Testosterone Measurement in Patients with Prostate Cancer

被引:34
作者
Schulman, Claude C. [1 ,2 ]
Irani, Jacques [3 ]
Morote, Juan [4 ]
Schalken, Jack A. [5 ]
Montorsi, Francesco [6 ]
Chlosta, Piotr L. [7 ]
Heidenreich, Axel [8 ]
机构
[1] Edith Cavell Clin, Dept Urol, B-1180 Brussels, Belgium
[2] Univ Brussels, Brussels, Belgium
[3] Hop Miletrie, Serv Urol, Poitiers, France
[4] Univ Autonoma Barcelona, Vall dHebron Hosp, Dept Urol, E-08193 Barcelona, Spain
[5] Radboud Univ Nijmegen, Med Ctr, Dept Urol, NL-6525 ED Nijmegen, Netherlands
[6] Univ Vita Salute San Raffaele, Dept Urol, Milan, Italy
[7] Inst Oncol, Dept Urol, Kielce, Poland
[8] Rhein Westfal TH Aachen, Dept Urol, Aachen, Germany
关键词
Androgen deprivation therapy; Androgen receptor; Luteinising hormone-releasing hormone agonist; Prostate cancer; Testosterone measurement; ANDROGEN-DEPRIVATION THERAPY; LOW SERUM TESTOSTERONE; RADICAL PROSTATECTOMY; REPLACEMENT THERAPY; TREATMENT FAILURE; HORMONE AGONISTS; RECEPTOR; CASTRATION; RISK; INTERMITTENT;
D O I
10.1016/j.eururo.2010.04.001
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Context: Serum testosterone measurement has no widely accepted place in the management of patients with prostate cancer (PCa). However, several potential clinical applications of serum testosterone determination can be envisaged. Objective: To review the role of testosterone and the androgen axis in the natural history of PCa and evaluate the evidence for the clinical application of serum testosterone measurement in patient screening, diagnosis, and management. Evidence acquisition: A Medline search retrieved original research and review articles relating to the androgen axis in PCa and the use of testosterone measurement for (1) assessing PCa risk in the general population, (2) adding to the specificity of prostate-specific antigen (PSA) testing, (3) determining tumour aggressiveness, (4) assessing the efficacy of androgen-deprivation therapy (ADT), and (5) optimising the scheduling of intermittent ADT. Relevant data were reviewed during a roundtable discussion, and consensus recommendations were agreed. Evidence synthesis: A body of data implicates the androgen axis in PCa throughout its natural history. Based on current evidence, serum testosterone measurement cannot be recommended for determining PCa risk, increasing specificity of PSA testing, or assessing tumour aggressiveness. In contrast, for patients receiving ADT, there is a clear rationale for serum testosterone monitoring to ensure that castration levels are achieved. Practical recommendations for testosterone measurement during ADT are outlined. If PSA is rising while on ADT, castration levels of serum testosterone must be demonstrated before hormonal independence can be assumed. Serum testosterone levels might be considered an additional trigger for therapy reinitiation in intermittent ADT schedules. Finally, future prospective studies should further evaluate the potential relevance of testosterone measurement as an independent assessment of prognosis and treatment decision in different disease stages. Conclusions: As a therapeutic target, serum testosterone levels should be monitored to verify response to ADT and confirm suspected castration independence. (C) 2010 European Association of Urology. Published by Elsevier B. V. All rights reserved.
引用
收藏
页码:65 / 74
页数:10
相关论文
共 69 条
[1]   FURTHER ANALYSES FROM THE REDUCE PROSTATE CANCER RISK REDUCTION TRIAL [J].
Andriole, Gerald ;
Bostwick, David ;
Brawley, Otis ;
Gomella, Leonard ;
Marberger, Michael ;
Montorsi, Francesco ;
Pettaway, Curtis ;
Tammela, Teuvo ;
Teloken, Claudio ;
Tindall, Donald ;
Teloken, Claudio ;
Tindall, Donald ;
Somerville, Matthew ;
Rittmaster, Roger .
JOURNAL OF UROLOGY, 2009, 181 (04) :555-555
[2]   TREATMENT FAILURE IS ASSOCIATED WITH DIFFERENT DOSING REGIMENS OF LEUTINIZING HORMONE RELEASING HORMONE AGONIST THERAPY FOR PROSTATE CANCER [J].
Blumberg, Jeremy M. ;
Kwon, Eric ;
Cheetham, T. Craig ;
Niu, Fang ;
Jacobsen, Steven J. ;
Shapiro, Charles E. ;
Williams, Stephen G. ;
Chien, Gary W. .
JOURNAL OF UROLOGY, 2009, 181 (04) :96-97
[3]   The role of intermittent androgen deprivation in prostate cancer [J].
Boccon-Gibod, Laurent ;
Hammerer, Peter ;
Madersbacher, Stephan ;
Mottet, Nicolas ;
Prayer-Galetti, Tommaso ;
Tunn, Ulf .
BJU INTERNATIONAL, 2007, 100 (04) :738-743
[4]   Intermittent Androgen Deprivation for Locally Advanced and Metastatic Prostate Cancer: Results from a Randomised Phase 3 Study of the South European Uroncological Group [J].
Calais da Silva, Fernando E. C. ;
Bono, Aldo V. ;
Whelan, Peter ;
Brausi, Maurizio ;
Marques Queimadelos, Anton ;
Portillo Martin, Jose A. ;
Kirkali, Ziya ;
Calais da Silva, Fernando M. V. ;
Robertson, Chris .
EUROPEAN UROLOGY, 2009, 55 (06) :1269-1277
[5]   Getting over testosterone: Postulating a fresh start for etiologic studies of prostate cancer [J].
Carpenter, William R. ;
Robinson, Whitney R. ;
Godley, Paul A. .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2008, 100 (03) :158-U5
[6]   A mechanism for hormone-independent prostate cancer through modulation of androgen receptor signaling by the HER-2/neu tyrosine kinase [J].
Craft, N ;
Shostak, Y ;
Carey, M ;
Sawyers, CL .
NATURE MEDICINE, 1999, 5 (03) :280-285
[7]   Mechanisms of androgen-refractory prostate cancer. [J].
Debes, JD ;
Tindall, DJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (15) :1488-1490
[8]   Androgen receptor structural and functional elements: Role and regulation in prostate cancer [J].
Dehm, Scott M. ;
Tindall, Donald J. .
MOLECULAR ENDOCRINOLOGY, 2007, 21 (12) :2855-2863
[9]   TESTOSTERONE AND 5-ALPHA-DIHYDROTESTOSTERONE INTERACT DIFFERENTLY WITH THE ANDROGEN RECEPTOR TO ENHANCE TRANSCRIPTION OF THE MMTV-CAT REPORTER GENE [J].
DESLYPERE, JP ;
YOUNG, M ;
WILSON, JD ;
MCPHAUL, MJ .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1992, 88 (1-3) :15-22
[10]   Obesity and prostate cancer: Making sense out of apparently conflicting data [J].
Freedland, Stephen J. ;
Platz, Elizabeth A. .
EPIDEMIOLOGIC REVIEWS, 2007, 29 :88-97