Predictive Factors of Somatostatin Receptor Ligand Response in Acromegaly-A Prospective Study.


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:
23 11 2022
Historique:
received: 09 05 2022
pubmed: 23 9 2022
medline: 25 11 2022
entrez: 22 9 2022
Statut: ppublish

Résumé

Somatostatin receptor ligands (SRLs) are the cornerstone medical treatments for acromegaly; however, many patients remain unresponsive to SRLs. Well-established predictive markers of response are needed. We aimed to explore the relationship between responsiveness to SRLs relative to somatostatin (SST)2A and 5 receptor expression, adenoma granularity, and T2-weighted magnetic resonance imaging (MRI) signal intensity (T2WSI). We conducted a multicentric, prospective, observational cohort study, in France. Forty-nine naïve patients (ie, patients without preoperative SRL treatment) with active acromegaly following surgery were treated with octreotide (group 1; n = 47), or pasireotide if uncontrolled under first-generation SRLs (group 2; n = 9). Data were collected at baseline and months 3 and 6. Biochemical measurements, immunohistochemistry studies, and MRI readings were centralized. In group 1, IGF-I decrease from baseline to month 6 positively correlated with SST2A immunoreactive score (IRS), P = 0.01. Densely granulated/intermediate adenomas had a greater IGF-I and GH decrease under octreotide compared with sparsely granulated adenomas (P = 0.02 and P = 0.006, respectively), and expressed greater levels of SST2A (P < 0.001), coupled with lower levels of SST5 (P = 0.004). T2WSI changed between preoperative MRI and month 6 MRI in one-half of the patients. Finally, SST5 IRS was higher in preoperative hyperintense compared with preoperative hypointense adenomas (P = 0.04), and most sparsely granulated and most hyperintense adenomas expressed high SST5 levels. We prospectively confirm that SST2A and adenoma granularity are good predictors of response to octreotide. We propose the IRS for scoring system harmonization. MRI sequences must be optimized to be able to use the T2WSI as a predictor of treatment response.

Identifiants

pubmed: 36136828
pii: 6711554
doi: 10.1210/clinem/dgac512
doi:

Substances chimiques

Receptors, Somatostatin 0
Octreotide RWM8CCW8GP
Insulin-Like Growth Factor I 67763-96-6
Ligands 0

Types de publication

Observational Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2982-2991

Subventions

Organisme : Novartis Pharma

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of the Endocrine Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Mirela-Diana Ilie (MD)

Inserm U1052, CNRS UMR5286, Claude Bernard Lyon 1 University, Cancer Research Center of Lyon, Lyon 69001, France.
Endocrinology Department, "C.I. Parhon" National Institute of Endocrinology, Bucharest 011863, Romania.

Antoine Tabarin (A)

Department of Endocrinology, Diabetes and Nutrition, Bordeaux University Hospital, Pessac 33600, France.

Alexandre Vasiljevic (A)

Inserm U1052, CNRS UMR5286, Claude Bernard Lyon 1 University, Cancer Research Center of Lyon, Lyon 69001, France.
Pathology Department, "Groupement Hospitalier Est" Hospices Civils de Lyon, Bron 69500, France.

Jean-François Bonneville (JF)

Departments of Medical Imaging and Endocrinology, Liège University Hospital, Liège 4000, Belgium.

Lucile Moreau-Grangé (L)

Department of Endocrinology, Diabetes and Metabolic Disorders, Rouen University Hospital, Rouen 76000, France.

Franck Schillo (F)

Department of Diabetes, Endocrinology and Nutrition, Besançon University Hospital, Besançon 25030, France.

Brigitte Delemer (B)

Department of Endocrinology, Diabetes and Nutrition, Reims University Hospital, Reims 51092, France.

Anne Barlier (A)

Laboratory of Molecular Biology, Conception University Hospital, AP-HM, Marseille 13005, France.
Aix-Marseille University, Inserm, MMG, Marseille 13011, France.

Dominique Figarella-Branger (D)

Pathology and Neuropathology Department, Timone University Hospital, AP-HM, Marseille 13005, France.

Ségolène Bisot-Locard (S)

Medical Oncology, Novartis, Rueil Malmaison 92563, France.

Alexandre Santos (A)

Medical Oncology, Novartis, Rueil Malmaison 92563, France.

Philippe Chanson (P)

Department of Endocrinology and Reproduction Disorders, Bicêtre Hospital, AP-HP, Le Kremlin-Bicêtre 94270, France.
Paris-Saclay University, Inserm, "Physiologie et Physiopathologie Endocriniennes", Le Kremlin-Bicêtre 91190, France.

Gérald Raverot (G)

Inserm U1052, CNRS UMR5286, Claude Bernard Lyon 1 University, Cancer Research Center of Lyon, Lyon 69001, France.
Endocrinology Department, "Groupement Hospitalier Est" Hospices Civils de Lyon, Bron 69500, France.

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Classifications MeSH