Cost-Effectiveness and Efficacy of a Novel Combination Regimen in Acromegaly: A Prospective, Randomized Trial.
Acromegaly
/ drug therapy
Adult
Cost-Benefit Analysis
Delayed-Action Preparations
Dosage Forms
Dose-Response Relationship, Drug
Drug Administration Schedule
Drug Costs
Drug Therapy, Combination
/ adverse effects
Female
Human Growth Hormone
/ administration & dosage
Humans
Male
Middle Aged
Octreotide
/ administration & dosage
Peptides, Cyclic
/ administration & dosage
Receptors, Somatostatin
/ agonists
Somatostatin
/ administration & dosage
Therapies, Investigational
/ adverse effects
Treatment Outcome
Acromegaly
combination therapy
pegvisomant
somatostatin receptor ligand
Journal
The Journal of clinical endocrinology and metabolism
ISSN: 1945-7197
Titre abrégé: J Clin Endocrinol Metab
Pays: United States
ID NLM: 0375362
Informations de publication
Date de publication:
01 09 2020
01 09 2020
Historique:
received:
17
04
2020
accepted:
07
07
2020
pubmed:
6
8
2020
medline:
24
2
2021
entrez:
6
8
2020
Statut:
ppublish
Résumé
Combination therapy with somatostatin receptor ligand (SRL) plus pegvisomant for patients with acromegaly is recommended after a maximizing dose on monotherapy. Lower-dose combination regimens are not well studied. To compare cost-effectiveness and efficacy of 3 lower-dose combination regimens in controlled and uncontrolled acromegaly. Prospective, randomized, open-label, parallel arm study at a tertiary referral pituitary center. Adults with acromegaly regardless of response to prior SRL and biochemical control status at baseline, stratified by an SRL dose required for insulin-like growth factor (IGF)-I normalization during any 3-month period within 12 months preceding enrollment. Combination therapy for 24 to 32 weeks on arm A, high-dose SRL (lanreotide 120 mg/octreotide long-acting release [LAR] 30 mg) plus weekly pegvisomant (40-160 mg/week); arm B, low-dose SRL (lanreotide 60 mg/octreotide LAR 10 mg) plus weekly pegvisomant; or arm C, low-dose SRL plus daily pegvisomant (15-60 mg/day). Monthly treatment cost in each arm in participants completing ≥ 24 weeks of therapy. Sixty patients were enrolled and 52 were evaluable. Fifty of 52 (96%) demonstrated IGF-I control regardless of prior SRL responsiveness (arm A, 14/15 [93.3%]; arm B, 22/23 [95.7%]; arm C, 14/14 [100%]). Arm B was least costly (mean, $9837 ± 1375 per month), arm C was most expensive (mean, $22543 ± 11158 per month), and arm A had an intermediate cost (mean, $14261 ± 1645 per month). Approximately 30% of patients required pegvisomant dose uptitration. Rates of adverse events were all < 10%. Low-dose SRL plus weekly pegvisomant represents a novel dosing option for achieving cost-effective, optimal biochemical control in patients with uncontrolled acromegaly requiring combination therapy.
Identifiants
pubmed: 32754748
pii: 5869881
doi: 10.1210/clinem/dgaa444
pii:
doi:
Substances chimiques
Delayed-Action Preparations
0
Dosage Forms
0
Peptides, Cyclic
0
Receptors, Somatostatin
0
lanreotide
0G3DE8943Y
Human Growth Hormone
12629-01-5
Somatostatin
51110-01-1
pegvisomant
N824AOU5XV
Octreotide
RWM8CCW8GP
Banques de données
ClinicalTrials.gov
['NCT01538966']
Types de publication
Journal Article
Randomized Controlled Trial
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
© Endocrine Society 2020. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.