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5α-reductase inhibitors impact prognosis of urothelial carcinoma
5α-reductase inhibitors (5-ARIs) inhibit the pathway of converting the testosterone to dihydrotestosterone and are widely used in benign prostatic hyperplasia patients. Since androgen receptor activation may play a role in urothelial tumorigenesis, we conducted this retrospective cohort study to det...
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Published in: | BMC cancer 2020-09, Vol.20 (1), p.872-7, Article 872 |
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description | 5α-reductase inhibitors (5-ARIs) inhibit the pathway of converting the testosterone to dihydrotestosterone and are widely used in benign prostatic hyperplasia patients. Since androgen receptor activation may play a role in urothelial tumorigenesis, we conducted this retrospective cohort study to determine whether 5α-reductase inhibitors (5-ARIs) administration is associated with bladder cancer mortality, bladder cancer recurrence and upper tract urothelial carcinoma mortality, using the Taiwan National Health Insurance database.
The data of this retrospective cohort study were sourced from the Longitudinal Health Insurance Database of Taiwan, compiled by the Taiwan National Health Insurance database from 1996 to 2010. It consists of 18,530 men with bladder cancer, of whom 474 were 5-ARIs recipients and 4384 men with upper tract urothelial carcinoma, of whom 109 were 5-ARIs recipients. Propensity Score Matching on the age and geographic data was done at the ratio of 1:10. We analyzed the odds ratios (OR) and 95% confidence interval (CI) of the risk of bladder cancer death, bladder cancer recurrence rate and upper tract urothelial carcinoma related death by the 5-ARIs administration.
Those who received 5-ARIs showed a lower risk of bladder cancer related death compared to nonusers in multivariable adjusted analysis (OR 0.835, 95% CI 0.71-0.98). However, there was no significant difference in the bladder cancer recurrence rate (OR 0.956, 95% CI 0.82-1.11) and upper tract urothelial carcinoma related mortality in multivariable adjusted analysis (OR 0.814, 95% CI 0.6-1.1).
Patients who receive 5-ARIs have lower bladder cancer related mortality compared to those who don't. 5-ARIs may prove to be a viable strategy to improve bladder cancer outcomes. |
doi_str_mv | 10.1186/s12885-020-07373-4 |
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The data of this retrospective cohort study were sourced from the Longitudinal Health Insurance Database of Taiwan, compiled by the Taiwan National Health Insurance database from 1996 to 2010. It consists of 18,530 men with bladder cancer, of whom 474 were 5-ARIs recipients and 4384 men with upper tract urothelial carcinoma, of whom 109 were 5-ARIs recipients. Propensity Score Matching on the age and geographic data was done at the ratio of 1:10. We analyzed the odds ratios (OR) and 95% confidence interval (CI) of the risk of bladder cancer death, bladder cancer recurrence rate and upper tract urothelial carcinoma related death by the 5-ARIs administration.
Those who received 5-ARIs showed a lower risk of bladder cancer related death compared to nonusers in multivariable adjusted analysis (OR 0.835, 95% CI 0.71-0.98). However, there was no significant difference in the bladder cancer recurrence rate (OR 0.956, 95% CI 0.82-1.11) and upper tract urothelial carcinoma related mortality in multivariable adjusted analysis (OR 0.814, 95% CI 0.6-1.1).
Patients who receive 5-ARIs have lower bladder cancer related mortality compared to those who don't. 5-ARIs may prove to be a viable strategy to improve bladder cancer outcomes.</description><identifier>ISSN: 1471-2407</identifier><identifier>EISSN: 1471-2407</identifier><identifier>DOI: 10.1186/s12885-020-07373-4</identifier><identifier>PMID: 32917158</identifier><language>eng</language><publisher>England: BioMed Central</publisher><subject>5-alpha Reductase Inhibitors - administration & dosage ; 5-alpha Reductase Inhibitors - adverse effects ; 5α-reductase inhibitors (5-ARIs) ; Age ; Aged ; Androgen receptor (AR) ; Androgen receptors ; Androgens ; Bladder cancer ; Cancer therapies ; Carcinoma - drug therapy ; Carcinoma - genetics ; Carcinoma - mortality ; Carcinoma - pathology ; Carcinoma, Transitional Cell - drug therapy ; Carcinoma, Transitional Cell - genetics ; Carcinoma, Transitional Cell - mortality ; Carcinoma, Transitional Cell - pathology ; Cholestenone 5 alpha-Reductase - genetics ; Codes ; Death ; Diabetes ; Dihydrotestosterone ; Drug dosages ; Dutasteride ; Dutasteride - administration & dosage ; Finasteride ; Finasteride - administration & dosage ; Health insurance ; Hospitals ; Humans ; Hyperplasia ; Hypertension ; Kidney diseases ; Male ; Medical diagnosis ; Medical prognosis ; Middle Aged ; Mortality ; Neoplasm Recurrence, Local - drug therapy ; Neoplasm Recurrence, Local - genetics ; Neoplasm Recurrence, Local - mortality ; Neoplasm Recurrence, Local - pathology ; Population ; Prognosis ; Prostate cancer ; Prostatic Hyperplasia - drug therapy ; Prostatic Hyperplasia - genetics ; Prostatic Hyperplasia - mortality ; Prostatic Hyperplasia - pathology ; Receptor mechanisms ; Receptors, Androgen - genetics ; Steroid 5α-reductase ; Taiwan - epidemiology ; Testosterone ; Tumorigenesis ; Upper tract urothelial carcinoma ; Urothelial carcinoma ; Urothelium - drug effects ; Urothelium - pathology</subject><ispartof>BMC cancer, 2020-09, Vol.20 (1), p.872-7, Article 872</ispartof><rights>2020. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c496t-33bf8b6af47bc559683fed9b87a05e1a2bb3caa0a387d31112d4e7d8415d14563</citedby><cites>FETCH-LOGICAL-c496t-33bf8b6af47bc559683fed9b87a05e1a2bb3caa0a387d31112d4e7d8415d14563</cites><orcidid>0000-0002-0429-7409 ; 0000-0003-2405-4874</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7488389/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2444112463?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25730,27900,27901,36988,44565,53765,53767</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32917158$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Chien-Sheng</creatorcontrib><creatorcontrib>Li, Ching-Chia</creatorcontrib><creatorcontrib>Juan, Yung-Shun</creatorcontrib><creatorcontrib>Wu, Wen-Jeng</creatorcontrib><creatorcontrib>Lee, Hsiang-Ying</creatorcontrib><title>5α-reductase inhibitors impact prognosis of urothelial carcinoma</title><title>BMC cancer</title><addtitle>BMC Cancer</addtitle><description>5α-reductase inhibitors (5-ARIs) inhibit the pathway of converting the testosterone to dihydrotestosterone and are widely used in benign prostatic hyperplasia patients. Since androgen receptor activation may play a role in urothelial tumorigenesis, we conducted this retrospective cohort study to determine whether 5α-reductase inhibitors (5-ARIs) administration is associated with bladder cancer mortality, bladder cancer recurrence and upper tract urothelial carcinoma mortality, using the Taiwan National Health Insurance database.
The data of this retrospective cohort study were sourced from the Longitudinal Health Insurance Database of Taiwan, compiled by the Taiwan National Health Insurance database from 1996 to 2010. It consists of 18,530 men with bladder cancer, of whom 474 were 5-ARIs recipients and 4384 men with upper tract urothelial carcinoma, of whom 109 were 5-ARIs recipients. Propensity Score Matching on the age and geographic data was done at the ratio of 1:10. We analyzed the odds ratios (OR) and 95% confidence interval (CI) of the risk of bladder cancer death, bladder cancer recurrence rate and upper tract urothelial carcinoma related death by the 5-ARIs administration.
Those who received 5-ARIs showed a lower risk of bladder cancer related death compared to nonusers in multivariable adjusted analysis (OR 0.835, 95% CI 0.71-0.98). However, there was no significant difference in the bladder cancer recurrence rate (OR 0.956, 95% CI 0.82-1.11) and upper tract urothelial carcinoma related mortality in multivariable adjusted analysis (OR 0.814, 95% CI 0.6-1.1).
Patients who receive 5-ARIs have lower bladder cancer related mortality compared to those who don't. 5-ARIs may prove to be a viable strategy to improve bladder cancer outcomes.</description><subject>5-alpha Reductase Inhibitors - administration & dosage</subject><subject>5-alpha Reductase Inhibitors - adverse effects</subject><subject>5α-reductase inhibitors (5-ARIs)</subject><subject>Age</subject><subject>Aged</subject><subject>Androgen receptor (AR)</subject><subject>Androgen receptors</subject><subject>Androgens</subject><subject>Bladder cancer</subject><subject>Cancer therapies</subject><subject>Carcinoma - drug therapy</subject><subject>Carcinoma - genetics</subject><subject>Carcinoma - mortality</subject><subject>Carcinoma - pathology</subject><subject>Carcinoma, Transitional Cell - drug therapy</subject><subject>Carcinoma, Transitional Cell - genetics</subject><subject>Carcinoma, Transitional Cell - mortality</subject><subject>Carcinoma, Transitional Cell - pathology</subject><subject>Cholestenone 5 alpha-Reductase - genetics</subject><subject>Codes</subject><subject>Death</subject><subject>Diabetes</subject><subject>Dihydrotestosterone</subject><subject>Drug dosages</subject><subject>Dutasteride</subject><subject>Dutasteride - administration & dosage</subject><subject>Finasteride</subject><subject>Finasteride - administration & dosage</subject><subject>Health insurance</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Hyperplasia</subject><subject>Hypertension</subject><subject>Kidney diseases</subject><subject>Male</subject><subject>Medical diagnosis</subject><subject>Medical prognosis</subject><subject>Middle Aged</subject><subject>Mortality</subject><subject>Neoplasm Recurrence, Local - drug therapy</subject><subject>Neoplasm Recurrence, Local - genetics</subject><subject>Neoplasm Recurrence, Local - mortality</subject><subject>Neoplasm Recurrence, Local - pathology</subject><subject>Population</subject><subject>Prognosis</subject><subject>Prostate cancer</subject><subject>Prostatic Hyperplasia - drug therapy</subject><subject>Prostatic Hyperplasia - genetics</subject><subject>Prostatic Hyperplasia - mortality</subject><subject>Prostatic Hyperplasia - pathology</subject><subject>Receptor mechanisms</subject><subject>Receptors, Androgen - genetics</subject><subject>Steroid 5α-reductase</subject><subject>Taiwan - epidemiology</subject><subject>Testosterone</subject><subject>Tumorigenesis</subject><subject>Upper tract urothelial carcinoma</subject><subject>Urothelial carcinoma</subject><subject>Urothelium - drug effects</subject><subject>Urothelium - pathology</subject><issn>1471-2407</issn><issn>1471-2407</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpVkc1O3DAQx62Kqny0L9BDFYlzqMeexM6lEkItICFxoWdr_JFdr7Lx1k6QeCxepM_UwFIEJ4_smd_8rR9jX4GfAej2ewGhdVNzwWuupJI1fmBHgApqgVwdvKkP2XEpG85Baa4_sUMpOlDQ6CN23vx9rHPws5uohCqO62jjlHKp4nZHbqp2Oa3GVGKpUl_NOU3rMEQaKkfZxTFt6TP72NNQwpeX84T9_vXz7uKqvrm9vL44v6kddu1US2l7bVvqUVnXNF2rZR98Z7Ui3gQgYa10RJykVl4CgPAYlNcIjQdsWnnCrvdcn2hjdjluKT-YRNE8X6S8MpSn6IZgJJchIHkRALHzlqzrrRKKE7edlriwfuxZu9lug3dhnDIN76DvX8a4Nqt0bxRqLXW3AE5fADn9mUOZzCbNeVz-bwQiLumxlUuX2He5nErJoX_dANw8KTR7hWZRaJ4Vmqds395mex3570z-A5w4mOI</recordid><startdate>20200911</startdate><enddate>20200911</enddate><creator>Wang, Chien-Sheng</creator><creator>Li, Ching-Chia</creator><creator>Juan, Yung-Shun</creator><creator>Wu, Wen-Jeng</creator><creator>Lee, Hsiang-Ying</creator><general>BioMed Central</general><general>BMC</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PIMPY</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-0429-7409</orcidid><orcidid>https://orcid.org/0000-0003-2405-4874</orcidid></search><sort><creationdate>20200911</creationdate><title>5α-reductase inhibitors impact prognosis of urothelial carcinoma</title><author>Wang, Chien-Sheng ; Li, Ching-Chia ; Juan, Yung-Shun ; Wu, Wen-Jeng ; Lee, Hsiang-Ying</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c496t-33bf8b6af47bc559683fed9b87a05e1a2bb3caa0a387d31112d4e7d8415d14563</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>5-alpha Reductase Inhibitors - administration & dosage</topic><topic>5-alpha Reductase Inhibitors - adverse effects</topic><topic>5α-reductase inhibitors (5-ARIs)</topic><topic>Age</topic><topic>Aged</topic><topic>Androgen receptor (AR)</topic><topic>Androgen receptors</topic><topic>Androgens</topic><topic>Bladder cancer</topic><topic>Cancer therapies</topic><topic>Carcinoma - drug therapy</topic><topic>Carcinoma - genetics</topic><topic>Carcinoma - mortality</topic><topic>Carcinoma - pathology</topic><topic>Carcinoma, Transitional Cell - drug therapy</topic><topic>Carcinoma, Transitional Cell - genetics</topic><topic>Carcinoma, Transitional Cell - mortality</topic><topic>Carcinoma, Transitional Cell - pathology</topic><topic>Cholestenone 5 alpha-Reductase - genetics</topic><topic>Codes</topic><topic>Death</topic><topic>Diabetes</topic><topic>Dihydrotestosterone</topic><topic>Drug dosages</topic><topic>Dutasteride</topic><topic>Dutasteride - administration & dosage</topic><topic>Finasteride</topic><topic>Finasteride - administration & dosage</topic><topic>Health insurance</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Hyperplasia</topic><topic>Hypertension</topic><topic>Kidney diseases</topic><topic>Male</topic><topic>Medical diagnosis</topic><topic>Medical prognosis</topic><topic>Middle Aged</topic><topic>Mortality</topic><topic>Neoplasm Recurrence, Local - drug therapy</topic><topic>Neoplasm Recurrence, Local - genetics</topic><topic>Neoplasm Recurrence, Local - mortality</topic><topic>Neoplasm Recurrence, Local - pathology</topic><topic>Population</topic><topic>Prognosis</topic><topic>Prostate cancer</topic><topic>Prostatic Hyperplasia - drug therapy</topic><topic>Prostatic Hyperplasia - genetics</topic><topic>Prostatic Hyperplasia - mortality</topic><topic>Prostatic Hyperplasia - pathology</topic><topic>Receptor mechanisms</topic><topic>Receptors, Androgen - genetics</topic><topic>Steroid 5α-reductase</topic><topic>Taiwan - epidemiology</topic><topic>Testosterone</topic><topic>Tumorigenesis</topic><topic>Upper tract urothelial carcinoma</topic><topic>Urothelial carcinoma</topic><topic>Urothelium - drug effects</topic><topic>Urothelium - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Chien-Sheng</creatorcontrib><creatorcontrib>Li, Ching-Chia</creatorcontrib><creatorcontrib>Juan, Yung-Shun</creatorcontrib><creatorcontrib>Wu, Wen-Jeng</creatorcontrib><creatorcontrib>Lee, Hsiang-Ying</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>ProQuest - Publicly Available Content Database</collection><collection>ProQuest Health & Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health & Nursing</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>BMC cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Chien-Sheng</au><au>Li, Ching-Chia</au><au>Juan, Yung-Shun</au><au>Wu, Wen-Jeng</au><au>Lee, Hsiang-Ying</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>5α-reductase inhibitors impact prognosis of urothelial carcinoma</atitle><jtitle>BMC cancer</jtitle><addtitle>BMC Cancer</addtitle><date>2020-09-11</date><risdate>2020</risdate><volume>20</volume><issue>1</issue><spage>872</spage><epage>7</epage><pages>872-7</pages><artnum>872</artnum><issn>1471-2407</issn><eissn>1471-2407</eissn><abstract>5α-reductase inhibitors (5-ARIs) inhibit the pathway of converting the testosterone to dihydrotestosterone and are widely used in benign prostatic hyperplasia patients. Since androgen receptor activation may play a role in urothelial tumorigenesis, we conducted this retrospective cohort study to determine whether 5α-reductase inhibitors (5-ARIs) administration is associated with bladder cancer mortality, bladder cancer recurrence and upper tract urothelial carcinoma mortality, using the Taiwan National Health Insurance database.
The data of this retrospective cohort study were sourced from the Longitudinal Health Insurance Database of Taiwan, compiled by the Taiwan National Health Insurance database from 1996 to 2010. It consists of 18,530 men with bladder cancer, of whom 474 were 5-ARIs recipients and 4384 men with upper tract urothelial carcinoma, of whom 109 were 5-ARIs recipients. Propensity Score Matching on the age and geographic data was done at the ratio of 1:10. We analyzed the odds ratios (OR) and 95% confidence interval (CI) of the risk of bladder cancer death, bladder cancer recurrence rate and upper tract urothelial carcinoma related death by the 5-ARIs administration.
Those who received 5-ARIs showed a lower risk of bladder cancer related death compared to nonusers in multivariable adjusted analysis (OR 0.835, 95% CI 0.71-0.98). However, there was no significant difference in the bladder cancer recurrence rate (OR 0.956, 95% CI 0.82-1.11) and upper tract urothelial carcinoma related mortality in multivariable adjusted analysis (OR 0.814, 95% CI 0.6-1.1).
Patients who receive 5-ARIs have lower bladder cancer related mortality compared to those who don't. 5-ARIs may prove to be a viable strategy to improve bladder cancer outcomes.</abstract><cop>England</cop><pub>BioMed Central</pub><pmid>32917158</pmid><doi>10.1186/s12885-020-07373-4</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-0429-7409</orcidid><orcidid>https://orcid.org/0000-0003-2405-4874</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 5-alpha Reductase Inhibitors - administration & dosage 5-alpha Reductase Inhibitors - adverse effects 5α-reductase inhibitors (5-ARIs) Age Aged Androgen receptor (AR) Androgen receptors Androgens Bladder cancer Cancer therapies Carcinoma - drug therapy Carcinoma - genetics Carcinoma - mortality Carcinoma - pathology Carcinoma, Transitional Cell - drug therapy Carcinoma, Transitional Cell - genetics Carcinoma, Transitional Cell - mortality Carcinoma, Transitional Cell - pathology Cholestenone 5 alpha-Reductase - genetics Codes Death Diabetes Dihydrotestosterone Drug dosages Dutasteride Dutasteride - administration & dosage Finasteride Finasteride - administration & dosage Health insurance Hospitals Humans Hyperplasia Hypertension Kidney diseases Male Medical diagnosis Medical prognosis Middle Aged Mortality Neoplasm Recurrence, Local - drug therapy Neoplasm Recurrence, Local - genetics Neoplasm Recurrence, Local - mortality Neoplasm Recurrence, Local - pathology Population Prognosis Prostate cancer Prostatic Hyperplasia - drug therapy Prostatic Hyperplasia - genetics Prostatic Hyperplasia - mortality Prostatic Hyperplasia - pathology Receptor mechanisms Receptors, Androgen - genetics Steroid 5α-reductase Taiwan - epidemiology Testosterone Tumorigenesis Upper tract urothelial carcinoma Urothelial carcinoma Urothelium - drug effects Urothelium - pathology |
title | 5α-reductase inhibitors impact prognosis of urothelial carcinoma |
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