Effectiveness and Safety of Eliglustat Treatment in Gaucher Disease: Real-life Unicentric Experience.


Journal

Clinical therapeutics
ISSN: 1879-114X
Titre abrégé: Clin Ther
Pays: United States
ID NLM: 7706726

Informations de publication

Date de publication:
Nov 2023
Historique:
received: 24 05 2023
revised: 01 08 2023
accepted: 15 08 2023
medline: 27 11 2023
pubmed: 19 9 2023
entrez: 18 9 2023
Statut: ppublish

Résumé

The therapy and management of Gaucher disease (GD) have radically changed with the use of substrate reduction therapy, of which eliglustat is the most widely known drug, allowing it to overcome the limits of enzyme replacement therapy (ERT). The rarity of GD and the limited use of eliglustat outside clinical trials require further study of its strengths and weaknesses. In this study, we evaluated the effectiveness and safety of eliglustat in a cohort of 12 patients with GD followed up in our center, reporting a reduction in both chitotriosidase (394.3 vs 181.1 nmol/h/mL, P = 0.027) and glucosylsphingosine values (45.1 vs 18.9 ng/mL, P <0.001) after at least 12 months of therapy compared with baseline, regardless of patient demographic characteristics and GD characteristics. There were no drug-related serious adverse effects and no drug-related cardiac events. Most adverse events were mild and transient, mainly dyspepsia and abdominal pain. Of interest, we reported an absence of statistical difference in terms of response regarding glucosylsphingosine reduction in relation to naive or prior exposure to ERT (P = 0.296), which was confirmed also when patients were placed in naive and treated groups for <5 vs >5 years (P = 0.667). The use of eliglustat immediately after diagnosis may guarantee the best treatment for patients with milder phenotypes or with aggressive disease after an initial stabilization with ERT compared with ERT, which cannot adequately remove the disease burden despite the apparent response, thus potentially reducing future complications caused by substrate deposits.

Identifiants

pubmed: 37722956
pii: S0149-2918(23)00312-0
doi: 10.1016/j.clinthera.2023.08.010
pii:
doi:

Substances chimiques

eliglustat DR40J4WA67
sphingosyl beta-glucoside 52050-17-6
Pyrrolidines 0
Psychosine 2238-90-6

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1105-1110

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest G. Giuffrida received consultancy fees from Sanofi Genzyme, and U. Markovic received consultancy fees from Sanofi Genzyme and Amgen. The other authors declare no relevant conflict of interest to declare. The authors have indicated that they have no other conflicts of interest regarding the content of this article.

Auteurs

Andrea Duminuco (A)

Hematology Unit with BMT, A.O.U. Policlinico "G.Rodolico-San Marco", Catania, Italy.

Manlio Fazio (M)

Hematology Unit with BMT, A.O.U. Policlinico "G.Rodolico-San Marco", Catania, Italy.

Stephanie Grasso (S)

Hematology Unit with BMT, A.O.U. Policlinico "G.Rodolico-San Marco", Catania, Italy.

Lara Gullo (L)

Hematology Unit with BMT, A.O.U. Policlinico "G.Rodolico-San Marco", Catania, Italy.

Carla Riccobene (C)

Hematology Unit with BMT, A.O.U. Policlinico "G.Rodolico-San Marco", Catania, Italy.

Valeria Calafiore (V)

U.O.C. Hematology and Oncology, Ospedali Riuniti Villa Sofia-Cervello, Palermo, Italy.

Uros Markovic (U)

Hematology Unit with BMT, A.O.U. Policlinico "G.Rodolico-San Marco", Catania, Italy.

Francesco Di Raimondo (F)

Hematology Unit with BMT, A.O.U. Policlinico "G.Rodolico-San Marco", Catania, Italy; Dipartimento di Specialità Medico-Chirurgiche, CHIRMED, Sezione di Ematologia, Università degli Studi di Catania, Catania, Italy.

Gaetano Giuffrida (G)

Hematology Unit with BMT, A.O.U. Policlinico "G.Rodolico-San Marco", Catania, Italy. Electronic address: gaegiuffrida@gmail.com.

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Classifications MeSH