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Trimodal therapy in T2‐4aN0M0 bladder cancer––How to select the best candidate?

The reported results of trimodal treatment (TMT) in muscle‐invasive bladder cancer vary widely. We attempted to characterize the profile of ideal candidates for this approach. Between 2000 and 2019, 105 patients (median age 78 years) with T2‐4aN0M0 bladder cancer were treated with TMT and analyzed r...

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Autores principales: Gofrit, Ofer N., Meirovitz, Amichay, Frank, Stephen, Rabinovich, Igal, Luwisch, Hemda, Yutkin, Vladimir, Neuman, Tzahi, Hidas, Guy, Duvdevani, Mordechai, Wygoda, Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7666756/
https://www.ncbi.nlm.nih.gov/pubmed/32960495
http://dx.doi.org/10.1002/cam4.3478
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author Gofrit, Ofer N.
Meirovitz, Amichay
Frank, Stephen
Rabinovich, Igal
Luwisch, Hemda
Yutkin, Vladimir
Neuman, Tzahi
Hidas, Guy
Duvdevani, Mordechai
Wygoda, Marc
author_facet Gofrit, Ofer N.
Meirovitz, Amichay
Frank, Stephen
Rabinovich, Igal
Luwisch, Hemda
Yutkin, Vladimir
Neuman, Tzahi
Hidas, Guy
Duvdevani, Mordechai
Wygoda, Marc
author_sort Gofrit, Ofer N.
collection PubMed
description The reported results of trimodal treatment (TMT) in muscle‐invasive bladder cancer vary widely. We attempted to characterize the profile of ideal candidates for this approach. Between 2000 and 2019, 105 patients (median age 78 years) with T2‐4aN0M0 bladder cancer were treated with TMT and analyzed retrospectively. Mean radiotherapy dose was 62 Gy (SD 8.4). Ten pretreatment prognostic parameters were evaluated including tumor diameter on pre‐TURBT CT. Multivariate analyses was performed and combination of parameters was studied. After a median follow‐up of 29 months, 53 patients (50.5%) developed recurrence and 70 patients (67.7%) died. Death was disease‐specific in 46 patients (65.7%). Tumor diameter was the most significant prognostic parameter with p < 0.0001 for overall, disease‐specific and recurrence‐free survivals. For every 1 cm increase in tumor diameter, the risk of disease‐specific mortality increased by 1.57. Age, cisplatin eligibility and the Charlson Comorbidity Index were significant predictors of overall survival but not of disease‐specific or recurrence‐free survival. Patients who were cisplatin‐eligible with a tumor diameter ≤3 cm had a 5‐year disease‐specific survival rate of 79.2% as opposed to 33.9% in patients without one of these features (p < 0.001). When tumor diameter exceeded 5 cm (irrelevant of all other parameters), 5‐year disease‐specific survival rate was only 28.2%. Patient profiles can accurately predict response to TMT. In cisplatin‐eligible patients with a tumor diameter ≤3 cm, TMT provides an excellent disease‐specific survival rate. In patients with a tumor diameter >5 cm TMT renders unacceptably poor treatment outcomes.
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spelling pubmed-76667562020-11-20 Trimodal therapy in T2‐4aN0M0 bladder cancer––How to select the best candidate? Gofrit, Ofer N. Meirovitz, Amichay Frank, Stephen Rabinovich, Igal Luwisch, Hemda Yutkin, Vladimir Neuman, Tzahi Hidas, Guy Duvdevani, Mordechai Wygoda, Marc Cancer Med Clinical Cancer Research The reported results of trimodal treatment (TMT) in muscle‐invasive bladder cancer vary widely. We attempted to characterize the profile of ideal candidates for this approach. Between 2000 and 2019, 105 patients (median age 78 years) with T2‐4aN0M0 bladder cancer were treated with TMT and analyzed retrospectively. Mean radiotherapy dose was 62 Gy (SD 8.4). Ten pretreatment prognostic parameters were evaluated including tumor diameter on pre‐TURBT CT. Multivariate analyses was performed and combination of parameters was studied. After a median follow‐up of 29 months, 53 patients (50.5%) developed recurrence and 70 patients (67.7%) died. Death was disease‐specific in 46 patients (65.7%). Tumor diameter was the most significant prognostic parameter with p < 0.0001 for overall, disease‐specific and recurrence‐free survivals. For every 1 cm increase in tumor diameter, the risk of disease‐specific mortality increased by 1.57. Age, cisplatin eligibility and the Charlson Comorbidity Index were significant predictors of overall survival but not of disease‐specific or recurrence‐free survival. Patients who were cisplatin‐eligible with a tumor diameter ≤3 cm had a 5‐year disease‐specific survival rate of 79.2% as opposed to 33.9% in patients without one of these features (p < 0.001). When tumor diameter exceeded 5 cm (irrelevant of all other parameters), 5‐year disease‐specific survival rate was only 28.2%. Patient profiles can accurately predict response to TMT. In cisplatin‐eligible patients with a tumor diameter ≤3 cm, TMT provides an excellent disease‐specific survival rate. In patients with a tumor diameter >5 cm TMT renders unacceptably poor treatment outcomes. John Wiley and Sons Inc. 2020-09-22 /pmc/articles/PMC7666756/ /pubmed/32960495 http://dx.doi.org/10.1002/cam4.3478 Text en © 2020 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Cancer Research
Gofrit, Ofer N.
Meirovitz, Amichay
Frank, Stephen
Rabinovich, Igal
Luwisch, Hemda
Yutkin, Vladimir
Neuman, Tzahi
Hidas, Guy
Duvdevani, Mordechai
Wygoda, Marc
Trimodal therapy in T2‐4aN0M0 bladder cancer––How to select the best candidate?
title Trimodal therapy in T2‐4aN0M0 bladder cancer––How to select the best candidate?
title_full Trimodal therapy in T2‐4aN0M0 bladder cancer––How to select the best candidate?
title_fullStr Trimodal therapy in T2‐4aN0M0 bladder cancer––How to select the best candidate?
title_full_unstemmed Trimodal therapy in T2‐4aN0M0 bladder cancer––How to select the best candidate?
title_short Trimodal therapy in T2‐4aN0M0 bladder cancer––How to select the best candidate?
title_sort trimodal therapy in t2‐4an0m0 bladder cancer––how to select the best candidate?
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7666756/
https://www.ncbi.nlm.nih.gov/pubmed/32960495
http://dx.doi.org/10.1002/cam4.3478
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