Laying the foundations for gene therapy in Italy for patients with haemophilia A: A Delphi consensus study

Autor: Giancarlo Castaman, Christian Carulli, Raimondo De Cristofaro, Marco Follino, Angelo Lupi, Maria Elisa Mancuso, Maria Francesca Mansueto, Angelo Claudio Molinari, Pietro Pasquetti, Cristina Santoro, Rita Carlotta Santoro, Sergio Siragusa, Luigi Piero Solimeno, Armando Tripodi, Ezio Zanon, Giovanni Di Minno
Přispěvatelé: Castaman, Giancarlo, Carulli, Christian, De Cristofaro, Raimondo, Follino, Marco, Lupi, Angelo, Mancuso, Maria Elisa, Mansueto, Maria Francesca, Molinari, Angelo Claudio, Pasquetti, Pietro, Santoro, Cristina, Santoro, Rita Carlotta, Siragusa, Sergio, Solimeno, Luigi Piero, Tripodi, Armando, Zanon, Ezio, Minno, Giovanni Di
Jazyk: angličtina
Rok vydání: 2023
Předmět:
Popis: IntroductionCurrent treatment for haemophilia A involves factor VIII replacement or non-replacement (emicizumab) therapies, neither of which permanently normalise factor VIII levels. Gene therapy using adeno-associated viral (AAV) vectors is an emerging long-term treatment strategy for people with severe haemophilia A (PwSHA) that is likely to be available for clinical use in the near future. AimThis article proposes practical guidelines for the assessment, treatment, and follow-up of potential PwSHA candidates for AAV-based gene therapy. MethodUsing the Delphi method, a working group of Italian stakeholders with expertise in and knowledge of the care of adults with haemophilia A analysed literature for AAV-based gene therapy and drafted a list of statements that were circulated to a panel of Italian peers. During two rounds of voting, panel members voted on their agreement with each statement to reach a consensus. ResultsThe Delphi process yielded 40 statements regarding haemophilia A gene therapy, across five topics: (1) organisational model; (2) multidisciplinary team; (3) patient engagement; (4) laboratory surveillance; and (5) patient follow-up and gene therapy outcomes. The consensus was reached for all 40 statements, with the second round of voting needed for five statements. ConclusionUse of the hub-and-spoke organisational model and multidisciplinary teams are expected to optimise patient selection for gene therapy, as well as the management of dosing and patient follow-up, patient engagement, laboratory surveillance, and patient expectations regarding outcomes. This approach should allow the benefits of AAV-based gene therapy for haemophilia A to be maximised.
Databáze: OpenAIRE