Non-metastatic castrate-resistant prostate cancer: a call for improved guidance on clinical management

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Non-metastatic castrate-resistant prostate cancer: a call for improved guidance on clinical management. / Rozet, Francois; Roumeguère, Thierry; Spahn, Martin; Beyersdorff, Dirk; Hammerer, Peter.

in: WORLD J UROL, Jahrgang 34, Nr. 11, 11.2016, S. 1505-1513.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

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@article{ddb048fa31fd4b248790fa3d3bbbf71e,
title = "Non-metastatic castrate-resistant prostate cancer: a call for improved guidance on clinical management",
abstract = "BACKGROUND: Guidelines on the clinical management of non-metastatic castrate-resistant prostate cancer (nmCRPC) generally focus on the need to continue androgen deprivation therapy and enrol patients into clinical trials of investigational agents. This guidance reflects the lack of clinical trial data with established agents in the nmCRPC patient population and the need for trials of new agents.AIM: To review the evidence base and consider ways of improving the management of nmCRPC.CONCLUSION: Upon the development of castrate resistance, it is essential to rule out the presence of metastases or micrometastases by optimising the use of bone scans and possibly newer procedures and techniques. When nmCRPC is established, management decisions should be individualised according to risk, but risk stratification in this diverse population is poorly defined. Currently, prostate-specific antigen (PSA) levels and PSA doubling time remain the best method of assessing the risk of progression and response to treatment in nmCRPC. However, optimising imaging protocols can also help assess the changing metastatic burden in patients with CRPC. Clinical trials of novel agents in nmCRPC are limited and have problems with enrolment, and therefore, improved risk stratification and imaging may be crucial to the improved management. The statements presented in this paper, reflecting the views of the authors, provide a discussion of the most recent evidence in nmCRPC and provide some advice on how to ensure these patients receive the best management available. However, there is an urgent need for more data on the management of nmCRPC.",
author = "Francois Rozet and Thierry Roumegu{\`e}re and Martin Spahn and Dirk Beyersdorff and Peter Hammerer",
year = "2016",
month = nov,
doi = "10.1007/s00345-016-1803-9",
language = "English",
volume = "34",
pages = "1505--1513",
journal = "WORLD J UROL",
issn = "0724-4983",
publisher = "Springer",
number = "11",

}

RIS

TY - JOUR

T1 - Non-metastatic castrate-resistant prostate cancer: a call for improved guidance on clinical management

AU - Rozet, Francois

AU - Roumeguère, Thierry

AU - Spahn, Martin

AU - Beyersdorff, Dirk

AU - Hammerer, Peter

PY - 2016/11

Y1 - 2016/11

N2 - BACKGROUND: Guidelines on the clinical management of non-metastatic castrate-resistant prostate cancer (nmCRPC) generally focus on the need to continue androgen deprivation therapy and enrol patients into clinical trials of investigational agents. This guidance reflects the lack of clinical trial data with established agents in the nmCRPC patient population and the need for trials of new agents.AIM: To review the evidence base and consider ways of improving the management of nmCRPC.CONCLUSION: Upon the development of castrate resistance, it is essential to rule out the presence of metastases or micrometastases by optimising the use of bone scans and possibly newer procedures and techniques. When nmCRPC is established, management decisions should be individualised according to risk, but risk stratification in this diverse population is poorly defined. Currently, prostate-specific antigen (PSA) levels and PSA doubling time remain the best method of assessing the risk of progression and response to treatment in nmCRPC. However, optimising imaging protocols can also help assess the changing metastatic burden in patients with CRPC. Clinical trials of novel agents in nmCRPC are limited and have problems with enrolment, and therefore, improved risk stratification and imaging may be crucial to the improved management. The statements presented in this paper, reflecting the views of the authors, provide a discussion of the most recent evidence in nmCRPC and provide some advice on how to ensure these patients receive the best management available. However, there is an urgent need for more data on the management of nmCRPC.

AB - BACKGROUND: Guidelines on the clinical management of non-metastatic castrate-resistant prostate cancer (nmCRPC) generally focus on the need to continue androgen deprivation therapy and enrol patients into clinical trials of investigational agents. This guidance reflects the lack of clinical trial data with established agents in the nmCRPC patient population and the need for trials of new agents.AIM: To review the evidence base and consider ways of improving the management of nmCRPC.CONCLUSION: Upon the development of castrate resistance, it is essential to rule out the presence of metastases or micrometastases by optimising the use of bone scans and possibly newer procedures and techniques. When nmCRPC is established, management decisions should be individualised according to risk, but risk stratification in this diverse population is poorly defined. Currently, prostate-specific antigen (PSA) levels and PSA doubling time remain the best method of assessing the risk of progression and response to treatment in nmCRPC. However, optimising imaging protocols can also help assess the changing metastatic burden in patients with CRPC. Clinical trials of novel agents in nmCRPC are limited and have problems with enrolment, and therefore, improved risk stratification and imaging may be crucial to the improved management. The statements presented in this paper, reflecting the views of the authors, provide a discussion of the most recent evidence in nmCRPC and provide some advice on how to ensure these patients receive the best management available. However, there is an urgent need for more data on the management of nmCRPC.

U2 - 10.1007/s00345-016-1803-9

DO - 10.1007/s00345-016-1803-9

M3 - SCORING: Journal article

C2 - 26988552

VL - 34

SP - 1505

EP - 1513

JO - WORLD J UROL

JF - WORLD J UROL

SN - 0724-4983

IS - 11

ER -