Impact of adjuvant androgen deprivation therapy after radical prostatectomy on the survival of patients with pathological T3b prostate cancer
Study Type – Therapy (case series) Level of Evidence 4 What’s known on the subject? and What does the study add? Adjuvant hormonal therapy is known to improve cancer specific survival in prostate cancer patients with lymph node positive disease. This study suggests that surgically treated prostate c...
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creator | Siddiqui, Sameer A. Boorjian, Stephen A. Blute, Michael L. Rangel, Laureano J. Bergstralh, Eric J. Karnes, Robert Jeffrey Frank, Igor |
description | Study Type – Therapy (case series)
Level of Evidence 4
What’s known on the subject? and What does the study add?
Adjuvant hormonal therapy is known to improve cancer specific survival in prostate cancer patients with lymph node positive disease.
This study suggests that surgically treated prostate cancer patients with seminal vesical invasion (pT3b) may have improved cancer specific survival if treated with adjuvant androgen deprivation therapy, similar to lymph node positive patients.
OBJECTIVE
To determine the impact of adjuvant androgen deprivation therapy (ADT) on survival in patients with seminal vesicle invasion (pT3b) at radical prostatectomy.
PATIENTS AND METHODS
We reviewed 12 115 patients who underwent radical prostatectomy between 1987 and 2002 to identify patients with pT3bN0 prostate cancer who received adjuvant ADT (n= 191). These patients were matched by clinical and pathological variables to a group of patients with pT3b prostate cancer who did not receive adjuvant ADT. Median postoperative follow‐up was 10 years. Clinical endpoints included biochemical progression‐free survival (BPFS), local recurrence‐free survival (LRFS), systemic progression‐free survival (SPFS), cancer‐specific survival (CSS) and overall survival.
RESULTS
Patients who underwent adjuvant ADT experienced improved 10‐year BPFS (60% vs 16%, P < 0.001), LRFS (87% vs 76%, P= 0.002), SPFS (91% vs 78%, P= 0.004) and CSS (94% vs 87%, P= 0.037). Overall survival was not significantly different between groups (75% vs 69%, P= 0.12). Both luteinizing hormone‐releasing hormone agonists (hazard ratio, 0.26; 95% CI, 0.15–0.46; P < 0.001) and bilateral orchiectomy (hazard ratio, 0.13; 95% CI, 0.06–0.31; P < 0.001) improved BPFS. When stratified by type of ADT (hormonal therapy vs orchiectomy), there was no difference in survival outcomes.
CONCLUSIONS
Adjuvant ADT improves local, and systemic control after radical prostatectomy for pT3b prostate cancer. There is no difference in survival between patients receiving medical hormonal therapy vs patients undergoing orchiectomy. Given the lack of improvement in overall survival, continued investigation is needed to identify the cohort of pT3b patients at highest risk for cancer progression and therefore most likely to benefit from a multimodal treatment approach. |
doi_str_mv | 10.1111/j.1464-410X.2010.09565.x |
format | Article |
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Level of Evidence 4
What’s known on the subject? and What does the study add?
Adjuvant hormonal therapy is known to improve cancer specific survival in prostate cancer patients with lymph node positive disease.
This study suggests that surgically treated prostate cancer patients with seminal vesical invasion (pT3b) may have improved cancer specific survival if treated with adjuvant androgen deprivation therapy, similar to lymph node positive patients.
OBJECTIVE
To determine the impact of adjuvant androgen deprivation therapy (ADT) on survival in patients with seminal vesicle invasion (pT3b) at radical prostatectomy.
PATIENTS AND METHODS
We reviewed 12 115 patients who underwent radical prostatectomy between 1987 and 2002 to identify patients with pT3bN0 prostate cancer who received adjuvant ADT (n= 191). These patients were matched by clinical and pathological variables to a group of patients with pT3b prostate cancer who did not receive adjuvant ADT. Median postoperative follow‐up was 10 years. Clinical endpoints included biochemical progression‐free survival (BPFS), local recurrence‐free survival (LRFS), systemic progression‐free survival (SPFS), cancer‐specific survival (CSS) and overall survival.
RESULTS
Patients who underwent adjuvant ADT experienced improved 10‐year BPFS (60% vs 16%, P < 0.001), LRFS (87% vs 76%, P= 0.002), SPFS (91% vs 78%, P= 0.004) and CSS (94% vs 87%, P= 0.037). Overall survival was not significantly different between groups (75% vs 69%, P= 0.12). Both luteinizing hormone‐releasing hormone agonists (hazard ratio, 0.26; 95% CI, 0.15–0.46; P < 0.001) and bilateral orchiectomy (hazard ratio, 0.13; 95% CI, 0.06–0.31; P < 0.001) improved BPFS. When stratified by type of ADT (hormonal therapy vs orchiectomy), there was no difference in survival outcomes.
CONCLUSIONS
Adjuvant ADT improves local, and systemic control after radical prostatectomy for pT3b prostate cancer. There is no difference in survival between patients receiving medical hormonal therapy vs patients undergoing orchiectomy. Given the lack of improvement in overall survival, continued investigation is needed to identify the cohort of pT3b patients at highest risk for cancer progression and therefore most likely to benefit from a multimodal treatment approach.</description><identifier>ISSN: 1464-4096</identifier><identifier>EISSN: 1464-410X</identifier><identifier>DOI: 10.1111/j.1464-410X.2010.09565.x</identifier><identifier>PMID: 21265985</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Aged ; Androgen Antagonists - therapeutic use ; androgen deprivation therapy ; Androgens - metabolism ; Antineoplastic agents ; Antineoplastic Agents, Hormonal - therapeutic use ; Biological and medical sciences ; Chemotherapy, Adjuvant ; Combined treatments (chemotherapy of immunotherapy associated with an other treatment) ; Epidemiologic Methods ; Gonadotropin-Releasing Hormone - agonists ; hormones ; Humans ; Male ; Medical sciences ; Middle Aged ; Neoplasm Invasiveness ; Neoplasm Recurrence, Local - prevention & control ; Nephrology. Urinary tract diseases ; Orchiectomy ; Pharmacology. Drug treatments ; Prostate - pathology ; prostate cancer ; Prostatectomy ; Prostatic Neoplasms - drug therapy ; Prostatic Neoplasms - mortality ; Prostatic Neoplasms - pathology ; Prostatic Neoplasms - surgery ; radical prostatectomy ; Seminal Vesicles - pathology ; survival ; Tumors of the urinary system ; Urinary tract. Prostate gland</subject><ispartof>BJU international, 2011-02, Vol.107 (3), p.383-388</ispartof><rights>2010 THE AUTHORS. JOURNAL COMPILATION © 2010 BJU INTERNATIONAL</rights><rights>2015 INIST-CNRS</rights><rights>2010 THE AUTHORS. JOURNAL COMPILATION © 2010 BJU INTERNATIONAL.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3985-bc411b8c2e69ab8b7c5461af59e9f45ec3862a715562acb2ff2739e5be63805c3</citedby><cites>FETCH-LOGICAL-c3985-bc411b8c2e69ab8b7c5461af59e9f45ec3862a715562acb2ff2739e5be63805c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1464-410X.2010.09565.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1464-410X.2010.09565.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23779124$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21265985$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Siddiqui, Sameer A.</creatorcontrib><creatorcontrib>Boorjian, Stephen A.</creatorcontrib><creatorcontrib>Blute, Michael L.</creatorcontrib><creatorcontrib>Rangel, Laureano J.</creatorcontrib><creatorcontrib>Bergstralh, Eric J.</creatorcontrib><creatorcontrib>Karnes, Robert Jeffrey</creatorcontrib><creatorcontrib>Frank, Igor</creatorcontrib><title>Impact of adjuvant androgen deprivation therapy after radical prostatectomy on the survival of patients with pathological T3b prostate cancer</title><title>BJU international</title><addtitle>BJU Int</addtitle><description>Study Type – Therapy (case series)
Level of Evidence 4
What’s known on the subject? and What does the study add?
Adjuvant hormonal therapy is known to improve cancer specific survival in prostate cancer patients with lymph node positive disease.
This study suggests that surgically treated prostate cancer patients with seminal vesical invasion (pT3b) may have improved cancer specific survival if treated with adjuvant androgen deprivation therapy, similar to lymph node positive patients.
OBJECTIVE
To determine the impact of adjuvant androgen deprivation therapy (ADT) on survival in patients with seminal vesicle invasion (pT3b) at radical prostatectomy.
PATIENTS AND METHODS
We reviewed 12 115 patients who underwent radical prostatectomy between 1987 and 2002 to identify patients with pT3bN0 prostate cancer who received adjuvant ADT (n= 191). These patients were matched by clinical and pathological variables to a group of patients with pT3b prostate cancer who did not receive adjuvant ADT. Median postoperative follow‐up was 10 years. Clinical endpoints included biochemical progression‐free survival (BPFS), local recurrence‐free survival (LRFS), systemic progression‐free survival (SPFS), cancer‐specific survival (CSS) and overall survival.
RESULTS
Patients who underwent adjuvant ADT experienced improved 10‐year BPFS (60% vs 16%, P < 0.001), LRFS (87% vs 76%, P= 0.002), SPFS (91% vs 78%, P= 0.004) and CSS (94% vs 87%, P= 0.037). Overall survival was not significantly different between groups (75% vs 69%, P= 0.12). Both luteinizing hormone‐releasing hormone agonists (hazard ratio, 0.26; 95% CI, 0.15–0.46; P < 0.001) and bilateral orchiectomy (hazard ratio, 0.13; 95% CI, 0.06–0.31; P < 0.001) improved BPFS. When stratified by type of ADT (hormonal therapy vs orchiectomy), there was no difference in survival outcomes.
CONCLUSIONS
Adjuvant ADT improves local, and systemic control after radical prostatectomy for pT3b prostate cancer. There is no difference in survival between patients receiving medical hormonal therapy vs patients undergoing orchiectomy. Given the lack of improvement in overall survival, continued investigation is needed to identify the cohort of pT3b patients at highest risk for cancer progression and therefore most likely to benefit from a multimodal treatment approach.</description><subject>Aged</subject><subject>Androgen Antagonists - therapeutic use</subject><subject>androgen deprivation therapy</subject><subject>Androgens - metabolism</subject><subject>Antineoplastic agents</subject><subject>Antineoplastic Agents, Hormonal - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Chemotherapy, Adjuvant</subject><subject>Combined treatments (chemotherapy of immunotherapy associated with an other treatment)</subject><subject>Epidemiologic Methods</subject><subject>Gonadotropin-Releasing Hormone - agonists</subject><subject>hormones</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neoplasm Invasiveness</subject><subject>Neoplasm Recurrence, Local - prevention & control</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Orchiectomy</subject><subject>Pharmacology. Drug treatments</subject><subject>Prostate - pathology</subject><subject>prostate cancer</subject><subject>Prostatectomy</subject><subject>Prostatic Neoplasms - drug therapy</subject><subject>Prostatic Neoplasms - mortality</subject><subject>Prostatic Neoplasms - pathology</subject><subject>Prostatic Neoplasms - surgery</subject><subject>radical prostatectomy</subject><subject>Seminal Vesicles - pathology</subject><subject>survival</subject><subject>Tumors of the urinary system</subject><subject>Urinary tract. Prostate gland</subject><issn>1464-4096</issn><issn>1464-410X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc9OGzEQxq2qqNC0r1D5UvWU1N5de9eHHtoIWhASlyBxs2a9Y7LR_qvtDeQheGe8JIQrvow9_n0zo28IoZwteDw_NwueyWyecXa3SFjMMiWkWDx-IGfHj4-vd6bkKfns_YaxmJDiEzlNeCKFKsQZebpsBzCB9pZCtRm30AUKXeX6e-xohYOrtxDqvqNhjQ6GHQUb0FEHVW2goYPrfYCAJvTtju4x6ke3jbJmKjpENXbB04c6rKfXum_6-xftKi2PemqgM-i-kBMLjcevhzgjtxfnq-W_-fXN38vl7-u5SePU89JknJeFSVAqKIsyNyKTHKxQqGwm0KSFTCDnQsRgysTaJE8VihJlWjBh0hn5sa8b-_8f0Qfd1t5g00CH_eh1keVC5SIXkSz2pImTeodWR0tacDvNmZ52oTd6sllPlutpF_plF_oxSr8dmoxli9VR-Gp-BL4fAPDREOuiB7V_49I8VzzJIvdrzz3UDe7ePYD-c3U73dJnkI-o4g</recordid><startdate>201102</startdate><enddate>201102</enddate><creator>Siddiqui, Sameer A.</creator><creator>Boorjian, Stephen A.</creator><creator>Blute, Michael L.</creator><creator>Rangel, Laureano J.</creator><creator>Bergstralh, Eric J.</creator><creator>Karnes, Robert Jeffrey</creator><creator>Frank, Igor</creator><general>Blackwell Publishing Ltd</general><general>Wiley-Blackwell</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>201102</creationdate><title>Impact of adjuvant androgen deprivation therapy after radical prostatectomy on the survival of patients with pathological T3b prostate cancer</title><author>Siddiqui, Sameer A. ; Boorjian, Stephen A. ; Blute, Michael L. ; Rangel, Laureano J. ; Bergstralh, Eric J. ; Karnes, Robert Jeffrey ; Frank, Igor</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3985-bc411b8c2e69ab8b7c5461af59e9f45ec3862a715562acb2ff2739e5be63805c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Aged</topic><topic>Androgen Antagonists - therapeutic use</topic><topic>androgen deprivation therapy</topic><topic>Androgens - metabolism</topic><topic>Antineoplastic agents</topic><topic>Antineoplastic Agents, Hormonal - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Chemotherapy, Adjuvant</topic><topic>Combined treatments (chemotherapy of immunotherapy associated with an other treatment)</topic><topic>Epidemiologic Methods</topic><topic>Gonadotropin-Releasing Hormone - agonists</topic><topic>hormones</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neoplasm Invasiveness</topic><topic>Neoplasm Recurrence, Local - prevention & control</topic><topic>Nephrology. Urinary tract diseases</topic><topic>Orchiectomy</topic><topic>Pharmacology. Drug treatments</topic><topic>Prostate - pathology</topic><topic>prostate cancer</topic><topic>Prostatectomy</topic><topic>Prostatic Neoplasms - drug therapy</topic><topic>Prostatic Neoplasms - mortality</topic><topic>Prostatic Neoplasms - pathology</topic><topic>Prostatic Neoplasms - surgery</topic><topic>radical prostatectomy</topic><topic>Seminal Vesicles - pathology</topic><topic>survival</topic><topic>Tumors of the urinary system</topic><topic>Urinary tract. Prostate gland</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Siddiqui, Sameer A.</creatorcontrib><creatorcontrib>Boorjian, Stephen A.</creatorcontrib><creatorcontrib>Blute, Michael L.</creatorcontrib><creatorcontrib>Rangel, Laureano J.</creatorcontrib><creatorcontrib>Bergstralh, Eric J.</creatorcontrib><creatorcontrib>Karnes, Robert Jeffrey</creatorcontrib><creatorcontrib>Frank, Igor</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>BJU international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Siddiqui, Sameer A.</au><au>Boorjian, Stephen A.</au><au>Blute, Michael L.</au><au>Rangel, Laureano J.</au><au>Bergstralh, Eric J.</au><au>Karnes, Robert Jeffrey</au><au>Frank, Igor</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of adjuvant androgen deprivation therapy after radical prostatectomy on the survival of patients with pathological T3b prostate cancer</atitle><jtitle>BJU international</jtitle><addtitle>BJU Int</addtitle><date>2011-02</date><risdate>2011</risdate><volume>107</volume><issue>3</issue><spage>383</spage><epage>388</epage><pages>383-388</pages><issn>1464-4096</issn><eissn>1464-410X</eissn><abstract>Study Type – Therapy (case series)
Level of Evidence 4
What’s known on the subject? and What does the study add?
Adjuvant hormonal therapy is known to improve cancer specific survival in prostate cancer patients with lymph node positive disease.
This study suggests that surgically treated prostate cancer patients with seminal vesical invasion (pT3b) may have improved cancer specific survival if treated with adjuvant androgen deprivation therapy, similar to lymph node positive patients.
OBJECTIVE
To determine the impact of adjuvant androgen deprivation therapy (ADT) on survival in patients with seminal vesicle invasion (pT3b) at radical prostatectomy.
PATIENTS AND METHODS
We reviewed 12 115 patients who underwent radical prostatectomy between 1987 and 2002 to identify patients with pT3bN0 prostate cancer who received adjuvant ADT (n= 191). These patients were matched by clinical and pathological variables to a group of patients with pT3b prostate cancer who did not receive adjuvant ADT. Median postoperative follow‐up was 10 years. Clinical endpoints included biochemical progression‐free survival (BPFS), local recurrence‐free survival (LRFS), systemic progression‐free survival (SPFS), cancer‐specific survival (CSS) and overall survival.
RESULTS
Patients who underwent adjuvant ADT experienced improved 10‐year BPFS (60% vs 16%, P < 0.001), LRFS (87% vs 76%, P= 0.002), SPFS (91% vs 78%, P= 0.004) and CSS (94% vs 87%, P= 0.037). Overall survival was not significantly different between groups (75% vs 69%, P= 0.12). Both luteinizing hormone‐releasing hormone agonists (hazard ratio, 0.26; 95% CI, 0.15–0.46; P < 0.001) and bilateral orchiectomy (hazard ratio, 0.13; 95% CI, 0.06–0.31; P < 0.001) improved BPFS. When stratified by type of ADT (hormonal therapy vs orchiectomy), there was no difference in survival outcomes.
CONCLUSIONS
Adjuvant ADT improves local, and systemic control after radical prostatectomy for pT3b prostate cancer. There is no difference in survival between patients receiving medical hormonal therapy vs patients undergoing orchiectomy. Given the lack of improvement in overall survival, continued investigation is needed to identify the cohort of pT3b patients at highest risk for cancer progression and therefore most likely to benefit from a multimodal treatment approach.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>21265985</pmid><doi>10.1111/j.1464-410X.2010.09565.x</doi><tpages>6</tpages></addata></record> |
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subjects | Aged Androgen Antagonists - therapeutic use androgen deprivation therapy Androgens - metabolism Antineoplastic agents Antineoplastic Agents, Hormonal - therapeutic use Biological and medical sciences Chemotherapy, Adjuvant Combined treatments (chemotherapy of immunotherapy associated with an other treatment) Epidemiologic Methods Gonadotropin-Releasing Hormone - agonists hormones Humans Male Medical sciences Middle Aged Neoplasm Invasiveness Neoplasm Recurrence, Local - prevention & control Nephrology. Urinary tract diseases Orchiectomy Pharmacology. Drug treatments Prostate - pathology prostate cancer Prostatectomy Prostatic Neoplasms - drug therapy Prostatic Neoplasms - mortality Prostatic Neoplasms - pathology Prostatic Neoplasms - surgery radical prostatectomy Seminal Vesicles - pathology survival Tumors of the urinary system Urinary tract. Prostate gland |
title | Impact of adjuvant androgen deprivation therapy after radical prostatectomy on the survival of patients with pathological T3b prostate cancer |
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