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Postoperative non-steroidal anti-inflammatory drug use and oncological outcomes of rectal cancer

BACKGROUND: Non-steroidal anti-inflammatory drugs (NSAIDs) are known to suppress the inflammatory response after surgery and are often used for pain control. This study aimed to investigate NSAID use after radical surgical resection for rectal cancer and long-term oncological outcomes. METHODS: A co...

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Autores principales: Grahn, O, Lundin, M, Lydrup, M-L, Angenete, E, Rutegård, M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7893477/
https://www.ncbi.nlm.nih.gov/pubmed/33609397
http://dx.doi.org/10.1093/bjsopen/zraa050
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author Grahn, O
Lundin, M
Lydrup, M-L
Angenete, E
Rutegård, M
author_facet Grahn, O
Lundin, M
Lydrup, M-L
Angenete, E
Rutegård, M
author_sort Grahn, O
collection PubMed
description BACKGROUND: Non-steroidal anti-inflammatory drugs (NSAIDs) are known to suppress the inflammatory response after surgery and are often used for pain control. This study aimed to investigate NSAID use after radical surgical resection for rectal cancer and long-term oncological outcomes. METHODS: A cohort of patients who underwent anterior resection for rectal cancer between 2007 and 2013 in 15 hospitals in Sweden was investigated retrospectively. Data were obtained from the Swedish Colorectal Cancer Registry and medical records; follow-up was undertaken until July 2019. Patients who received NSAID treatment for at least 2 days after surgery were compared with controls who did not, and the primary outcome was recurrence-free survival. Cox regression modelling with confounder adjustment, propensity score matching, and an instrumental variables approach were used; missing data were handled by multiple imputation. RESULTS: The cohort included 1341 patients, 362 (27.0 per cent) of whom received NSAIDs after operation. In analyses using conventional regression and propensity score matching, there was no significant association between postoperative NSAID use and recurrence-free survival (adjusted hazard ratio (HR) 1.02, 0.79 to 1.33). The instrumental variables approach, including individual hospital as the instrumental variable and clinicopathological variables as co-variables, suggested a potential improvement in the NSAID group (HR 0.61, 0.38 to 0.99). CONCLUSION: Conventional modelling did not demonstrate an association between postoperative NSAID use and recurrence-free survival in patients with rectal cancer, although an instrumental variables approach suggested a potential benefit.
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spelling pubmed-78934772021-02-24 Postoperative non-steroidal anti-inflammatory drug use and oncological outcomes of rectal cancer Grahn, O Lundin, M Lydrup, M-L Angenete, E Rutegård, M BJS Open Original Article BACKGROUND: Non-steroidal anti-inflammatory drugs (NSAIDs) are known to suppress the inflammatory response after surgery and are often used for pain control. This study aimed to investigate NSAID use after radical surgical resection for rectal cancer and long-term oncological outcomes. METHODS: A cohort of patients who underwent anterior resection for rectal cancer between 2007 and 2013 in 15 hospitals in Sweden was investigated retrospectively. Data were obtained from the Swedish Colorectal Cancer Registry and medical records; follow-up was undertaken until July 2019. Patients who received NSAID treatment for at least 2 days after surgery were compared with controls who did not, and the primary outcome was recurrence-free survival. Cox regression modelling with confounder adjustment, propensity score matching, and an instrumental variables approach were used; missing data were handled by multiple imputation. RESULTS: The cohort included 1341 patients, 362 (27.0 per cent) of whom received NSAIDs after operation. In analyses using conventional regression and propensity score matching, there was no significant association between postoperative NSAID use and recurrence-free survival (adjusted hazard ratio (HR) 1.02, 0.79 to 1.33). The instrumental variables approach, including individual hospital as the instrumental variable and clinicopathological variables as co-variables, suggested a potential improvement in the NSAID group (HR 0.61, 0.38 to 0.99). CONCLUSION: Conventional modelling did not demonstrate an association between postoperative NSAID use and recurrence-free survival in patients with rectal cancer, although an instrumental variables approach suggested a potential benefit. Oxford University Press 2021-02-15 /pmc/articles/PMC7893477/ /pubmed/33609397 http://dx.doi.org/10.1093/bjsopen/zraa050 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of BJS Society Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Article
Grahn, O
Lundin, M
Lydrup, M-L
Angenete, E
Rutegård, M
Postoperative non-steroidal anti-inflammatory drug use and oncological outcomes of rectal cancer
title Postoperative non-steroidal anti-inflammatory drug use and oncological outcomes of rectal cancer
title_full Postoperative non-steroidal anti-inflammatory drug use and oncological outcomes of rectal cancer
title_fullStr Postoperative non-steroidal anti-inflammatory drug use and oncological outcomes of rectal cancer
title_full_unstemmed Postoperative non-steroidal anti-inflammatory drug use and oncological outcomes of rectal cancer
title_short Postoperative non-steroidal anti-inflammatory drug use and oncological outcomes of rectal cancer
title_sort postoperative non-steroidal anti-inflammatory drug use and oncological outcomes of rectal cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7893477/
https://www.ncbi.nlm.nih.gov/pubmed/33609397
http://dx.doi.org/10.1093/bjsopen/zraa050
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