Radiotherapy after radical prostatectomy: immediate or early delayed?
Background Biochemical recurrence after radical prostatectomy (RP) is associated with risk indicators, including Gleason score, preoperative PSA level, tumor stage, seminal vesicle invasion, and positive surgical margins. The 5-year biochemical progression rate among predisposed patients is as high...
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Veröffentlicht in: | Strahlentherapie und Onkologie 2012-12, Vol.188 (12), p.1096-1101 |
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description | Background
Biochemical recurrence after radical prostatectomy (RP) is associated with risk indicators, including Gleason score, preoperative PSA level, tumor stage, seminal vesicle invasion, and positive surgical margins. The 5-year biochemical progression rate among predisposed patients is as high as 50–70%. Post-RP treatment options include adjuvant radiotherapy (ART, for men with undetectable PSA) or salvage radiotherapy (SRT, for PSA persisting or re-rising above detection threshold). Presently, there are no published randomized trials evaluating ART vs. SRT directly.
Methods
Published data on ART and SRT were reviewed to allow a comparison of the two treatment approaches.
Results
Three randomized phase III trials demonstrated an almost 20% absolute benefit for biochemical progression-free survival after ART (60–64 Gy) compared to a “wait and see” policy. The greatest benefit was achieved in patients with positive margins and pT3 tumors.
SRT can be offered to patients with elevated PSA after RP. In 30–70% of SRT patients, PSA will decrease to an undetectable level, thus giving a second curative chance. The rate of side effects for both treatments is comparably low.
The role of irradiation of pelvic lymph nodes and the additional use of hormone therapy and radiation dose are discussed.
Conclusion
It remains unclear whether early SRT initiated after PSA failure is equivalent to ART. Where SRT is indicated, it should be started as early as possible. |
doi_str_mv | 10.1007/s00066-012-0234-9 |
format | Article |
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Biochemical recurrence after radical prostatectomy (RP) is associated with risk indicators, including Gleason score, preoperative PSA level, tumor stage, seminal vesicle invasion, and positive surgical margins. The 5-year biochemical progression rate among predisposed patients is as high as 50–70%. Post-RP treatment options include adjuvant radiotherapy (ART, for men with undetectable PSA) or salvage radiotherapy (SRT, for PSA persisting or re-rising above detection threshold). Presently, there are no published randomized trials evaluating ART vs. SRT directly.
Methods
Published data on ART and SRT were reviewed to allow a comparison of the two treatment approaches.
Results
Three randomized phase III trials demonstrated an almost 20% absolute benefit for biochemical progression-free survival after ART (60–64 Gy) compared to a “wait and see” policy. The greatest benefit was achieved in patients with positive margins and pT3 tumors.
SRT can be offered to patients with elevated PSA after RP. In 30–70% of SRT patients, PSA will decrease to an undetectable level, thus giving a second curative chance. The rate of side effects for both treatments is comparably low.
The role of irradiation of pelvic lymph nodes and the additional use of hormone therapy and radiation dose are discussed.
Conclusion
It remains unclear whether early SRT initiated after PSA failure is equivalent to ART. Where SRT is indicated, it should be started as early as possible.</description><identifier>ISSN: 0179-7158</identifier><identifier>EISSN: 1439-099X</identifier><identifier>DOI: 10.1007/s00066-012-0234-9</identifier><identifier>PMID: 23128897</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>Biomarkers, Tumor - blood ; Combined Modality Therapy ; Disease-Free Survival ; Follow-Up Studies ; Guideline Adherence ; Humans ; Lymphatic Irradiation ; Magnetic Resonance Imaging ; Male ; Medicine ; Medicine & Public Health ; Neoplasm Grading ; Neoplasm Recurrence, Local - pathology ; Neoplasm Recurrence, Local - radiotherapy ; Neoplasm Recurrence, Local - surgery ; Neoplasm Staging ; Neoplasm, Residual - pathology ; Neoplasm, Residual - radiotherapy ; Neoplasm, Residual - surgery ; Oncology ; Original Article ; Prostate-Specific Antigen - blood ; Prostatectomy ; Prostatic Neoplasms - mortality ; Prostatic Neoplasms - pathology ; Prostatic Neoplasms - radiotherapy ; Prostatic Neoplasms - surgery ; Radiotherapy ; Radiotherapy Dosage ; Radiotherapy Planning, Computer-Assisted ; Radiotherapy, Adjuvant - methods ; Randomized Controlled Trials as Topic ; Salvage Therapy - methods ; Time-to-Treatment</subject><ispartof>Strahlentherapie und Onkologie, 2012-12, Vol.188 (12), p.1096-1101</ispartof><rights>Urban & Vogel 2012</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c372t-3499906812a61efbacd957725cda07b0244f6749d35dd06dcb722535ed7ec4a93</citedby><cites>FETCH-LOGICAL-c372t-3499906812a61efbacd957725cda07b0244f6749d35dd06dcb722535ed7ec4a93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00066-012-0234-9$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00066-012-0234-9$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>315,781,785,27929,27930,41493,42562,51324</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23128897$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bottke, D.</creatorcontrib><creatorcontrib>Bartkowiak, D.</creatorcontrib><creatorcontrib>Schrader, M.</creatorcontrib><creatorcontrib>Wiegel, T.</creatorcontrib><title>Radiotherapy after radical prostatectomy: immediate or early delayed?</title><title>Strahlentherapie und Onkologie</title><addtitle>Strahlenther Onkol</addtitle><addtitle>Strahlenther Onkol</addtitle><description>Background
Biochemical recurrence after radical prostatectomy (RP) is associated with risk indicators, including Gleason score, preoperative PSA level, tumor stage, seminal vesicle invasion, and positive surgical margins. The 5-year biochemical progression rate among predisposed patients is as high as 50–70%. Post-RP treatment options include adjuvant radiotherapy (ART, for men with undetectable PSA) or salvage radiotherapy (SRT, for PSA persisting or re-rising above detection threshold). Presently, there are no published randomized trials evaluating ART vs. SRT directly.
Methods
Published data on ART and SRT were reviewed to allow a comparison of the two treatment approaches.
Results
Three randomized phase III trials demonstrated an almost 20% absolute benefit for biochemical progression-free survival after ART (60–64 Gy) compared to a “wait and see” policy. The greatest benefit was achieved in patients with positive margins and pT3 tumors.
SRT can be offered to patients with elevated PSA after RP. In 30–70% of SRT patients, PSA will decrease to an undetectable level, thus giving a second curative chance. The rate of side effects for both treatments is comparably low.
The role of irradiation of pelvic lymph nodes and the additional use of hormone therapy and radiation dose are discussed.
Conclusion
It remains unclear whether early SRT initiated after PSA failure is equivalent to ART. Where SRT is indicated, it should be started as early as possible.</description><subject>Biomarkers, Tumor - blood</subject><subject>Combined Modality Therapy</subject><subject>Disease-Free Survival</subject><subject>Follow-Up Studies</subject><subject>Guideline Adherence</subject><subject>Humans</subject><subject>Lymphatic Irradiation</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Neoplasm Grading</subject><subject>Neoplasm Recurrence, Local - pathology</subject><subject>Neoplasm Recurrence, Local - radiotherapy</subject><subject>Neoplasm Recurrence, Local - surgery</subject><subject>Neoplasm Staging</subject><subject>Neoplasm, Residual - pathology</subject><subject>Neoplasm, Residual - radiotherapy</subject><subject>Neoplasm, Residual - surgery</subject><subject>Oncology</subject><subject>Original Article</subject><subject>Prostate-Specific Antigen - blood</subject><subject>Prostatectomy</subject><subject>Prostatic Neoplasms - mortality</subject><subject>Prostatic Neoplasms - pathology</subject><subject>Prostatic Neoplasms - radiotherapy</subject><subject>Prostatic Neoplasms - surgery</subject><subject>Radiotherapy</subject><subject>Radiotherapy Dosage</subject><subject>Radiotherapy Planning, Computer-Assisted</subject><subject>Radiotherapy, Adjuvant - methods</subject><subject>Randomized Controlled Trials as Topic</subject><subject>Salvage Therapy - methods</subject><subject>Time-to-Treatment</subject><issn>0179-7158</issn><issn>1439-099X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNp1kEtLxDAUhYMozjj6A9xIwXX05tGkcSMyjA8YEETBXUiTVDu00zHpLPrvzdBR3MhdhHtzck7uh9A5gSsCIK8jAAiBgVAMlHGsDtCUcKYwKPV-iKZApMKS5MUEncS4AiCCK36MJpQRWhRKTtHixbi66z99MJshM1XvQxbSyJom24Qu9qb3tu_a4Sar29a7OvVZFzJvQjNkzjdm8O72FB1Vpon-bH_O0Nv94nX-iJfPD0_zuyW2TNIeM66UAlEQagTxVWmsU7mUNLfOgCyBcl4JyZVjuXMgnC0lpTnLvZPecqPYDF2OvulrX1sfe73qtmGdIjXhVKRSgicVGVU2LRCDr_Qm1K0Jgyagd-D0CE4ncHoHTu-cL_bO2zKt-fvih1QS0FEQ09X6w4c_0f-6fgNCmXgY</recordid><startdate>20121201</startdate><enddate>20121201</enddate><creator>Bottke, D.</creator><creator>Bartkowiak, D.</creator><creator>Schrader, M.</creator><creator>Wiegel, T.</creator><general>Springer-Verlag</general><general>Springer Nature B.V</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>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FG</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20121201</creationdate><title>Radiotherapy after radical prostatectomy: immediate or early delayed?</title><author>Bottke, D. ; Bartkowiak, D. ; Schrader, M. ; Wiegel, T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c372t-3499906812a61efbacd957725cda07b0244f6749d35dd06dcb722535ed7ec4a93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Biomarkers, Tumor - blood</topic><topic>Combined Modality Therapy</topic><topic>Disease-Free Survival</topic><topic>Follow-Up Studies</topic><topic>Guideline Adherence</topic><topic>Humans</topic><topic>Lymphatic Irradiation</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Neoplasm Grading</topic><topic>Neoplasm Recurrence, Local - pathology</topic><topic>Neoplasm Recurrence, Local - radiotherapy</topic><topic>Neoplasm Recurrence, Local - surgery</topic><topic>Neoplasm Staging</topic><topic>Neoplasm, Residual - pathology</topic><topic>Neoplasm, Residual - radiotherapy</topic><topic>Neoplasm, Residual - surgery</topic><topic>Oncology</topic><topic>Original Article</topic><topic>Prostate-Specific Antigen - blood</topic><topic>Prostatectomy</topic><topic>Prostatic Neoplasms - mortality</topic><topic>Prostatic Neoplasms - pathology</topic><topic>Prostatic Neoplasms - radiotherapy</topic><topic>Prostatic Neoplasms - surgery</topic><topic>Radiotherapy</topic><topic>Radiotherapy Dosage</topic><topic>Radiotherapy Planning, Computer-Assisted</topic><topic>Radiotherapy, Adjuvant - methods</topic><topic>Randomized Controlled Trials as Topic</topic><topic>Salvage Therapy - methods</topic><topic>Time-to-Treatment</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bottke, D.</creatorcontrib><creatorcontrib>Bartkowiak, D.</creatorcontrib><creatorcontrib>Schrader, M.</creatorcontrib><creatorcontrib>Wiegel, T.</creatorcontrib><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>Nursing & Allied Health Database</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>ProQuest SciTech Collection</collection><collection>ProQuest Technology 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>Advanced Technologies & Aerospace Collection</collection><collection>Proquest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</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><jtitle>Strahlentherapie und Onkologie</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bottke, D.</au><au>Bartkowiak, D.</au><au>Schrader, M.</au><au>Wiegel, T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Radiotherapy after radical prostatectomy: immediate or early delayed?</atitle><jtitle>Strahlentherapie und Onkologie</jtitle><stitle>Strahlenther Onkol</stitle><addtitle>Strahlenther Onkol</addtitle><date>2012-12-01</date><risdate>2012</risdate><volume>188</volume><issue>12</issue><spage>1096</spage><epage>1101</epage><pages>1096-1101</pages><issn>0179-7158</issn><eissn>1439-099X</eissn><abstract>Background
Biochemical recurrence after radical prostatectomy (RP) is associated with risk indicators, including Gleason score, preoperative PSA level, tumor stage, seminal vesicle invasion, and positive surgical margins. The 5-year biochemical progression rate among predisposed patients is as high as 50–70%. Post-RP treatment options include adjuvant radiotherapy (ART, for men with undetectable PSA) or salvage radiotherapy (SRT, for PSA persisting or re-rising above detection threshold). Presently, there are no published randomized trials evaluating ART vs. SRT directly.
Methods
Published data on ART and SRT were reviewed to allow a comparison of the two treatment approaches.
Results
Three randomized phase III trials demonstrated an almost 20% absolute benefit for biochemical progression-free survival after ART (60–64 Gy) compared to a “wait and see” policy. The greatest benefit was achieved in patients with positive margins and pT3 tumors.
SRT can be offered to patients with elevated PSA after RP. In 30–70% of SRT patients, PSA will decrease to an undetectable level, thus giving a second curative chance. The rate of side effects for both treatments is comparably low.
The role of irradiation of pelvic lymph nodes and the additional use of hormone therapy and radiation dose are discussed.
Conclusion
It remains unclear whether early SRT initiated after PSA failure is equivalent to ART. Where SRT is indicated, it should be started as early as possible.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>23128897</pmid><doi>10.1007/s00066-012-0234-9</doi><tpages>6</tpages></addata></record> |
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subjects | Biomarkers, Tumor - blood Combined Modality Therapy Disease-Free Survival Follow-Up Studies Guideline Adherence Humans Lymphatic Irradiation Magnetic Resonance Imaging Male Medicine Medicine & Public Health Neoplasm Grading Neoplasm Recurrence, Local - pathology Neoplasm Recurrence, Local - radiotherapy Neoplasm Recurrence, Local - surgery Neoplasm Staging Neoplasm, Residual - pathology Neoplasm, Residual - radiotherapy Neoplasm, Residual - surgery Oncology Original Article Prostate-Specific Antigen - blood Prostatectomy Prostatic Neoplasms - mortality Prostatic Neoplasms - pathology Prostatic Neoplasms - radiotherapy Prostatic Neoplasms - surgery Radiotherapy Radiotherapy Dosage Radiotherapy Planning, Computer-Assisted Radiotherapy, Adjuvant - methods Randomized Controlled Trials as Topic Salvage Therapy - methods Time-to-Treatment |
title | Radiotherapy after radical prostatectomy: immediate or early delayed? |
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