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Chronic Treatment with Somatostatin Analogues in Recurrent Type 1 Gastric Neuroendocrine Tumors

Background: Type 1 gastric neuroendocrine tumors (GC-1) represent an uncommon subtype of neoplasms. Endoscopic resection has been proposed as the treatment of choice; active surveillance may be performed in those smaller than 1 cm, while gastric surgery may be performed for those with frequent recur...

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Autores principales: Sebastian-Valles, Fernando, Bernaldo Madrid, Blanca, Sager, Carolina, Carrillo López, Elena, Mera Carreiro, Sara, Ávila Antón, Laura, García, Noelia Sánchez-Maroto, Sampedro-Nuñez, Miguel Antonio, Pérez, Jose Ángel Díaz, Marazuela, Mónica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10045480/
https://www.ncbi.nlm.nih.gov/pubmed/36979851
http://dx.doi.org/10.3390/biomedicines11030872
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author Sebastian-Valles, Fernando
Bernaldo Madrid, Blanca
Sager, Carolina
Carrillo López, Elena
Mera Carreiro, Sara
Ávila Antón, Laura
García, Noelia Sánchez-Maroto
Sampedro-Nuñez, Miguel Antonio
Pérez, Jose Ángel Díaz
Marazuela, Mónica
author_facet Sebastian-Valles, Fernando
Bernaldo Madrid, Blanca
Sager, Carolina
Carrillo López, Elena
Mera Carreiro, Sara
Ávila Antón, Laura
García, Noelia Sánchez-Maroto
Sampedro-Nuñez, Miguel Antonio
Pérez, Jose Ángel Díaz
Marazuela, Mónica
author_sort Sebastian-Valles, Fernando
collection PubMed
description Background: Type 1 gastric neuroendocrine tumors (GC-1) represent an uncommon subtype of neoplasms. Endoscopic resection has been proposed as the treatment of choice; active surveillance may be performed in those smaller than 1 cm, while gastric surgery may be performed for those with frequent recurrences. The antiproliferative effect of somatostatin analogues (SSA) is well known, and their action on GC-1s has been postulated as a chronic treatment to reduce recurrence. Methods: A two-centered, retrospective, observational study that included nine patients (55.6% women) diagnosed with GC-1, receiving long-term treatment with SSA, with a median follow-up from baseline of 22 months, was undertaken. Endoscopic follow-up, extension study, and analytical values of chromogranin A (Cg A) and gastrin were collected. Results: In total, 88.9% of patients presented partial or complete response. Treatment with SSA was the only independent factor with a trend to prevent tumor recurrence (Odds Ratio 0.054; p = 0.005). A nonsignificant tendency toward a decrease in CgA and gastrin was observed; lack of significance was probably related to concomitant treatment with proton pump inhibitors in some patients. Conclusions: Chronic treatment with SSA is a feasible option for recurrent GC-1s that are difficult to manage using endoscopy or gastrectomy. Randomized clinical trials to provide more scientific evidence are still needed.
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spelling pubmed-100454802023-03-29 Chronic Treatment with Somatostatin Analogues in Recurrent Type 1 Gastric Neuroendocrine Tumors Sebastian-Valles, Fernando Bernaldo Madrid, Blanca Sager, Carolina Carrillo López, Elena Mera Carreiro, Sara Ávila Antón, Laura García, Noelia Sánchez-Maroto Sampedro-Nuñez, Miguel Antonio Pérez, Jose Ángel Díaz Marazuela, Mónica Biomedicines Article Background: Type 1 gastric neuroendocrine tumors (GC-1) represent an uncommon subtype of neoplasms. Endoscopic resection has been proposed as the treatment of choice; active surveillance may be performed in those smaller than 1 cm, while gastric surgery may be performed for those with frequent recurrences. The antiproliferative effect of somatostatin analogues (SSA) is well known, and their action on GC-1s has been postulated as a chronic treatment to reduce recurrence. Methods: A two-centered, retrospective, observational study that included nine patients (55.6% women) diagnosed with GC-1, receiving long-term treatment with SSA, with a median follow-up from baseline of 22 months, was undertaken. Endoscopic follow-up, extension study, and analytical values of chromogranin A (Cg A) and gastrin were collected. Results: In total, 88.9% of patients presented partial or complete response. Treatment with SSA was the only independent factor with a trend to prevent tumor recurrence (Odds Ratio 0.054; p = 0.005). A nonsignificant tendency toward a decrease in CgA and gastrin was observed; lack of significance was probably related to concomitant treatment with proton pump inhibitors in some patients. Conclusions: Chronic treatment with SSA is a feasible option for recurrent GC-1s that are difficult to manage using endoscopy or gastrectomy. Randomized clinical trials to provide more scientific evidence are still needed. MDPI 2023-03-13 /pmc/articles/PMC10045480/ /pubmed/36979851 http://dx.doi.org/10.3390/biomedicines11030872 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sebastian-Valles, Fernando
Bernaldo Madrid, Blanca
Sager, Carolina
Carrillo López, Elena
Mera Carreiro, Sara
Ávila Antón, Laura
García, Noelia Sánchez-Maroto
Sampedro-Nuñez, Miguel Antonio
Pérez, Jose Ángel Díaz
Marazuela, Mónica
Chronic Treatment with Somatostatin Analogues in Recurrent Type 1 Gastric Neuroendocrine Tumors
title Chronic Treatment with Somatostatin Analogues in Recurrent Type 1 Gastric Neuroendocrine Tumors
title_full Chronic Treatment with Somatostatin Analogues in Recurrent Type 1 Gastric Neuroendocrine Tumors
title_fullStr Chronic Treatment with Somatostatin Analogues in Recurrent Type 1 Gastric Neuroendocrine Tumors
title_full_unstemmed Chronic Treatment with Somatostatin Analogues in Recurrent Type 1 Gastric Neuroendocrine Tumors
title_short Chronic Treatment with Somatostatin Analogues in Recurrent Type 1 Gastric Neuroendocrine Tumors
title_sort chronic treatment with somatostatin analogues in recurrent type 1 gastric neuroendocrine tumors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10045480/
https://www.ncbi.nlm.nih.gov/pubmed/36979851
http://dx.doi.org/10.3390/biomedicines11030872
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