Machine Learning-based Prediction Model for Treatment of Acromegaly With First-generation Somatostatin Receptor Ligands.
Acromegaly
/ blood
Adult
Aged
Biomarkers
/ blood
Clinical Decision Rules
Drug Monitoring
/ methods
Female
Human Growth Hormone
/ blood
Humans
Insulin-Like Growth Factor I
/ metabolism
Keratins
Ligands
Logistic Models
Machine Learning
Male
Middle Aged
Predictive Value of Tests
Receptors, Somatostatin
/ administration & dosage
Treatment Outcome
Young Adult
acromegaly
biomarker
machine learning
precision medicine
prediction model
somatostatin receptor
somatostatin receptor ligands
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:
16 06 2021
16 06 2021
Historique:
received:
03
12
2020
pubmed:
10
3
2021
medline:
5
10
2021
entrez:
9
3
2021
Statut:
ppublish
Résumé
Artificial intelligence (AI), in particular machine learning (ML), may be used to deeply analyze biomarkers of response to first-generation somatostatin receptor ligands (fg-SRLs) in the treatment of acromegaly. To develop a prediction model of therapeutic response of acromegaly to fg-SRL. Patients with acromegaly not cured by primary surgical treatment and who had adjuvant therapy with fg-SRL for at least 6 months after surgery were included. Patients were considered controlled if they presented growth hormone (GH) <1.0 ng/mL and normal age-adjusted insulin-like growth factor (IGF)-I levels. Six AI models were evaluated: logistic regression, k-nearest neighbor classifier, support vector machine, gradient-boosted classifier, random forest, and multilayer perceptron. The features included in the analysis were age at diagnosis, sex, GH, and IGF-I levels at diagnosis and at pretreatment, somatostatin receptor subtype 2 and 5 (SST2 and SST5) protein expression and cytokeratin granulation pattern (GP). A total of 153 patients were analyzed. Controlled patients were older (P = .002), had lower GH at diagnosis (P = .01), had lower pretreatment GH and IGF-I (P < .001), and more frequently harbored tumors that were densely granulated (P = .014) or highly expressed SST2 (P < .001). The model that performed best was the support vector machine with the features SST2, SST5, GP, sex, age, and pretreatment GH and IGF-I levels. It had an accuracy of 86.3%, positive predictive value of 83.3% and negative predictive value of 87.5%. We developed a ML-based prediction model with high accuracy that has the potential to improve medical management of acromegaly, optimize biochemical control, decrease long-term morbidities and mortality, and reduce health services costs.
Identifiants
pubmed: 33686418
pii: 6158816
doi: 10.1210/clinem/dgab125
doi:
Substances chimiques
Biomarkers
0
IGF1 protein, human
0
Ligands
0
Receptors, Somatostatin
0
SSTR2 protein, human
0
Human Growth Hormone
12629-01-5
Insulin-Like Growth Factor I
67763-96-6
Keratins
68238-35-7
somatostatin receptor 5
8X85ZJG6XJ
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
2047-2056Informations de copyright
© The Author(s) 2021. Published by Oxford University Press on behalf of the Endocrine Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.