Benchikh El Fegoun; Aidan Cooper; Erik Scalfaro; Andreas Tiede
Journal:  Thromb Haemost       Date:  2021-12-05       Impact factor: 6.681

6.  Health-related quality-of-life and treatment satisfaction of individuals with hemophilia A treated with turoctocog alfa pegol (N8-GP): a new recombinant extended half-life FVIII.

Authors:  Susan Kearney; Leslie J Raffini; Tan P Pham; Xin Ying Lee; Sylvia von Mackensen; Andrea Landorph; Hideyuki Takedani; Johannes Oldenburg
Journal:  Patient Prefer Adherence       Date:  2019-04-09       Impact factor: 2.711

7.  Health-related quality of life in paediatric haemophilia B patients treated with rIX-FP.

Authors:  Sylvia von Mackensen; Jinesh Shah; Wilfried Seifert; Gili Kenet
Journal:  Haemophilia       Date:  2018-11-14       Impact factor: 4.287

Review 8.  Achieving the unimaginable: Health equity in haemophilia.

Authors:  Mark W Skinner; Diane Nugent; Pam Wilton; Brian O'Mahony; Gerry Dolan; Jamie O'Hara; Erik Berntorp
Journal:  Haemophilia       Date:  2019-11-13       Impact factor: 4.287

9.  The impact of extended half-life versus conventional factor product on hemophilia caregiver burden.

Authors:  Carolyn E Schwartz; Victoria E Powell; Jun Su; Jie Zhang; Adi Eldar-Lissai
Journal:  Qual Life Res       Date:  2018-02-01       Impact factor: 4.147

Review 10.  Updates in clinical trial data of extended half-life recombinant factor IX products for the treatment of haemophilia B.

Authors:  Johnny N Mahlangu
Journal:  Ther Adv Hematol       Date:  2018-10-05
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.