TY - JOUR
T1 - Screening for prostate cancer (Review)
AU - Ilic, Dragan
AU - Neuberger, Molly
AU - Djulbegovic, Mia
AU - Dahm, Phillip
PY - 2013
Y1 - 2013
N2 - Prostate cancer is one of the most prevalent forms of cancer in men worldwide. Screening for prostate cancer implies that diagnostic
tests be performed in the absence of any symptoms or indications of disease. These tests include the digital rectal examination (DRE),
the prostate-specific antigen (PSA) blood test and transrectal ultrasound (TRUS) guided biopsy. Screening aims to identify cancers
at an early and treatable stage, therefore increasing the chances of successful treatment while also improving a patient?s future quality
of life. This review identified five relevant studies, comprised of 341,342 participants in total. Two of the studies were assessed to
be of low risk of bias, whilst the remaining three had more substantive methodological weaknesses. Meta-analysis of all five included
studies demonstrated no statistically significant reduction in prostate cancer-specific mortality (risk ratio (RR) 1.00, 95 confidence
interval (CI) 0.86 to 1.17). Meta-analysis of the two low risk of bias studies indicated no significant reduction in prostate cancerspecific
mortality (RR 0.96, 95 CI 0.70 to 1.30). Only one study included in this review (ERSPC) reported a significant 21 relative
reduction (95 CI 31 to 8 ) in prostate cancer-specific mortality in a pre-specified subgroup of men. These results were primarily
driven by two countries within the ERSPC study that had very high prostate cancer mortality rates and unusually large reduction
Screening for prostate cancer (Review) 2
Copyright ? 2013 The Cochrane Collaboration. Published by JohnWiley Sons, Ltd.
estimates. Among men aged 55 to 69 years in the ERSPC study, the study authors reported that 1055 men would need to be screened
to prevent one additional death from prostate cancer during a median follow-up duration of 11 years. Harms included overdiagnosis
and harms associated with overtreatment, including false-positive results for the PSA test, infection, bleeding, and pain associated with
subsequent biopsy.
AB - Prostate cancer is one of the most prevalent forms of cancer in men worldwide. Screening for prostate cancer implies that diagnostic
tests be performed in the absence of any symptoms or indications of disease. These tests include the digital rectal examination (DRE),
the prostate-specific antigen (PSA) blood test and transrectal ultrasound (TRUS) guided biopsy. Screening aims to identify cancers
at an early and treatable stage, therefore increasing the chances of successful treatment while also improving a patient?s future quality
of life. This review identified five relevant studies, comprised of 341,342 participants in total. Two of the studies were assessed to
be of low risk of bias, whilst the remaining three had more substantive methodological weaknesses. Meta-analysis of all five included
studies demonstrated no statistically significant reduction in prostate cancer-specific mortality (risk ratio (RR) 1.00, 95 confidence
interval (CI) 0.86 to 1.17). Meta-analysis of the two low risk of bias studies indicated no significant reduction in prostate cancerspecific
mortality (RR 0.96, 95 CI 0.70 to 1.30). Only one study included in this review (ERSPC) reported a significant 21 relative
reduction (95 CI 31 to 8 ) in prostate cancer-specific mortality in a pre-specified subgroup of men. These results were primarily
driven by two countries within the ERSPC study that had very high prostate cancer mortality rates and unusually large reduction
Screening for prostate cancer (Review) 2
Copyright ? 2013 The Cochrane Collaboration. Published by JohnWiley Sons, Ltd.
estimates. Among men aged 55 to 69 years in the ERSPC study, the study authors reported that 1055 men would need to be screened
to prevent one additional death from prostate cancer during a median follow-up duration of 11 years. Harms included overdiagnosis
and harms associated with overtreatment, including false-positive results for the PSA test, infection, bleeding, and pain associated with
subsequent biopsy.
UR - http://onlinelibrary.wiley.com/doi/10.1002/14651858.CD004720.pub3/pdf
U2 - 10.1002/14651858.CD004720.pub3
DO - 10.1002/14651858.CD004720.pub3
M3 - Article
SN - 1469-493X
VL - 2013
SP - 1
EP - 78
JO - Cochrane Database of Systematic Reviews
JF - Cochrane Database of Systematic Reviews
IS - 1
ER -