Preference of acromegaly patients for treatment attributes in Spain.


Journal

Endocrine
ISSN: 1559-0100
Titre abrégé: Endocrine
Pays: United States
ID NLM: 9434444

Informations de publication

Date de publication:
11 2023
Historique:
received: 04 04 2023
accepted: 19 07 2023
medline: 2 10 2023
pubmed: 29 7 2023
entrez: 28 7 2023
Statut: ppublish

Résumé

Acromegaly is a rare disease caused by increased growth hormone secretion and a subsequent increase in insulin-like growth factor I (IGF-I) levels. Patients display multiple comorbidities that affect their quality of life (QoL). Treatment aims to maintain good biochemical control, tumour control and reduce the risk of comorbidities; however, their impact on QoL has been overlooked until recently. We interviewed patients to explore their preferences with regard to treatment attributes. A cross-sectional study based on interviews and a discrete choice experiment (DCE) in a Spanish cohort. Adult patients diagnosed with acromegaly ≥1 year before the start of the study and under treatment were included. Treatment attributes were collected from patient testimony during face-to-face interviews. Then, a DCE was performed to elicit patient preferences for certain treatment attributes. Sixty-seven patients completed the study. QoL improvement was the most important treatment attribute (37%), followed by IGF-I control (20%), blood sugar control (17%) and tumour control (13%). Secondary attributes were pain associated with the route of administration (7%), diarrhoea (2%), administration method (2%) and storage conditions (2%). We then calculated the theoretical share of preference for existing treatments, based on the individual preference utility for each attribute and level. Pegvisomant obtained the highest share of preference overall, and the highest preference as a second-line treatment (53 and 95%, respectively). QoL greatly influences patient treatment preference. Since acromegaly patients are informed and aware of their disease, treatment choices should always be shared with patients.

Identifiants

pubmed: 37507554
doi: 10.1007/s12020-023-03462-z
pii: 10.1007/s12020-023-03462-z
pmc: PMC10543785
doi:

Substances chimiques

Insulin-Like Growth Factor I 67763-96-6

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

379-389

Informations de copyright

© 2023. The Author(s).

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Auteurs

Carmen Fajardo (C)

Endocrinology Department, La Ribera University Hospital, Alzira, Valencia, Spain.

Cristina Álvarez-Escola (C)

Endocrinology Department, La Paz University Hospital, Madrid, Spain.

Betina Biagetti (B)

Diabetes and Metabolism Research Unit, Vall d'Hebron University Hospital and Vall d'Hebron Research Institute (VHIR), Universidad Autónoma de Barcelona, Barcelona, Spain.

Rogelio Garcia-Centeno (R)

Endocrinology Department, Gregorio Marañon University Hospital, Madrid, Spain.

Raquel Ciriza (R)

Spanish Association of People Affected by Acromegaly (Asociación de pacientes Afectados por Acromegalia), Huesca, Spain.

Laura Sánchez-Cenizo (L)

Medical Affairs Department, Pfizer S.L.U, Alcobendas, Madrid, Spain.

Marcos Díaz-Muñoz (M)

Medical Affairs Department, Pfizer S.L.U, Alcobendas, Madrid, Spain. marcos.diaz@pfizer.com.

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Classifications MeSH