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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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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. |
format | Online Article Text |
id | pubmed-10045480 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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