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人腺激肽释放酶与游离前列腺特异性抗原(PSA)的联合检测可提高总PSA中度升高患者前列腺癌与良性前列腺增生之间的鉴别能力。

The combination of human glandular kallikrein and free prostate-specific antigen (PSA) enhances discrimination between prostate cancer and benign prostatic hyperplasia in patients with moderately increased total PSA.

作者信息

Magklara A, Scorilas A, Catalona W J, Diamandis E P

机构信息

Department of Pathology and Laboratory Medicine, Mount Sinai Hospital, Toronto, Ontario, Canada M5G 1X5.

出版信息

Clin Chem. 1999 Nov;45(11):1960-6.

Abstract

BACKGROUND

Prostate-specific antigen (PSA) is the most reliable tumor marker available and is widely used for the diagnosis and management of prostate cancer. Unfortunately, PSA cannot distinguish efficiently between benign and malignant disease of the prostate, especially within the range of 4-10 microg/L. Among the refinements developed to enhance PSA specificity is the free/total PSA ratio, which is useful in discriminating between the two diseases within the diagnostic "gray zone". Recent data indicate that human glandular kallikrein (hK2), a protein with high homology to PSA, may be an additional serum marker for the diagnosis and monitoring of prostate cancer.

METHODS

We analyzed 206 serum samples (all before treatment was initiated) from men with histologically confirmed benign prostatic hyperplasia (n = 100) or prostatic carcinoma (n = 106) with total PSA in the range of 2.5-10 microg/L. Total and free PSA and hK2 were measured with noncompetitive immunological procedures. Statistical analysis was performed to investigate the potential utility of the various markers or their combinations in discriminating between benign prostatic hyperplasia and prostatic carcinoma.

RESULTS

hK2 concentrations were not statistically different between the two groups of patients. There was a strong positive correlation between hK2 and free PSA in the whole patient population. hK2/free PSA ratio (area under the curve = 0.69) was stronger predictor of prostate cancer than the free/total PSA ratio (area under the curve = 0.64). At 95% specificity, the hK2/free PSA ratio identified 30% of patients with total PSA between 2.5-10 microg/L who had cancer. At 95% specificity, the hK2/free PSA ratio identified 25% of patients with total PSA between 2.5 and 4.5 microg/L who had cancer.

CONCLUSIONS

Our data suggest that hK2 in combination with free and total PSA can enhance the biochemical detection of prostate cancer in patients with moderately increased total PSA concentrations. More specifically, the hK2/free PSA ratio appears to be valuable in identifying a subset of patients with total PSA between 2.5 and 4.5 microg/L who have high probability of cancer and who should be considered for biopsy.

摘要

背景

前列腺特异性抗原(PSA)是目前最可靠的肿瘤标志物,广泛应用于前列腺癌的诊断和治疗。不幸的是,PSA无法有效区分前列腺的良性和恶性疾病,尤其是在4 - 10μg/L范围内。为提高PSA特异性而开发的改进方法之一是游离/总PSA比值,它有助于在诊断“灰色地带”区分这两种疾病。最近的数据表明,人腺体激肽释放酶(hK2),一种与PSA具有高度同源性的蛋白质,可能是用于前列腺癌诊断和监测的另一种血清标志物。

方法

我们分析了206份血清样本(均在开始治疗前),这些样本来自组织学确诊为良性前列腺增生(n = 100)或前列腺癌(n = 106)的男性,其总PSA范围为2.5 - 10μg/L。采用非竞争性免疫程序测量总PSA、游离PSA和hK2。进行统计分析以研究各种标志物或其组合在区分良性前列腺增生和前列腺癌方面的潜在效用。

结果

两组患者的hK2浓度无统计学差异。在整个患者群体中,hK2与游离PSA之间存在强正相关。hK2/游离PSA比值(曲线下面积 = 0.69)比游离/总PSA比值(曲线下面积 = 0.64)更能预测前列腺癌。在95%的特异性下,hK2/游离PSA比值可识别出总PSA在2.5 - 10μg/L之间的癌症患者中的30%。在95%的特异性下, hK2/游离PSA比值可识别出总PSA在2.5至4.5μg/L之间的癌症患者中的25%。

结论

我们的数据表明,hK2与游离PSA和总PSA联合使用可提高总PSA浓度中度升高患者前列腺癌的生化检测率。更具体地说,hK2/游离PSA比值在识别总PSA在2.5至4.5μg/L之间且癌症可能性高、应考虑进行活检的患者亚组方面似乎很有价值。

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