Switching between Enzyme Replacement Therapies and Substrate Reduction Therapies in Patients with Gaucher Disease: Data from the Gaucher Outcome Survey (GOS).

Gaucher disease enzyme replacement therapy substrate reduction therapy treatment switch

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
31 Aug 2022
Historique:
received: 14 07 2022
revised: 27 08 2022
accepted: 30 08 2022
entrez: 9 9 2022
pubmed: 10 9 2022
medline: 10 9 2022
Statut: epublish

Résumé

Switching between enzyme replacement therapies (ERT) and substrate reduction therapies (SRT) in patients with type 1 Gaucher disease (GD1) is not uncommon; however, the reasons for switchng treatments have not been explored in detail. Data from the Gaucher Outcome Survey (GOS), an international registry for patients with confirmed GD, were used to evaluate the reasons for, and consequences of, switching between these treatment types. Of the 1843 patients enrolled in GOS on 25 February 2020, 245 had undergone a treatment switch: 222 from initial ERT to SRT (of whom 88 later switched back to ERT) and 23 from initial SRT to ERT. The most common reasons for ERT-SRT switching were duration of infusion (25.4%), drug shortage (22.0%), and adverse events (AEs; 11.9%), and for SRT-ERT switching, AEs (63.6%), lack of beneficial effect (16.4%), and participation in a clinical trial (9.1%). Bodyweight and hematologic parameters largely remained stable before and after switching between ERT and SRT, although with substantial variation between patients. These findings contribute to understanding why treatment switching occurs in patients with GD, and may help physicians recognize the real-world impact of treatment switching between ERT and SRT for patients with GD.

Identifiants

pubmed: 36079085
pii: jcm11175158
doi: 10.3390/jcm11175158
pmc: PMC9457166
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Shire Human Genetic Therapies, a Takeda company
ID : NA

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Auteurs

Derralynn A Hughes (DA)

LSD Unit, Royal Free London NHS Foundation Trust, University College London, London NW3 2QG, UK.

Patrick Deegan (P)

Addenbrookes Hospital, Cambridge CB2 0QQ, UK.

Pilar Giraldo (P)

CIBER de Enfermedades Raras, IIS Aragon, 50009 Zaragoza, Spain.
Translational Research Unit, IIS Aragon, 50009 Zaragoza, Spain.

Özlem Göker-Alpan (Ö)

Lysosomal Disorders Unit and Center for Clinical Trials, O&O Alpan LLC, Fairfax, VA 22030, USA.

Heather Lau (H)

Department of Neurology, New York University School of Medicine, New York, NY 10016, USA.

Elena Lukina (E)

Department of Orphan Diseases, National Research Center for Hematology, 125167 Moscow, Russia.

Shoshana Revel-Vilk (S)

Gaucher Unit, Shaare Zedek Medical Center, Jerusalem 9103102, Israel.
The Faculty of Medicine, Hebrew University, Jerusalem 9112102, Israel.

Maurizio Scarpa (M)

Centre for Rare Diseases, Academic Medical Centre Hospital of Udine, 33100 Udine, Italy.

Jaco Botha (J)

Takeda Pharmaceuticals International AG, 8152 Zurich, Switzerland.

Noga Gadir (N)

LSD Unit, Royal Free London NHS Foundation Trust, University College London, London NW3 2QG, UK.

Ari Zimran (A)

Gaucher Unit, Shaare Zedek Medical Center, Jerusalem 9103102, Israel.
The Faculty of Medicine, Hebrew University, Jerusalem 9112102, Israel.

Classifications MeSH