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Minimally Invasive Surgery for Pelvic Exenteration in Primary Colorectal Cancer

BACKGROUND: Minimally invasive surgery (MIS) for pelvic exenteration is not a well-established technique. The aim was to assess the safety and feasibility of MIS for pelvic exenteration in locally advanced primary colorectal cancer and to compare the perioperative outcomes with open surgery. METHODS...

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Autores principales: Kumar, Naveena AN, Sasi, Sajith P., Shinde, Rajesh S., Verma, Kamlesh, Sugoor, Pavan, Desouza, Ashwin, Engineer, Reena, Saklani, Avanish
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society of Laparoendoscopic Surgeons 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7347395/
https://www.ncbi.nlm.nih.gov/pubmed/32714002
http://dx.doi.org/10.4293/JSLS.2020.00026
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author Kumar, Naveena AN
Sasi, Sajith P.
Shinde, Rajesh S.
Verma, Kamlesh
Sugoor, Pavan
Desouza, Ashwin
Engineer, Reena
Saklani, Avanish
author_facet Kumar, Naveena AN
Sasi, Sajith P.
Shinde, Rajesh S.
Verma, Kamlesh
Sugoor, Pavan
Desouza, Ashwin
Engineer, Reena
Saklani, Avanish
author_sort Kumar, Naveena AN
collection PubMed
description BACKGROUND: Minimally invasive surgery (MIS) for pelvic exenteration is not a well-established technique. The aim was to assess the safety and feasibility of MIS for pelvic exenteration in locally advanced primary colorectal cancer and to compare the perioperative outcomes with open surgery. METHODS: This is a retrospective analysis of patients, who had undergone pelvic exenteration for primary colorectal adenocarcinoma from May 2013 to July 2018. The short-term outcomes like perioperative details and histopathological characteristics were compared between the two groups. RESULTS: MIS was performed in 23 patients and open pelvic exenteration was carried out in 72 patients. The mean operative time was significantly more in the MIS group (640 vs. 432 min, p = 0.00). The intraoperative blood loss (900 vs. 1550 ml, p = 0.00) and the requirement for blood transfusion (170 vs. 250 ml, p = 0.03) was significantly less in the MIS group. The overall morbidity (60% vs. 49%, p = 0.306) was comparable between the two groups. The median length of hospital stay in the MIS group was 11 d, compared to 12 d in the open surgery group, (p = 0.634). The rate of R0 resection (87% vs. 89%, p = 0.668) was comparable between the two groups. CONCLUSION: MIS is feasible and safe for total pelvic exenteration and posterior exenteration in carefully selected locally advanced primary colorectal cancer, when performed by an experienced surgical team in high volume centers. An R0 resection with adequate margin can be achieved with good perioperative outcomes in MIS. Long-term oncological outcomes would require further follow up to confirm.
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spelling pubmed-73473952020-07-23 Minimally Invasive Surgery for Pelvic Exenteration in Primary Colorectal Cancer Kumar, Naveena AN Sasi, Sajith P. Shinde, Rajesh S. Verma, Kamlesh Sugoor, Pavan Desouza, Ashwin Engineer, Reena Saklani, Avanish JSLS Research Article BACKGROUND: Minimally invasive surgery (MIS) for pelvic exenteration is not a well-established technique. The aim was to assess the safety and feasibility of MIS for pelvic exenteration in locally advanced primary colorectal cancer and to compare the perioperative outcomes with open surgery. METHODS: This is a retrospective analysis of patients, who had undergone pelvic exenteration for primary colorectal adenocarcinoma from May 2013 to July 2018. The short-term outcomes like perioperative details and histopathological characteristics were compared between the two groups. RESULTS: MIS was performed in 23 patients and open pelvic exenteration was carried out in 72 patients. The mean operative time was significantly more in the MIS group (640 vs. 432 min, p = 0.00). The intraoperative blood loss (900 vs. 1550 ml, p = 0.00) and the requirement for blood transfusion (170 vs. 250 ml, p = 0.03) was significantly less in the MIS group. The overall morbidity (60% vs. 49%, p = 0.306) was comparable between the two groups. The median length of hospital stay in the MIS group was 11 d, compared to 12 d in the open surgery group, (p = 0.634). The rate of R0 resection (87% vs. 89%, p = 0.668) was comparable between the two groups. CONCLUSION: MIS is feasible and safe for total pelvic exenteration and posterior exenteration in carefully selected locally advanced primary colorectal cancer, when performed by an experienced surgical team in high volume centers. An R0 resection with adequate margin can be achieved with good perioperative outcomes in MIS. Long-term oncological outcomes would require further follow up to confirm. Society of Laparoendoscopic Surgeons 2020 /pmc/articles/PMC7347395/ /pubmed/32714002 http://dx.doi.org/10.4293/JSLS.2020.00026 Text en © 2020 by JSLS, Journal of the Society of Laparoscopic & Robotic Surgeons. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives License (http://creativecommons.org/licenses/by-nc-nd/3.0/us/), which permits for noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited and is not altered in any way.
spellingShingle Research Article
Kumar, Naveena AN
Sasi, Sajith P.
Shinde, Rajesh S.
Verma, Kamlesh
Sugoor, Pavan
Desouza, Ashwin
Engineer, Reena
Saklani, Avanish
Minimally Invasive Surgery for Pelvic Exenteration in Primary Colorectal Cancer
title Minimally Invasive Surgery for Pelvic Exenteration in Primary Colorectal Cancer
title_full Minimally Invasive Surgery for Pelvic Exenteration in Primary Colorectal Cancer
title_fullStr Minimally Invasive Surgery for Pelvic Exenteration in Primary Colorectal Cancer
title_full_unstemmed Minimally Invasive Surgery for Pelvic Exenteration in Primary Colorectal Cancer
title_short Minimally Invasive Surgery for Pelvic Exenteration in Primary Colorectal Cancer
title_sort minimally invasive surgery for pelvic exenteration in primary colorectal cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7347395/
https://www.ncbi.nlm.nih.gov/pubmed/32714002
http://dx.doi.org/10.4293/JSLS.2020.00026
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