Morote Robles J, de Torres Mateos J A
Arch Esp Urol. 1989;42 Suppl 2:124-30.
The authors analyzed 3,079 serum determinations for prostate specific antigen (PSA) and prostatic acid phosphatase (PAP) that had been performed in 1,470 patients. The control group was comprised of 370 patients, 444 comprised the patient group with benign non-prostatic disease, 201 had malignant nonprostatic disease, 290 had benign prostatic disease (85 uncomplicated benign prostatic hypertrophy, 125 complicated benign prostatic hypertrophy, 50 acute prostatitis, 30 chronic prostatitis), 78 had untreated prostate carcinoma, and 165 were patients with prostate carcinoma under treatment. Quantification of PSA and PAP was performed by double antibody radioimmunoassay. The upper limit for normal values was set at 10 ng/ml. for PSA and 2.5 ng/ml. for PAP. Statistical analyses were performed with a personal computer using the SPSC program. Non-parametric tests were utilized throughout in the absence of a normal distribution of values for both tumor markers. In the control group, no significant differences in PSA and PAP levels were observed relative to the age group for the female patients; however, for the male patients, a significant increase was observed after age 15 for both markers. Furthermore, after age 50 PAP values became stable whereas a slight increase was observed for PSA. With regard to tumor mass, a significant correlation was found between PSA levels and the different patient groups while no remarkable differences were observed for PAP levels in those patients without or with single metastasis. We can conclude from the foregoing findings that PSA is currently the most useful tumor marker in diagnosing, staging, and monitoring prostate cancer. However, we believe that PSA and PAP are different manifestations of the prostate cell.(ABSTRACT TRUNCATED AT 250 WORDS)
作者分析了1470例患者的3079次血清前列腺特异性抗原(PSA)和前列腺酸性磷酸酶(PAP)检测结果。对照组由370例患者组成,444例为患有良性非前列腺疾病的患者组,201例患有恶性非前列腺疾病,290例患有良性前列腺疾病(85例无并发症的良性前列腺增生,125例有并发症的良性前列腺增生,50例急性前列腺炎,30例慢性前列腺炎),78例为未治疗的前列腺癌患者,165例为正在接受治疗的前列腺癌患者。PSA和PAP的定量检测采用双抗体放射免疫分析法。PSA的正常值上限设定为10 ng/ml,PAP为2.5 ng/ml。使用个人计算机通过SPSC程序进行统计分析。由于两种肿瘤标志物的值均未呈正态分布,因此自始至终都采用非参数检验。在对照组中,女性患者的PSA和PAP水平在各年龄组之间未观察到显著差异;然而,对于男性患者,两种标志物在15岁以后均显著升高。此外,50岁以后PAP值趋于稳定,而PSA则略有升高。关于肿瘤肿块,PSA水平与不同患者组之间存在显著相关性,而在无转移或有单个转移的患者中,PAP水平未观察到明显差异。从上述研究结果我们可以得出结论,目前PSA是诊断、分期和监测前列腺癌最有用的肿瘤标志物。然而,我们认为PSA和PAP是前列腺细胞的不同表现形式。(摘要截短于250字)