Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/45401
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dc.contributor.authorRavi, Praful-
dc.contributor.authorXie, Wanling-
dc.contributor.authorBUYSE, Marc-
dc.contributor.authorHalabi, Susan-
dc.contributor.authorKantoff, Philip W.-
dc.contributor.authorSartor, Oliver-
dc.contributor.authorAttard, Gert-
dc.contributor.authorClarke, Noel-
dc.contributor.authorD'Amico, Anthony-
dc.contributor.authorDignam, James-
dc.contributor.authorJames, Nicholas-
dc.contributor.authorFizazi, Karim-
dc.contributor.authorGillessen, Silke-
dc.contributor.authorParulekar, Wendy-
dc.contributor.authorSandler, Howard-
dc.contributor.authorSpratt, Daniel E.-
dc.contributor.authorSydes, Matthew R.-
dc.contributor.authorTombal, Bertrand-
dc.contributor.authorWilliams, Scott-
dc.contributor.authorSweeney, Christopher J.-
dc.date.accessioned2025-02-25T10:58:55Z-
dc.date.available2025-02-25T10:58:55Z-
dc.date.issued2025-
dc.date.submitted2025-02-24T15:55:59Z-
dc.identifier.citationEuropean urology, 87 (2) , p. 217 -224-
dc.identifier.urihttp://hdl.handle.net/1942/45401-
dc.description.abstractBackground and objective: Radiotherapy (RT) and long-term androgen deprivation therapy (ltADT; 18-36 mo) is a standard of care in the treatment of high-risk localized/locoregional prostate cancer (HRLPC). We evaluated the outcomes in patients treated with RT + ltADT to identify which patients have poorer prognosis with standard therapy. Methods: Individual patient data from patients with HRLPC (as defined by any of the following three risk factors [RFs] in the context of cN0 disease-Gleason score >= 8, cT3-4, and prostate-specific antigen [PSA] >20 ng/ml, or cN1 disease) treated with RT and ltADT in randomized controlled trials collated by the Intermediate Clinical Endpoints in Cancer of the Prostate group. The outcome measures of interest were metastasis- free survival (MFS), overall survival (OS), time to metastasis, and prostate cancer- specific mortality. Multivariable Cox and Fine-Gray regression estimated hazard ratios (HRs) for the three RFs and cN1 disease. Key findings and limitations: A total of 3604 patients from ten trials were evaluated, with a median PSA value of 24 ng/ml. Gleason score >= 8 (MFS HR = 1.45; OS HR = 1.42), cN1 disease (MFS HR = 1.86; OS HR = 1.77), cT3-4 disease (MFS HR = 1.28; OS HR = 1.22), and PSA >20 ng/ml (MFS HR = 1.30; OS HR = 1.21) were associated with poorer outcomes. Adjusted 5-yr MFS rates were 83% and 78%, and 10-yr MFS rates were 63% and 53% for patients with one and two to three RFs, respectively; corresponding 10-yr adjusted OS rates were 67% and 60%, respectively. In cN1 patients, adjusted 5- and 10-yr MFS rates were 67% and 36%, respectively, and 10-yr OS was 47%. Conclusions and clinical implications: HRLPC patients with two to three RFs (and cN0) or cN1 disease had the poorest outcomes on RT and ltADT. This will help in counseling patients treated in routine practice and in guiding adjuvant trials in HRLPC. Patient summary: Radiotherapy and long-term hormone therapy are standard treatments for high-risk and locoregional prostate cancer. In this report, we defined prognostic groups within high-risk/locoregional prostate cancer and showed that outcomes to standard therapy are poorest in those with two or more "high-risk"factors or evidence of lymph node involvement. Such patients may therefore be the best candidates for intensification of treatment. (c) 2024 European Association of Urology. Published by Elsevier B.V. All rights are reserved, including those for text and data mining, AI training, and similar technologies.-
dc.description.sponsorshipFunding This work was funded by the Prostate Cancer Foundation Challenge Award, and grants from Astellas Pharma, Pfizer, Janssen Pharmaceuticals, Millennium Pharmaceuticals, Sotio, Bayer, Dendreon, and Sanofi. Acknowledgments: This manuscript was prepared using data from Dataset RTOG-9902 from the NCTN Data Archive of the National Cancer Institute’s (NCI’s) National Clinical Trials Network (NCTN). Data were originally collected from clinical trial NCT00004054. All analyses and conclusions in this manuscript are the sole responsibility of the authors and do not necessarily reflect the opinions or views of the clinical trial investigators, the NCTN, or the NCI.-
dc.language.isoen-
dc.publisherELSEVIER-
dc.rights2024 European Association of Urology. Published by Elsevier B.V. All rights are reserved, including those for text and data mining, AI training, and similar technologies.-
dc.subject.otherHigh-risk prostate cancer-
dc.subject.otherRisk stratification-
dc.subject.otherMetastasis-free survival-
dc.subject.otherOverall survival-
dc.subject.otherRadiotherapy-
dc.subject.otherAndrogen deprivation therapy-
dc.titleRefining Risk Stratification of High-risk and Locoregional Prostate Cancer: A Pooled Analysis of Randomized Trials-
dc.typeJournal Contribution-
dc.identifier.epage224-
dc.identifier.issue2-
dc.identifier.spage217-
dc.identifier.volume87-
local.format.pages8-
local.bibliographicCitation.jcatA1-
dc.description.notesRavi, P (corresponding author), 450 Brookline Ave, Boston, MA 02215 USA.; Sweeney, CJ (corresponding author), Level 9 AHMS Bldg,North Terrace, Adelaide, SA, Australia.-
dc.description.notespraful_ravi@dfci.harvard.edu; christopher.sweeney@adelaide.edu.au-
local.publisher.placeRADARWEG 29, 1043 NX AMSTERDAM, NETHERLANDS-
local.type.refereedRefereed-
local.type.specifiedArticle-
dc.identifier.doi10.1016/j.eururo.2024.04.038-
dc.identifier.pmid38777647-
dc.identifier.isi001416311000001-
dc.contributor.orcidJames, Nicholas/0000-0002-7314-8204; Sydes, Matthew/0000-0002-9323-1371;-
dc.contributor.orcidHalabi, Susan/0000-0003-4135-2777-
local.provider.typewosris-
local.description.affiliation[Ravi, Praful; Xie, Wanling; D'Amico, Anthony] Dana Farber Canc Inst, Boston, MA USA.-
local.description.affiliation[Buyse, Marc] IDDI, Louvain La Neuve, Belgium.-
local.description.affiliation[Buyse, Marc] Hasselt Univ, I BioStat, Hasselt, Belgium.-
local.description.affiliation[Halabi, Susan] Duke Univ, Durham, NC USA.-
local.description.affiliation[Kantoff, Philip W.] Convergent Therapeut, Cambridge, MA USA.-
local.description.affiliation[Sartor, Oliver] Mayo Clin, Rochester, MN USA.-
local.description.affiliation[Attard, Gert] UCL, London, England.-
local.description.affiliation[Clarke, Noel] Christie NHS Fdn Trust, Manchester, England.-
local.description.affiliation[D'Amico, Anthony] Brigham & Womens Hosp, Boston, MA USA.-
local.description.affiliation[Dignam, James] Univ Chicago, Chicago, IL USA.-
local.description.affiliation[James, Nicholas] Inst Canc Res, London, England.-
local.description.affiliation[James, Nicholas] Royal Marsden NHS Fdn Trust, London, England.-
local.description.affiliation[Fizazi, Karim] Univ Paris Saclay, Inst Gustave Roussy, Villejuif, France.-
local.description.affiliation[Gillessen, Silke] Oncol Inst Southern Switzerland, EOC, Bellinzona, Switzerland.-
local.description.affiliation[Gillessen, Silke] Univ Svizzera Italiana, Lugano, Switzerland.-
local.description.affiliation[Parulekar, Wendy] Queens Univ, Kingston, ON, Canada.-
local.description.affiliation[Sandler, Howard] Cedars Sinai Med Ctr, Los Angeles, CA USA.-
local.description.affiliation[Spratt, Daniel E.] Case Western Reserve Univ, Univ Hosp Siedman Canc Ctr, Cleveland, OH USA.-
local.description.affiliation[Sydes, Matthew R.] UCL, Inst Clin Trials & Methodol, MRC Clin Trials Unit UCL, London, England.-
local.description.affiliation[Tombal, Bertrand] Clin Univ St Luc, Brussels, Belgium.-
local.description.affiliation[Williams, Scott] Peter MacCallum Canc Ctr, Melbourne, Australia.-
local.description.affiliation[Sweeney, Christopher J.] Univ Adelaide, South Australian Immunogenom Canc Inst, Adelaide, SA, Australia.-
local.description.affiliation[Kantoff, Philip W.] Mem Sloan Kettering Canc Ctr, New York, NY USA.-
local.description.affiliation[Ravi, Praful] 450 Brookline Ave, Boston, MA 02215 USA.-
local.uhasselt.internationalyes-
item.accessRightsRestricted Access-
item.fullcitationRavi, Praful; Xie, Wanling; BUYSE, Marc; Halabi, Susan; Kantoff, Philip W.; Sartor, Oliver; Attard, Gert; Clarke, Noel; D'Amico, Anthony; Dignam, James; James, Nicholas; Fizazi, Karim; Gillessen, Silke; Parulekar, Wendy; Sandler, Howard; Spratt, Daniel E.; Sydes, Matthew R.; Tombal, Bertrand; Williams, Scott & Sweeney, Christopher J. (2025) Refining Risk Stratification of High-risk and Locoregional Prostate Cancer: A Pooled Analysis of Randomized Trials. In: European urology, 87 (2) , p. 217 -224.-
item.fulltextWith Fulltext-
item.contributorRavi, Praful-
item.contributorXie, Wanling-
item.contributorBUYSE, Marc-
item.contributorHalabi, Susan-
item.contributorKantoff, Philip W.-
item.contributorSartor, Oliver-
item.contributorAttard, Gert-
item.contributorClarke, Noel-
item.contributorD'Amico, Anthony-
item.contributorDignam, James-
item.contributorJames, Nicholas-
item.contributorFizazi, Karim-
item.contributorGillessen, Silke-
item.contributorParulekar, Wendy-
item.contributorSandler, Howard-
item.contributorSpratt, Daniel E.-
item.contributorSydes, Matthew R.-
item.contributorTombal, Bertrand-
item.contributorWilliams, Scott-
item.contributorSweeney, Christopher J.-
crisitem.journal.issn0302-2838-
crisitem.journal.eissn1873-7560-
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