Real-World Efficacy and Safety of Plasma-Derived Von Willebrand Factor-Containing Factor VIII Concentrates in Patients With Von Willebrand Disease in Italy.

bleeding plasma-derived von Willebrand factor / factor VIII concentrate secondary long-term prophylaxis surgery von Willebrand disease

Journal

Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis
ISSN: 1938-2723
Titre abrégé: Clin Appl Thromb Hemost
Pays: United States
ID NLM: 9508125

Informations de publication

Date de publication:
21 Jul 2024
Historique:
medline: 21 7 2024
pubmed: 21 7 2024
entrez: 21 7 2024
Statut: aheadofprint

Résumé

Plasma-derived von Willebrand factor-containing factor VIII concentrates (pd-VWF/FVIII-C) are the mainstay of treatment in von Willebrand disease (VWD). Real-world data on efficacy and safety of these pd-VWF/FVIII-C are required. To retrospectively evaluate the efficacy and safety of pd-VWF/FVIII-C (Fanhdi® and Alphanate®, Grifols) in clinical practice in Italy. A multicentric, observational, retrospective study at 10 Italian centers was conducted. Eligible patients diagnosed with inherited VWD (ISTH criteria) were treated with either Fanhdi® or Alphanate® for bleeding episodes, prevention of surgical bleeding and secondary long-term prophylaxis (SLTP) according to clinical practice with medical records collected from January 2007 to December 2019. Efficacy/safety of pd-VWF/FVIII-C was assessed according to FDA-agreed objective criteria following regulatory procedures. Fifty-seven patients (M/F: 21/36) were enrolled in the study with the following VWD types: VWD1 (n = 29, 52%), VWD2A (n = 10, 18%), VWD2B (n = 7, 12%), VWD2M (n = 2, 4%), VWD2N (n = 1, 2%), VWD2 unclassified (n = 1, 2%), and VWD3 (n = 7, 12%). These pd-VWF/FVIII-C were used to manage 58 bleeding episodes (n = 24 patients), 100 surgeries (n = 47 patients), and 7 SLTP (n = 6 patients). Global clinical efficacy with these pd-VWF/FVIII-C was reported to be excellent/good in 85% of bleeding episodes, 98% of surgeries, and 100% of SLTP. As far as safety, no adverse-drug-related episodes, immunogenic or thrombotic events were reported. This study confirmed that Fanhdi® and Alphanate® were effective and safe in the management of bleeding episodes, the prevention of bleeding during surgeries and for SLTP in Italian patients with inherited VWD.

Identifiants

pubmed: 39033425
doi: 10.1177/10760296241264541
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

10760296241264541

Déclaration de conflit d'intérêts

Declaration of Conflicting InterestsR. Mir is full-time employee of Grifols. E. Mairal is a former full-time employee of Grifols. A.B. Federici has been involved in advisory boards of Baxalta/Shire/Takeda, CSL Behring, Grifols, Kedrion, LFB and Octapharma with honoraria related to VWD. The remaining authors declare that there is no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Auteurs

Augusto B Federici (AB)

Department of Haematology and Haemotherapy, Luigi Sacco Hospital, Milano, Italy.

Rita Carlotta Santoro (RC)

Haemophilia Centre, Haemostasis and Thrombosis Unit, Department of Haemato-Oncology, Azienda Ospedaliero-Universitaria Dulbecco, Catanzaro, Italy.

Cristina Santoro (C)

Department of Hematology, University Hospital Policlinico Umberto I, Rome, Italy.

Lisa Pieri (L)

Center for Bleeding Disorders and Coagulation, Department of Oncology, Careggi University Hospital, Florence, Italy.

Roberto Mario Santi (RM)

SSD Thrombosis and Hemostasis Center, Azienda Ospedaliera "SS Antonio e Biagio e C. Arrigo", Alessandria, Italy.

Giovanni Barillari (G)

Center for Hemorrhagic and Thrombotic Diseases, Udine General and University Hospital "S. Maria della Misericordia", Udine, Italy.

Alessandra Borchiellini (A)

Regional Reference Center for Thrombotic and Haemorrhagic Disorders of Hematology, Division Department of Hematology and Oncology, A.O.U. Città della Salute e della Scienza di Torino, Torino, Italy.

Alberto Tosetto (A)

Hemophilia and Thrombosis Center, Hematology Department, San Bortolo Hospital, Vicenza, Italy.

Ezio Zanon (E)

Haemophilia Center, Department of Medicine, University of Padua Medical School, Padua, Italy.

Raimondo De Cristofaro (R)

Thrombotic and Hemorrhagic Diseases Center and Department of Translational Medicine and Surgery, Catholic University of the S. Heart, School of Medicine, Roma, Italy.

Esther Mairal (E)

Scientific and Medical Affairs Department, Grifols, Barcelona, Spain.

Roser Mir (R)

Scientific and Medical Affairs Department, Grifols, Barcelona, Spain.

Classifications MeSH