Babaian R J, Camps J L, Frangos D N, Ramirez E I, Tenney D M, Hassell J S, Fritsche H A
Department of Urology, University of Texas M.D. Anderson Cancer Center, Houston 77030.
Cancer. 1991 Apr 15;67(8):2200-6. doi: 10.1002/1097-0142(19910415)67:8<2200::aid-cncr2820670833>3.0.co;2-e.
The authors evaluated 440 men with clinically staged and untreated prostate cancer with a monoclonal prostate-specific antigen (PSA) assay. The serum PSA value correlated significantly with both the stage and grade of disease (P less than 0.00005). The relationships between PSA and consecutive Stages A, B, C, and D2 (alpha = 0.15) and between progressive Gleason's scores 2 to 4, 5 to 7, and 8 to 10 (alpha = 0.15) were statistically significant. Also statistically significant was the correlation between serum PSA level and intracapsular versus extracapsular disease (P less than 0.00005), although no one value can be used to differentiate reliably between patients in these two categories. The probability of clinically detectable metastasis (Stage D2) is 85% if the serum PSA level is greater than 30; however, 12% of patients without clinical evidence of metastases (Stages A, B, and C) have such a serum PSA value. Despite the statistically significant association between PSA and tumor differentiation and volume as reflected by tumor grade and clinical stage, this marker cannot be used to determine either for an individual patient.
作者使用单克隆前列腺特异性抗原(PSA)检测法对440例未经治疗且临床分期的前列腺癌男性患者进行了评估。血清PSA值与疾病的分期和分级均显著相关(P<0.00005)。PSA与连续的A、B、C和D2期(α=0.15)以及Gleason评分2至4、5至7和8至10的进展情况(α=0.15)之间的关系具有统计学意义。血清PSA水平与包膜内和包膜外疾病之间的相关性也具有统计学意义(P<0.00005),尽管无法用单一值可靠地区分这两类患者。如果血清PSA水平大于30,临床可检测到转移(D2期)的概率为85%;然而,12%没有转移临床证据(A、B和C期)的患者也有这样的血清PSA值。尽管PSA与肿瘤分级和临床分期所反映的肿瘤分化及体积之间存在统计学上的显著关联,但该标志物不能用于为个体患者确定(肿瘤分化及体积)。