Liu Xin, Tang Jie, Fei Xiang, Li Qiu-Yang
Ultrasonography Department of Nan Lou Clinical Medicine Division, Chinese PLA General Hospital, China.
Dept. of Ultrasonography, Chinese PLA General Hospital, 28 Fuxing Road, Beijing, China.
Iran J Public Health. 2015 Nov;44(11):1466-72.
We aimed to value the usefulness of free to total prostate-specific antigen and Prostate-specific antigen (PSA) density for prostate cancer in the patients with PSA levels of 4.0 ng/ml or less.
A total of 343 subjects with PSA levels of 4.0 ng/ml or less were biopsied. All patients were divided into four groups according to the PSA levels: 0 to 1.0 ng/ml, 1.1 to 2.0 ng/ml, 2.1 to 3.0 ng/ml, and 3.1 to 4.0 ng/ml. The reliability of cancer detection in relation to the f/t PSA ratio and PSAD were estimated.
Overall, 65 people were diagnosed with prostate cancer. The detection rate was 16.28%、17.17%, 21.82%, 25.00% in subjects with PSA levels of 0 to 1.0 ng/ml, 1.1 to 2.0 ng/ml, 2.1 to 3.0 ng/ml, and 3.1 to 4.0 ng/ml, respectively. The f/t PSA ratio was significantly lower in patients with prostate cancer and PSA levels of 2.1 to 4.0 ng/ml (P<0.05). The PSAD had no statistical significance between the two groups.
Routine prostate biopsy should be undertaken if the f/t PSA ratio less than 15% with /without abnormal DRE/TRUS findings.
我们旨在评估游离前列腺特异性抗原与总前列腺特异性抗原比值(f/t PSA)以及前列腺特异性抗原密度(PSAD)在前列腺特异性抗原(PSA)水平为4.0 ng/ml及以下的患者中对前列腺癌的诊断价值。
对343例PSA水平为4.0 ng/ml及以下的受试者进行活检。所有患者根据PSA水平分为四组:0至1.0 ng/ml、1.1至2.0 ng/ml、2.1至3.0 ng/ml和3.1至4.0 ng/ml。评估f/t PSA比值和PSAD与癌症检测的相关性。
总体而言,65人被诊断为前列腺癌。PSA水平在0至1.0 ng/ml、1.1至2.0 ng/ml、2.1至3.0 ng/ml和3.1至4.0 ng/ml的受试者中,癌症检出率分别为16.28%、17.17%、21.82%、25.00%。PSA水平在2.1至4.0 ng/ml的前列腺癌患者中,f/t PSA比值显著更低(P<0.05)。两组之间PSAD无统计学意义。
若f/t PSA比值小于15%,无论直肠指检(DRE)/经直肠超声检查(TRUS)结果是否异常,均应进行常规前列腺活检。