Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/22737
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dc.contributor.authorMoris, Lisa-
dc.contributor.authorCumberbatch, Marcus G-
dc.contributor.authorVan den Broeck, Thomas-
dc.contributor.authorGandaglia, Giorgio-
dc.contributor.authorFossati, Nicola-
dc.contributor.authorKelly, Brian-
dc.contributor.authorPal, Raj-
dc.contributor.authorBriers, Erik-
dc.contributor.authorCornford, Philip-
dc.contributor.authorDe Santis, Maria-
dc.contributor.authorFanti, Stefano-
dc.contributor.authorGillessen, Silke-
dc.contributor.authorGrummet, Jeremy P-
dc.contributor.authorHenry, Ann M-
dc.contributor.authorLam, Thomas B L-
dc.contributor.authorLardas, Michael-
dc.contributor.authorLiew, Matthew-
dc.contributor.authorMason, Malcolm D-
dc.contributor.authorOmar, Muhammad Imran-
dc.contributor.authorRouvière, Olivier-
dc.contributor.authorSchoots, Ivo G-
dc.contributor.authorTilki, Derya-
dc.contributor.authorvan den Bergh, Roderick C N-
dc.contributor.authorvan Der Kwast, Theodorus H-
dc.contributor.authorvan Der Poel, Henk G-
dc.contributor.authorWillemse, Peter-Paul M-
dc.contributor.authorYuan, Cathy Y-
dc.contributor.authorKonety, Badrinath-
dc.contributor.authorDorff, Tanya-
dc.contributor.authorJain, Suneil-
dc.contributor.authorMottet, Nicolas-
dc.contributor.authorWiegel, Thomas-
dc.date2020-03-04-
dc.date.accessioned2020-03-10T22:06:18Z-
dc.date.available2020-03-10T22:06:18Z-
dc.date.issued2020-05-
dc.identifier.citationEuropean Urology 2020; 77(5): 614-627-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/22737-
dc.description.abstractThe optimal treatment for men with high-risk localized or locally advanced prostate cancer (PCa) remains unknown. To perform a systematic review of the existing literature on the effectiveness of the different primary treatment modalities for high-risk localized and locally advanced PCa. The primary oncological outcome is the development of distant metastases at ≥5 yr of follow-up. Secondary oncological outcomes are PCa-specific mortality, overall mortality, biochemical recurrence, and need for salvage treatment with ≥5 yr of follow-up. Nononcological outcomes are quality of life (QoL), functional outcomes, and treatment-related side effects reported. Medline, Medline In-Process, Embase, and the Cochrane Central Register of Randomized Controlled Trials were searched. All comparative (randomized and nonrandomized) studies published between January 2000 and May 2019 with at least 50 participants in each arm were included. Studies reporting on high-risk localized PCa (International Society of Urologic Pathologists [ISUP] grade 4-5 [Gleason score {GS} 8-10] or prostate-specific antigen [PSA] >20 ng/ml or ≥ cT2c) and/or locally advanced PCa (any PSA, cT3-4 or cN+, any ISUP grade/GS) or where subanalyses were performed on either group were included. The following primary local treatments were mandated: radical prostatectomy (RP), external beam radiotherapy (EBRT) (≥64 Gy), brachytherapy (BT), or multimodality treatment combining any of the local treatments above (±any systemic treatment). Risk of bias (RoB) and confounding factors were assessed for each study. A narrative synthesis was performed. Overall, 90 studies met the inclusion criteria. RoB and confounding factors revealed high RoB for selection, performance, and detection bias, and low RoB for correction of initial PSA and biopsy GS. When comparing RP with EBRT, retrospective series suggested an advantage for RP, although with a low level of evidence. Both RT and RP should be seen as part of a multimodal treatment plan with possible addition of (postoperative) RT and/or androgen deprivation therapy (ADT), respectively. High levels of evidence exist for EBRT treatment, with several randomized clinical trials showing superior outcome for adding long-term ADT or BT to EBRT. No clear cutoff can be proposed for RT dose, but higher RT doses by means of dose escalation schemes result in an improved biochemical control. Twenty studies reported data on QoL, with RP resulting mainly in genitourinary toxicity and sexual dysfunction, and EBRT in bowel problems. Based on the results of this systematic review, both RP as part of multimodal treatment and EBRT + long-term ADT can be recommended as primary treatment in high-risk and locally advanced PCa. For high-risk PCa, EBRT + BT can also be offered despite more grade 3 toxicity. Interestingly, for selected patients, for example, those with higher comorbidity, a shorter duration of ADT might be an option. For locally advanced PCa, EBRT + BT shows promising result but still needs further validation. In this setting, it is important that patients are aware that the offered therapy will most likely be in the context a multimodality treatment plan. In particular, if radiation is used, the combination of local with systemic treatment provides the best outcome, provided the patient is fit enough to receive both. Until the results of the SPCG15 trial are known, the optimal local treatment remains a matter of debate. Patients should at all times be fully informed about all available options, and the likelihood of a multimodal approach including the potential side effects of both local and systemic treatment. We reviewed the literature to see whether the evidence from clinical studies would tell us the best way of curing men with aggressive prostate cancer that had not spread to other parts of the body such as lymph glands or bones. Based on the results of this systematic review, there is good evidence that both surgery and radiation therapy are good treatment options, in terms of prolonging life and preserving quality of life, provided they are combined with other treatments. In the case of surgery this means including radiotherapy (RT), and in the case of RT this means either hormonal therapy or combined RT and brachytherapy.-
dc.language.isoeng-
dc.subjectBrachytherapy-
dc.subjectExternal beam radiotherapy-
dc.subjectLocalized-
dc.subjectLocally advanced-
dc.subjectModality treatment-
dc.subjectPrimary therapy-
dc.subjectProstate cancer-
dc.subjectRadical prostatectomy-
dc.subjectSystematic review-
dc.subjectSystemic treatment-
dc.titleBenefits and Risks of Primary Treatments for High-risk Localized and Locally Advanced Prostate Cancer: An International Multidisciplinary Systematic Review.-
dc.typeJournal Article-
dc.identifier.journaltitleEuropean urology-
dc.identifier.affiliationAcademic Urology Unit, University of Aberdeen, Aberdeen, UKen
dc.identifier.affiliationLaboratory of Molecular Endocrinology, KU Leuven, Leuven, Belgium-
dc.identifier.affiliationDepartment of Urology, Aberdeen Royal Infirmary, Aberdeen, UKen
dc.identifier.affiliationDepartment of Medical Oncology and Developmental Therapeutics, City of Hope, Duarte, CA, USAen
dc.identifier.affiliationDepartment of Urology, University Hospital Hamburg-Eppendorf, Hamburg, Germanyen
dc.identifier.affiliationMartini-Klinik Prostate Cancer Center, University Hospital Hamburg-Eppendorf, Hamburg, Germanyen
dc.identifier.affiliationDivision of Cancer Sciences, University of Manchester and The Christie, Manchester, UKen
dc.identifier.affiliationDepartment of Medical Oncology and Haematology, Cantonal Hospital St. Gallen, University of Bern, Bern, Switzerlanden
dc.identifier.affiliationCentre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, UKen
dc.identifier.affiliationDepartment of Urology, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationNorthern Ireland Cancer Centre, Belfast Health and Social Care Trust, Belfast, UKen
dc.identifier.affiliationHospices Civils de Lyon, Department of Urinary and Vascular Imaging, Hôpital Edouard Herriot, Lyon, Franceen
dc.identifier.affiliationFaculté de Médecine Lyon Est, Université Lyon 1, Université de Lyon, Lyon, Franceen
dc.identifier.affiliationDepartment of Medicine, University of Southern California (USC) Keck School of Medicine and Norris Comprehensive Cancer Center (NCCC), Los Angeles, CA, USAen
dc.identifier.affiliationAcademic Urology Unit, University of Sheffield, Sheffield, UK-
dc.identifier.affiliationDepartment of Surgery, Central Clinical School, Monash University, Australiaen
dc.identifier.affiliationDepartment of Urology, University Hospitals Leuven, Leuven, Belgium-
dc.identifier.affiliationUnit of Urology, Division of Oncology, Urological Research Institute, IRCCS Ospedale San Raffaele, Milan, Italy-
dc.identifier.affiliationBristol Urological Institute, Southmead Hospital, Bristol, UK-
dc.identifier.affiliationPatient Advocate, Hasselt, Belgium-
dc.identifier.affiliationRoyal Liverpool and Broadgreen Hospitals NHS Trust, Liverpool, UK-
dc.identifier.affiliationDepartment of Urology, Charité University Hospital, Berlin, Germany-
dc.identifier.affiliationDepartment of Nuclear Medicine, Policlinico S. Orsola, University of Bologna, Italy-
dc.identifier.affiliationLeeds Cancer Centre, St. James's University Hospital and University of Leeds, Leeds, UK-
dc.identifier.affiliationDepartment of Urology, Leto Hospital, Athens, Greece-
dc.identifier.affiliationDepartment of Urology, Wrightington, Wigan and Leigh NHS Foundation Trust, Wigan, UK-
dc.identifier.affiliationDivision of Cancer & Genetics, School of Medicine Cardiff University, Velindre Cancer Centre, Cardiff, UK-
dc.identifier.affiliationAcademic Urology Unit, University of Aberdeen, Aberdeen, UK-
dc.identifier.affiliationDepartment of Radiology & Nuclear Medicine, Erasmus MC University Medical Center, Rotterdam, The Netherlands-
dc.identifier.affiliationDepartment of Urology, Antonius Hospital, Utrecht, The Netherlands-
dc.identifier.affiliationDepartment of Pathology, Erasmus MC University Medical Center, Rotterdam, The Netherlands-
dc.identifier.affiliationDepartment of Urology, Netherlands Cancer Institute, Amsterdam, The Netherlands-
dc.identifier.affiliationDepartment of Oncological Urology, University Medical Center, Utrecht Cancer Center, Utrecht, The Netherlands-
dc.identifier.affiliationDepartment of Medicine, Health Science Centre, McMaster University, Hamilton, ON, Canada-
dc.identifier.affiliationUniversity of Minnesota, Minneapolis, MN, USA-
dc.identifier.affiliationDepartment of Urology, University Hospital, St. Etienne, France-
dc.identifier.affiliationDepartment of Radiation Oncology, University Hospital Ulm, Ulm, Germany-
dc.identifier.doi10.1016/j.eururo.2020.01.033-
dc.identifier.pubmedid32146018-
dc.type.austinJournal Article-
dc.type.austinReview-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
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