首页> 外文期刊>International Urology and Nephrology >Prospective evaluation of prostate specific antigen (PSA), PSA density, free-to-total PSA ratio and a new formula (prostate malignancy index) for detecting prostate cancer and preventing negative biopsies in patients with normal rectal examinations a
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Prospective evaluation of prostate specific antigen (PSA), PSA density, free-to-total PSA ratio and a new formula (prostate malignancy index) for detecting prostate cancer and preventing negative biopsies in patients with normal rectal examinations a

机译:前瞻性评估前列腺特异性抗原(PSA),PSA密度,游离总PSA比和新公式(前列腺恶性指数),用于在正常直肠检查的患者中检测前列腺癌并预防活检阴性

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OBJECTIVE: To improve the specificity and sensitivity of prostatic cancer detection, we prospectively evaluated total prostate specific antigen (PSA) level, PSA density, free-to-total PSA ratio and a new formula called prostate malignancy index (PMI) as a discriminator of prostate cancer in patients with intermediate PSA levels and normal digital rectal examinations. MATERIALS AND METHODS: Between November 1995 and October 1997, 95 patients who had serum PSA levels of 4.0 to 10.0 ng/ml with normal digital rectal examinations were prospectively evaluated. All patients underwent one or two times transrectal ultrasound guided prostate biopsies. Based on age specific reference range of PSA, PSA density and % free PSA ratio, PMI was calculated for each patient. The free and total serum PSA concentrations were determined by an Immulite assay system. (Diagnostic Product Corp., Los Angeles, California). RESULTS: Overall 20 of 95 (21%) patients had prostate cancer. There were no significant differences in patient mean age and mean total PSA between those with benign and those with malignant biopsies (p>0.05). However, there were significant differences in mean PSAD, mean free-to-total PSA ratio and mean PMI (p<0.01, p<0.05, p<0.01, respectively). Benign condition specificities for PM index, percent free PSA, PSA density and total PSA at a 90% sensitivity for prostate cancer were 48%, 10.6%, 8% and 4%, respectively. Of 95 patients, 27 (28.4%) had a PMI of equal or more than 3.1, including 12 of 75 (16%) with negative biopsy and 15 of 20 (75%) with positive biopsy. Furthermore a cutoff MI 0.86 P correctly identified 24% of benign cases without missing any prostate cancer cases. The comparison of receiver operating characteristic (ROC) curve areas showed that PMI was better than total PSA (p<0.01). Although, the area under the ROC curve of % free PSA and PSAD were higher than the area of total PSA, these differences were not statistically significant (p>0.05). CONCLUSIONS: We concluded that the prostate malignancy index could be utilized to differentiate benign conditions from prostate cancer in patients with intermediate PSA levels and normal digital rectal examination. Also significant numbers of negative biopsies can be prevented in these patients.
机译:目的:为了提高前列腺癌检测的特异性和敏感性,我们前瞻性评估了总前列腺特异性抗原(PSA)水平,PSA密度,总PSA比率和一种新的公式,称为前列腺恶性指数(PMI)作为鉴别指标。 PSA水平中等且直肠指检正常的前列腺癌患者。材料与方法:从1995年11月至1997年10月,对95例血清PSA水平在4.0到10.0 ng / ml的患者进行了直肠指检,这些患者均经过前瞻性评估。所有患者均接受一两次经直肠超声引导的前列腺活检。根据PSA的年龄特定参考范围,PSA密度和游离PSA百分比百分比,计算每位患者的PMI。通过Immulite测定系统确定游离和总血清PSA浓度。 (诊断产品公司,加利福尼亚州洛杉矶)。结果:95名患者中有20名(21%)患有前列腺癌。良性和恶性活检患者的平均年龄和平均总PSA无显着差异(p> 0.05)。但是,平均PSAD,平均总PSA比率和平均PMI存在显着差异(分别为p <0.01,p <0.05,p <0.01)。前列腺癌的敏感性为90%时,PM指数,游离PSA百分比,PSA密度和总PSA的良性条件特异性分别为48%,10.6%,8%和4%。在95名患者中,有27名(28.4%)的PMI等于或大于3.1,包括75名中的12名(16%)活检阴性和20名中的15名(75%)活检阳性。此外,临界MI 0.86 P可以正确识别出24%的良性病例,而不会遗漏任何前列腺癌病例。接收器工作特性曲线区域的比较显示,PMI优于总PSA(p <0.01)。尽管%游离PSA和PSAD的ROC曲线下面积高于总PSA面积,但这些差异在统计学上无统计学意义(p> 0.05)。结论:我们得出结论,在PSA水平中等且直肠指检正常的患者中,前列腺恶性指数可用于区分良性疾病与前列腺癌。在这些患者中,还可以防止大量的阴性活检。

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