Active Surveillance for Low-risk Prostate Cancer in African American Men: A Multi-institutional Experience

Objective To compare the outcomes of active surveillance (AS) series between African American men (AAM) and non-AAM diagnosed with low-risk prostate cancer at 3 medical centers. Methods Between 2005 and 2012, 214 men accepted AS on the basis of favorable clinical features and parameters after initia...

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Veröffentlicht in:Urology (Ridgewood, N.J.) N.J.), 2014-02, Vol.83 (2), p.364-368
Hauptverfasser: Odom, Brian D, Mir, M.C, Hughes, Scott, Senechal, Cedric, Santy, Alexis, Eyraud, Remi, Stephenson, Andrew J, Ylitalo, Kelly, Miocinovic, Ranko
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container_end_page 368
container_issue 2
container_start_page 364
container_title Urology (Ridgewood, N.J.)
container_volume 83
creator Odom, Brian D
Mir, M.C
Hughes, Scott
Senechal, Cedric
Santy, Alexis
Eyraud, Remi
Stephenson, Andrew J
Ylitalo, Kelly
Miocinovic, Ranko
description Objective To compare the outcomes of active surveillance (AS) series between African American men (AAM) and non-AAM diagnosed with low-risk prostate cancer at 3 medical centers. Methods Between 2005 and 2012, 214 men accepted AS on the basis of favorable clinical features and parameters after initial and repeat biopsy. Failure was defined as increase in Gleason score >6, total positive cores >33%, maximum cancer volume in any core >50%, or a prostate-specific antigen >10 ng/mL. Disease progression and overall AS failure were compared between the 2 groups. Results Of 214 men, 75 were excluded, leaving 67 AAM and 72 non-AAM on AS. Median age at diagnosis was 64 and 67 years for AAM and non-AAM, respectively, and median follow-up was 34 and 46 months, respectively. During this time, 44 AAM (66%) remained on AS, and 23 (34%) underwent treatment, of whom 6 (26%) were treated by patient choice and 17 (74%) because of disease progression. In the non-AAM group, 59 (82%) men remained on AS, and 13 (18%) underwent treatment, 8 (62%) were treated by patient choice and 5 (38%) because of disease progression. The 3-year freedom from overall treatment was 74% and did not differ by race ( P  = .06). The 3-year freedom from disease progression was 85%, where AAM were at significantly higher risk of disease progression (hazard ratio = 3.8; 95% confidence interval: 1.4-10.4; P  = .01). Conclusion Our study suggests a higher disease progression rate in AAM who choose AS for low-risk prostate cancer compared with non-AAM, signifying a potential need for closer follow-up and more stringent enrollment criteria in AAM.
doi_str_mv 10.1016/j.urology.2013.09.038
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Methods Between 2005 and 2012, 214 men accepted AS on the basis of favorable clinical features and parameters after initial and repeat biopsy. Failure was defined as increase in Gleason score &gt;6, total positive cores &gt;33%, maximum cancer volume in any core &gt;50%, or a prostate-specific antigen &gt;10 ng/mL. Disease progression and overall AS failure were compared between the 2 groups. Results Of 214 men, 75 were excluded, leaving 67 AAM and 72 non-AAM on AS. Median age at diagnosis was 64 and 67 years for AAM and non-AAM, respectively, and median follow-up was 34 and 46 months, respectively. During this time, 44 AAM (66%) remained on AS, and 23 (34%) underwent treatment, of whom 6 (26%) were treated by patient choice and 17 (74%) because of disease progression. In the non-AAM group, 59 (82%) men remained on AS, and 13 (18%) underwent treatment, 8 (62%) were treated by patient choice and 5 (38%) because of disease progression. The 3-year freedom from overall treatment was 74% and did not differ by race ( P  = .06). The 3-year freedom from disease progression was 85%, where AAM were at significantly higher risk of disease progression (hazard ratio = 3.8; 95% confidence interval: 1.4-10.4; P  = .01). Conclusion Our study suggests a higher disease progression rate in AAM who choose AS for low-risk prostate cancer compared with non-AAM, signifying a potential need for closer follow-up and more stringent enrollment criteria in AAM.</description><identifier>ISSN: 0090-4295</identifier><identifier>EISSN: 1527-9995</identifier><identifier>DOI: 10.1016/j.urology.2013.09.038</identifier><identifier>PMID: 24286600</identifier><identifier>CODEN: URGYAZ</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>African Americans ; Aged ; Biological and medical sciences ; Disease Progression ; Gynecology. Andrology. Obstetrics ; Humans ; Male ; Male genital diseases ; Medical sciences ; Middle Aged ; Nephrology. Urinary tract diseases ; Prostatic Neoplasms - therapy ; Retrospective Studies ; Risk Assessment ; Tumors ; Tumors of the urinary system ; Urinary tract. Prostate gland ; Urology ; Watchful Waiting</subject><ispartof>Urology (Ridgewood, N.J.), 2014-02, Vol.83 (2), p.364-368</ispartof><rights>Elsevier Inc.</rights><rights>2014 Elsevier Inc.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2014 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c450t-99f8bf1b7691ed97dbca5f248afd8785d87866ec8a2e0a9927037b9713ddf5083</citedby><cites>FETCH-LOGICAL-c450t-99f8bf1b7691ed97dbca5f248afd8785d87866ec8a2e0a9927037b9713ddf5083</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.urology.2013.09.038$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,782,786,3554,27933,27934,46004</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=28302303$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24286600$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Odom, Brian D</creatorcontrib><creatorcontrib>Mir, M.C</creatorcontrib><creatorcontrib>Hughes, Scott</creatorcontrib><creatorcontrib>Senechal, Cedric</creatorcontrib><creatorcontrib>Santy, Alexis</creatorcontrib><creatorcontrib>Eyraud, Remi</creatorcontrib><creatorcontrib>Stephenson, Andrew J</creatorcontrib><creatorcontrib>Ylitalo, Kelly</creatorcontrib><creatorcontrib>Miocinovic, Ranko</creatorcontrib><title>Active Surveillance for Low-risk Prostate Cancer in African American Men: A Multi-institutional Experience</title><title>Urology (Ridgewood, N.J.)</title><addtitle>Urology</addtitle><description>Objective To compare the outcomes of active surveillance (AS) series between African American men (AAM) and non-AAM diagnosed with low-risk prostate cancer at 3 medical centers. Methods Between 2005 and 2012, 214 men accepted AS on the basis of favorable clinical features and parameters after initial and repeat biopsy. Failure was defined as increase in Gleason score &gt;6, total positive cores &gt;33%, maximum cancer volume in any core &gt;50%, or a prostate-specific antigen &gt;10 ng/mL. Disease progression and overall AS failure were compared between the 2 groups. Results Of 214 men, 75 were excluded, leaving 67 AAM and 72 non-AAM on AS. Median age at diagnosis was 64 and 67 years for AAM and non-AAM, respectively, and median follow-up was 34 and 46 months, respectively. During this time, 44 AAM (66%) remained on AS, and 23 (34%) underwent treatment, of whom 6 (26%) were treated by patient choice and 17 (74%) because of disease progression. In the non-AAM group, 59 (82%) men remained on AS, and 13 (18%) underwent treatment, 8 (62%) were treated by patient choice and 5 (38%) because of disease progression. The 3-year freedom from overall treatment was 74% and did not differ by race ( P  = .06). The 3-year freedom from disease progression was 85%, where AAM were at significantly higher risk of disease progression (hazard ratio = 3.8; 95% confidence interval: 1.4-10.4; P  = .01). Conclusion Our study suggests a higher disease progression rate in AAM who choose AS for low-risk prostate cancer compared with non-AAM, signifying a potential need for closer follow-up and more stringent enrollment criteria in AAM.</description><subject>African Americans</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Disease Progression</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Male</subject><subject>Male genital diseases</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Prostatic Neoplasms - therapy</subject><subject>Retrospective Studies</subject><subject>Risk Assessment</subject><subject>Tumors</subject><subject>Tumors of the urinary system</subject><subject>Urinary tract. Prostate gland</subject><subject>Urology</subject><subject>Watchful Waiting</subject><issn>0090-4295</issn><issn>1527-9995</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFks-O0zAQxi0EYrsLjwDKBYlLwtjOP3MAVdUuIHUF0sLZcpwxcpvGxXYKfRuehSfDoQUkLlw8lvz7xjPfDCFPKBQUaP1iU0zeDe7zsWBAeQGiAN7eIwtasSYXQlT3yQJAQF4yUV2QyxA2AFDXdfOQXLCStXUNsCDbpY72gNnd5A9oh0GNGjPjfLZ2X3Nvwzb74F2IKmK2mt98ZsdsabzVKsUdni63OL7Mlj--305DtLkdQ7RxitaNasiuv-0ThUn7iDwwagj4-ByvyKeb64-rt_n6_Zt3q-U612UFMRVv2s7QrqkFxV40fadVZVjZKtO3TVvNR12jbhVDUEKwBnjTiYbyvjcVtPyKPD_l3Xv3ZcIQ5c4GjXNz6KYgaZk0NIFNQqsTqlOXwaORe293yh8lBTn7LDfy7LOcfZYgZPI56Z6ev5i6HfZ_VL-NTcCzM6CCVoPxyTwb_nItB8aBJ-71icNkyMGil0H_Mqu3HnWUvbP_LeXVPxn0YMc0lmGLRwwbN_k0htS1DEyCvJuXYt4JylOSlJf_BLsktMU</recordid><startdate>20140201</startdate><enddate>20140201</enddate><creator>Odom, Brian D</creator><creator>Mir, M.C</creator><creator>Hughes, Scott</creator><creator>Senechal, Cedric</creator><creator>Santy, Alexis</creator><creator>Eyraud, Remi</creator><creator>Stephenson, Andrew J</creator><creator>Ylitalo, Kelly</creator><creator>Miocinovic, Ranko</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</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>7X8</scope></search><sort><creationdate>20140201</creationdate><title>Active Surveillance for Low-risk Prostate Cancer in African American Men: A Multi-institutional Experience</title><author>Odom, Brian D ; Mir, M.C ; Hughes, Scott ; Senechal, Cedric ; Santy, Alexis ; Eyraud, Remi ; Stephenson, Andrew J ; Ylitalo, Kelly ; Miocinovic, Ranko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c450t-99f8bf1b7691ed97dbca5f248afd8785d87866ec8a2e0a9927037b9713ddf5083</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>African Americans</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Disease Progression</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>Male</topic><topic>Male genital diseases</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Nephrology. Urinary tract diseases</topic><topic>Prostatic Neoplasms - therapy</topic><topic>Retrospective Studies</topic><topic>Risk Assessment</topic><topic>Tumors</topic><topic>Tumors of the urinary system</topic><topic>Urinary tract. Prostate gland</topic><topic>Urology</topic><topic>Watchful Waiting</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Odom, Brian D</creatorcontrib><creatorcontrib>Mir, M.C</creatorcontrib><creatorcontrib>Hughes, Scott</creatorcontrib><creatorcontrib>Senechal, Cedric</creatorcontrib><creatorcontrib>Santy, Alexis</creatorcontrib><creatorcontrib>Eyraud, Remi</creatorcontrib><creatorcontrib>Stephenson, Andrew J</creatorcontrib><creatorcontrib>Ylitalo, Kelly</creatorcontrib><creatorcontrib>Miocinovic, Ranko</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Urology (Ridgewood, N.J.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Odom, Brian D</au><au>Mir, M.C</au><au>Hughes, Scott</au><au>Senechal, Cedric</au><au>Santy, Alexis</au><au>Eyraud, Remi</au><au>Stephenson, Andrew J</au><au>Ylitalo, Kelly</au><au>Miocinovic, Ranko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Active Surveillance for Low-risk Prostate Cancer in African American Men: A Multi-institutional Experience</atitle><jtitle>Urology (Ridgewood, N.J.)</jtitle><addtitle>Urology</addtitle><date>2014-02-01</date><risdate>2014</risdate><volume>83</volume><issue>2</issue><spage>364</spage><epage>368</epage><pages>364-368</pages><issn>0090-4295</issn><eissn>1527-9995</eissn><coden>URGYAZ</coden><abstract>Objective To compare the outcomes of active surveillance (AS) series between African American men (AAM) and non-AAM diagnosed with low-risk prostate cancer at 3 medical centers. Methods Between 2005 and 2012, 214 men accepted AS on the basis of favorable clinical features and parameters after initial and repeat biopsy. Failure was defined as increase in Gleason score &gt;6, total positive cores &gt;33%, maximum cancer volume in any core &gt;50%, or a prostate-specific antigen &gt;10 ng/mL. Disease progression and overall AS failure were compared between the 2 groups. Results Of 214 men, 75 were excluded, leaving 67 AAM and 72 non-AAM on AS. Median age at diagnosis was 64 and 67 years for AAM and non-AAM, respectively, and median follow-up was 34 and 46 months, respectively. During this time, 44 AAM (66%) remained on AS, and 23 (34%) underwent treatment, of whom 6 (26%) were treated by patient choice and 17 (74%) because of disease progression. In the non-AAM group, 59 (82%) men remained on AS, and 13 (18%) underwent treatment, 8 (62%) were treated by patient choice and 5 (38%) because of disease progression. The 3-year freedom from overall treatment was 74% and did not differ by race ( P  = .06). The 3-year freedom from disease progression was 85%, where AAM were at significantly higher risk of disease progression (hazard ratio = 3.8; 95% confidence interval: 1.4-10.4; P  = .01). Conclusion Our study suggests a higher disease progression rate in AAM who choose AS for low-risk prostate cancer compared with non-AAM, signifying a potential need for closer follow-up and more stringent enrollment criteria in AAM.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>24286600</pmid><doi>10.1016/j.urology.2013.09.038</doi><tpages>5</tpages></addata></record>
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subjects African Americans
Aged
Biological and medical sciences
Disease Progression
Gynecology. Andrology. Obstetrics
Humans
Male
Male genital diseases
Medical sciences
Middle Aged
Nephrology. Urinary tract diseases
Prostatic Neoplasms - therapy
Retrospective Studies
Risk Assessment
Tumors
Tumors of the urinary system
Urinary tract. Prostate gland
Urology
Watchful Waiting
title Active Surveillance for Low-risk Prostate Cancer in African American Men: A Multi-institutional Experience
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