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IDEAL study: A real-world assessment of pattern of use and clinical outcomes with recombinant coagulation factor IX albumin fusion protein (rIX-FP) in patients with haemophilia B in Italy.
Tagliaferri, Annarita; Molinari, Angelo Claudio; Peyvandi, Flora; Coppola, Antonio; Demartis, Francesco; Biasoli, Chiara; Borchiellini, Alessandra; Cultrera, Dorina; De Cristofaro, Raimondo; Daniele, Filomena; Giordano, Paola; Marchesini, Emanuela; Margaglione, Maurizio; Marino, Renato; Pollio, Berardino; Radossi, Paolo; Santoro, Cristina; Santoro, Rita Carlotta; Siragusa, Sergio; Sottilotta, Gianluca; Tosetto, Alberto; Piscitelli, Lydia; Villa, Maria Rosaria; Zanon, Ezio; Finardi, Adele; Schiavetti, Irene; Vaccari, Daniella; Castaman, Giancarlo.
Afiliação
  • Tagliaferri A; Regional Reference Centre for Inherited Bleeding Disorders, University Hospital of Parma, Parma, Italy.
  • Molinari AC; Regional Reference Centre for Haemorrhagic Diseases, IRCCS Istituto Giannina Gaslini, Genova, Italy.
  • Peyvandi F; Department of Pathophysiology and Transplantation, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Haemophilia and Thrombosis Centre, Università degli Studi di Milano, Milan, Italy.
  • Coppola A; Regional Reference Centre for Inherited Bleeding Disorders, University Hospital of Parma, Parma, Italy.
  • Demartis F; Department of Oncology, Centre for Bleeding Disorders and Coagulation, Careggi University Hospital, Florence, Italy.
  • Biasoli C; Haemophilia and Transfusion Centre, "Bufalini" Hospital, Cesena, Italy.
  • Borchiellini A; Regional Reference Centre for Bleeding and Thrombotic Disorders, "Città della Salute e della Scienza" University Hospital, Turin, Italy.
  • Cultrera D; Haemophilia Regional Reference Centre, Haematology Unit, Policlinico "G. Rodolico - S. Marco" Hospital, Catania, Italy.
  • De Cristofaro R; Haemorrhagic and Thrombotic Disease Service, Area of Haematological and Oncological Sciences, IRCCS Fondazione Policlinico Universitario "A. Gemelli", Rome, Italy.
  • Daniele F; Haemostasis and Thrombosis Service, Ospedale Civile dell'Annunziata, Cosenza, Italy.
  • Giordano P; "B. Trambusti" General and Specialised Paediatrics Unit, "Giovanni XXIII" Hospital, University of Bari, Bari, Italy.
  • Marchesini E; Haemophilia Centre, Internal and Cardiovascular Medicine, "Santa Maria della Misericordia" University Hospital, Perugia, Italy.
  • Margaglione M; Department of Clinical and Experimental Medicine, University of Foggia, Foggia, Italy.
  • Marino R; Haemophilia and Thrombosis Centre, University Hospital, Bari, Italy.
  • Pollio B; Regional Reference Centre for Inherited Bleeding and Thrombotic Disorders, Transfusion Medicine, "Regina Margherita" Children Hospital, Turin, Italy.
  • Radossi P; Onco-Haematology Unit, Istituto Oncologico Veneto, Castelfranco Veneto Hospital, Castelfranco Veneto, Italy.
  • Santoro C; Department of Haematology, University Hospital Policlinico Umberto I, Rome, Italy.
  • Santoro RC; Regional Reference Centre for Haemophilia and Coagulation Diseases, Azienda Ospedaliera Pugliese-Ciaccio, Catanzaro, Italy.
  • Siragusa S; Haematology Unit, Thrombosis and Haemostasis Reference Regional Centre, University of Palermo, Palermo, Italy.
  • Sottilotta G; Haemophilia Centre, Grande Ospedale Metropolitano, Reggio Calabria, Italy.
  • Tosetto A; Haematology Department, Haemostasis and Thrombosis Unit, San Bortolo Hospital, Vicenza, Italy.
  • Piscitelli L; SSD Congenital Haemorrhagic Diseases, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
  • Villa MR; Haemophilia and Thrombosis Centre, Haematology Unit, "Ospedale del Mare" Hospital, Naples, Italy.
  • Zanon E; Department of Medicine, Haemophilia Centre, University Hospital of Padua, Padua, Italy.
  • Finardi A; CSL Behring, Milan, Italy.
  • Schiavetti I; Hippocrates Research, Genova, Italy.
  • Vaccari D; Department of Health Sciences, University of Genoa, Genoa, Italy.
  • Castaman G; Hippocrates Research, Genova, Italy.
Haemophilia ; 29(1): 135-144, 2023 Jan.
Article em En | MEDLINE | ID: mdl-36423202
ABSTRACT

INTRODUCTION:

Factor IX replacement therapy is used for treatment and prophylaxis of bleeding in haemophilia B. rIX-FP is an extended half-life albumin-fusion protein, which, in clinical studies, has demonstrated prolonged dosing intervals up to 21 days for routine prophylaxis, providing therapeutic benefit.

AIMS:

To describe dosing frequency and consumption (primary endpoint), efficacy and safety of rIX-FP treatment during routine clinical practice in Italy.

METHODS:

Patients with moderate/severe haemophilia B on prophylaxis with rIX-FP for ≥6 months, were enrolled in this observational study from October 2017 to February 2019 and followed-up for 2 years. Descriptive analysis included prospective and retrospective data (12 months prior to switching to rIX-FP).

RESULTS:

Data were collected from 59 male patients (median age 30.1 years) enrolled by 23 Italian centres. Of them, 50 were on prophylaxis during the entire observation period and completed the study. The infusion frequency changed from 2-3 times/week in 86.0% of patients with previous treatment, to less than once a week in 84.0% of patients treated with rIX-FP at the 2nd-year follow-up. The annual number of infusions decreased by about 70%, whereas the mean FIX activity trough level increased from 3.8% to 14.4% (mean > 10% in all the infusion regimens). Median Annualised Bleeding Rate of .0 was achieved across all prophylaxis regimens. Subjects with zero bleedings increased from 66.0% to 78.0% with rIX-FP.

CONCLUSION:

Treatment with rIX-FP reduced infusion frequency, while providing higher FIX trough levels with substantial benefit in terms of annualised bleeding rate and a good safety profile.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fator IX / Hemofilia B Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fator IX / Hemofilia B Idioma: En Ano de publicação: 2023 Tipo de documento: Article