Preference of acromegaly patients for treatment attributes in Spain.
Acromegaly
Growth hormone
Preferences
Quality of life
Treatment
Journal
Endocrine
ISSN: 1559-0100
Titre abrégé: Endocrine
Pays: United States
ID NLM: 9434444
Informations de publication
Date de publication:
11 2023
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
379-389Informations de copyright
© 2023. The Author(s).
Références
Clin Endocrinol (Oxf). 2017 Jun;86(6):806-815
pubmed: 28316090
Adv Ther. 2021 Feb;38(2):969-993
pubmed: 33432541
Clin Endocrinol (Oxf). 1994 Jul;41(1):95-102
pubmed: 8050136
Neuroendocrinology. 2020;110(9-10):882-888
pubmed: 32101858
Endocrine. 2022 Feb;75(2):525-536
pubmed: 34668173
J Clin Endocrinol Metab. 2008 Jun;93(6):2035-41
pubmed: 18381584
Pituitary. 2021 Feb;24(1):1-13
pubmed: 33079318
Endocrine. 2017 Jan;55(1):247-255
pubmed: 27896545
Drug Discov Today. 2019 Jul;24(7):1324-1331
pubmed: 31077814
J Clin Endocrinol Metab. 2014 May;99(5):1825-33
pubmed: 24606084
Ann Endocrinol (Paris). 2021 Dec;82(6):582-589
pubmed: 34256010
Front Endocrinol (Lausanne). 2018 Jul 06;9:358
pubmed: 30034367
BMC Med Inform Decis Mak. 2020 Jun 19;20(1):114
pubmed: 32560655
Endocr Connect. 2020 Oct;9(10):971-977
pubmed: 33048063
N Engl J Med. 2000 Apr 20;342(16):1171-7
pubmed: 10770982
Pituitary. 2020 Apr;23(2):129-139
pubmed: 31823249
J Clin Endocrinol Metab. 2014 Nov;99(11):3933-51
pubmed: 25356808
Pituitary. 2017 Dec;20(6):692-701
pubmed: 28887782
J Clin Endocrinol Metab. 2011 Nov;96(11):3550-8
pubmed: 21917873
Nat Rev Dis Primers. 2019 Mar 21;5(1):20
pubmed: 30899019
Pituitary. 2017 Feb;20(1):185-188
pubmed: 27730455
Indian J Endocrinol Metab. 2020 Sep-Oct;24(5):402-405
pubmed: 33489844
Clin Endocrinol (Oxf). 2015 Jul;83(1):3-14
pubmed: 25640882
J Clin Endocrinol Metab. 2008 Oct;93(10):3853-9
pubmed: 18647806
Eur J Endocrinol. 2017 Jul;177(1):R13-R26
pubmed: 28351913
Pituitary. 2019 Feb;22(1):62-69
pubmed: 30627944
Cochrane Database Syst Rev. 2008 Apr 16;(2):CD000011
pubmed: 18425859
Endocr Connect. 2016 Jul;5(4):167-73
pubmed: 27458240
BMC Health Serv Res. 2017 Jul 11;17(1):476
pubmed: 28697796
Lancet Diabetes Endocrinol. 2014 Nov;2(11):875-84
pubmed: 25260838
Eur J Endocrinol. 2021 Aug 27;185(4):525-538
pubmed: 34342594
Pituitary. 2014 Dec;17(6):557-63
pubmed: 24337714
Endocrinol Diabetes Nutr (Engl Ed). 2018 May;65(5):297-305
pubmed: 29653911
Neuroendocrinology. 2016;103(1):106-11
pubmed: 25661974
PLoS One. 2012;7(5):e36411
pubmed: 22574156
Clin Endocrinol (Oxf). 2005 Jul;63(1):103-10
pubmed: 15963069
Pituitary. 2016 Oct;19(5):536-43
pubmed: 27405306
F1000Res. 2020 Jul 29;9:
pubmed: 32765836
Clin Endocrinol (Oxf). 2002 Aug;57(2):251-8
pubmed: 12153605