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BMJ 2007;335:1139 (1 December), doi:10.1136/bmj.39381.436829.BE (published 15 November 2007)
J Athene Lane, senior research fellow1, Joanne Howson, lead research nurse2, Jenny L Donovan, professor1, John R Goepel, consultant histopathologist3, Daniel J Dedman, public health information specialist4, Liz Down, research associate1, Emma L Turner, research associate1, David E Neal, professor of surgical oncology5, Freddie C Hamdy, professor, head of urology and oncology2
1 Department of Social Medicine, University of Bristol, 2 Academic Urology Unit, Section of Oncology, University of Sheffield, Royal Hallamshire Hospital, Sheffield, S10 2JF , 3 Sheffield Teaching Hospitals NHS Foundation Trust, Royal Hallamshire Hospital, 4 North West Public Health Observatory, Liverpool John Moores University, Liverpool, 5 Oncology Centre, Addenbrooke's Hospital, Cambridge
Correspondence to: F C Hamdy f.c.hamdy{at}sheffield.ac.uk
Design Prospective cohort nested within a randomised controlled trial, with two years of follow-up.
Setting Eight general practices in a UK city.
Participants 1299 unselected men aged 45-49.
Intervention Prostate biopsies for participants with a prostate specific antigen level of 1.5 ng/ml or more and the possibility of randomisation to three treatments for those with localised prostate cancer.
Main outcome measures Uptake of testing for prostate specific antigen; positive predictive value of prostate specific antigen; and prevalence of prostate cancer, TNM disease stage, and histological grade (Gleason score).
Results 442 of 1299 men agreed to be tested for prostate specific antigen (34%) and 54 (12%) had a raised level. The positive predictive value for prostate specific antigen was 21.3%. Ten cases of prostate cancer were detected (2.3%) with eight having at least two positive results in biopsy cores and three showing perineural invasion. One tumour was of high volume (cT2c), Gleason score 7, with a positive result on digital rectal examination; nine tumours were cT1c, Gleason score 6, and eight had a negative result on digital rectal examination. Five of the nine eligible participants (55%) agreed to be randomised. No biochemical disease progression in the form of a rising prostate specific antigen level occurred in two years of follow-up.
Conclusions Men younger than 50 will accept testing for prostate cancer but at a much lower rate than older men. Using an age based threshold of 1.5 ng/ml, the prevalence of prostate cancer was similar to that in older men (3.0 ng/ml threshold) and some cancers of potential clinical significance were found.
Trial registration Current Controlled Trials ISRCTN20141297
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