Anatomical patterns of recurrence following biochemical relapse after post‐prostatectomy salvage radiation therapy: a multi‐institutional study

Objectives To characterise the frequency and detailed anatomical sites of failure for patients receiving post‐radical prostatectomy (RP) salvage radiation therapy (SRT). Patients and Methods A multi‐institutional retrospective study was performed on 574 men who underwent SRT between 1986 and 2013. A...

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Veröffentlicht in:BJU international 2017-09, Vol.120 (3), p.351-357
Hauptverfasser: Jackson, William C., Desai, Neil B., Abugharib, Ahmed E., Tumati, Vasu, Dess, Robert T., Lee, Jae Y., Zhao, Shuang G., Soliman, Moaaz, Folkert, Michael, Laine, Aaron, Hannan, Raquibul, Zumsteg, Zachary S., Sandler, Howard, Hamstra, Daniel A., Montgomery, Jeffrey S., Miller, David C., Kozminski, Mike A., Hollenbeck, Brent K., Hearn, Jason W., Palapattu, Ganesh, Tomlins, Scott A., Mehra, Rohit, Morgan, Todd M., Feng, Felix Y., Spratt, Daniel E.
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container_end_page 357
container_issue 3
container_start_page 351
container_title BJU international
container_volume 120
creator Jackson, William C.
Desai, Neil B.
Abugharib, Ahmed E.
Tumati, Vasu
Dess, Robert T.
Lee, Jae Y.
Zhao, Shuang G.
Soliman, Moaaz
Folkert, Michael
Laine, Aaron
Hannan, Raquibul
Zumsteg, Zachary S.
Sandler, Howard
Hamstra, Daniel A.
Montgomery, Jeffrey S.
Miller, David C.
Kozminski, Mike A.
Hollenbeck, Brent K.
Hearn, Jason W.
Palapattu, Ganesh
Tomlins, Scott A.
Mehra, Rohit
Morgan, Todd M.
Feng, Felix Y.
Spratt, Daniel E.
description Objectives To characterise the frequency and detailed anatomical sites of failure for patients receiving post‐radical prostatectomy (RP) salvage radiation therapy (SRT). Patients and Methods A multi‐institutional retrospective study was performed on 574 men who underwent SRT between 1986 and 2013. Anatomical recurrence patterns were classified as lymphotrophic (lymph nodes only), osteotrophic (bone only), or multifocal if both were present. Isolated first failure sites were defined as sites of initial clinically detected recurrence that remained isolated for at least 3 months. Results The median follow‐up after SRT was 6.8 years. The 8‐year rates of local, regional, and distant failure for patients undergoing SRT were 2%, 6%, and 21%, respectively. Of the 22% men (128 of 574) who developed a clinically detectable recurrence, 17%, 50%, and 31% were lymphotrophic, osteotrophic, and multifocal, respectively. The trophic nature of metastases was prognostic for distant metastases‐free survival (DMFS) and prostate cancer‐specific survival (PCSS); the 10‐year rates of DMFS were 18%, 5%, and 7% (P < 0.01), and PCSS were 78%, 68%, and 56% (P < 0.01), for lymphotrophic, osteotrophic, and multifocal failure patterns, respectively. Conclusions We demonstrate that trophism for metastatic site has significant prognostic impact on PCSS in men treated with SRT. Radiographic local failure is an uncommon event after SRT when compared to historical data of patients treated with surgery monotherapy. However, distant failure remains a challenge in this patient population and warrants further therapeutic investigation.
doi_str_mv 10.1111/bju.13792
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Patients and Methods A multi‐institutional retrospective study was performed on 574 men who underwent SRT between 1986 and 2013. Anatomical recurrence patterns were classified as lymphotrophic (lymph nodes only), osteotrophic (bone only), or multifocal if both were present. Isolated first failure sites were defined as sites of initial clinically detected recurrence that remained isolated for at least 3 months. Results The median follow‐up after SRT was 6.8 years. The 8‐year rates of local, regional, and distant failure for patients undergoing SRT were 2%, 6%, and 21%, respectively. Of the 22% men (128 of 574) who developed a clinically detectable recurrence, 17%, 50%, and 31% were lymphotrophic, osteotrophic, and multifocal, respectively. The trophic nature of metastases was prognostic for distant metastases‐free survival (DMFS) and prostate cancer‐specific survival (PCSS); the 10‐year rates of DMFS were 18%, 5%, and 7% (P &lt; 0.01), and PCSS were 78%, 68%, and 56% (P &lt; 0.01), for lymphotrophic, osteotrophic, and multifocal failure patterns, respectively. Conclusions We demonstrate that trophism for metastatic site has significant prognostic impact on PCSS in men treated with SRT. Radiographic local failure is an uncommon event after SRT when compared to historical data of patients treated with surgery monotherapy. However, distant failure remains a challenge in this patient population and warrants further therapeutic investigation.</description><identifier>ISSN: 1464-4096</identifier><identifier>EISSN: 1464-410X</identifier><identifier>DOI: 10.1111/bju.13792</identifier><identifier>PMID: 28139024</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Aged ; Cancer surgery ; Humans ; Kaplan-Meier Estimate ; Lymph nodes ; Male ; Metastases ; Metastasis ; Middle Aged ; Neoplasm Recurrence, Local - epidemiology ; patterns of failure ; PCSM ; Prostate cancer ; Prostate-Specific Antigen - blood ; ProstateCancer ; Prostatectomy ; Prostatectomy - statistics &amp; numerical data ; Prostatic Neoplasms - epidemiology ; Prostatic Neoplasms - pathology ; Prostatic Neoplasms - therapy ; Radiation therapy ; radical prostatectomy ; Retrospective Studies ; salvage radiotherapy ; Salvage Therapy ; Surgery ; Survival ; Treatment Failure ; Urological surgery</subject><ispartof>BJU international, 2017-09, Vol.120 (3), p.351-357</ispartof><rights>2017 The Authors BJU International © 2017 BJU International Published by John Wiley &amp; Sons Ltd</rights><rights>2017 The Authors BJU International © 2017 BJU International Published by John Wiley &amp; Sons Ltd.</rights><rights>BJUI © 2017 BJU International</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3882-da4f9cf9849e4ba3d094885fe03049a7b8b72d70baf8ac78002bad174e37ab3</citedby><cites>FETCH-LOGICAL-c3882-da4f9cf9849e4ba3d094885fe03049a7b8b72d70baf8ac78002bad174e37ab3</cites><orcidid>0000-0002-5973-4741 ; 0000-0003-3908-6166</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fbju.13792$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fbju.13792$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28139024$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jackson, William C.</creatorcontrib><creatorcontrib>Desai, Neil B.</creatorcontrib><creatorcontrib>Abugharib, Ahmed E.</creatorcontrib><creatorcontrib>Tumati, Vasu</creatorcontrib><creatorcontrib>Dess, Robert T.</creatorcontrib><creatorcontrib>Lee, Jae Y.</creatorcontrib><creatorcontrib>Zhao, Shuang G.</creatorcontrib><creatorcontrib>Soliman, Moaaz</creatorcontrib><creatorcontrib>Folkert, Michael</creatorcontrib><creatorcontrib>Laine, Aaron</creatorcontrib><creatorcontrib>Hannan, Raquibul</creatorcontrib><creatorcontrib>Zumsteg, Zachary S.</creatorcontrib><creatorcontrib>Sandler, Howard</creatorcontrib><creatorcontrib>Hamstra, Daniel A.</creatorcontrib><creatorcontrib>Montgomery, Jeffrey S.</creatorcontrib><creatorcontrib>Miller, David C.</creatorcontrib><creatorcontrib>Kozminski, Mike A.</creatorcontrib><creatorcontrib>Hollenbeck, Brent K.</creatorcontrib><creatorcontrib>Hearn, Jason W.</creatorcontrib><creatorcontrib>Palapattu, Ganesh</creatorcontrib><creatorcontrib>Tomlins, Scott A.</creatorcontrib><creatorcontrib>Mehra, Rohit</creatorcontrib><creatorcontrib>Morgan, Todd M.</creatorcontrib><creatorcontrib>Feng, Felix Y.</creatorcontrib><creatorcontrib>Spratt, Daniel E.</creatorcontrib><title>Anatomical patterns of recurrence following biochemical relapse after post‐prostatectomy salvage radiation therapy: a multi‐institutional study</title><title>BJU international</title><addtitle>BJU Int</addtitle><description>Objectives To characterise the frequency and detailed anatomical sites of failure for patients receiving post‐radical prostatectomy (RP) salvage radiation therapy (SRT). Patients and Methods A multi‐institutional retrospective study was performed on 574 men who underwent SRT between 1986 and 2013. Anatomical recurrence patterns were classified as lymphotrophic (lymph nodes only), osteotrophic (bone only), or multifocal if both were present. Isolated first failure sites were defined as sites of initial clinically detected recurrence that remained isolated for at least 3 months. Results The median follow‐up after SRT was 6.8 years. The 8‐year rates of local, regional, and distant failure for patients undergoing SRT were 2%, 6%, and 21%, respectively. Of the 22% men (128 of 574) who developed a clinically detectable recurrence, 17%, 50%, and 31% were lymphotrophic, osteotrophic, and multifocal, respectively. The trophic nature of metastases was prognostic for distant metastases‐free survival (DMFS) and prostate cancer‐specific survival (PCSS); the 10‐year rates of DMFS were 18%, 5%, and 7% (P &lt; 0.01), and PCSS were 78%, 68%, and 56% (P &lt; 0.01), for lymphotrophic, osteotrophic, and multifocal failure patterns, respectively. Conclusions We demonstrate that trophism for metastatic site has significant prognostic impact on PCSS in men treated with SRT. Radiographic local failure is an uncommon event after SRT when compared to historical data of patients treated with surgery monotherapy. However, distant failure remains a challenge in this patient population and warrants further therapeutic investigation.</description><subject>Aged</subject><subject>Cancer surgery</subject><subject>Humans</subject><subject>Kaplan-Meier Estimate</subject><subject>Lymph nodes</subject><subject>Male</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Middle Aged</subject><subject>Neoplasm Recurrence, Local - epidemiology</subject><subject>patterns of failure</subject><subject>PCSM</subject><subject>Prostate cancer</subject><subject>Prostate-Specific Antigen - blood</subject><subject>ProstateCancer</subject><subject>Prostatectomy</subject><subject>Prostatectomy - statistics &amp; numerical data</subject><subject>Prostatic Neoplasms - epidemiology</subject><subject>Prostatic Neoplasms - pathology</subject><subject>Prostatic Neoplasms - therapy</subject><subject>Radiation therapy</subject><subject>radical prostatectomy</subject><subject>Retrospective Studies</subject><subject>salvage radiotherapy</subject><subject>Salvage Therapy</subject><subject>Surgery</subject><subject>Survival</subject><subject>Treatment Failure</subject><subject>Urological surgery</subject><issn>1464-4096</issn><issn>1464-410X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc1qFjEUhgex2FpdeAMScKOLr00y6UzirhZ_WgouVHA3nGRO2nxkfsyPZXZeguAdeiXm67QuBLM5IXnOw-G8VfWM0SNWzrHe5iNWt4o_qA6YaMRGMPr14f2dqma_ehzjltLy0Jw8qva5ZLWiXBxUv05HSNPgDHgyQ0oYxkgmSwKaHAKOBomdvJ9u3HhFtJvMNa5wQA9zRAK29JB5iun3j59zKBUSmqJcSAT_Ha6QBOgdJDeNJF1jgHl5TYAM2SdXWtwYk0t5912sMeV-eVLtWfARn97Vw-rTu7efzz5sLj--Pz87vdyYWkq-6UFYZaySQqHQUPdUCSlPLNKaCgWtlrrlfUs1WAmmlZRyDT1rBdYt6Pqwerlay9DfMsbUDS4a9B5GnHLsmGxqzhRvZUFf_INupxzKvIVSXO1WyZpCvVopU7YQA9puDm6AsHSMdrucupJTd5tTYZ_fGbMesP9L3gdTgOMVuHEel_-bujcXX1blHxFoou4</recordid><startdate>201709</startdate><enddate>201709</enddate><creator>Jackson, William C.</creator><creator>Desai, Neil B.</creator><creator>Abugharib, Ahmed E.</creator><creator>Tumati, Vasu</creator><creator>Dess, Robert T.</creator><creator>Lee, Jae Y.</creator><creator>Zhao, Shuang G.</creator><creator>Soliman, Moaaz</creator><creator>Folkert, Michael</creator><creator>Laine, Aaron</creator><creator>Hannan, Raquibul</creator><creator>Zumsteg, Zachary S.</creator><creator>Sandler, Howard</creator><creator>Hamstra, Daniel A.</creator><creator>Montgomery, Jeffrey S.</creator><creator>Miller, David C.</creator><creator>Kozminski, Mike A.</creator><creator>Hollenbeck, Brent K.</creator><creator>Hearn, Jason W.</creator><creator>Palapattu, Ganesh</creator><creator>Tomlins, Scott A.</creator><creator>Mehra, Rohit</creator><creator>Morgan, Todd M.</creator><creator>Feng, Felix Y.</creator><creator>Spratt, Daniel E.</creator><general>Wiley Subscription Services, Inc</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>7QP</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-5973-4741</orcidid><orcidid>https://orcid.org/0000-0003-3908-6166</orcidid></search><sort><creationdate>201709</creationdate><title>Anatomical patterns of recurrence following biochemical relapse after post‐prostatectomy salvage radiation therapy: a multi‐institutional study</title><author>Jackson, William C. ; 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numerical data</topic><topic>Prostatic Neoplasms - epidemiology</topic><topic>Prostatic Neoplasms - pathology</topic><topic>Prostatic Neoplasms - therapy</topic><topic>Radiation therapy</topic><topic>radical prostatectomy</topic><topic>Retrospective Studies</topic><topic>salvage radiotherapy</topic><topic>Salvage Therapy</topic><topic>Surgery</topic><topic>Survival</topic><topic>Treatment Failure</topic><topic>Urological surgery</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jackson, William C.</creatorcontrib><creatorcontrib>Desai, Neil B.</creatorcontrib><creatorcontrib>Abugharib, Ahmed E.</creatorcontrib><creatorcontrib>Tumati, Vasu</creatorcontrib><creatorcontrib>Dess, Robert T.</creatorcontrib><creatorcontrib>Lee, Jae Y.</creatorcontrib><creatorcontrib>Zhao, Shuang G.</creatorcontrib><creatorcontrib>Soliman, Moaaz</creatorcontrib><creatorcontrib>Folkert, Michael</creatorcontrib><creatorcontrib>Laine, Aaron</creatorcontrib><creatorcontrib>Hannan, Raquibul</creatorcontrib><creatorcontrib>Zumsteg, Zachary S.</creatorcontrib><creatorcontrib>Sandler, Howard</creatorcontrib><creatorcontrib>Hamstra, Daniel A.</creatorcontrib><creatorcontrib>Montgomery, Jeffrey S.</creatorcontrib><creatorcontrib>Miller, David C.</creatorcontrib><creatorcontrib>Kozminski, Mike A.</creatorcontrib><creatorcontrib>Hollenbeck, Brent K.</creatorcontrib><creatorcontrib>Hearn, Jason W.</creatorcontrib><creatorcontrib>Palapattu, Ganesh</creatorcontrib><creatorcontrib>Tomlins, Scott A.</creatorcontrib><creatorcontrib>Mehra, Rohit</creatorcontrib><creatorcontrib>Morgan, Todd M.</creatorcontrib><creatorcontrib>Feng, Felix Y.</creatorcontrib><creatorcontrib>Spratt, Daniel E.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>BJU international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jackson, William C.</au><au>Desai, Neil B.</au><au>Abugharib, Ahmed E.</au><au>Tumati, Vasu</au><au>Dess, Robert T.</au><au>Lee, Jae Y.</au><au>Zhao, Shuang G.</au><au>Soliman, Moaaz</au><au>Folkert, Michael</au><au>Laine, Aaron</au><au>Hannan, Raquibul</au><au>Zumsteg, Zachary S.</au><au>Sandler, Howard</au><au>Hamstra, Daniel A.</au><au>Montgomery, Jeffrey S.</au><au>Miller, David C.</au><au>Kozminski, Mike A.</au><au>Hollenbeck, Brent K.</au><au>Hearn, Jason W.</au><au>Palapattu, Ganesh</au><au>Tomlins, Scott A.</au><au>Mehra, Rohit</au><au>Morgan, Todd M.</au><au>Feng, Felix Y.</au><au>Spratt, Daniel E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Anatomical patterns of recurrence following biochemical relapse after post‐prostatectomy salvage radiation therapy: a multi‐institutional study</atitle><jtitle>BJU international</jtitle><addtitle>BJU Int</addtitle><date>2017-09</date><risdate>2017</risdate><volume>120</volume><issue>3</issue><spage>351</spage><epage>357</epage><pages>351-357</pages><issn>1464-4096</issn><eissn>1464-410X</eissn><abstract>Objectives To characterise the frequency and detailed anatomical sites of failure for patients receiving post‐radical prostatectomy (RP) salvage radiation therapy (SRT). Patients and Methods A multi‐institutional retrospective study was performed on 574 men who underwent SRT between 1986 and 2013. Anatomical recurrence patterns were classified as lymphotrophic (lymph nodes only), osteotrophic (bone only), or multifocal if both were present. Isolated first failure sites were defined as sites of initial clinically detected recurrence that remained isolated for at least 3 months. Results The median follow‐up after SRT was 6.8 years. The 8‐year rates of local, regional, and distant failure for patients undergoing SRT were 2%, 6%, and 21%, respectively. Of the 22% men (128 of 574) who developed a clinically detectable recurrence, 17%, 50%, and 31% were lymphotrophic, osteotrophic, and multifocal, respectively. The trophic nature of metastases was prognostic for distant metastases‐free survival (DMFS) and prostate cancer‐specific survival (PCSS); the 10‐year rates of DMFS were 18%, 5%, and 7% (P &lt; 0.01), and PCSS were 78%, 68%, and 56% (P &lt; 0.01), for lymphotrophic, osteotrophic, and multifocal failure patterns, respectively. Conclusions We demonstrate that trophism for metastatic site has significant prognostic impact on PCSS in men treated with SRT. Radiographic local failure is an uncommon event after SRT when compared to historical data of patients treated with surgery monotherapy. However, distant failure remains a challenge in this patient population and warrants further therapeutic investigation.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>28139024</pmid><doi>10.1111/bju.13792</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-5973-4741</orcidid><orcidid>https://orcid.org/0000-0003-3908-6166</orcidid><oa>free_for_read</oa></addata></record>
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subjects Aged
Cancer surgery
Humans
Kaplan-Meier Estimate
Lymph nodes
Male
Metastases
Metastasis
Middle Aged
Neoplasm Recurrence, Local - epidemiology
patterns of failure
PCSM
Prostate cancer
Prostate-Specific Antigen - blood
ProstateCancer
Prostatectomy
Prostatectomy - statistics & numerical data
Prostatic Neoplasms - epidemiology
Prostatic Neoplasms - pathology
Prostatic Neoplasms - therapy
Radiation therapy
radical prostatectomy
Retrospective Studies
salvage radiotherapy
Salvage Therapy
Surgery
Survival
Treatment Failure
Urological surgery
title Anatomical patterns of recurrence following biochemical relapse after post‐prostatectomy salvage radiation therapy: a multi‐institutional study
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