Literature DB >> 19660851

Prostate cancer mortality reduction by prostate-specific antigen-based screening adjusted for nonattendance and contamination in the European Randomised Study of Screening for Prostate Cancer (ERSPC).

Monique J Roobol1, Melissa Kerkhof, Fritz H Schröder, Jack Cuzick, Peter Sasieni, Matti Hakama, Ulf Hakan Stenman, Stefano Ciatto, Vera Nelen, Maciej Kwiatkowski, Marcos Lujan, Hans Lilja, Marco Zappa, Louis Denis, Franz Recker, Antonio Berenguer, Mirja Ruutu, Paula Kujala, Chris H Bangma, Gunnar Aus, Teuvo L J Tammela, Arnauld Villers, Xavier Rebillard, Sue M Moss, Harry J de Koning, Jonas Hugosson, Anssi Auvinen.   

Abstract

BACKGROUND: Prostate-specific antigen (PSA) based screening for prostate cancer (PCa) has been shown to reduce prostate specific mortality by 20% in an intention to screen (ITS) analysis in a randomised trial (European Randomised Study of Screening for Prostate Cancer [ERSPC]). This effect may be diluted by nonattendance in men randomised to the screening arm and contamination in men randomised to the control arm.
OBJECTIVE: To assess the magnitude of the PCa-specific mortality reduction after adjustment for nonattendance and contamination. DESIGN, SETTING, AND PARTICIPANTS: We analysed the occurrence of PCa deaths during an average follow-up of 9 yr in 162,243 men 55-69 yr of age randomised in seven participating centres of the ERSPC. Centres were also grouped according to the type of randomisation (ie, before or after informed written consent). INTERVENTION: Nonattendance was defined as nonattending the initial screening round in ERSPC. The estimate of contamination was based on PSA use in controls in ERSPC Rotterdam. MEASUREMENTS: Relative risks (RRs) with 95% confidence intervals (CIs) were compared between an ITS analysis and analyses adjusting for nonattendance and contamination using a statistical method developed for this purpose. RESULTS AND LIMITATIONS: In the ITS analysis, the RR of PCa death in men allocated to the intervention arm relative to the control arm was 0.80 (95% CI, 0.68-0.96). Adjustment for nonattendance resulted in a RR of 0.73 (95% CI, 0.58-0.93), and additional adjustment for contamination using two different estimates led to estimated reductions of 0.69 (95% CI, 0.51-0.92) to 0.71 (95% CI, 0.55-0.93), respectively. Contamination data were obtained through extrapolation of single-centre data. No heterogeneity was found between the groups of centres.
CONCLUSIONS: PSA screening reduces the risk of dying of PCa by up to 31% in men actually screened. This benefit should be weighed against a degree of overdiagnosis and overtreatment inherent in PCa screening.

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Year:  2009        PMID: 19660851     DOI: 10.1016/j.eururo.2009.07.018

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


  49 in total

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2.  What is the true mortality benefit of prostate-specific antigen screening?

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3.  What is the true number needed to screen and treat to save a life with prostate-specific antigen testing?

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4.  Prostate-specific antigen screening can be beneficial to younger and at-risk men.

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5.  The number of tPSA tests continues to rise and variation in testing practices persists: a survey of laboratory services in Ireland 2008-2010.

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6.  Expected population impacts of discontinued prostate-specific antigen screening.

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8.  Prostate cancer screening characteristics in men with BRCA1/2 mutations attending a high-risk prevention clinic.

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9.  Reducing prostate cancer racial disparity: evidence for aggressive early prostate cancer PSA testing of African American men.

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10.  Overdetection, overtreatment and costs in prostate-specific antigen screening for prostate cancer.

Authors:  E A M Heijnsdijk; A der Kinderen; E M Wever; G Draisma; M J Roobol; H J de Koning
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