Individual Treatment Trials-Do Experts Know and Use This Option to Improve the Treatability of Mucopolysaccharidosis?

ESITT MPS decision analysis framework model expert survey individual treatment trials mucopolysaccharidosis n-of-1 precision medicine rare disease treatment

Journal

Pharmaceuticals (Basel, Switzerland)
ISSN: 1424-8247
Titre abrégé: Pharmaceuticals (Basel)
Pays: Switzerland
ID NLM: 101238453

Informations de publication

Date de publication:
09 Mar 2023
Historique:
received: 16 02 2023
revised: 03 03 2023
accepted: 05 03 2023
medline: 30 3 2023
entrez: 29 3 2023
pubmed: 30 3 2023
Statut: epublish

Résumé

Mucopolysaccharidoses (MPS) are a group of rare, heterogeneous, lysosomal storage disorders. Patients show a broad spectrum of clinical features with a substantial unmet medical need. Individual treatment trials (ITTs) might be a valid, time- and cost-efficient way to facilitate personalized medicine in the sense of drug repurposing in MPS. However, this treatment option has so far hardly been used-at least hardly been reported or published. Therefore, we aimed to investigate the awareness and utilization of ITTs among MPS clinicians, as well as the potential challenges and innovative approaches to overcome key hurdles, by using an international expert survey on ITTs, namely, ESITT. Although 74% (20/27) were familiar with the concept of ITTs, only 37% (10/27) ever used it, and subsequently only 15% (2/16) published their results. The indicated hurdles of ITTs in MPS were mainly the lack of time and know-how. An evidence-based tool, which provides resources and expertise needed for high-quality ITTs, was highly appreciated by the vast majority (89%; 23/26). The ESITT highlights a serious deficiency of ITT implementation in MPS-a promising option to improve its treatability. Furthermore, we discuss the challenges and innovative approaches to overcome key barriers to ITTs in MPS.

Identifiants

pubmed: 36986515
pii: ph16030416
doi: 10.3390/ph16030416
pmc: PMC10058611
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Anna-Maria Wiesinger (AM)

Department of Medical Science, Institute of Congenital Metabolic Diseases, Paracelsus Medical University, 5020 Salzburg, Austria.
Department of Rare Diseases, European Reference Network for Hereditary Metabolic Diseases, MetabERN, 33100 Udine, Italy.

Hannah Strobl (H)

Department of Medical Science, Institute of Congenital Metabolic Diseases, Paracelsus Medical University, 5020 Salzburg, Austria.

Florian B Lagler (FB)

Department of Medical Science, Institute of Congenital Metabolic Diseases, Paracelsus Medical University, 5020 Salzburg, Austria.
Department of Rare Diseases, European Reference Network for Hereditary Metabolic Diseases, MetabERN, 33100 Udine, Italy.

Classifications MeSH