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Prophylactic urethral stenting with Memokath(®) 028SW in prostate cancer patients undergoing prostate (125)I seed implants: phase I/II study
PURPOSE: To study the feasibility/toxicity of urethral stenting with the Memokath(®) 028SW stent in patients undergoing prostate implant (PI) for prostate adenocarcinoma. MATERIAL AND METHODS: An Investigational Device Exemption from the Food and Drug Administration (FDA) and institutional review bo...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Termedia Publishing House
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5108832/ https://www.ncbi.nlm.nih.gov/pubmed/27877196 http://dx.doi.org/10.5114/jcb.2011.21038 |
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author | Chao, Samuel T. Angermeier, Kenneth Klein, Eric A. Reddy, Chandana A. Ulchaker, James C. Stephenson, Andrew Campbell, Steven Ciezki, Jay P. |
author_facet | Chao, Samuel T. Angermeier, Kenneth Klein, Eric A. Reddy, Chandana A. Ulchaker, James C. Stephenson, Andrew Campbell, Steven Ciezki, Jay P. |
author_sort | Chao, Samuel T. |
collection | PubMed |
description | PURPOSE: To study the feasibility/toxicity of urethral stenting with the Memokath(®) 028SW stent in patients undergoing prostate implant (PI) for prostate adenocarcinoma. MATERIAL AND METHODS: An Investigational Device Exemption from the Food and Drug Administration (FDA) and institutional review board (IRB) approval were obtained. Twenty patients enrolled. Baseline American Urological Association (AUA) score was obtained prior to PI. Follow-up information was obtained with weekly phone calls for the first 12 weeks and biweekly calls for the next 12 weeks to assess toxicity and AUA score. Removal of the stent was planned at six months after PI, or earlier due to excessive toxicity/patient request. RESULTS: Median age was 66.5 years. The median prostate volume was 39 cc (range: 10-90). The median baseline AUA score was 7.5 (range: 1-21). Three patients required intermittent self-catheterization (ISC) within 3 days after PI. No patients required ISC beyond day 3 after PI. The median duration of ISC was 1 day (range: 1-2). AUA scores returned to baseline values 6 weeks after PI. The week 6 AUA score was 10 (range: 4-16). Seven patients (35%) underwent early removal because of patient preference. The reasons were: incontinence (n = 3), discomfort (n = 2), hematuria (n = 1), and obstructive symptoms (n = 1). The median time of stent removal in these patients was 13.9 weeks (range: 0.9-21.4). Thirteen patients (65%) had ISC and/or urinary catheterization post stent removal. Median time for ISC use was 10 days (range: 1-90). CONCLUSIONS: Urethral stenting with Memokath(®) in patients undergoing PI was feasible, but resulted in relatively high rate of urinary incontinence and discomfort. Given the adverse effects experienced by patients of this study, further studies should focus only on patients with highest risk of urinary obstruction from PI or those with obstruction needing ISC. |
format | Online Article Text |
id | pubmed-5108832 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Termedia Publishing House |
record_format | MEDLINE/PubMed |
spelling | pubmed-51088322016-11-22 Prophylactic urethral stenting with Memokath(®) 028SW in prostate cancer patients undergoing prostate (125)I seed implants: phase I/II study Chao, Samuel T. Angermeier, Kenneth Klein, Eric A. Reddy, Chandana A. Ulchaker, James C. Stephenson, Andrew Campbell, Steven Ciezki, Jay P. J Contemp Brachytherapy Original Article PURPOSE: To study the feasibility/toxicity of urethral stenting with the Memokath(®) 028SW stent in patients undergoing prostate implant (PI) for prostate adenocarcinoma. MATERIAL AND METHODS: An Investigational Device Exemption from the Food and Drug Administration (FDA) and institutional review board (IRB) approval were obtained. Twenty patients enrolled. Baseline American Urological Association (AUA) score was obtained prior to PI. Follow-up information was obtained with weekly phone calls for the first 12 weeks and biweekly calls for the next 12 weeks to assess toxicity and AUA score. Removal of the stent was planned at six months after PI, or earlier due to excessive toxicity/patient request. RESULTS: Median age was 66.5 years. The median prostate volume was 39 cc (range: 10-90). The median baseline AUA score was 7.5 (range: 1-21). Three patients required intermittent self-catheterization (ISC) within 3 days after PI. No patients required ISC beyond day 3 after PI. The median duration of ISC was 1 day (range: 1-2). AUA scores returned to baseline values 6 weeks after PI. The week 6 AUA score was 10 (range: 4-16). Seven patients (35%) underwent early removal because of patient preference. The reasons were: incontinence (n = 3), discomfort (n = 2), hematuria (n = 1), and obstructive symptoms (n = 1). The median time of stent removal in these patients was 13.9 weeks (range: 0.9-21.4). Thirteen patients (65%) had ISC and/or urinary catheterization post stent removal. Median time for ISC use was 10 days (range: 1-90). CONCLUSIONS: Urethral stenting with Memokath(®) in patients undergoing PI was feasible, but resulted in relatively high rate of urinary incontinence and discomfort. Given the adverse effects experienced by patients of this study, further studies should focus only on patients with highest risk of urinary obstruction from PI or those with obstruction needing ISC. Termedia Publishing House 2011-03-31 2011-03 /pmc/articles/PMC5108832/ /pubmed/27877196 http://dx.doi.org/10.5114/jcb.2011.21038 Text en Copyright: © 2011 Termedia Sp. z o. o. http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license. |
spellingShingle | Original Article Chao, Samuel T. Angermeier, Kenneth Klein, Eric A. Reddy, Chandana A. Ulchaker, James C. Stephenson, Andrew Campbell, Steven Ciezki, Jay P. Prophylactic urethral stenting with Memokath(®) 028SW in prostate cancer patients undergoing prostate (125)I seed implants: phase I/II study |
title | Prophylactic urethral stenting with Memokath(®) 028SW in prostate cancer patients undergoing prostate (125)I seed implants: phase I/II study |
title_full | Prophylactic urethral stenting with Memokath(®) 028SW in prostate cancer patients undergoing prostate (125)I seed implants: phase I/II study |
title_fullStr | Prophylactic urethral stenting with Memokath(®) 028SW in prostate cancer patients undergoing prostate (125)I seed implants: phase I/II study |
title_full_unstemmed | Prophylactic urethral stenting with Memokath(®) 028SW in prostate cancer patients undergoing prostate (125)I seed implants: phase I/II study |
title_short | Prophylactic urethral stenting with Memokath(®) 028SW in prostate cancer patients undergoing prostate (125)I seed implants: phase I/II study |
title_sort | prophylactic urethral stenting with memokath(®) 028sw in prostate cancer patients undergoing prostate (125)i seed implants: phase i/ii study |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5108832/ https://www.ncbi.nlm.nih.gov/pubmed/27877196 http://dx.doi.org/10.5114/jcb.2011.21038 |
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