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 |
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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 |
format | Article |
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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.</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 & 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 & Sons Ltd</rights><rights>2017 The Authors BJU International © 2017 BJU International Published by John Wiley & 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 < 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.</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 & 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. ; 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.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3882-da4f9cf9849e4ba3d094885fe03049a7b8b72d70baf8ac78002bad174e37ab3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Aged</topic><topic>Cancer surgery</topic><topic>Humans</topic><topic>Kaplan-Meier Estimate</topic><topic>Lymph nodes</topic><topic>Male</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Middle Aged</topic><topic>Neoplasm Recurrence, Local - epidemiology</topic><topic>patterns of failure</topic><topic>PCSM</topic><topic>Prostate cancer</topic><topic>Prostate-Specific Antigen - blood</topic><topic>ProstateCancer</topic><topic>Prostatectomy</topic><topic>Prostatectomy - statistics & 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 & 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 < 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.</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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