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The therapeutic response of somatotropinomas according to the T2-weighted signal intensity on the MRI

BACKGROUND AND AIM: Identifying the predictive factors of tumoral and hormonal answer of somatotropinomas to the medical treatment with somatostatin analogs represent an important element for treatment management. The aim of this study was to assess the therapeutic answer of the somatotropinomas acc...

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Autores principales: Scânteie, Carla-Liana, Leucuţa, Daniel-Corneliu, Ghervan, Cristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Iuliu Hatieganu University of Medicine and Pharmacy 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9389873/
https://www.ncbi.nlm.nih.gov/pubmed/36105498
http://dx.doi.org/10.15386/mpr-1299
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author Scânteie, Carla-Liana
Leucuţa, Daniel-Corneliu
Ghervan, Cristina
author_facet Scânteie, Carla-Liana
Leucuţa, Daniel-Corneliu
Ghervan, Cristina
author_sort Scânteie, Carla-Liana
collection PubMed
description BACKGROUND AND AIM: Identifying the predictive factors of tumoral and hormonal answer of somatotropinomas to the medical treatment with somatostatin analogs represent an important element for treatment management. The aim of this study was to assess the therapeutic answer of the somatotropinomas according to the T2-weighted signal intensity on the MRI. METHODS: We included 31 acromegalic patients, mean age 51.35 ± 10.37 years, who underwent surgery. The patients were divided according to the T2-weighted MRI signal intensity - hypointense, hyperintense and isointense - of the GH-secreting pituitary adenoma and were evaluated after surgery, 3, 6 and 12 months with somatostatin analogs therapy. RESULTS: 16 (51.61%) somatropinomas were hypointense, 9 (29.03%) were hyperintense and 6 (19.35%) were isointense. The median IGF-1 and GH level decreased significantly in macroadenomas (p<0.001, p<0.001, respectively), whereas GH decreased significantly only in microadenomas (p=0.010). A significant statistical correlation was found between IGF-1 or GH levels and tumor volume before surgery (Spearman=0.38, p<0.001; Spearman=0.64, p<0.001, respectively) and after surgery (Spearman=0.61, p=0.001; Spearman=0.74, p<0.001). The percentage of optimally controlled patients increased from 12.9% after surgery, to 28.57% after 12 months with somatostatin analogs. The highest percentage of optimally controlled patients with somatostatin analogs treatment was in hypointense somatotropinomas (50%). CONCLUSION: The T2-weighted MRI signal intensity classifies the somatotropinomas into groups with certain evolutive and medical treatment response particularities, of which we found that the hypointense somatotropinomas have a better therapeutic response after surgery and after long-term treatment with somatostatin analogs.
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spelling pubmed-93898732022-09-13 The therapeutic response of somatotropinomas according to the T2-weighted signal intensity on the MRI Scânteie, Carla-Liana Leucuţa, Daniel-Corneliu Ghervan, Cristina Med Pharm Rep Original Research BACKGROUND AND AIM: Identifying the predictive factors of tumoral and hormonal answer of somatotropinomas to the medical treatment with somatostatin analogs represent an important element for treatment management. The aim of this study was to assess the therapeutic answer of the somatotropinomas according to the T2-weighted signal intensity on the MRI. METHODS: We included 31 acromegalic patients, mean age 51.35 ± 10.37 years, who underwent surgery. The patients were divided according to the T2-weighted MRI signal intensity - hypointense, hyperintense and isointense - of the GH-secreting pituitary adenoma and were evaluated after surgery, 3, 6 and 12 months with somatostatin analogs therapy. RESULTS: 16 (51.61%) somatropinomas were hypointense, 9 (29.03%) were hyperintense and 6 (19.35%) were isointense. The median IGF-1 and GH level decreased significantly in macroadenomas (p<0.001, p<0.001, respectively), whereas GH decreased significantly only in microadenomas (p=0.010). A significant statistical correlation was found between IGF-1 or GH levels and tumor volume before surgery (Spearman=0.38, p<0.001; Spearman=0.64, p<0.001, respectively) and after surgery (Spearman=0.61, p=0.001; Spearman=0.74, p<0.001). The percentage of optimally controlled patients increased from 12.9% after surgery, to 28.57% after 12 months with somatostatin analogs. The highest percentage of optimally controlled patients with somatostatin analogs treatment was in hypointense somatotropinomas (50%). CONCLUSION: The T2-weighted MRI signal intensity classifies the somatotropinomas into groups with certain evolutive and medical treatment response particularities, of which we found that the hypointense somatotropinomas have a better therapeutic response after surgery and after long-term treatment with somatostatin analogs. Iuliu Hatieganu University of Medicine and Pharmacy 2021-10 2021-10-30 /pmc/articles/PMC9389873/ /pubmed/36105498 http://dx.doi.org/10.15386/mpr-1299 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License
spellingShingle Original Research
Scânteie, Carla-Liana
Leucuţa, Daniel-Corneliu
Ghervan, Cristina
The therapeutic response of somatotropinomas according to the T2-weighted signal intensity on the MRI
title The therapeutic response of somatotropinomas according to the T2-weighted signal intensity on the MRI
title_full The therapeutic response of somatotropinomas according to the T2-weighted signal intensity on the MRI
title_fullStr The therapeutic response of somatotropinomas according to the T2-weighted signal intensity on the MRI
title_full_unstemmed The therapeutic response of somatotropinomas according to the T2-weighted signal intensity on the MRI
title_short The therapeutic response of somatotropinomas according to the T2-weighted signal intensity on the MRI
title_sort therapeutic response of somatotropinomas according to the t2-weighted signal intensity on the mri
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9389873/
https://www.ncbi.nlm.nih.gov/pubmed/36105498
http://dx.doi.org/10.15386/mpr-1299
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