Published online Nov 24, 2015. doi: 10.5410/wjcu.v4.i3.97
Peer-review started: February 22, 2015
First decision: May 13, 2015
Revised: May 29, 2015
Accepted: July 21, 2015
Article in press: July 23, 2015
Published online: November 24, 2015
Processing time: 282 Days and 8.1 Hours
At 13 years of follow-up, the European Randomized Study of Screening for Prostate Cancer shows a 21% decrease in prostate cancer deaths in the prostate-specific antigen-screened group compared to control. This difference increases to 27% when non compliance is taken into account. The benefits of screening compared to control are higher at 28% (compared to 21%) when duration of follow-up ranges between 8 and 12 years. Such data obtained following an average rate of one screening performed once every 5.7 years in quite impressive and strongly supports the use of screening for a successful fight against a cancer which grows to an advanced and non curable stage without any specific sign or symptom.
Core tip: The wide use of prostate-specific antigen for screening of prostate cancer is a major issue preventing the recruitment of true unscreened controls in studies on prostate cancer screening. This is why only studies performed some time ago can meet this requirement of a small contamination of the control group. The European Randomized Study on Screening for Prostate Cancer had a contamination of 23%-40%, thus permitting to see, at 13 years of follow-up, a 21% decrease in prostate cancer deaths in the screened group compared to no screening. The earlier Quebec trial had a contamination of only 7% with a 62% decrease in death from prostate cancer at a median follow-up of 7.9 years. A contamination of 85% of the control group prevented the United States PLCO trial from providing reliable data. The data obtained in the European and Quebec trials are strong arguments for a major positive impact of early diagnosis which needs screening for a successful fight against prostate cancer.