Low endogenous testosterone levels are associated with the extend of lymphnodal invasion at radical prostatectomy and extended pelvic lymph node dissection
Objective To investigate clinical factors associated to lymphnodal metastasis load in patients who underwent to radical prostatectomy (RP) and extended pelvic lymph node dissection (ePLND). Materials and methods Between November 2014 and December 2019, ET was measured in 617 consecutive patients not...
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creator | Porcaro, Antonio Benito Cerrato, Clara Tafuri, Alessandro Bianchi, Alberto Gallina, Sebastian Orlando, Rossella Amigoni, Nelia Rizzetto, Riccardo Gozzo, Alessandra Migliorini, Filippo Zecchini Antoniolli, Stefano Monaco, Carmelo Brunelli, Matteo Cerruto, Maria Angela Antonelli, Alessandro |
description | Objective
To investigate clinical factors associated to lymphnodal metastasis load in patients who underwent to radical prostatectomy (RP) and extended pelvic lymph node dissection (ePLND).
Materials and methods
Between November 2014 and December 2019, ET was measured in 617 consecutive patients not under androgen deprivation therapy who underwent RP and ePLND. Lymphnode invasion (LNI) was codified as not present (
N
= 0) or with one (
N
= 1) or more than one metastatic node (
N
> 1). The risk of multiple pelvic lymph node metastasis (
N
> 1, mPLNM) was assessed by comparing it to the other two groups (
N
> 1 vs.
N
= 0 and
N
> 1 vs.
N
= 1). Then, we assessed the association between ET and lymphnode invasion for standard predictors, such as PSA, percentage of biopsy positive cores (BPC), tumor stage greater than 1 (cT > 1) and tumor grade group greater than two (ISUP > 2).
Results
Overall, LNI was detected in 70 patients (11.3%) of whom 39 (6.3%) with
N
= 1 and 31 (5%) with
N
> 1. On multivariate analysis, ET was inversely associated with the risk of
N
> 1 when compared to both
N
= 0 (odds ratio, OR 0.997; CI 0.994–1;
p
= 0.027) as well as with
N
= 1 cases (OR 0.994; 95% CI 0.989–1.000;
p
= 0.015).
Conclusions
In clinical PCa, the risk of mPLNM was increased by low ET levels. As ET decreased, patients had an increased likelihood of mPLNM. Because of the inverse association between ET and mPLNM, higher ET levels were protective against aggressive disease. The influence of locally advanced PCa with high metastatic load on ET levels needs to be explored by controlled trials. |
doi_str_mv | 10.1007/s11255-021-02938-z |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8463355</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2548907373</sourcerecordid><originalsourceid>FETCH-LOGICAL-c474t-83127c6b6794e19c09e2b9911ef3b1a555d0f13c15705cbdf7090c485b9404ec3</originalsourceid><addsrcrecordid>eNp9kUtv1DAUhSMEokPhD7BAltiwCfiZxBskVPGSRmIDa8txbmZcJXawPdNO_wp_lgsp5bFgYVnyPeezfU5VPWX0JaO0fZUZ40rVlDNcWnT1zb1qw1Qraq46eb_aUEFZzRouzqpHOV9SSnVH6cPqTEjOO97QTfVtG68IhCHuIMRDJgVyiblAigHIBEeYMrEJiM05Om8LDOTKlz0peyBwXdBJ4kim07zsQxzsRHw42uxjILaQZAfv8GxJiESvK3E-EYue1YqwBaajdyuAIAHI4HNGJSIeVw9GO2V4crufV1_evf188aHefnr_8eLNtnaylaXuBOOta_qm1RKYdlQD77VmDEbRM6uUGujIhMNkqHL9MLZUUyc71WtJJThxXr1eucuhn2FwEEqyk1mSn206mWi9-XsS_N7s4tF0shFCKQS8uAWk-PWACZrZZwfTZANgqIYr2Wnailag9Pk_0st4SAG_h6q2YZJpzlDFV5XD5HKC8e4xjJof3Zu1e4Pdm5_dmxs0PfvzG3eWX2WjQKyCjKOwg_T77v9gvwPFcL80</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2576141921</pqid></control><display><type>article</type><title>Low endogenous testosterone levels are associated with the extend of lymphnodal invasion at radical prostatectomy and extended pelvic lymph node dissection</title><source>MEDLINE</source><source>SpringerLink Journals - AutoHoldings</source><creator>Porcaro, Antonio Benito ; Cerrato, Clara ; Tafuri, Alessandro ; Bianchi, Alberto ; Gallina, Sebastian ; Orlando, Rossella ; Amigoni, Nelia ; Rizzetto, Riccardo ; Gozzo, Alessandra ; Migliorini, Filippo ; Zecchini Antoniolli, Stefano ; Monaco, Carmelo ; Brunelli, Matteo ; Cerruto, Maria Angela ; Antonelli, Alessandro</creator><creatorcontrib>Porcaro, Antonio Benito ; Cerrato, Clara ; Tafuri, Alessandro ; Bianchi, Alberto ; Gallina, Sebastian ; Orlando, Rossella ; Amigoni, Nelia ; Rizzetto, Riccardo ; Gozzo, Alessandra ; Migliorini, Filippo ; Zecchini Antoniolli, Stefano ; Monaco, Carmelo ; Brunelli, Matteo ; Cerruto, Maria Angela ; Antonelli, Alessandro</creatorcontrib><description>Objective
To investigate clinical factors associated to lymphnodal metastasis load in patients who underwent to radical prostatectomy (RP) and extended pelvic lymph node dissection (ePLND).
Materials and methods
Between November 2014 and December 2019, ET was measured in 617 consecutive patients not under androgen deprivation therapy who underwent RP and ePLND. Lymphnode invasion (LNI) was codified as not present (
N
= 0) or with one (
N
= 1) or more than one metastatic node (
N
> 1). The risk of multiple pelvic lymph node metastasis (
N
> 1, mPLNM) was assessed by comparing it to the other two groups (
N
> 1 vs.
N
= 0 and
N
> 1 vs.
N
= 1). Then, we assessed the association between ET and lymphnode invasion for standard predictors, such as PSA, percentage of biopsy positive cores (BPC), tumor stage greater than 1 (cT > 1) and tumor grade group greater than two (ISUP > 2).
Results
Overall, LNI was detected in 70 patients (11.3%) of whom 39 (6.3%) with
N
= 1 and 31 (5%) with
N
> 1. On multivariate analysis, ET was inversely associated with the risk of
N
> 1 when compared to both
N
= 0 (odds ratio, OR 0.997; CI 0.994–1;
p
= 0.027) as well as with
N
= 1 cases (OR 0.994; 95% CI 0.989–1.000;
p
= 0.015).
Conclusions
In clinical PCa, the risk of mPLNM was increased by low ET levels. As ET decreased, patients had an increased likelihood of mPLNM. Because of the inverse association between ET and mPLNM, higher ET levels were protective against aggressive disease. The influence of locally advanced PCa with high metastatic load on ET levels needs to be explored by controlled trials.</description><identifier>ISSN: 0301-1623</identifier><identifier>EISSN: 1573-2584</identifier><identifier>DOI: 10.1007/s11255-021-02938-z</identifier><identifier>PMID: 34228260</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Aged ; Biopsy ; Cancer surgery ; Clinical trials ; Humans ; Lymph Node Excision - methods ; Lymph nodes ; Lymphatic Metastasis ; Lymphatic system ; Male ; Medicine ; Medicine & Public Health ; Metastases ; Metastasis ; Middle Aged ; Multivariate analysis ; Nephrology ; Patients ; Pelvis ; Prostate cancer ; Prostatectomy ; Prostatectomy - methods ; Prostatic Neoplasms - blood ; Prostatic Neoplasms - pathology ; Prostatic Neoplasms - surgery ; Retrospective Studies ; Testosterone ; Testosterone - blood ; Urological surgery ; Urology ; Urology - Original Paper</subject><ispartof>International urology and nephrology, 2021-10, Vol.53 (10), p.2027-2039</ispartof><rights>The Author(s) 2021</rights><rights>2021. The Author(s).</rights><rights>The Author(s) 2021. This work is published 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><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-83127c6b6794e19c09e2b9911ef3b1a555d0f13c15705cbdf7090c485b9404ec3</citedby><cites>FETCH-LOGICAL-c474t-83127c6b6794e19c09e2b9911ef3b1a555d0f13c15705cbdf7090c485b9404ec3</cites><orcidid>0000-0002-7890-040X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11255-021-02938-z$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11255-021-02938-z$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34228260$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Porcaro, Antonio Benito</creatorcontrib><creatorcontrib>Cerrato, Clara</creatorcontrib><creatorcontrib>Tafuri, Alessandro</creatorcontrib><creatorcontrib>Bianchi, Alberto</creatorcontrib><creatorcontrib>Gallina, Sebastian</creatorcontrib><creatorcontrib>Orlando, Rossella</creatorcontrib><creatorcontrib>Amigoni, Nelia</creatorcontrib><creatorcontrib>Rizzetto, Riccardo</creatorcontrib><creatorcontrib>Gozzo, Alessandra</creatorcontrib><creatorcontrib>Migliorini, Filippo</creatorcontrib><creatorcontrib>Zecchini Antoniolli, Stefano</creatorcontrib><creatorcontrib>Monaco, Carmelo</creatorcontrib><creatorcontrib>Brunelli, Matteo</creatorcontrib><creatorcontrib>Cerruto, Maria Angela</creatorcontrib><creatorcontrib>Antonelli, Alessandro</creatorcontrib><title>Low endogenous testosterone levels are associated with the extend of lymphnodal invasion at radical prostatectomy and extended pelvic lymph node dissection</title><title>International urology and nephrology</title><addtitle>Int Urol Nephrol</addtitle><addtitle>Int Urol Nephrol</addtitle><description>Objective
To investigate clinical factors associated to lymphnodal metastasis load in patients who underwent to radical prostatectomy (RP) and extended pelvic lymph node dissection (ePLND).
Materials and methods
Between November 2014 and December 2019, ET was measured in 617 consecutive patients not under androgen deprivation therapy who underwent RP and ePLND. Lymphnode invasion (LNI) was codified as not present (
N
= 0) or with one (
N
= 1) or more than one metastatic node (
N
> 1). The risk of multiple pelvic lymph node metastasis (
N
> 1, mPLNM) was assessed by comparing it to the other two groups (
N
> 1 vs.
N
= 0 and
N
> 1 vs.
N
= 1). Then, we assessed the association between ET and lymphnode invasion for standard predictors, such as PSA, percentage of biopsy positive cores (BPC), tumor stage greater than 1 (cT > 1) and tumor grade group greater than two (ISUP > 2).
Results
Overall, LNI was detected in 70 patients (11.3%) of whom 39 (6.3%) with
N
= 1 and 31 (5%) with
N
> 1. On multivariate analysis, ET was inversely associated with the risk of
N
> 1 when compared to both
N
= 0 (odds ratio, OR 0.997; CI 0.994–1;
p
= 0.027) as well as with
N
= 1 cases (OR 0.994; 95% CI 0.989–1.000;
p
= 0.015).
Conclusions
In clinical PCa, the risk of mPLNM was increased by low ET levels. As ET decreased, patients had an increased likelihood of mPLNM. Because of the inverse association between ET and mPLNM, higher ET levels were protective against aggressive disease. The influence of locally advanced PCa with high metastatic load on ET levels needs to be explored by controlled trials.</description><subject>Aged</subject><subject>Biopsy</subject><subject>Cancer surgery</subject><subject>Clinical trials</subject><subject>Humans</subject><subject>Lymph Node Excision - methods</subject><subject>Lymph nodes</subject><subject>Lymphatic Metastasis</subject><subject>Lymphatic system</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Middle Aged</subject><subject>Multivariate analysis</subject><subject>Nephrology</subject><subject>Patients</subject><subject>Pelvis</subject><subject>Prostate cancer</subject><subject>Prostatectomy</subject><subject>Prostatectomy - methods</subject><subject>Prostatic Neoplasms - blood</subject><subject>Prostatic Neoplasms - pathology</subject><subject>Prostatic Neoplasms - surgery</subject><subject>Retrospective Studies</subject><subject>Testosterone</subject><subject>Testosterone - blood</subject><subject>Urological surgery</subject><subject>Urology</subject><subject>Urology - Original Paper</subject><issn>0301-1623</issn><issn>1573-2584</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kUtv1DAUhSMEokPhD7BAltiwCfiZxBskVPGSRmIDa8txbmZcJXawPdNO_wp_lgsp5bFgYVnyPeezfU5VPWX0JaO0fZUZ40rVlDNcWnT1zb1qw1Qraq46eb_aUEFZzRouzqpHOV9SSnVH6cPqTEjOO97QTfVtG68IhCHuIMRDJgVyiblAigHIBEeYMrEJiM05Om8LDOTKlz0peyBwXdBJ4kim07zsQxzsRHw42uxjILaQZAfv8GxJiESvK3E-EYue1YqwBaajdyuAIAHI4HNGJSIeVw9GO2V4crufV1_evf188aHefnr_8eLNtnaylaXuBOOta_qm1RKYdlQD77VmDEbRM6uUGujIhMNkqHL9MLZUUyc71WtJJThxXr1eucuhn2FwEEqyk1mSn206mWi9-XsS_N7s4tF0shFCKQS8uAWk-PWACZrZZwfTZANgqIYr2Wnailag9Pk_0st4SAG_h6q2YZJpzlDFV5XD5HKC8e4xjJof3Zu1e4Pdm5_dmxs0PfvzG3eWX2WjQKyCjKOwg_T77v9gvwPFcL80</recordid><startdate>20211001</startdate><enddate>20211001</enddate><creator>Porcaro, Antonio Benito</creator><creator>Cerrato, Clara</creator><creator>Tafuri, Alessandro</creator><creator>Bianchi, Alberto</creator><creator>Gallina, Sebastian</creator><creator>Orlando, Rossella</creator><creator>Amigoni, Nelia</creator><creator>Rizzetto, Riccardo</creator><creator>Gozzo, Alessandra</creator><creator>Migliorini, Filippo</creator><creator>Zecchini Antoniolli, Stefano</creator><creator>Monaco, Carmelo</creator><creator>Brunelli, Matteo</creator><creator>Cerruto, Maria Angela</creator><creator>Antonelli, Alessandro</creator><general>Springer Netherlands</general><general>Springer Nature B.V</general><scope>C6C</scope><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>7QP</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-7890-040X</orcidid></search><sort><creationdate>20211001</creationdate><title>Low endogenous testosterone levels are associated with the extend of lymphnodal invasion at radical prostatectomy and extended pelvic lymph node dissection</title><author>Porcaro, Antonio Benito ; Cerrato, Clara ; Tafuri, Alessandro ; Bianchi, Alberto ; Gallina, Sebastian ; Orlando, Rossella ; Amigoni, Nelia ; Rizzetto, Riccardo ; Gozzo, Alessandra ; Migliorini, Filippo ; Zecchini Antoniolli, Stefano ; Monaco, Carmelo ; Brunelli, Matteo ; Cerruto, Maria Angela ; Antonelli, Alessandro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-83127c6b6794e19c09e2b9911ef3b1a555d0f13c15705cbdf7090c485b9404ec3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Aged</topic><topic>Biopsy</topic><topic>Cancer surgery</topic><topic>Clinical trials</topic><topic>Humans</topic><topic>Lymph Node Excision - methods</topic><topic>Lymph nodes</topic><topic>Lymphatic Metastasis</topic><topic>Lymphatic system</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Middle Aged</topic><topic>Multivariate analysis</topic><topic>Nephrology</topic><topic>Patients</topic><topic>Pelvis</topic><topic>Prostate cancer</topic><topic>Prostatectomy</topic><topic>Prostatectomy - methods</topic><topic>Prostatic Neoplasms - blood</topic><topic>Prostatic Neoplasms - pathology</topic><topic>Prostatic Neoplasms - surgery</topic><topic>Retrospective Studies</topic><topic>Testosterone</topic><topic>Testosterone - blood</topic><topic>Urological surgery</topic><topic>Urology</topic><topic>Urology - Original Paper</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Porcaro, Antonio Benito</creatorcontrib><creatorcontrib>Cerrato, Clara</creatorcontrib><creatorcontrib>Tafuri, Alessandro</creatorcontrib><creatorcontrib>Bianchi, Alberto</creatorcontrib><creatorcontrib>Gallina, Sebastian</creatorcontrib><creatorcontrib>Orlando, Rossella</creatorcontrib><creatorcontrib>Amigoni, Nelia</creatorcontrib><creatorcontrib>Rizzetto, Riccardo</creatorcontrib><creatorcontrib>Gozzo, Alessandra</creatorcontrib><creatorcontrib>Migliorini, Filippo</creatorcontrib><creatorcontrib>Zecchini Antoniolli, Stefano</creatorcontrib><creatorcontrib>Monaco, Carmelo</creatorcontrib><creatorcontrib>Brunelli, Matteo</creatorcontrib><creatorcontrib>Cerruto, Maria Angela</creatorcontrib><creatorcontrib>Antonelli, Alessandro</creatorcontrib><collection>Springer Nature OA Free Journals</collection><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>Calcium & Calcified Tissue Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International urology and nephrology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Porcaro, Antonio Benito</au><au>Cerrato, Clara</au><au>Tafuri, Alessandro</au><au>Bianchi, Alberto</au><au>Gallina, Sebastian</au><au>Orlando, Rossella</au><au>Amigoni, Nelia</au><au>Rizzetto, Riccardo</au><au>Gozzo, Alessandra</au><au>Migliorini, Filippo</au><au>Zecchini Antoniolli, Stefano</au><au>Monaco, Carmelo</au><au>Brunelli, Matteo</au><au>Cerruto, Maria Angela</au><au>Antonelli, Alessandro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Low endogenous testosterone levels are associated with the extend of lymphnodal invasion at radical prostatectomy and extended pelvic lymph node dissection</atitle><jtitle>International urology and nephrology</jtitle><stitle>Int Urol Nephrol</stitle><addtitle>Int Urol Nephrol</addtitle><date>2021-10-01</date><risdate>2021</risdate><volume>53</volume><issue>10</issue><spage>2027</spage><epage>2039</epage><pages>2027-2039</pages><issn>0301-1623</issn><eissn>1573-2584</eissn><abstract>Objective
To investigate clinical factors associated to lymphnodal metastasis load in patients who underwent to radical prostatectomy (RP) and extended pelvic lymph node dissection (ePLND).
Materials and methods
Between November 2014 and December 2019, ET was measured in 617 consecutive patients not under androgen deprivation therapy who underwent RP and ePLND. Lymphnode invasion (LNI) was codified as not present (
N
= 0) or with one (
N
= 1) or more than one metastatic node (
N
> 1). The risk of multiple pelvic lymph node metastasis (
N
> 1, mPLNM) was assessed by comparing it to the other two groups (
N
> 1 vs.
N
= 0 and
N
> 1 vs.
N
= 1). Then, we assessed the association between ET and lymphnode invasion for standard predictors, such as PSA, percentage of biopsy positive cores (BPC), tumor stage greater than 1 (cT > 1) and tumor grade group greater than two (ISUP > 2).
Results
Overall, LNI was detected in 70 patients (11.3%) of whom 39 (6.3%) with
N
= 1 and 31 (5%) with
N
> 1. On multivariate analysis, ET was inversely associated with the risk of
N
> 1 when compared to both
N
= 0 (odds ratio, OR 0.997; CI 0.994–1;
p
= 0.027) as well as with
N
= 1 cases (OR 0.994; 95% CI 0.989–1.000;
p
= 0.015).
Conclusions
In clinical PCa, the risk of mPLNM was increased by low ET levels. As ET decreased, patients had an increased likelihood of mPLNM. Because of the inverse association between ET and mPLNM, higher ET levels were protective against aggressive disease. The influence of locally advanced PCa with high metastatic load on ET levels needs to be explored by controlled trials.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>34228260</pmid><doi>10.1007/s11255-021-02938-z</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-7890-040X</orcidid><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; SpringerLink Journals - AutoHoldings |
subjects | Aged Biopsy Cancer surgery Clinical trials Humans Lymph Node Excision - methods Lymph nodes Lymphatic Metastasis Lymphatic system Male Medicine Medicine & Public Health Metastases Metastasis Middle Aged Multivariate analysis Nephrology Patients Pelvis Prostate cancer Prostatectomy Prostatectomy - methods Prostatic Neoplasms - blood Prostatic Neoplasms - pathology Prostatic Neoplasms - surgery Retrospective Studies Testosterone Testosterone - blood Urological surgery Urology Urology - Original Paper |
title | Low endogenous testosterone levels are associated with the extend of lymphnodal invasion at radical prostatectomy and extended pelvic lymph node dissection |
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