Efficacy of silodosin in patients undergoing brachytherapy: a randomized trial involving a pressure flow study
Purpose The purpose of the study is to investigate the efficacy of an alpha-1 adrenergic receptor antagonist (silodosin) for the treatment of lower urinary tract symptoms (LUTS) associated with interstitial 125 I implantation for prostate cancer. Methods This randomized single-center study involved...
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Published in: | World journal of urology Vol. 32; no. 6; pp. 1423 - 1432 |
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Main Authors: | , , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
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Springer Berlin Heidelberg
01-12-2014
Springer Nature B.V |
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Abstract | Purpose
The purpose of the study is to investigate the efficacy of an alpha-1 adrenergic receptor antagonist (silodosin) for the treatment of lower urinary tract symptoms (LUTS) associated with interstitial
125
I implantation for prostate cancer.
Methods
This randomized single-center study involved 105 patients (53 with and 52 without silodosin). Silodosin was postoperatively administered, daily, for 6 months (8 mg/day). Urinary symptoms and pressure flow were evaluated preoperatively and postoperatively at 1, 3, 6, and 12 months.
Results
At 12 months, interstitial
125
I implantation had induced a significant decrease in prostate volume (28.3 ± 11.1–20.5 ± 8.1 g in the silodosin group and 26.1 ± 9.7–17.7 ± 4.9 g in the controls) and the prostate-specific antigen level (7.1 ± 3.6–1.4 ± 1.7 ng/mL in the silodosin group and 8.1 ± 4.3–1.3 ± 1.2 ng/mL in the controls). Significant improvements in the international prostate symptom voiding subscores at 6 months and quality of life at 3 months were observed in those receiving silodosin. The pressure flow studies demonstrated that silodosin had significantly enlarged the bladder capacity when the first non-voiding contraction was seen at 3 and 12 months (3M: 127.1 ± 74.8 vs. 118.2 ± 83.9 mL,
p
= 0.001; 12M: 123.7 ± 79.3 vs. 100.3 ± 73.4 mL,
p
= 0.01); however, there were no improvements in the bladder outlet obstruction index (BOOI) or urinary flow.
Conclusions
Silodosin temporarily improved LUTS, but did not improve the BOOI after
125
I implantation in the prostate. |
---|---|
AbstractList | The purpose of the study is to investigate the efficacy of an alpha-1 adrenergic receptor antagonist (silodosin) for the treatment of lower urinary tract symptoms (LUTS) associated with interstitial (125)I implantation for prostate cancer.
This randomized single-center study involved 105 patients (53 with and 52 without silodosin). Silodosin was postoperatively administered, daily, for 6 months (8 mg/day). Urinary symptoms and pressure flow were evaluated preoperatively and postoperatively at 1, 3, 6, and 12 months.
At 12 months, interstitial (125)I implantation had induced a significant decrease in prostate volume (28.3 ± 11.1-20.5 ± 8.1 g in the silodosin group and 26.1 ± 9.7-17.7 ± 4.9 g in the controls) and the prostate-specific antigen level (7.1 ± 3.6-1.4 ± 1.7 ng/mL in the silodosin group and 8.1 ± 4.3-1.3 ± 1.2 ng/mL in the controls). Significant improvements in the international prostate symptom voiding subscores at 6 months and quality of life at 3 months were observed in those receiving silodosin. The pressure flow studies demonstrated that silodosin had significantly enlarged the bladder capacity when the first non-voiding contraction was seen at 3 and 12 months (3M: 127.1 ± 74.8 vs. 118.2 ± 83.9 mL, p = 0.001; 12M: 123.7 ± 79.3 vs. 100.3 ± 73.4 mL, p = 0.01); however, there were no improvements in the bladder outlet obstruction index (BOOI) or urinary flow.
Silodosin temporarily improved LUTS, but did not improve the BOOI after (125)I implantation in the prostate. Purpose The purpose of the study is to investigate the efficacy of an alpha-1 adrenergic receptor antagonist (silodosin) for the treatment of lower urinary tract symptoms (LUTS) associated with interstitial 125 I implantation for prostate cancer. Methods This randomized single-center study involved 105 patients (53 with and 52 without silodosin). Silodosin was postoperatively administered, daily, for 6 months (8 mg/day). Urinary symptoms and pressure flow were evaluated preoperatively and postoperatively at 1, 3, 6, and 12 months. Results At 12 months, interstitial 125 I implantation had induced a significant decrease in prostate volume (28.3 ± 11.1–20.5 ± 8.1 g in the silodosin group and 26.1 ± 9.7–17.7 ± 4.9 g in the controls) and the prostate-specific antigen level (7.1 ± 3.6–1.4 ± 1.7 ng/mL in the silodosin group and 8.1 ± 4.3–1.3 ± 1.2 ng/mL in the controls). Significant improvements in the international prostate symptom voiding subscores at 6 months and quality of life at 3 months were observed in those receiving silodosin. The pressure flow studies demonstrated that silodosin had significantly enlarged the bladder capacity when the first non-voiding contraction was seen at 3 and 12 months (3M: 127.1 ± 74.8 vs. 118.2 ± 83.9 mL, p = 0.001; 12M: 123.7 ± 79.3 vs. 100.3 ± 73.4 mL, p = 0.01); however, there were no improvements in the bladder outlet obstruction index (BOOI) or urinary flow. Conclusions Silodosin temporarily improved LUTS, but did not improve the BOOI after 125 I implantation in the prostate. The purpose of the study is to investigate the efficacy of an alpha-1 adrenergic receptor antagonist (silodosin) for the treatment of lower urinary tract symptoms (LUTS) associated with interstitial ^sup 125^I implantation for prostate cancer. This randomized single-center study involved 105 patients (53 with and 52 without silodosin). Silodosin was postoperatively administered, daily, for 6 months (8 mg/day). Urinary symptoms and pressure flow were evaluated preoperatively and postoperatively at 1, 3, 6, and 12 months. At 12 months, interstitial ^sup 125^I implantation had induced a significant decrease in prostate volume (28.3 ± 11.1-20.5 ± 8.1 g in the silodosin group and 26.1 ± 9.7-17.7 ± 4.9 g in the controls) and the prostate-specific antigen level (7.1 ± 3.6-1.4 ± 1.7 ng/mL in the silodosin group and 8.1 ± 4.3-1.3 ± 1.2 ng/mL in the controls). Significant improvements in the international prostate symptom voiding subscores at 6 months and quality of life at 3 months were observed in those receiving silodosin. The pressure flow studies demonstrated that silodosin had significantly enlarged the bladder capacity when the first non-voiding contraction was seen at 3 and 12 months (3M: 127.1 ± 74.8 vs. 118.2 ± 83.9 mL, p = 0.001; 12M: 123.7 ± 79.3 vs. 100.3 ± 73.4 mL, p = 0.01); however, there were no improvements in the bladder outlet obstruction index (BOOI) or urinary flow. Silodosin temporarily improved LUTS, but did not improve the BOOI after ^sup 125^I implantation in the prostate.[PUBLICATION ABSTRACT] |
Author | Saito, Yoshitaka Hayashi, Taiji Nakamatsu, Kiyoshi Yamamoto, Yutaka Sugimoto, Koichi Tsuji, Hidenori Minami, Takafumi Nozawa, Masahiro Ishii, Tokumi Shimizu, Nobutaka Yoshimura, Kazuhiro Uemura, Hirotsugu |
Author_xml | – sequence: 1 givenname: Nobutaka surname: Shimizu fullname: Shimizu, Nobutaka email: shimizun@med.kindai.ac.jp organization: Department of Urology, Faculty of Medicine, Kinki University – sequence: 2 givenname: Takafumi surname: Minami fullname: Minami, Takafumi organization: Department of Urology, Faculty of Medicine, Kinki University – sequence: 3 givenname: Koichi surname: Sugimoto fullname: Sugimoto, Koichi organization: Department of Urology, Faculty of Medicine, Kinki University – sequence: 4 givenname: Yoshitaka surname: Saito fullname: Saito, Yoshitaka organization: Department of Urology, Faculty of Medicine, Kinki University – sequence: 5 givenname: Yutaka surname: Yamamoto fullname: Yamamoto, Yutaka organization: Department of Urology, Faculty of Medicine, Kinki University – sequence: 6 givenname: Taiji surname: Hayashi fullname: Hayashi, Taiji organization: Department of Urology, Faculty of Medicine, Kinki University – sequence: 7 givenname: Hidenori surname: Tsuji fullname: Tsuji, Hidenori organization: Department of Urology, Faculty of Medicine, Kinki University – sequence: 8 givenname: Masahiro surname: Nozawa fullname: Nozawa, Masahiro organization: Department of Urology, Faculty of Medicine, Kinki University – sequence: 9 givenname: Kazuhiro surname: Yoshimura fullname: Yoshimura, Kazuhiro organization: Department of Urology, Faculty of Medicine, Kinki University – sequence: 10 givenname: Tokumi surname: Ishii fullname: Ishii, Tokumi organization: Department of Urology, Faculty of Medicine, Kinki University – sequence: 11 givenname: Hirotsugu surname: Uemura fullname: Uemura, Hirotsugu organization: Department of Urology, Faculty of Medicine, Kinki University – sequence: 12 givenname: Kiyoshi surname: Nakamatsu fullname: Nakamatsu, Kiyoshi organization: Department of Radiology, Faculty of Medicine, Kinki University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/24435207$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1007_s00345_020_03398_3 crossref_primary_10_1007_s11934_021_01048_8 crossref_primary_10_1186_s13014_014_0302_7 crossref_primary_10_2147_DDDT_S373659 crossref_primary_10_1016_j_brachy_2017_12_004 crossref_primary_10_1016_j_brachy_2021_07_006 crossref_primary_10_1007_s12325_018_0854_2 crossref_primary_10_1111_luts_12402 crossref_primary_10_1016_j_brachy_2017_05_009 crossref_primary_10_1111_ijcp_12693 crossref_primary_10_1007_s11884_014_0279_y crossref_primary_10_1016_j_brachy_2014_09_009 |
Cites_doi | 10.1016/S0360-3016(01)02812-7 10.1016/S0302-2838(02)00019-2 10.1002/nau.10066 10.1111/j.1464-410X.2005.05346.x 10.1016/j.ijrobp.2004.09.036 10.1016/j.radonc.2007.05.020 10.1016/j.juro.2013.03.110 10.1016/S0022-5347(01)62542-4 10.1016/S0360-3016(01)02657-8 10.1111/j.1464-410X.2011.10814.x 10.1016/S0090-4295(02)02142-8 10.1111/j.1464-410X.2011.10623.x 10.1016/S0090-4295(02)01840-X 10.1016/j.juro.2009.08.030 10.1200/JCO.1996.14.2.449 10.1016/j.ijrobp.2011.04.026 10.1111/j.1464-410X.2011.10800.x 10.1016/S0360-3016(99)00069-3 10.1016/j.urology.2009.05.045 10.1016/j.radonc.2008.12.009 10.1093/jjco/hyr184 10.1097/01.coc.0000225412.24750.4c 10.1016/j.ijrobp.2005.01.040 10.1200/JCO.2009.25.3245 10.1016/j.juro.2006.10.018 10.1200/JCO.1999.17.2.517 10.1016/S0360-3016(99)00525-8 10.1016/S0360-3016(02)02726-8 10.1111/j.1464-410X.2011.10827.x 10.1111/j.1442-2042.2011.02957.x |
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Keywords | Pressure flow study Brachytherapy Prostatic neoplasms Alpha-1 antagonists Silodosin |
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The purpose of the study is to investigate the efficacy of an alpha-1 adrenergic receptor antagonist (silodosin) for the treatment of lower urinary... The purpose of the study is to investigate the efficacy of an alpha-1 adrenergic receptor antagonist (silodosin) for the treatment of lower urinary tract... |
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SubjectTerms | Adrenergic alpha-1 Receptor Antagonists - therapeutic use Aged Brachytherapy - adverse effects Humans Indoles - therapeutic use Lower Urinary Tract Symptoms - drug therapy Lower Urinary Tract Symptoms - etiology Lower Urinary Tract Symptoms - physiopathology Male Medicine Medicine & Public Health Middle Aged Nephrology Oncology Original Article Prostatic Neoplasms - pathology Prostatic Neoplasms - physiopathology Prostatic Neoplasms - radiotherapy Quality of Life Treatment Outcome Urinary Bladder Neck Obstruction - drug therapy Urinary Bladder Neck Obstruction - etiology Urinary Bladder Neck Obstruction - physiopathology Urodynamics Urology |
Title | Efficacy of silodosin in patients undergoing brachytherapy: a randomized trial involving a pressure flow study |
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