ForsideAZ MedicaOnkologiOptimal predictors of prostate cancer
AstraZeneca nettsteder

Optimal predictors of prostate cancer on repeat prostate biopsy: A prospective study of 1,051 men

  • Percent free PSA was the most accurate predictor of prostate cancer in repeat biopsy specimens
  • Repeat biopsies are recommended in men with percent free PSA <30% or transition zone PSA density 0.26ng/ml/cc.
All urology clinics have their share of patients with benign histology following prostate biopsy who have a persistently raised PSA. Urologists and patients alike wonder what to do about this worrying phenomenon. The information from a number of studies tells us that some of these patients have a persistent cancer and so must get a repeat biopsy with a resultant cancer pick-up rate of approximately 20%.

This study improves on the data from a number of smaller retrospective studies as it is large (1051 patients), prospective and systematic. It shows that by using a specific percent free PSA threshold (33%) the sensitivity of the biopsy can increase to 95% and its use can result in the dramatic reduction in the number of patients requiring repeat biopsy (in excess of 40% reduction).

This kind of improvement in outcome from detection/biopsy would undoubtedly make the lot of the patient and urologist easier and potentially save a considerable amount of money. Perhaps it is time to consider a general move to the use of percent free PSA in UK clinics when this situation arises.

Although the Prostate Specific Antigen (PSA) test is an important biological marker for prostate cancer its use is limited in serum PSA range 4-10ng/ml, as there is considerable overlap of patients with prostate cancer and those with benign disease. However this can mean that a large percentage of patients will undergo unnecessary prostatic biopsy. This paper reports on a prospective study to evaluate the ability of PSA, PSA density, transition zone PSA density and percent free PSA to improve sensitivity and specificity of PSA testing compared to the use of total PSA measurements alone.

Between January 1997 and March 1999 a total of 1051 men (aged 48-77 years), who had undergone repeat prostatic biopsy after initial results were negative for prostate carcinoma, were enrolled into the study. All subject to total serum PSA value between 4-10ng/ml. Blood samples were taken for PSA measurements before any prostate manipulation. All patients underwent digital rectal examination and transrectal ultrasound guided sextant biopsy with 2 additional transition zone biopsies. In 254 patients biopsy specimens were also taken from suspicious areas identified during investigations. Subjects with negative initial biopsy results underwent repeat biopsies after 6 weeks.

In 231 subjects (22%) initial biopsy results were positive for prostate cancer, these men had significantly higher total PSA, PSA density and transitional zone PSA density. The remaining 820 men were diagnosed with benign prostate hyperplasia, and underwent repeat biopsies at 6 weeks, at which point 10% were determined to have prostate cancer. Percent free PSA and transition zone PSA density were most accurate predictors of carcinoma in this group. Assessing sensitivity and specificity it was observed that a cut-off of 30% percent free PSA and 0.26ng/ml/cc transition zone PSA density, would have detected 90% of cancers whilst avoiding 505 unnecessary repeat biopsies. Using receiver operating characteristics (ROC) analysis it was found that when initial and repeat biopsy results were combined, the area under the curve was 82.7% for transition zone PSA density and 74.2% for percent free PSA, making transistion zone PSA density a better predictor of repeat biopsy results.

In the repeat biopsy group and overall (initial plus repeat biopsy group) percent free PSA resulted in a higher rate of cancer detection. It was recommended that percent free PSA and/or transition zone PSA density should be determined in patients with total serum PSA between 4-10ng/ml.

Supported by an educational grant from AstraZeneca

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Publisert 01.11.2001
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