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Sequential Intravesical Gemcitabine and Docetaxel for the Salvage Treatment of Non-Muscle Invasive Bladder Cancer

BACKGROUND: Bacillus Calmette-Guerin (BCG) is the most effective intravesical therapy for non-muscle invasive bladder cancer (NMIBC), but patients can fail or supply shortages can develop. For BCG failures, radical cystectomy is recommended. However, in patients who desire bladder preservation or ar...

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Autores principales: Steinberg, Ryan L., Thomas, Lewis J., O’Donnell, Michael A., Nepple, Kenneth G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6218180/
https://www.ncbi.nlm.nih.gov/pubmed/30561441
http://dx.doi.org/10.3233/BLC-150008
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author Steinberg, Ryan L.
Thomas, Lewis J.
O’Donnell, Michael A.
Nepple, Kenneth G.
author_facet Steinberg, Ryan L.
Thomas, Lewis J.
O’Donnell, Michael A.
Nepple, Kenneth G.
author_sort Steinberg, Ryan L.
collection PubMed
description BACKGROUND: Bacillus Calmette-Guerin (BCG) is the most effective intravesical therapy for non-muscle invasive bladder cancer (NMIBC), but patients can fail or supply shortages can develop. For BCG failures, radical cystectomy is recommended. However, in patients who desire bladder preservation or are poor surgical candidates, alternative salvage intravesical therapies should be explored. OBJECTIVE: To determine whether dual sequential intravesical gemcitabine and docetaxel is effective in treating NMIBC. METHODS: We evaluated our initial experience with 45 patients treated with intravesical gemcitabine and docetaxel between June 2009 and May 2014. Patients were treated with 6 weekly instillations of gemcitabine (1 gram of gemcitabine in 50 ml of sterile water) followed immediately by docetaxel (37.5 mg of docetaxel in 50 mL of saline). Treatment success was defined as no bladder cancer recurrence and no cystectomy. Intention-to-treat analysis was performed using the Kaplan Meier method. RESULTS: Forty-five patients received treatment with a median overall follow-up of 15 months. Median follow up for treatment success was 6 months in all patients and 13 months for responders. Five patients were unable to tolerate a full induction course. Treatment success was 66% at first surveillance, 54% at 1 year, and 34% at 2 years after initiating induction. Ten patients received cystectomy (median of 5.6 months from starting induction) with no positive margins or lymph nodes on final pathology. CONCLUSIONS: Sequential dual intravesical gemcitabine and docetaxel can salvage some patients in a challenging NMIBC cohort.
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spelling pubmed-62181802018-11-09 Sequential Intravesical Gemcitabine and Docetaxel for the Salvage Treatment of Non-Muscle Invasive Bladder Cancer Steinberg, Ryan L. Thomas, Lewis J. O’Donnell, Michael A. Nepple, Kenneth G. Bladder Cancer Research Report BACKGROUND: Bacillus Calmette-Guerin (BCG) is the most effective intravesical therapy for non-muscle invasive bladder cancer (NMIBC), but patients can fail or supply shortages can develop. For BCG failures, radical cystectomy is recommended. However, in patients who desire bladder preservation or are poor surgical candidates, alternative salvage intravesical therapies should be explored. OBJECTIVE: To determine whether dual sequential intravesical gemcitabine and docetaxel is effective in treating NMIBC. METHODS: We evaluated our initial experience with 45 patients treated with intravesical gemcitabine and docetaxel between June 2009 and May 2014. Patients were treated with 6 weekly instillations of gemcitabine (1 gram of gemcitabine in 50 ml of sterile water) followed immediately by docetaxel (37.5 mg of docetaxel in 50 mL of saline). Treatment success was defined as no bladder cancer recurrence and no cystectomy. Intention-to-treat analysis was performed using the Kaplan Meier method. RESULTS: Forty-five patients received treatment with a median overall follow-up of 15 months. Median follow up for treatment success was 6 months in all patients and 13 months for responders. Five patients were unable to tolerate a full induction course. Treatment success was 66% at first surveillance, 54% at 1 year, and 34% at 2 years after initiating induction. Ten patients received cystectomy (median of 5.6 months from starting induction) with no positive margins or lymph nodes on final pathology. CONCLUSIONS: Sequential dual intravesical gemcitabine and docetaxel can salvage some patients in a challenging NMIBC cohort. IOS Press 2015-04-30 /pmc/articles/PMC6218180/ /pubmed/30561441 http://dx.doi.org/10.3233/BLC-150008 Text en © 2015 – IOS Press and the authors. All rights reserved 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 (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Report
Steinberg, Ryan L.
Thomas, Lewis J.
O’Donnell, Michael A.
Nepple, Kenneth G.
Sequential Intravesical Gemcitabine and Docetaxel for the Salvage Treatment of Non-Muscle Invasive Bladder Cancer
title Sequential Intravesical Gemcitabine and Docetaxel for the Salvage Treatment of Non-Muscle Invasive Bladder Cancer
title_full Sequential Intravesical Gemcitabine and Docetaxel for the Salvage Treatment of Non-Muscle Invasive Bladder Cancer
title_fullStr Sequential Intravesical Gemcitabine and Docetaxel for the Salvage Treatment of Non-Muscle Invasive Bladder Cancer
title_full_unstemmed Sequential Intravesical Gemcitabine and Docetaxel for the Salvage Treatment of Non-Muscle Invasive Bladder Cancer
title_short Sequential Intravesical Gemcitabine and Docetaxel for the Salvage Treatment of Non-Muscle Invasive Bladder Cancer
title_sort sequential intravesical gemcitabine and docetaxel for the salvage treatment of non-muscle invasive bladder cancer
topic Research Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6218180/
https://www.ncbi.nlm.nih.gov/pubmed/30561441
http://dx.doi.org/10.3233/BLC-150008
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