Cost-Effectiveness and Efficacy of a Novel Combination Regimen in Acromegaly: A Prospective, Randomized Trial.


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
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.

Auteurs

Vivien Bonert (V)

Pituitary Center, Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, California.

James Mirocha (J)

Biostatistics and Bioinformatics Research Center, Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, California.

John Carmichael (J)

Division of Endocrinology and Metabolism, Keck School of Medicine, University of Southern California, Los Angeles, California.

Kevin C J Yuen (KCJ)

Department of Neuroendocrinology and Neurosurgery, Barrow Neurological Institute, University of Arizona College of Medicine and Creighton School of Medicine, Phoenix, Arizona.

Takako Araki (T)

Division of Diabetes, Endocrinology and Metabolism, University of Minnesota, Minneapolis, Minnesota.

Shlomo Melmed (S)

Pituitary Center, Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, California.

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Classifications MeSH