Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/104853
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dc.contributor.authorMuralidhar, V.-
dc.contributor.authorCatalano, P.-
dc.contributor.authorReznor, G.-
dc.contributor.authorMahal, B.-
dc.contributor.authorChoueiri, T.-
dc.contributor.authorSweeney, C.-
dc.contributor.authorMartin, N.-
dc.contributor.authorBeard, C.-
dc.contributor.authorChen, Y.-
dc.contributor.authorNezolosky, M.-
dc.contributor.authorHoffman, K.-
dc.contributor.authorFeng, F.-
dc.contributor.authorTrinh, Q.-
dc.contributor.authorNguyen, P.-
dc.date.issued2016-
dc.identifier.citationJournal of the National Comprehensive Cancer Network : JNCCN, 2016; 14(4):421-428-
dc.identifier.issn1540-1405-
dc.identifier.issn1540-1413-
dc.identifier.urihttp://hdl.handle.net/2440/104853-
dc.description.abstractThe current NCCN Clinical Practice Guidelines in Oncology for Prostate Cancer recommend long-term androgen deprivation therapy (ADT) for all men with high-risk prostate cancer treated with external-beam radiation therapy (EBRT). We determined whether the use of long-term ADT varied by the recently defined subcategories of high-risk disease (favorable, other, and very high) versus unfavorable intermediate-risk disease.We identified 5,524 patients with unfavorable-risk prostate cancer diagnosed from 2004 to 2007 and managed with EBRT using the SEER-Medicare linked database. Patients were stratified by risk group: unfavorable intermediate-risk, favorable high-risk (previously defined and validated as clinical stage T1c, Gleason score of 4 + 4 = 8, and prostate-specific antigen [PSA] level <10 ng/mL, or clinical stage T1c, Gleason score of 6, and PSA level >20 ng/mL), very-high-risk (clinical stage T3b-T4 or primary Gleason pattern 5), or other high risk (ie, neither favorable nor very high). We used multivariable competing risks regression to estimate the rates of long-term (≥2 years) ADT by group.Men with favorable high-risk prostate cancer were significantly less likely to receive long-term ADT than those with other high-risk disease (15.4% vs 24.6%, adjusted hazard ratio [AHR], 0.68; 95% CI, 0.60-0.76;P<.001), and similarly likely as those with unfavorable intermediate-risk disease (AHR, 1.10; 95% CI, 0.99-1.23;P=.087). Other high-risk disease was less likely to receive long-term ADT than very high-risk cancer (24.6% vs 30.8%; AHR, 0.83; 95% CI, 0.74-0.93;P=.002).Despite current guidelines, patients with EBRT-managed high-risk prostate cancer received significantly different rates of long-course ADT based on subclassification. Our results suggest that oncologists view these patients as a heterogeneous group with favorable high-risk cancer warranting less aggressive therapy than other high-risk or very high-risk disease.-
dc.description.statementofresponsibilityVinayak Muralidhar, Brandon Arvin Virgil Mahal, Gally Reznor, Toni K. Choueiri, Christopher Sweeney, Neil E. Martin, Peter F. Orio, Yu-Wei Chen, Michelle Daniel Nezolosky, Karen E. Hoffman, Felix Yi-Chung Feng, Quoc-Dien Trinh, Paul L. Nguyen-
dc.language.isoen-
dc.publisherJones and Barlett Publishers-
dc.rightsCopyright © 2016 by the National Comprehensive Cancer Network.-
dc.source.urihttp://dx.doi.org/10.6004/jnccn.2016.0048-
dc.subjectAndrogen deprivation therapy; African-American men; cardiovascular-disease; radiation-therapy; trial; radiotherapy; suppression; mortality; duration-
dc.titleVariation in national use of long-term ADT by disease aggressiveness among men with unfavorable-risk prostate cancer-
dc.typeJournal article-
dc.identifier.doi10.6004/jnccn.2016.0048-
pubs.publication-statusPublished-
dc.identifier.orcidSweeney, C. [0000-0002-0398-6018]-
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