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Differences in Cancer-Specific Mortality after Trimodal Therapy for T2N0M0 Bladder Cancer according to Histological Subtype

SIMPLE SUMMARY: Trimodal therapy represents an accepted treatment option for non-metastatic muscle-invasive bladder cancer, which is an alternative to radical cystectomy. Evidence regarding trimodal therapy efficacy has predominantly, or even exclusively, been applied to urothelial carcinoma of the...

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Autores principales: Barletta, Francesco, Tappero, Stefano, Panunzio, Andrea, Incesu, Reha-Baris, Cano Garcia, Cristina, Piccinelli, Mattia Luca, Tian, Zhe, Gandaglia, Giorgio, Moschini, Marco, Terrone, Carlo, Antonelli, Alessandro, Tilki, Derya, Chun, Felix K. H., de Cobelli, Ottavio, Saad, Fred, Shariat, Shahrokh F., Montorsi, Francesco, Briganti, Alberto, Karakiewicz, Pierre I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9736026/
https://www.ncbi.nlm.nih.gov/pubmed/36497246
http://dx.doi.org/10.3390/cancers14235766
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author Barletta, Francesco
Tappero, Stefano
Panunzio, Andrea
Incesu, Reha-Baris
Cano Garcia, Cristina
Piccinelli, Mattia Luca
Tian, Zhe
Gandaglia, Giorgio
Moschini, Marco
Terrone, Carlo
Antonelli, Alessandro
Tilki, Derya
Chun, Felix K. H.
de Cobelli, Ottavio
Saad, Fred
Shariat, Shahrokh F.
Montorsi, Francesco
Briganti, Alberto
Karakiewicz, Pierre I.
author_facet Barletta, Francesco
Tappero, Stefano
Panunzio, Andrea
Incesu, Reha-Baris
Cano Garcia, Cristina
Piccinelli, Mattia Luca
Tian, Zhe
Gandaglia, Giorgio
Moschini, Marco
Terrone, Carlo
Antonelli, Alessandro
Tilki, Derya
Chun, Felix K. H.
de Cobelli, Ottavio
Saad, Fred
Shariat, Shahrokh F.
Montorsi, Francesco
Briganti, Alberto
Karakiewicz, Pierre I.
author_sort Barletta, Francesco
collection PubMed
description SIMPLE SUMMARY: Trimodal therapy represents an accepted treatment option for non-metastatic muscle-invasive bladder cancer, which is an alternative to radical cystectomy. Evidence regarding trimodal therapy efficacy has predominantly, or even exclusively, been applied to urothelial carcinoma of the urinary bladder patients. To address this void, we tested for differences in cancer-specific mortality in trimodal therapy-treated bladder cancer patients, according to histological subtype, namely urothelial carcinoma vs. neuroendocrine carcinoma vs. squamous cell carcinoma vs. adenocarcinoma. ABSTRACT: We aimed at assessing the impact of non-urothelial variant histology (VH), relative to urothelial carcinoma of the urinary bladder (UCUB), on cancer-specific mortality (CSM) in T2N0M0 bladder cancer patients treated with trimodal therapy (TMT). TMT patients treated for T2N0M0 bladder cancer were identified within the Surveillance, Epidemiology, and End Results database (2000−2018). Patients who underwent TMT received trans-urethral resection of the bladder tumor, chemotherapy, and radiotherapy. CSM-FS rates were tested using Kaplan–Meier plots and multivariable Cox-regression (MCR) models according to histological subtype: UCUB vs. neuroendocrine carcinoma vs. squamous cell carcinoma vs. adenocarcinoma. A total of 3846 T2N0MO bladder cancer patients treated with TMT were identified. Of these, 3627 (94.3%) harbored UCUB, while 105 (2.7%), 85 (2.2%), and 29 (0.8%) harbored neuroendocrine carcinoma, squamous cell carcinoma, and adenocarcinoma, respectively. In Kaplan–Meier analyses, 3-yr CSM-FS rates were 57% for UCUB, 51% for neuroendocrine carcinoma, 35% for squamous cell carcinoma, and 60% for adenocarcinoma (p-value < 0.0001). In MCR models, only squamous cell carcinoma exhibited higher CSM than UCUB (HR 1.98, 95%CI 1.5–2.61, p-value < 0.001). Despite the small number of observations, squamous cell carcinoma distinguished itself from UCUB based on worse survival in T2N0M0 patients after TMT.
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spelling pubmed-97360262022-12-11 Differences in Cancer-Specific Mortality after Trimodal Therapy for T2N0M0 Bladder Cancer according to Histological Subtype Barletta, Francesco Tappero, Stefano Panunzio, Andrea Incesu, Reha-Baris Cano Garcia, Cristina Piccinelli, Mattia Luca Tian, Zhe Gandaglia, Giorgio Moschini, Marco Terrone, Carlo Antonelli, Alessandro Tilki, Derya Chun, Felix K. H. de Cobelli, Ottavio Saad, Fred Shariat, Shahrokh F. Montorsi, Francesco Briganti, Alberto Karakiewicz, Pierre I. Cancers (Basel) Article SIMPLE SUMMARY: Trimodal therapy represents an accepted treatment option for non-metastatic muscle-invasive bladder cancer, which is an alternative to radical cystectomy. Evidence regarding trimodal therapy efficacy has predominantly, or even exclusively, been applied to urothelial carcinoma of the urinary bladder patients. To address this void, we tested for differences in cancer-specific mortality in trimodal therapy-treated bladder cancer patients, according to histological subtype, namely urothelial carcinoma vs. neuroendocrine carcinoma vs. squamous cell carcinoma vs. adenocarcinoma. ABSTRACT: We aimed at assessing the impact of non-urothelial variant histology (VH), relative to urothelial carcinoma of the urinary bladder (UCUB), on cancer-specific mortality (CSM) in T2N0M0 bladder cancer patients treated with trimodal therapy (TMT). TMT patients treated for T2N0M0 bladder cancer were identified within the Surveillance, Epidemiology, and End Results database (2000−2018). Patients who underwent TMT received trans-urethral resection of the bladder tumor, chemotherapy, and radiotherapy. CSM-FS rates were tested using Kaplan–Meier plots and multivariable Cox-regression (MCR) models according to histological subtype: UCUB vs. neuroendocrine carcinoma vs. squamous cell carcinoma vs. adenocarcinoma. A total of 3846 T2N0MO bladder cancer patients treated with TMT were identified. Of these, 3627 (94.3%) harbored UCUB, while 105 (2.7%), 85 (2.2%), and 29 (0.8%) harbored neuroendocrine carcinoma, squamous cell carcinoma, and adenocarcinoma, respectively. In Kaplan–Meier analyses, 3-yr CSM-FS rates were 57% for UCUB, 51% for neuroendocrine carcinoma, 35% for squamous cell carcinoma, and 60% for adenocarcinoma (p-value < 0.0001). In MCR models, only squamous cell carcinoma exhibited higher CSM than UCUB (HR 1.98, 95%CI 1.5–2.61, p-value < 0.001). Despite the small number of observations, squamous cell carcinoma distinguished itself from UCUB based on worse survival in T2N0M0 patients after TMT. MDPI 2022-11-23 /pmc/articles/PMC9736026/ /pubmed/36497246 http://dx.doi.org/10.3390/cancers14235766 Text en © 2022 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
Barletta, Francesco
Tappero, Stefano
Panunzio, Andrea
Incesu, Reha-Baris
Cano Garcia, Cristina
Piccinelli, Mattia Luca
Tian, Zhe
Gandaglia, Giorgio
Moschini, Marco
Terrone, Carlo
Antonelli, Alessandro
Tilki, Derya
Chun, Felix K. H.
de Cobelli, Ottavio
Saad, Fred
Shariat, Shahrokh F.
Montorsi, Francesco
Briganti, Alberto
Karakiewicz, Pierre I.
Differences in Cancer-Specific Mortality after Trimodal Therapy for T2N0M0 Bladder Cancer according to Histological Subtype
title Differences in Cancer-Specific Mortality after Trimodal Therapy for T2N0M0 Bladder Cancer according to Histological Subtype
title_full Differences in Cancer-Specific Mortality after Trimodal Therapy for T2N0M0 Bladder Cancer according to Histological Subtype
title_fullStr Differences in Cancer-Specific Mortality after Trimodal Therapy for T2N0M0 Bladder Cancer according to Histological Subtype
title_full_unstemmed Differences in Cancer-Specific Mortality after Trimodal Therapy for T2N0M0 Bladder Cancer according to Histological Subtype
title_short Differences in Cancer-Specific Mortality after Trimodal Therapy for T2N0M0 Bladder Cancer according to Histological Subtype
title_sort differences in cancer-specific mortality after trimodal therapy for t2n0m0 bladder cancer according to histological subtype
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9736026/
https://www.ncbi.nlm.nih.gov/pubmed/36497246
http://dx.doi.org/10.3390/cancers14235766
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