dc.contributor.author | Gillessen, S | |
dc.contributor.author | Attard, G | |
dc.contributor.author | Beer, TM | |
dc.contributor.author | Beltran, H | |
dc.contributor.author | Bossi, A | |
dc.contributor.author | Bristow, R | |
dc.contributor.author | Carver, B | |
dc.contributor.author | Castellano, D | |
dc.contributor.author | Chung, BH | |
dc.contributor.author | Clarke, N | |
dc.contributor.author | Daugaard, G | |
dc.contributor.author | Davis, ID | |
dc.contributor.author | de Bono, J | |
dc.contributor.author | Borges Dos Reis, R | |
dc.contributor.author | Drake, CG | |
dc.contributor.author | Eeles, R | |
dc.contributor.author | Efstathiou, E | |
dc.contributor.author | Evans, CP | |
dc.contributor.author | Fanti, S | |
dc.contributor.author | Feng, F | |
dc.contributor.author | Fizazi, K | |
dc.contributor.author | Frydenberg, M | |
dc.contributor.author | Gleave, M | |
dc.contributor.author | Halabi, S | |
dc.contributor.author | Heidenreich, A | |
dc.contributor.author | Higano, CS | |
dc.contributor.author | James, N | |
dc.contributor.author | Kantoff, P | |
dc.contributor.author | Kellokumpu-Lehtinen, P-L | |
dc.contributor.author | Khauli, RB | |
dc.contributor.author | Kramer, G | |
dc.contributor.author | Logothetis, C | |
dc.contributor.author | Maluf, F | |
dc.contributor.author | Morgans, AK | |
dc.contributor.author | Morris, MJ | |
dc.contributor.author | Mottet, N | |
dc.contributor.author | Murthy, V | |
dc.contributor.author | Oh, W | |
dc.contributor.author | Ost, P | |
dc.contributor.author | Padhani, AR | |
dc.contributor.author | Parker, C | |
dc.contributor.author | Pritchard, CC | |
dc.contributor.author | Roach, M | |
dc.contributor.author | Rubin, MA | |
dc.contributor.author | Ryan, C | |
dc.contributor.author | Saad, F | |
dc.contributor.author | Sartor, O | |
dc.contributor.author | Scher, H | |
dc.contributor.author | Sella, A | |
dc.contributor.author | Shore, N | |
dc.contributor.author | Smith, M | |
dc.contributor.author | Soule, H | |
dc.contributor.author | Sternberg, CN | |
dc.contributor.author | Suzuki, H | |
dc.contributor.author | Sweeney, C | |
dc.contributor.author | Sydes, MR | |
dc.contributor.author | Tannock, I | |
dc.contributor.author | Tombal, B | |
dc.contributor.author | Valdagni, R | |
dc.contributor.author | Wiegel, T | |
dc.contributor.author | Omlin, A | |
dc.date.accessioned | 2017-07-19T14:54:48Z | |
dc.date.issued | 2018-02-01 | |
dc.identifier.citation | European urology, 2018, 73 (2), pp. 178 - 211 | |
dc.identifier.issn | 0302-2838 | |
dc.identifier.uri | https://repository.icr.ac.uk/handle/internal/715 | |
dc.identifier.eissn | 1873-7560 | |
dc.identifier.doi | 10.1016/j.eururo.2017.06.002 | |
dc.description.abstract | BACKGROUND: In advanced prostate cancer (APC), successful drug development as well as advances in imaging and molecular characterisation have resulted in multiple areas where there is lack of evidence or low level of evidence. The Advanced Prostate Cancer Consensus Conference (APCCC) 2017 addressed some of these topics. OBJECTIVE: To present the report of APCCC 2017. DESIGN, SETTING, AND PARTICIPANTS: Ten important areas of controversy in APC management were identified: high-risk localised and locally advanced prostate cancer; "oligometastatic" prostate cancer; castration-naïve and castration-resistant prostate cancer; the role of imaging in APC; osteoclast-targeted therapy; molecular characterisation of blood and tissue; genetic counselling/testing; side effects of systemic treatment(s); global access to prostate cancer drugs. A panel of 60 international prostate cancer experts developed the program and the consensus questions. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: The panel voted publicly but anonymously on 150 predefined questions, which have been developed following a modified Delphi process. RESULTS AND LIMITATIONS: Voting is based on panellist opinion, and thus is not based on a standard literature review or meta-analysis. The outcomes of the voting had varying degrees of support, as reflected in the wording of this article, as well as in the detailed voting results recorded in Supplementary data. CONCLUSIONS: The presented expert voting results can be used for support in areas of management of men with APC where there is no high-level evidence, but individualised treatment decisions should as always be based on all of the data available, including disease extent and location, prior therapies regardless of type, host factors including comorbidities, as well as patient preferences, current and emerging evidence, and logistical and economic constraints. Inclusion of men with APC in clinical trials should be strongly encouraged. Importantly, APCCC 2017 again identified important areas in need of trials specifically designed to address them. PATIENT SUMMARY: The second Advanced Prostate Cancer Consensus Conference APCCC 2017 did provide a forum for discussion and debates on current treatment options for men with advanced prostate cancer. The aim of the conference is to bring the expertise of world experts to care givers around the world who see less patients with prostate cancer. The conference concluded with a discussion and voting of the expert panel on predefined consensus questions, targeting areas of primary clinical relevance. The results of these expert opinion votes are embedded in the clinical context of current treatment of men with advanced prostate cancer and provide a practical guide to clinicians to assist in the discussions with men with prostate cancer as part of a shared and multidisciplinary decision-making process. | |
dc.format | Print-Electronic | |
dc.format.extent | 178 - 211 | |
dc.language | eng | |
dc.language.iso | eng | |
dc.publisher | ELSEVIER SCIENCE BV | |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/4.0 | |
dc.subject | Humans | |
dc.subject | Prostatic Neoplasms | |
dc.subject | Neoplasm Staging | |
dc.subject | Male | |
dc.subject | Practice Guidelines as Topic | |
dc.title | Management of Patients with Advanced Prostate Cancer: The Report of the Advanced Prostate Cancer Consensus Conference APCCC 2017. | |
dc.type | Journal Article | |
dcterms.dateAccepted | 2017-06-01 | |
rioxxterms.versionofrecord | 10.1016/j.eururo.2017.06.002 | |
rioxxterms.licenseref.uri | https://creativecommons.org/licenses/by-nc-nd/4.0 | |
rioxxterms.licenseref.startdate | 2018-02 | |
rioxxterms.type | Journal Article/Review | |
dc.relation.isPartOf | European urology | |
pubs.issue | 2 | |
pubs.notes | Not known | |
pubs.organisational-group | /ICR | |
pubs.organisational-group | /ICR/Primary Group | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Clinical Studies | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Clinical Studies/Prostate Cancer Targeted Therapy Group | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Genetics and Epidemiology | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Genetics and Epidemiology/Oncogenetics | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Molecular Pathology | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Molecular Pathology/Treatment Resistance | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Oncogenetics | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Prostate and Bladder Cancer Research | |
pubs.organisational-group | /ICR/Primary Group/Royal Marsden Clinical Units | |
pubs.organisational-group | /ICR | |
pubs.organisational-group | /ICR/Primary Group | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Clinical Studies | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Clinical Studies/Prostate Cancer Targeted Therapy Group | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Genetics and Epidemiology | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Genetics and Epidemiology/Oncogenetics | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Molecular Pathology | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Molecular Pathology/Treatment Resistance | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Oncogenetics | |
pubs.organisational-group | /ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Prostate and Bladder Cancer Research | |
pubs.organisational-group | /ICR/Primary Group/Royal Marsden Clinical Units | |
pubs.publication-status | Published | |
pubs.volume | 73 | |
pubs.embargo.terms | Not known | |
icr.researchteam | Prostate Cancer Targeted Therapy Group | |
icr.researchteam | Treatment Resistance | |
icr.researchteam | Oncogenetics | |
icr.researchteam | Prostate and Bladder Cancer Research | |
dc.contributor.icrauthor | De Bono, Johann | |
dc.contributor.icrauthor | Eeles, Rosalind | |
dc.contributor.icrauthor | James, Nicholas | |