Catalona W J, Smith D S, Wolfert R L, Wang T J, Rittenhouse H G, Ratliff T L, Nadler R B
Department of Surgery, Washington University School of Medicine, St Louis, MO, USA.
JAMA. 1995 Oct 18;274(15):1214-20.
To evaluate measurement of percentage of free prostate-specific antigen (PSA) in serum to improve the specificity of prostate cancer screening in men with serum PSA levels between 4.1 and 10.0 ng/mL.
Retrospective, nonrandomized analysis using a research assay for measuring free PSA in frozen serum from men with a spectrum of prostate sizes and digital rectal examination results.
General community outpatient prostate cancer screening program at a university center.
One hundred thirteen men aged 50 years or older, 99% of whom were white, with serum PSA concentrations of 4.1 to 10.0 ng/mL, including 63 men with histologically confirmed benign prostatic hyperplasia, 30 with prostate cancer with an enlarged gland, and 20 with cancer with a normal-sized gland. All study volunteers had undergone prostatic ultrasonography and biopsy.
Percentage of free PSA in serum and percentage of free PSA cutoff that maintained at least 90% sensitivity for prostate cancer detection.
Median percentage of free PSA was 9.2% in men with cancer and a normal-sized gland, 15.9% in men with cancer and an enlarged gland, and 18.8% in men with benign prostatic hyperplasia (P < .001). The percentage of free PSA cutoff was higher in men with an enlarged gland and in those with a palpably benign gland. In men with an enlarged, palpably benign gland, a free PSA cutoff of 23.4% or lower detected at least 90% of cancers and would have eliminated 31.3% of negative biopsies.
Measurement of percentage of free serum PSA improves specificity of prostate cancer screening in selected men with elevated total serum PSA levels and can reduce unnecessary prostate biopsies with minimal effects on the cancer detection rate; however, further studies are needed to define optimal cutoffs. Final evaluation of PSA screening also must consider the ability of current treatments to improve the prognosis of screen-detected prostate cancer.
评估血清中游离前列腺特异性抗原(PSA)百分比的测定,以提高血清PSA水平在4.1至10.0 ng/mL之间男性前列腺癌筛查的特异性。
采用研究检测法对不同前列腺大小和直肠指检结果男性的冻存血清中游离PSA进行测量的回顾性、非随机分析。
大学中心的普通社区门诊前列腺癌筛查项目。
113名50岁及以上男性,其中99%为白人,血清PSA浓度为4.1至10.0 ng/mL,包括63名经组织学证实为良性前列腺增生的男性、30名前列腺癌且腺体增大的男性以及20名前列腺癌且腺体大小正常的男性。所有研究志愿者均接受了前列腺超声检查和活检。
血清中游离PSA的百分比以及维持前列腺癌检测至少90%敏感性的游离PSA临界值百分比。
前列腺癌且腺体大小正常的男性中游离PSA的中位数百分比为9.2%,前列腺癌且腺体增大的男性中为15.9%,良性前列腺增生的男性中为18.8%(P <.001)。游离PSA临界值百分比在腺体增大的男性和可触及为良性腺体的男性中更高。在腺体增大且可触及为良性腺体的男性中,游离PSA临界值为23.4%或更低可检测出至少90%的癌症,且可减少31.3%的阴性活检。
测定血清游离PSA百分比可提高特定血清总PSA水平升高男性前列腺癌筛查的特异性,并可减少不必要的前列腺活检,对癌症检出率影响最小;然而,需要进一步研究来确定最佳临界值。PSA筛查的最终评估还必须考虑当前治疗改善筛查发现的前列腺癌预后的能力。