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Downstaging and survival after Neoadjuvant chemotherapy for bladder cancer in Norway; a population-based study
BACKGROUND: Neoadjuvant chemotherapy (NAC) before radical cystectomy is associated with pathological downstaging (DS) and improved overall survival (OS) in patients with muscle-invasive bladder cancer (MIBC). Population-based studies have not unequivocally shown improved survival. The aim of this po...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9746207/ https://www.ncbi.nlm.nih.gov/pubmed/36510166 http://dx.doi.org/10.1186/s12885-022-10394-w |
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author | Møller, Christina Tanem Støer, Nathalie C. Blindheim, Augun Berge, Viktor Tafjord, Gunnar Fosså, Sophie D. Andreassen, Bettina Kulle |
author_facet | Møller, Christina Tanem Støer, Nathalie C. Blindheim, Augun Berge, Viktor Tafjord, Gunnar Fosså, Sophie D. Andreassen, Bettina Kulle |
author_sort | Møller, Christina Tanem |
collection | PubMed |
description | BACKGROUND: Neoadjuvant chemotherapy (NAC) before radical cystectomy is associated with pathological downstaging (DS) and improved overall survival (OS) in patients with muscle-invasive bladder cancer (MIBC). Population-based studies have not unequivocally shown improved survival. The aim of this population-based study was to evaluate the effect of NAC on DS and OS in Norwegian patients with MIBC. METHODS: Patients in the Cancer Registry of Norway undergoing radical cystectomy (2008–2015) with or without NAC diagnosed with MIBC between 2008 and 2012 were included. Follow-up data were available until 31 December 2019. Logistic regression estimated the odds of DS with NAC, and a Cox model investigated the effect of DS on OS. Cox models, a mediator analysis and an instrumental variable approach were used to investigate the effect of NAC on OS. RESULTS: A total of 575 patients were included. NAC was administered to 82 (14%) patients. Compared to cystectomy only, NAC increased the proportion (43% vs. 22%) and the odds of DS (OR 2.51, CI 1.37–4.60, p = 0.003). Independent of NAC, the proportion of pN0 was higher in patients with DS (89% vs. 60%) and DS yielded a 78% mortality risk reduction (HR 0.22, CI 0.15–0.34, p = 1.9∙10–12), compared to patients without DS. We did not find an association between NAC and OS, neither by Cox regression (HR 1.16, CI 0.80–1.68, p = 0.417) nor by an instrumental variable approach (HR = 0.56, CI = 0.07–4.57, p = 0.586). The mediation analysis (p = 0.026) confirmed an indirect effect of NAC on OS through DS. Limitations include limited information of the primary tumour, details of NAC treatment and treatment indications. CONCLUSIONS: NAC increases the probability of DS and is indirectly associated to OS. DS is related to the absence of regional lymph node metastases and is associated with an OS benefit. Improved staging and biomarkers are needed to identify patients most likely to achieve DS and to benefit from NAC. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-022-10394-w. |
format | Online Article Text |
id | pubmed-9746207 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-97462072022-12-14 Downstaging and survival after Neoadjuvant chemotherapy for bladder cancer in Norway; a population-based study Møller, Christina Tanem Støer, Nathalie C. Blindheim, Augun Berge, Viktor Tafjord, Gunnar Fosså, Sophie D. Andreassen, Bettina Kulle BMC Cancer Research BACKGROUND: Neoadjuvant chemotherapy (NAC) before radical cystectomy is associated with pathological downstaging (DS) and improved overall survival (OS) in patients with muscle-invasive bladder cancer (MIBC). Population-based studies have not unequivocally shown improved survival. The aim of this population-based study was to evaluate the effect of NAC on DS and OS in Norwegian patients with MIBC. METHODS: Patients in the Cancer Registry of Norway undergoing radical cystectomy (2008–2015) with or without NAC diagnosed with MIBC between 2008 and 2012 were included. Follow-up data were available until 31 December 2019. Logistic regression estimated the odds of DS with NAC, and a Cox model investigated the effect of DS on OS. Cox models, a mediator analysis and an instrumental variable approach were used to investigate the effect of NAC on OS. RESULTS: A total of 575 patients were included. NAC was administered to 82 (14%) patients. Compared to cystectomy only, NAC increased the proportion (43% vs. 22%) and the odds of DS (OR 2.51, CI 1.37–4.60, p = 0.003). Independent of NAC, the proportion of pN0 was higher in patients with DS (89% vs. 60%) and DS yielded a 78% mortality risk reduction (HR 0.22, CI 0.15–0.34, p = 1.9∙10–12), compared to patients without DS. We did not find an association between NAC and OS, neither by Cox regression (HR 1.16, CI 0.80–1.68, p = 0.417) nor by an instrumental variable approach (HR = 0.56, CI = 0.07–4.57, p = 0.586). The mediation analysis (p = 0.026) confirmed an indirect effect of NAC on OS through DS. Limitations include limited information of the primary tumour, details of NAC treatment and treatment indications. CONCLUSIONS: NAC increases the probability of DS and is indirectly associated to OS. DS is related to the absence of regional lymph node metastases and is associated with an OS benefit. Improved staging and biomarkers are needed to identify patients most likely to achieve DS and to benefit from NAC. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-022-10394-w. BioMed Central 2022-12-12 /pmc/articles/PMC9746207/ /pubmed/36510166 http://dx.doi.org/10.1186/s12885-022-10394-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Møller, Christina Tanem Støer, Nathalie C. Blindheim, Augun Berge, Viktor Tafjord, Gunnar Fosså, Sophie D. Andreassen, Bettina Kulle Downstaging and survival after Neoadjuvant chemotherapy for bladder cancer in Norway; a population-based study |
title | Downstaging and survival after Neoadjuvant chemotherapy for bladder cancer in Norway; a population-based study |
title_full | Downstaging and survival after Neoadjuvant chemotherapy for bladder cancer in Norway; a population-based study |
title_fullStr | Downstaging and survival after Neoadjuvant chemotherapy for bladder cancer in Norway; a population-based study |
title_full_unstemmed | Downstaging and survival after Neoadjuvant chemotherapy for bladder cancer in Norway; a population-based study |
title_short | Downstaging and survival after Neoadjuvant chemotherapy for bladder cancer in Norway; a population-based study |
title_sort | downstaging and survival after neoadjuvant chemotherapy for bladder cancer in norway; a population-based study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9746207/ https://www.ncbi.nlm.nih.gov/pubmed/36510166 http://dx.doi.org/10.1186/s12885-022-10394-w |
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