Literature DB >> 19249153

Intermittent androgen deprivation for locally advanced and metastatic prostate cancer: results from a randomised phase 3 study of the South European Uroncological Group.

Fernando E C Calais da Silva1, Aldo V Bono, Peter Whelan, Maurizio Brausi, Anton Marques Queimadelos, Jose A Portillo Martin, Ziya Kirkali, Fernando M V Calais da Silva, Chris Robertson.   

Abstract

BACKGROUND: Few randomised studies have compared intermittent hormonal therapy (IHT) with continuous therapy for the treatment of advanced prostate cancer (PCa).
OBJECTIVE: To determine whether intermittent therapy is associated with a shorter time to progression. DESIGN, SETTING, AND PARTICIPANTS: 766 patients with locally advanced or metastatic PCa received a 3-mo induction treatment. The 626 patients whose prostate-specific antigen (PSA) level decreased to <4 ng/ml or to 80% below the initial value were randomised. INTERVENTION: Patients received cyproterone acetate (CPA) 200mg for 2 wk and then monthly depot injections of a luteinising hormone-releasing hormone (LHRH) analogue plus 200mg of CPA daily during induction. Patients randomised to the intermittent arm ceased treatment, while those randomised to the continuous arm received 200mg of CPA daily plus an LHRH analogue. MEASUREMENTS: Primary outcome measurement was time to subjective or objective progression. Secondary outcomes were survival and quality of life (QoL). Time off therapy in the intermittent arm was also recorded. RESULTS AND LIMITATIONS: 127 patients from the intermittent arm and 107 patients from the continuous arm progressed, with a hazard ratio (HR) of 0.81 (95% confidence interval [CI]: 0.63-1.05, p=0.11). There was no difference in survival, with an HR of 0.99 (95% CI: 0.80-1.23) and 170 deaths in the intermittent arm and 169 deaths in the continuous arm. The greater number of cancer deaths in the intermittent treatment arm (106 vs 84) was balanced by a greater number of cardiovascular deaths in the continuous arm (52 vs 41). Side-effects were more pronounced in the continuous arm. Men treated with intermittent therapy reported better sexual function. Median time off therapy for the intermittent patients was 52 wk (95% CI: 39.4-65.7).
CONCLUSIONS: IHT should be considered for use in routine practice because it is associated with no reduction in survival, no clinically meaningful impairment in QoL, better sexual activity, and considerable economic benefit to the individual and the community.

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Year:  2009        PMID: 19249153     DOI: 10.1016/j.eururo.2009.02.016

Source DB:  PubMed          Journal:  Eur Urol        ISSN: 0302-2838            Impact factor:   20.096


  64 in total

Review 1.  [Intermittent androgen deprivation as therapy for androgen-sensitive prostate cancer. Sense or nonsense?].

Authors:  P Thelen; R-H Ringert; H Loertzer; A Strauß
Journal:  Urologe A       Date:  2012-09       Impact factor: 0.639

2.  Efficacy of intermittent androgen deprivation therapy vs conventional continuous androgen deprivation therapy for advanced prostate cancer: a meta-analysis.

Authors:  Huei-Ting Tsai; David F Penson; Kepher H Makambi; John H Lynch; Stephen K Van Den Eeden; Arnold L Potosky
Journal:  Urology       Date:  2013-08       Impact factor: 2.649

3.  Intermittent androgen deprivation--questions remain.

Authors:  Daniel Keizman; Michael A Carducci
Journal:  Nat Rev Urol       Date:  2009-08       Impact factor: 14.432

4.  Evolution of the clinical presentation of men undergoing radical prostatectomy for high-risk prostate cancer.

Authors:  Phillip M Pierorazio; Ashley E Ross; Misop Han; Jonathan I Epstein; Alan W Partin; Edward M Schaeffer
Journal:  BJU Int       Date:  2011-08-22       Impact factor: 5.588

Review 5.  The role of intermittent androgen deprivation therapy in the management of biochemically recurrent or metastatic prostate cancer.

Authors:  Jasbir Jaswal; Juanita Crook
Journal:  Curr Urol Rep       Date:  2015-03       Impact factor: 3.092

6.  Urological cancer. The benefits of intermittent androgen-deprivation therapy.

Authors:  Timur Mitin; Jason A Efstathiou; William U Shipley
Journal:  Nat Rev Clin Oncol       Date:  2012-11-20       Impact factor: 66.675

7.  Urological cancer: walking the tightrope of survival and quality of life with ADT.

Authors:  Matthew J Resnick
Journal:  Nat Rev Clin Oncol       Date:  2013-05-07       Impact factor: 66.675

8.  Preoperative characteristics of high-Gleason disease predictive of favourable pathological and clinical outcomes at radical prostatectomy.

Authors:  Phillip M Pierorazio; Ashley E Ross; Brian M Lin; Jonathan I Epstein; Misop Han; Patrick C Walsh; Alan W Partin; Christian P Pavlovich; Edward M Schaeffer
Journal:  BJU Int       Date:  2012-02-28       Impact factor: 5.588

9.  PET/CT imaging and the oligometastatic prostate cancer patient: an opportunity for a curative approach with high-dose radiotherapy?

Authors:  Raymond Miralbell; Franz Buchegger
Journal:  Eur J Nucl Med Mol Imaging       Date:  2014-07       Impact factor: 9.236

10.  Influence of serum testosterone on urinary continence and sexual activity in patients undergoing radical prostatectomy for clinically localized prostate cancer.

Authors:  M Gacci; G Corona; G Apolone; A Apolone; M Lanciotti; N Tosi; S Giancane; L Masieri; S Serni; M Maggi; M Carini
Journal:  Prostate Cancer Prostatic Dis       Date:  2010-03-09       Impact factor: 5.554

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