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Small Bowel Neuroendocrine Tumors—10-Year Experience of the Ottawa Hospital (TOH)

(1) Aim: The prevalence and incidence of small bowel NETs have increased significantly over the past two decades. This study aims to report the 10-year experience of SB-NET management at a regional cancer center in Canada. (2) Materials and methods: We conducted a retrospective study of the clinical...

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Autores principales: Alfagih, Abdulhameed, AlJassim, Abdulaziz, Alqahtani, Nasser, Vickers, Michael, Goodwin, Rachel, Asmis, Timothy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10453717/
https://www.ncbi.nlm.nih.gov/pubmed/37623025
http://dx.doi.org/10.3390/curroncol30080544
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author Alfagih, Abdulhameed
AlJassim, Abdulaziz
Alqahtani, Nasser
Vickers, Michael
Goodwin, Rachel
Asmis, Timothy
author_facet Alfagih, Abdulhameed
AlJassim, Abdulaziz
Alqahtani, Nasser
Vickers, Michael
Goodwin, Rachel
Asmis, Timothy
author_sort Alfagih, Abdulhameed
collection PubMed
description (1) Aim: The prevalence and incidence of small bowel NETs have increased significantly over the past two decades. This study aims to report the 10-year experience of SB-NET management at a regional cancer center in Canada. (2) Materials and methods: We conducted a retrospective study of the clinical and pathological data of patients diagnosed with biopsy-proven SB-NET at The Ottawa Hospital (TOH), Ottawa, Canada between 2011 and 2021. We report the clinicopathological characteristics of these patients, as well as their outcomes data, including survival rates. (3) Results: Between 2011 and 2021, a total of 177 SB-NET cases were identified with 51% (n = 91) of cases being males. The most common sites of the tumors were the ileum 53% (n = 94), followed by the duodenum 9% (n = 16) and jejunum 7% (n = 12). Approximately 24% (n = 42) of the patients had symptoms for over six months prior to diagnosis and 18% (n = 32) had functioning SB-NET during the course of the disease. The majority of patients had locally advanced or metastatic disease at the time of presentation with stage III, and stage IV representing 42% (n = 75), and 41% (n = 73) respectively. The majority of patients 84% (n = 148) had well-differentiated histology. One hundred twenty patients underwent surgical resection of the primary tumor including 28 patients (16%) with limited metastatic disease. A total of 21 patients (18%) had recurrence after curative surgery. A total of 62 patients (35%) received first-line somatostatin analog (SSA) therapy for unresectable disease and seven patients had PRRT after progression on SSA. Five years OS was 100%, 91%, 97%, and 73% for stages I, II, III, and IV respectively. In univariate analysis, carcinoid symptoms, T stage, and differentiation were significant predictors for worse overall survival, but not RFS. (4) Conclusions: Compared to published historical controls, our study suggests improvement in the 5-year survival rate of SB-NETs over the last 10 years.
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spelling pubmed-104537172023-08-26 Small Bowel Neuroendocrine Tumors—10-Year Experience of the Ottawa Hospital (TOH) Alfagih, Abdulhameed AlJassim, Abdulaziz Alqahtani, Nasser Vickers, Michael Goodwin, Rachel Asmis, Timothy Curr Oncol Article (1) Aim: The prevalence and incidence of small bowel NETs have increased significantly over the past two decades. This study aims to report the 10-year experience of SB-NET management at a regional cancer center in Canada. (2) Materials and methods: We conducted a retrospective study of the clinical and pathological data of patients diagnosed with biopsy-proven SB-NET at The Ottawa Hospital (TOH), Ottawa, Canada between 2011 and 2021. We report the clinicopathological characteristics of these patients, as well as their outcomes data, including survival rates. (3) Results: Between 2011 and 2021, a total of 177 SB-NET cases were identified with 51% (n = 91) of cases being males. The most common sites of the tumors were the ileum 53% (n = 94), followed by the duodenum 9% (n = 16) and jejunum 7% (n = 12). Approximately 24% (n = 42) of the patients had symptoms for over six months prior to diagnosis and 18% (n = 32) had functioning SB-NET during the course of the disease. The majority of patients had locally advanced or metastatic disease at the time of presentation with stage III, and stage IV representing 42% (n = 75), and 41% (n = 73) respectively. The majority of patients 84% (n = 148) had well-differentiated histology. One hundred twenty patients underwent surgical resection of the primary tumor including 28 patients (16%) with limited metastatic disease. A total of 21 patients (18%) had recurrence after curative surgery. A total of 62 patients (35%) received first-line somatostatin analog (SSA) therapy for unresectable disease and seven patients had PRRT after progression on SSA. Five years OS was 100%, 91%, 97%, and 73% for stages I, II, III, and IV respectively. In univariate analysis, carcinoid symptoms, T stage, and differentiation were significant predictors for worse overall survival, but not RFS. (4) Conclusions: Compared to published historical controls, our study suggests improvement in the 5-year survival rate of SB-NETs over the last 10 years. MDPI 2023-08-09 /pmc/articles/PMC10453717/ /pubmed/37623025 http://dx.doi.org/10.3390/curroncol30080544 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
Alfagih, Abdulhameed
AlJassim, Abdulaziz
Alqahtani, Nasser
Vickers, Michael
Goodwin, Rachel
Asmis, Timothy
Small Bowel Neuroendocrine Tumors—10-Year Experience of the Ottawa Hospital (TOH)
title Small Bowel Neuroendocrine Tumors—10-Year Experience of the Ottawa Hospital (TOH)
title_full Small Bowel Neuroendocrine Tumors—10-Year Experience of the Ottawa Hospital (TOH)
title_fullStr Small Bowel Neuroendocrine Tumors—10-Year Experience of the Ottawa Hospital (TOH)
title_full_unstemmed Small Bowel Neuroendocrine Tumors—10-Year Experience of the Ottawa Hospital (TOH)
title_short Small Bowel Neuroendocrine Tumors—10-Year Experience of the Ottawa Hospital (TOH)
title_sort small bowel neuroendocrine tumors—10-year experience of the ottawa hospital (toh)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10453717/
https://www.ncbi.nlm.nih.gov/pubmed/37623025
http://dx.doi.org/10.3390/curroncol30080544
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