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dc.contributor.advisorStephen Freedland, MD and Dan Kirsch, MD/Urology, Duke University
dc.contributor.authorMithal, Prabhakar
dc.contributor.authorHoward, Lauren E.
dc.contributor.authorAronson, William J.
dc.contributor.authorTerris, Martha K.
dc.contributor.authorCooperberg, Matthew R.
dc.contributor.authorKane, Christopher J.
dc.contributor.authorAmling, Christopher L.
dc.contributor.authorFreedland, Stephen J.
dc.date2022-08-11T08:10:55.000
dc.date.accessioned2022-08-23T17:24:54Z
dc.date.available2022-08-23T17:24:54Z
dc.date.issued2016-02-01
dc.date.submitted2016-04-20
dc.identifier.citationBJU Int. 2016 Feb;117(2):244-8. doi: 10.1111/bju.13181. Epub 2015 Jun 23. <a href="http://dx.doi.org/10.1111/bju.13181">Link to article on publisher's site</a>
dc.identifier.issn1464-4096 (Linking)
dc.identifier.doi10.1111/bju.13181
dc.identifier.pmid26010160
dc.identifier.urihttp://hdl.handle.net/20.500.14038/49291
dc.description<p>Prabhakar Mithal participated in this study as a medical student as part of the Senior Scholars research program at the University of Massachusetts Medical School.</p>
dc.description.abstractOBJECTIVE: To assess the impact of positive surgical margins (PSMs) on long-term outcomes after radical prostatectomy (RP), including metastasis, castrate-resistant prostate cancer (CRPC), and prostate cancer-specific mortality (PCSM). PATIENTS AND METHODS: Retrospective study of 4 051 men in the Shared Equal Access Regional Cancer Hospital (SEARCH) cohort treated by RP from 1988 to 2013. Proportional hazard models were used to estimate hazard ratios (HRs) of PSMs in predicting biochemical recurrence (BCR), CRPC, metastases, and PCSM. To determine if PSMs were more predictive in certain patients, analyses were stratified by pathological Gleason score, stage, and preoperative prostate-specific antigen (PSA) level. RESULTS: The median (interquartile range) follow-up was 6.6 (3.2-10.6) years and 1 127 patients had > 10 years of follow-up. During this time, 302 (32%) men had BCR, 112 (3%) developed CRPC, 144 (4%) developed metastases, and 83 (2%) died from prostate cancer. There were 1 600 (40%) men with PSMs. In unadjusted models, PSMs were significantly associated with all adverse outcomes: BCR, CRPC, metastases and PCSM (all P < /= 0.001). After adjusting for demographic and pathological characteristics, PSMs were associated with increased risk of only BCR (HR 1.98, P < 0.001), and not CRPC, metastases, or PCSM (HR < /=1.29, P > 0.18). Similar results were seen when stratified by pathological Gleason score, stage, or PSA level, and when patients who underwent adjuvant radiotherapy were excluded. CONCLUSIONS: PSMs after RP are not an independent risk factor for CRPC, metastasis, or PCSM overall or within any subset. In the absence of other high-risk features, PSMs alone may not be an indication for adjuvant radiotherapy.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=26010160&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1111/bju.13181
dc.subjectadjuvant radiotherapy
dc.subjectdisease progression
dc.subjectprostate cancer
dc.subjectprostatectomy
dc.subjectNeoplasms
dc.subjectOncology
dc.subjectSurgery
dc.titlePositive surgical margins in radical prostatectomy patients do not predict long-term oncological outcomes: results from the Shared Equal Access Regional Cancer Hospital (SEARCH) cohort
dc.typeJournal Article
dc.source.journaltitleBJU international
dc.source.volume117
dc.source.issue2
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/ssp/233
dc.identifier.contextkey8497988
html.description.abstract<p>OBJECTIVE: To assess the impact of positive surgical margins (PSMs) on long-term outcomes after radical prostatectomy (RP), including metastasis, castrate-resistant prostate cancer (CRPC), and prostate cancer-specific mortality (PCSM).</p> <p>PATIENTS AND METHODS: Retrospective study of 4 051 men in the Shared Equal Access Regional Cancer Hospital (SEARCH) cohort treated by RP from 1988 to 2013. Proportional hazard models were used to estimate hazard ratios (HRs) of PSMs in predicting biochemical recurrence (BCR), CRPC, metastases, and PCSM. To determine if PSMs were more predictive in certain patients, analyses were stratified by pathological Gleason score, stage, and preoperative prostate-specific antigen (PSA) level.</p> <p>RESULTS: The median (interquartile range) follow-up was 6.6 (3.2-10.6) years and 1 127 patients had > 10 years of follow-up. During this time, 302 (32%) men had BCR, 112 (3%) developed CRPC, 144 (4%) developed metastases, and 83 (2%) died from prostate cancer. There were 1 600 (40%) men with PSMs. In unadjusted models, PSMs were significantly associated with all adverse outcomes: BCR, CRPC, metastases and PCSM (all P < /= 0.001). After adjusting for demographic and pathological characteristics, PSMs were associated with increased risk of only BCR (HR 1.98, P < 0.001), and not CRPC, metastases, or PCSM (HR < /=1.29, P > 0.18). Similar results were seen when stratified by pathological Gleason score, stage, or PSA level, and when patients who underwent adjuvant radiotherapy were excluded.</p> <p>CONCLUSIONS: PSMs after RP are not an independent risk factor for CRPC, metastasis, or PCSM overall or within any subset. In the absence of other high-risk features, PSMs alone may not be an indication for adjuvant radiotherapy.</p>
dc.identifier.submissionpathssp/233
dc.contributor.departmentSchool of Medicine
dc.contributor.departmentSenior Scholars Program
dc.source.pages244-8


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