Wu J T, Liu G H, Zhang P, Stephenson R A
Department of Pathology, University of Utah Health Sciences Complex, Salt Lake City 84108, USA.
J Clin Lab Anal. 1998;12(1):26-31. doi: 10.1002/(sici)1098-2825(1998)12:1<26::aid-jcla5>3.0.co;2-h.
We have measured the serum concentration of prostate specific antigen (tPSA) and determined the percent free PSA (% fPSA) in serial specimens from 64 patients with prostate cancer, 35 patients with benign prostate hyperplasia (BPH), and 3 patients with prostitis. We found that the % fPSAs were not a constant for individual patients during the course of the disease. When we compared only the % fPSA of the first specimen of serial specimens from individual patients, who were largely untreated, 37% of BPH specimens were above 22%, whereas only 1.6% cancer samples were above that value. We also found that 67% of cancer specimens and 14% of BPH samples were below 8%, respectively. Although % fPSA distribution pattern remained similar between two types of specimens, less differentiation was found between BPH and prostate cancer in random specimens compared to the study using first specimens of an individual patient's serial samples. Percent fPSA apparently are affected by treatment. However, the most important benefit for the determination of % fPSA appears to be the sensitivity of % fPSA to identify occult tumors when the tPSAs were in the normal concentration range. Determination of % fPSA also seems to improve the specificity of tPSA, not only during screening for the differentiation between BPH and prostate cancer, but also during monitoring of treatment and recurrence.
我们测定了64例前列腺癌患者、35例良性前列腺增生(BPH)患者和3例前列腺炎患者系列样本中的血清前列腺特异性抗原(tPSA)浓度,并测定了游离PSA百分比(%fPSA)。我们发现,在疾病过程中,%fPSA对个体患者而言并非恒定不变。当我们仅比较个体患者系列样本中首个样本的%fPSA时(这些患者大多未接受治疗),37%的BPH样本高于22%,而只有1.6%的癌症样本高于该值。我们还发现,分别有67%的癌症样本和14%的BPH样本低于8%。尽管两种类型样本之间的%fPSA分布模式保持相似,但与使用个体患者系列样本首个样本的研究相比,随机样本中BPH和前列腺癌之间的差异较小。%fPSA显然受治疗影响。然而,测定%fPSA最重要的益处似乎在于,当tPSA处于正常浓度范围时,%fPSA识别隐匿性肿瘤的敏感性。测定%fPSA似乎还能提高tPSA的特异性,不仅在筛查BPH和前列腺癌的鉴别诊断时如此,在治疗和复发监测期间也是如此。