Literature DB >> 29886751

Prophylactic versus on-demand treatments for hemophilia: advantages and drawbacks.

Giancarlo Castaman1, Silvia Linari1.   

Abstract

INTRODUCTION: Early long-term prophylaxis is the standard of care to prevent joint bleeding and chronic arthropathy in patients with severe hemophilia. Areas covered: Despite the obvious prophylaxis advantages upon the clinical outcomes, there are still several drawbacks to be addressed for the optimal patients' compliance. Frequency of treatment due to short half-life of conventional FVIII and FIX concentrates, difficult venous access, adherence to the prescribed therapy and costs may represent significant critical issues. The development of inhibitors also makes replacement therapy ineffective, preventing patients from receiving long-term prophylaxis. This paper will review these drawbacks and the tools to overcome these limitations, mainly thanks to the use of extended half-life products and the development of novel non-conventional therapeutic approaches. Expert commentary: The use of extended half-life products may help in reducing the burden of the frequent intravenous administration and in better tailoring an individualized prophylaxis. The development of novel therapeutic approaches, like the bi-specific antibody mimicking the coagulation function of FVIII or inhibition of anticoagulant proteins may facilitate prophylaxis treatment not only in patients with inhibitors, but also in severe hemophilia patients without inhibitors. Exciting opportunities are emerging for improving prophylaxis in hemophilia.

Entities:  

Keywords:  Hemophilia; bleeding; challenge; extended half-life concentrates; novel therapeutic approaches; prophylaxis; replacement therapy

Mesh:

Substances:

Year:  2018        PMID: 29886751     DOI: 10.1080/17474086.2018.1486704

Source DB:  PubMed          Journal:  Expert Rev Hematol        ISSN: 1747-4094            Impact factor:   2.929


  3 in total

1.  LongHest project: A prospective, observational study of extended half-life treatment in the musculoskeletal health of patients with severe haemophilia A.

Authors:  Rubén Cuesta-Barriuso; Raúl Pérez-Llanes; Elena Donoso-Úbeda; Roberto Ucero-Lozano
Journal:  Haemophilia       Date:  2022-05-13       Impact factor: 4.263

2.  The risk of venipuncture in newborn with severe hemophilia: Case report of a large elbow hemorrhage and literature review of compartment syndrome.

Authors:  Giuseppe Lassandro; Anna Amoruso; Valentina Palladino; Viviana Valeria Palmieri; Paola Giordano
Journal:  Hematol Rep       Date:  2021-06-09

3.  Recombinant factor VIII Fc fusion protein for the treatment of severe haemophilia A: Final results from the ASPIRE extension study.

Authors:  Beatrice Nolan; Johnny Mahlangu; Ingrid Pabinger; Guy Young; Barbara A Konkle; Chris Barnes; Keiji Nogami; Elena Santagostino; K John Pasi; Liane Khoo; Bent Winding; Huixing Yuan; Joachim Fruebis; Dan Rudin; Johannes Oldenburg
Journal:  Haemophilia       Date:  2020-03-30       Impact factor: 4.287

  3 in total

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