The significance of circulating tumor cells in prostate cancer patients undergoing adjuvant or salvage radiation therapy
Background: Following radical prostatectomy, success of adjuvant and salvage radiation therapy (RT) is dependent on the absence of micrometastatic disease. However, reliable prognostic/predictive factors for determining this are lacking. Therefore, novel biomarkers are needed to assist with clinical...
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creator | Lowes, L E Lock, M Rodrigues, G D’Souza, D Bauman, G Ahmad, B Venkatesan, V Allan, A L Sexton, T |
description | Background:
Following radical prostatectomy, success of adjuvant and salvage radiation therapy (RT) is dependent on the absence of micrometastatic disease. However, reliable prognostic/predictive factors for determining this are lacking. Therefore, novel biomarkers are needed to assist with clinical decision-making in this setting. Enumeration of circulating tumor cells (CTCs) using the regulatory-approved CellSearch System (CSS) is prognostic in metastatic prostate cancer. We hypothesize that CTCs may also be prognostic in the post-prostatectomy setting.
Methods:
Patient blood samples (
n
=55) were processed on the CSS to enumerate CTCs at 0, 6, 12 and 24 months after completion of RT. CTC values were correlated with predictive/prognostic factors and progression-free survival.
Results:
CTC status (presence/absence) correlated significantly with positive margins (increased likelihood of CTC
neg
disease;
P
=0.032), and trended toward significance with the presence of seminal vesicle invasion (CTC
pos
;
P
=0.113) and extracapsular extension (CTC
neg
;
P
=0.116). Although there was a trend toward a decreased time to biochemical failure (BCF) in baseline CTC-positive patients (
n
=9), this trend was not significant (hazard ratio (HR)=0.3505;
P
=0.166). However, CTC-positive status at any point (
n
=16) predicted for time to BCF (HR=0.2868;
P
=0.0437).
Conclusions:
One caveat of this study is the small sample size utilized (
n
=55) and the low number of patients with CTC-positive disease (
n
=16). However, our results suggest that CTCs may be indicative of disseminated disease and assessment of CTCs during RT may be helpful in clinical decision-making to determine, which patients may benefit from RT versus those who may benefit more from systemic treatments. |
doi_str_mv | 10.1038/pcan.2015.36 |
format | Article |
fullrecord | <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4788488</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A435191167</galeid><sourcerecordid>A435191167</sourcerecordid><originalsourceid>FETCH-LOGICAL-c618t-785d279aa84aa51eb771334249f791f1ebfbb816d31530e88481c4640fe72ae13</originalsourceid><addsrcrecordid>eNptkk1v1DAQhiMEoqVw44wsISEO7GLHju1cKlUVX1IlLuVszTqTxKusHexkRf89DlvKLqp8sDV-5vXM6ymK14yuGeX642jBr0vKqjWXT4pzJpRcVZLqp_nMZbVSuirPihcpbSmlNavp8-KslCXXJefnxa_bHklynXety0IWSWiJddHOA0zOd2SadyESi8OQiPNkjCFNMCH5A0cyZgr9lMjsG4xdWFKg2c578BPJiQmGPXRIIjQuo8GTqccI493L4lkLQ8JX9_tF8ePzp9vrr6ub71--XV_drKxkelqqb0pVA2gBUDHcKMU4F6WoW1WzNgfazUYz2XBWcYpaC82skIK2qEpAxi-Ky4PuOG922NhcbITBjNHtIN6ZAM6c3njXmy7sjVCLmM4C7-8FYvg5Y5rMzqXFD_AY5mSY4iWnSlQ8o2__Q7dhjj63lykpc-FU6H9UBwMa59uQ37WLqLkSvGI1Y1Jlav0IlVeDO2eDx9bl-EnCu6OEHmGY-hSGeTE9nYIfDqDNf5kitg9mMGqWkTLLSJllpAyXGX9zbOAD_HeGMrA6AClf-Q7jUdePCf4Gl5nWtQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1766133048</pqid></control><display><type>article</type><title>The significance of circulating tumor cells in prostate cancer patients undergoing adjuvant or salvage radiation therapy</title><source>MEDLINE</source><source>Springer Nature - Complete Springer Journals</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>Lowes, L E ; Lock, M ; Rodrigues, G ; D’Souza, D ; Bauman, G ; Ahmad, B ; Venkatesan, V ; Allan, A L ; Sexton, T</creator><creatorcontrib>Lowes, L E ; Lock, M ; Rodrigues, G ; D’Souza, D ; Bauman, G ; Ahmad, B ; Venkatesan, V ; Allan, A L ; Sexton, T</creatorcontrib><description>Background:
Following radical prostatectomy, success of adjuvant and salvage radiation therapy (RT) is dependent on the absence of micrometastatic disease. However, reliable prognostic/predictive factors for determining this are lacking. Therefore, novel biomarkers are needed to assist with clinical decision-making in this setting. Enumeration of circulating tumor cells (CTCs) using the regulatory-approved CellSearch System (CSS) is prognostic in metastatic prostate cancer. We hypothesize that CTCs may also be prognostic in the post-prostatectomy setting.
Methods:
Patient blood samples (
n
=55) were processed on the CSS to enumerate CTCs at 0, 6, 12 and 24 months after completion of RT. CTC values were correlated with predictive/prognostic factors and progression-free survival.
Results:
CTC status (presence/absence) correlated significantly with positive margins (increased likelihood of CTC
neg
disease;
P
=0.032), and trended toward significance with the presence of seminal vesicle invasion (CTC
pos
;
P
=0.113) and extracapsular extension (CTC
neg
;
P
=0.116). Although there was a trend toward a decreased time to biochemical failure (BCF) in baseline CTC-positive patients (
n
=9), this trend was not significant (hazard ratio (HR)=0.3505;
P
=0.166). However, CTC-positive status at any point (
n
=16) predicted for time to BCF (HR=0.2868;
P
=0.0437).
Conclusions:
One caveat of this study is the small sample size utilized (
n
=55) and the low number of patients with CTC-positive disease (
n
=16). However, our results suggest that CTCs may be indicative of disseminated disease and assessment of CTCs during RT may be helpful in clinical decision-making to determine, which patients may benefit from RT versus those who may benefit more from systemic treatments.</description><identifier>ISSN: 1365-7852</identifier><identifier>EISSN: 1476-5608</identifier><identifier>DOI: 10.1038/pcan.2015.36</identifier><identifier>PMID: 26238233</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>14/1 ; 14/63 ; 631/67/1059 ; 631/67/589/466 ; 692/308/575 ; 692/53/2422 ; 82/80 ; Biomarkers, Tumor ; Biomedical and Life Sciences ; Biomedicine ; Cancer Research ; Care and treatment ; Cell Count ; Complications and side effects ; Follow-Up Studies ; Health aspects ; Humans ; Male ; Metastasis ; Neoplasm Grading ; Neoplasm Staging ; Neoplastic Cells, Circulating - pathology ; Original ; original-article ; Prostate cancer ; Prostate-Specific Antigen - blood ; Prostatic Neoplasms - mortality ; Prostatic Neoplasms - pathology ; Prostatic Neoplasms - radiotherapy ; Radiotherapy ; Radiotherapy, Adjuvant ; Risk factors ; Salvage Therapy ; Survival Analysis ; Treatment Outcome</subject><ispartof>Prostate cancer and prostatic diseases, 2015-12, Vol.18 (4), p.358-364</ispartof><rights>The Author(s) 2015</rights><rights>COPYRIGHT 2015 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Dec 2015</rights><rights>Copyright © 2015 Macmillan Publishers Limited 2015 Macmillan Publishers Limited</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c618t-785d279aa84aa51eb771334249f791f1ebfbb816d31530e88481c4640fe72ae13</citedby><cites>FETCH-LOGICAL-c618t-785d279aa84aa51eb771334249f791f1ebfbb816d31530e88481c4640fe72ae13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/pcan.2015.36$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/pcan.2015.36$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26238233$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lowes, L E</creatorcontrib><creatorcontrib>Lock, M</creatorcontrib><creatorcontrib>Rodrigues, G</creatorcontrib><creatorcontrib>D’Souza, D</creatorcontrib><creatorcontrib>Bauman, G</creatorcontrib><creatorcontrib>Ahmad, B</creatorcontrib><creatorcontrib>Venkatesan, V</creatorcontrib><creatorcontrib>Allan, A L</creatorcontrib><creatorcontrib>Sexton, T</creatorcontrib><title>The significance of circulating tumor cells in prostate cancer patients undergoing adjuvant or salvage radiation therapy</title><title>Prostate cancer and prostatic diseases</title><addtitle>Prostate Cancer Prostatic Dis</addtitle><addtitle>Prostate Cancer Prostatic Dis</addtitle><description>Background:
Following radical prostatectomy, success of adjuvant and salvage radiation therapy (RT) is dependent on the absence of micrometastatic disease. However, reliable prognostic/predictive factors for determining this are lacking. Therefore, novel biomarkers are needed to assist with clinical decision-making in this setting. Enumeration of circulating tumor cells (CTCs) using the regulatory-approved CellSearch System (CSS) is prognostic in metastatic prostate cancer. We hypothesize that CTCs may also be prognostic in the post-prostatectomy setting.
Methods:
Patient blood samples (
n
=55) were processed on the CSS to enumerate CTCs at 0, 6, 12 and 24 months after completion of RT. CTC values were correlated with predictive/prognostic factors and progression-free survival.
Results:
CTC status (presence/absence) correlated significantly with positive margins (increased likelihood of CTC
neg
disease;
P
=0.032), and trended toward significance with the presence of seminal vesicle invasion (CTC
pos
;
P
=0.113) and extracapsular extension (CTC
neg
;
P
=0.116). Although there was a trend toward a decreased time to biochemical failure (BCF) in baseline CTC-positive patients (
n
=9), this trend was not significant (hazard ratio (HR)=0.3505;
P
=0.166). However, CTC-positive status at any point (
n
=16) predicted for time to BCF (HR=0.2868;
P
=0.0437).
Conclusions:
One caveat of this study is the small sample size utilized (
n
=55) and the low number of patients with CTC-positive disease (
n
=16). However, our results suggest that CTCs may be indicative of disseminated disease and assessment of CTCs during RT may be helpful in clinical decision-making to determine, which patients may benefit from RT versus those who may benefit more from systemic treatments.</description><subject>14/1</subject><subject>14/63</subject><subject>631/67/1059</subject><subject>631/67/589/466</subject><subject>692/308/575</subject><subject>692/53/2422</subject><subject>82/80</subject><subject>Biomarkers, Tumor</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cancer Research</subject><subject>Care and treatment</subject><subject>Cell Count</subject><subject>Complications and side effects</subject><subject>Follow-Up Studies</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Male</subject><subject>Metastasis</subject><subject>Neoplasm Grading</subject><subject>Neoplasm Staging</subject><subject>Neoplastic Cells, Circulating - pathology</subject><subject>Original</subject><subject>original-article</subject><subject>Prostate cancer</subject><subject>Prostate-Specific Antigen - blood</subject><subject>Prostatic Neoplasms - mortality</subject><subject>Prostatic Neoplasms - pathology</subject><subject>Prostatic Neoplasms - radiotherapy</subject><subject>Radiotherapy</subject><subject>Radiotherapy, Adjuvant</subject><subject>Risk factors</subject><subject>Salvage Therapy</subject><subject>Survival Analysis</subject><subject>Treatment Outcome</subject><issn>1365-7852</issn><issn>1476-5608</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNptkk1v1DAQhiMEoqVw44wsISEO7GLHju1cKlUVX1IlLuVszTqTxKusHexkRf89DlvKLqp8sDV-5vXM6ymK14yuGeX642jBr0vKqjWXT4pzJpRcVZLqp_nMZbVSuirPihcpbSmlNavp8-KslCXXJefnxa_bHklynXety0IWSWiJddHOA0zOd2SadyESi8OQiPNkjCFNMCH5A0cyZgr9lMjsG4xdWFKg2c578BPJiQmGPXRIIjQuo8GTqccI493L4lkLQ8JX9_tF8ePzp9vrr6ub71--XV_drKxkelqqb0pVA2gBUDHcKMU4F6WoW1WzNgfazUYz2XBWcYpaC82skIK2qEpAxi-Ky4PuOG922NhcbITBjNHtIN6ZAM6c3njXmy7sjVCLmM4C7-8FYvg5Y5rMzqXFD_AY5mSY4iWnSlQ8o2__Q7dhjj63lykpc-FU6H9UBwMa59uQ37WLqLkSvGI1Y1Jlav0IlVeDO2eDx9bl-EnCu6OEHmGY-hSGeTE9nYIfDqDNf5kitg9mMGqWkTLLSJllpAyXGX9zbOAD_HeGMrA6AClf-Q7jUdePCf4Gl5nWtQ</recordid><startdate>20151201</startdate><enddate>20151201</enddate><creator>Lowes, L E</creator><creator>Lock, M</creator><creator>Rodrigues, G</creator><creator>D’Souza, D</creator><creator>Bauman, G</creator><creator>Ahmad, B</creator><creator>Venkatesan, V</creator><creator>Allan, A L</creator><creator>Sexton, T</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</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>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>M7Z</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20151201</creationdate><title>The significance of circulating tumor cells in prostate cancer patients undergoing adjuvant or salvage radiation therapy</title><author>Lowes, L E ; Lock, M ; Rodrigues, G ; D’Souza, D ; Bauman, G ; Ahmad, B ; Venkatesan, V ; Allan, A L ; Sexton, T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c618t-785d279aa84aa51eb771334249f791f1ebfbb816d31530e88481c4640fe72ae13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>14/1</topic><topic>14/63</topic><topic>631/67/1059</topic><topic>631/67/589/466</topic><topic>692/308/575</topic><topic>692/53/2422</topic><topic>82/80</topic><topic>Biomarkers, Tumor</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cancer Research</topic><topic>Care and treatment</topic><topic>Cell Count</topic><topic>Complications and side effects</topic><topic>Follow-Up Studies</topic><topic>Health aspects</topic><topic>Humans</topic><topic>Male</topic><topic>Metastasis</topic><topic>Neoplasm Grading</topic><topic>Neoplasm Staging</topic><topic>Neoplastic Cells, Circulating - pathology</topic><topic>Original</topic><topic>original-article</topic><topic>Prostate cancer</topic><topic>Prostate-Specific Antigen - blood</topic><topic>Prostatic Neoplasms - mortality</topic><topic>Prostatic Neoplasms - pathology</topic><topic>Prostatic Neoplasms - radiotherapy</topic><topic>Radiotherapy</topic><topic>Radiotherapy, Adjuvant</topic><topic>Risk factors</topic><topic>Salvage Therapy</topic><topic>Survival Analysis</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lowes, L E</creatorcontrib><creatorcontrib>Lock, M</creatorcontrib><creatorcontrib>Rodrigues, G</creatorcontrib><creatorcontrib>D’Souza, D</creatorcontrib><creatorcontrib>Bauman, G</creatorcontrib><creatorcontrib>Ahmad, B</creatorcontrib><creatorcontrib>Venkatesan, V</creatorcontrib><creatorcontrib>Allan, A L</creatorcontrib><creatorcontrib>Sexton, T</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>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>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science 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 Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Prostate cancer and prostatic diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lowes, L E</au><au>Lock, M</au><au>Rodrigues, G</au><au>D’Souza, D</au><au>Bauman, G</au><au>Ahmad, B</au><au>Venkatesan, V</au><au>Allan, A L</au><au>Sexton, T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The significance of circulating tumor cells in prostate cancer patients undergoing adjuvant or salvage radiation therapy</atitle><jtitle>Prostate cancer and prostatic diseases</jtitle><stitle>Prostate Cancer Prostatic Dis</stitle><addtitle>Prostate Cancer Prostatic Dis</addtitle><date>2015-12-01</date><risdate>2015</risdate><volume>18</volume><issue>4</issue><spage>358</spage><epage>364</epage><pages>358-364</pages><issn>1365-7852</issn><eissn>1476-5608</eissn><abstract>Background:
Following radical prostatectomy, success of adjuvant and salvage radiation therapy (RT) is dependent on the absence of micrometastatic disease. However, reliable prognostic/predictive factors for determining this are lacking. Therefore, novel biomarkers are needed to assist with clinical decision-making in this setting. Enumeration of circulating tumor cells (CTCs) using the regulatory-approved CellSearch System (CSS) is prognostic in metastatic prostate cancer. We hypothesize that CTCs may also be prognostic in the post-prostatectomy setting.
Methods:
Patient blood samples (
n
=55) were processed on the CSS to enumerate CTCs at 0, 6, 12 and 24 months after completion of RT. CTC values were correlated with predictive/prognostic factors and progression-free survival.
Results:
CTC status (presence/absence) correlated significantly with positive margins (increased likelihood of CTC
neg
disease;
P
=0.032), and trended toward significance with the presence of seminal vesicle invasion (CTC
pos
;
P
=0.113) and extracapsular extension (CTC
neg
;
P
=0.116). Although there was a trend toward a decreased time to biochemical failure (BCF) in baseline CTC-positive patients (
n
=9), this trend was not significant (hazard ratio (HR)=0.3505;
P
=0.166). However, CTC-positive status at any point (
n
=16) predicted for time to BCF (HR=0.2868;
P
=0.0437).
Conclusions:
One caveat of this study is the small sample size utilized (
n
=55) and the low number of patients with CTC-positive disease (
n
=16). However, our results suggest that CTCs may be indicative of disseminated disease and assessment of CTCs during RT may be helpful in clinical decision-making to determine, which patients may benefit from RT versus those who may benefit more from systemic treatments.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>26238233</pmid><doi>10.1038/pcan.2015.36</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Springer Nature - Complete Springer Journals; EZB-FREE-00999 freely available EZB journals |
subjects | 14/1 14/63 631/67/1059 631/67/589/466 692/308/575 692/53/2422 82/80 Biomarkers, Tumor Biomedical and Life Sciences Biomedicine Cancer Research Care and treatment Cell Count Complications and side effects Follow-Up Studies Health aspects Humans Male Metastasis Neoplasm Grading Neoplasm Staging Neoplastic Cells, Circulating - pathology Original original-article Prostate cancer Prostate-Specific Antigen - blood Prostatic Neoplasms - mortality Prostatic Neoplasms - pathology Prostatic Neoplasms - radiotherapy Radiotherapy Radiotherapy, Adjuvant Risk factors Salvage Therapy Survival Analysis Treatment Outcome |
title | The significance of circulating tumor cells in prostate cancer patients undergoing adjuvant or salvage radiation therapy |
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