Cargando…

FRI296 Somatostatin Receptor 5 Staining In Prolactinomas

Disclosure: S. Mehta: None. R.A. Feelders: Advisory Board Member; Self; Corcept. Research Investigator; Self; Recordati, Strongbridge. L.J. Hofland: None. C. Campana: None. S.J. Neggers: None. X. Li: None. K. Wright: None. S. Skwiersky: None. J.D. Goldberg: None. H. Kim: None. D. Zagzag: None. N. Ag...

Descripción completa

Detalles Bibliográficos
Autores principales: Mehta, Sonal, Feelders, Richard Abraham, Hofland, Leo J, Campana, Claudia, Neggers, Sebastian J CM M, Li, Xiaochun, Wright, Kyla, Skwiersky, Samara, Goldberg, Judith D, Kim, Hyon, Zagzag, David, Agrawal, Nidhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10554113/
http://dx.doi.org/10.1210/jendso/bvad114.1231
_version_ 1785116335017033728
author Mehta, Sonal
Feelders, Richard Abraham
Hofland, Leo J
Campana, Claudia
Neggers, Sebastian J CM M
Li, Xiaochun
Wright, Kyla
Skwiersky, Samara
Goldberg, Judith D
Kim, Hyon
Zagzag, David
Agrawal, Nidhi
author_facet Mehta, Sonal
Feelders, Richard Abraham
Hofland, Leo J
Campana, Claudia
Neggers, Sebastian J CM M
Li, Xiaochun
Wright, Kyla
Skwiersky, Samara
Goldberg, Judith D
Kim, Hyon
Zagzag, David
Agrawal, Nidhi
author_sort Mehta, Sonal
collection PubMed
description Disclosure: S. Mehta: None. R.A. Feelders: Advisory Board Member; Self; Corcept. Research Investigator; Self; Recordati, Strongbridge. L.J. Hofland: None. C. Campana: None. S.J. Neggers: None. X. Li: None. K. Wright: None. S. Skwiersky: None. J.D. Goldberg: None. H. Kim: None. D. Zagzag: None. N. Agrawal: Research Investigator; Self; Chiasma, Ascendis, Recordati. The vast majority of prolactinomas are treated with dopamine agonists (DA) with excellent response, however DA resistance occurs in about 15% of prolactinomas. Surgery and radiotherapy are alternative treatments for these patients, but are not always successful. Somatostatin (SST) receptors have been studied with growing interest in prolactinomas. There are five SST receptor subtypes and mRNA expression analysis of prolactinomas has shown high expression of SST5 in comparison to SST1 and 2. The somatostatin analog, Pasireotide, which has a 40-fold greater binding affinity to SST5 compared to SST2 receptors, shows promising results in individual case reports of DA resistant and aggressive prolactinomas. This two-center retrospective cohort study investigated dopamine 2 (D2R), SST2a and SST5 receptor expression in surgical specimens of DA resistant prolactinomas. The study included consecutive surgical cases of adult patients with a diagnosis of DA-resistant prolactinoma at NYU Langone Health and Erasmus MC. DA resistance was defined as a failure to achieve normal prolactin (PRL) levels on maximally tolerated dopamine agonist doses and/or a failure to achieve 50% reduction in tumor size on coronal view. Co-secreting pituitary tumors were excluded to keep the somatostatin receptor analysis specific to prolactinomas. Receptor expression was scored on the basis of the well validated immunoreactivity score (IRS). This was done independently by two investigators by calculating the product of the percentage of positive cells and the intensity of the staining. 34 patients with average age 41.6 years and 19 (56%) males and 15 females are included in this analysis. Results: means (SDs) of pre-op PRL, pre-op image tumor size transverse and post-op PRL follow-up are respectively 1796 (4772) ng/mL in 33 patients; 2.23(1.61) cm in 15 patients; 108 (117) ng/mL in 17 patients. 31/33(94%) patients used DA preoperatively at various doses; 25/34 (74%) were DA resistant. Other indications include DA intolerance, apoplexy, cerebrospinal fluid leak. D2R was expressed in 94.1% (95% CI: 80.8%, 99.2%) of the cases. SST5 is expressed 61.8% (95% CI: 43.6%, 77.9%) of the prolactinomas and at a high level in a subset of SST5 positive cases. Only 17.6% (95% CI: 6.7%, 34.5%) of the prolactinomas express SST2a. SST5 expression has previously been studied in prolactinomas with variable expression. We show in this retrospective two center study a higher expression of SST5 receptor staining than previously demonstrated analyses and suggest SST5 staining to consider Pasireotide use in a subset of these patients. Larger prospective studies are needed to validate these findings. Presentation: Friday, June 16, 2023
format Online
Article
Text
id pubmed-10554113
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-105541132023-10-06 FRI296 Somatostatin Receptor 5 Staining In Prolactinomas Mehta, Sonal Feelders, Richard Abraham Hofland, Leo J Campana, Claudia Neggers, Sebastian J CM M Li, Xiaochun Wright, Kyla Skwiersky, Samara Goldberg, Judith D Kim, Hyon Zagzag, David Agrawal, Nidhi J Endocr Soc Neuroendocrinology & Pituitary Disclosure: S. Mehta: None. R.A. Feelders: Advisory Board Member; Self; Corcept. Research Investigator; Self; Recordati, Strongbridge. L.J. Hofland: None. C. Campana: None. S.J. Neggers: None. X. Li: None. K. Wright: None. S. Skwiersky: None. J.D. Goldberg: None. H. Kim: None. D. Zagzag: None. N. Agrawal: Research Investigator; Self; Chiasma, Ascendis, Recordati. The vast majority of prolactinomas are treated with dopamine agonists (DA) with excellent response, however DA resistance occurs in about 15% of prolactinomas. Surgery and radiotherapy are alternative treatments for these patients, but are not always successful. Somatostatin (SST) receptors have been studied with growing interest in prolactinomas. There are five SST receptor subtypes and mRNA expression analysis of prolactinomas has shown high expression of SST5 in comparison to SST1 and 2. The somatostatin analog, Pasireotide, which has a 40-fold greater binding affinity to SST5 compared to SST2 receptors, shows promising results in individual case reports of DA resistant and aggressive prolactinomas. This two-center retrospective cohort study investigated dopamine 2 (D2R), SST2a and SST5 receptor expression in surgical specimens of DA resistant prolactinomas. The study included consecutive surgical cases of adult patients with a diagnosis of DA-resistant prolactinoma at NYU Langone Health and Erasmus MC. DA resistance was defined as a failure to achieve normal prolactin (PRL) levels on maximally tolerated dopamine agonist doses and/or a failure to achieve 50% reduction in tumor size on coronal view. Co-secreting pituitary tumors were excluded to keep the somatostatin receptor analysis specific to prolactinomas. Receptor expression was scored on the basis of the well validated immunoreactivity score (IRS). This was done independently by two investigators by calculating the product of the percentage of positive cells and the intensity of the staining. 34 patients with average age 41.6 years and 19 (56%) males and 15 females are included in this analysis. Results: means (SDs) of pre-op PRL, pre-op image tumor size transverse and post-op PRL follow-up are respectively 1796 (4772) ng/mL in 33 patients; 2.23(1.61) cm in 15 patients; 108 (117) ng/mL in 17 patients. 31/33(94%) patients used DA preoperatively at various doses; 25/34 (74%) were DA resistant. Other indications include DA intolerance, apoplexy, cerebrospinal fluid leak. D2R was expressed in 94.1% (95% CI: 80.8%, 99.2%) of the cases. SST5 is expressed 61.8% (95% CI: 43.6%, 77.9%) of the prolactinomas and at a high level in a subset of SST5 positive cases. Only 17.6% (95% CI: 6.7%, 34.5%) of the prolactinomas express SST2a. SST5 expression has previously been studied in prolactinomas with variable expression. We show in this retrospective two center study a higher expression of SST5 receptor staining than previously demonstrated analyses and suggest SST5 staining to consider Pasireotide use in a subset of these patients. Larger prospective studies are needed to validate these findings. Presentation: Friday, June 16, 2023 Oxford University Press 2023-10-05 /pmc/articles/PMC10554113/ http://dx.doi.org/10.1210/jendso/bvad114.1231 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Neuroendocrinology & Pituitary
Mehta, Sonal
Feelders, Richard Abraham
Hofland, Leo J
Campana, Claudia
Neggers, Sebastian J CM M
Li, Xiaochun
Wright, Kyla
Skwiersky, Samara
Goldberg, Judith D
Kim, Hyon
Zagzag, David
Agrawal, Nidhi
FRI296 Somatostatin Receptor 5 Staining In Prolactinomas
title FRI296 Somatostatin Receptor 5 Staining In Prolactinomas
title_full FRI296 Somatostatin Receptor 5 Staining In Prolactinomas
title_fullStr FRI296 Somatostatin Receptor 5 Staining In Prolactinomas
title_full_unstemmed FRI296 Somatostatin Receptor 5 Staining In Prolactinomas
title_short FRI296 Somatostatin Receptor 5 Staining In Prolactinomas
title_sort fri296 somatostatin receptor 5 staining in prolactinomas
topic Neuroendocrinology & Pituitary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10554113/
http://dx.doi.org/10.1210/jendso/bvad114.1231
work_keys_str_mv AT mehtasonal fri296somatostatinreceptor5staininginprolactinomas
AT feeldersrichardabraham fri296somatostatinreceptor5staininginprolactinomas
AT hoflandleoj fri296somatostatinreceptor5staininginprolactinomas
AT campanaclaudia fri296somatostatinreceptor5staininginprolactinomas
AT neggerssebastianjcmm fri296somatostatinreceptor5staininginprolactinomas
AT lixiaochun fri296somatostatinreceptor5staininginprolactinomas
AT wrightkyla fri296somatostatinreceptor5staininginprolactinomas
AT skwierskysamara fri296somatostatinreceptor5staininginprolactinomas
AT goldbergjudithd fri296somatostatinreceptor5staininginprolactinomas
AT kimhyon fri296somatostatinreceptor5staininginprolactinomas
AT zagzagdavid fri296somatostatinreceptor5staininginprolactinomas
AT agrawalnidhi fri296somatostatinreceptor5staininginprolactinomas