Tellier J L, Chatal J F, Bourdin S, Auvigne J, Etienne P, Faye R
J Urol (Paris). 1981;87(3):169-73.
Radioimmunological estimation of prostatic acid phosphatase was carried out in 72 reference subjects, 46 patients with benign prostatic hypertrophy, 106 patients with untreated prostatic carcinoma and 25 patients with a carcinoma of some other origin. The mean concentration in non-acidified serum was 1.3 +/- 0.4 (M +/- SD) ng/ml for the reference group and 1.6 +/- 0.8 ng/ml for the benign hypertrophy group. The upper limit of discriminatory values for the diagnosis of prostatic carcinoma was fixed at 3 ng/ml. Taking this value, the overall percentage of positive results for carcinoma of the prostate was 61% (65/106). The number of cases with a value greater than 3 ng/ml was 3/18 (17%) for stage A, 8/27 (30%) for stage B, 7/13 (54%) for stage C and 47/48 (98%) for stage D. 8% (2/25) of carcinomas of another origin gave a positive result. The results of estimation using the radioimmunological technique were compared with those obtained by the measurement of enzyme activity using para nitro-phenyl phosphate as a substrate in 34 untreated prostatic carcinomas (all stages mixed together). When measurements by both techniques were carried out under the same ideal conditions using fresh sera as soon as possible after the blood was drawn, the result was abnormal in 10 cases out of 12 (83%) for the radioimmunological method and in 8 cases out of 12 (67%) for the measurement of enzyme activity. By contrast, under routine conditions, the positive percentage figures were 77% (17/22) for the radioimmunological technique and only 36% (8/22) for the measurement of enzyme activity. It would thus appear that radioimmunological measurement is more reliable than the measurement of enzyme activity.
对72名参照对象、46例良性前列腺增生患者、106例未经治疗的前列腺癌患者以及25例其他来源癌症患者进行了前列腺酸性磷酸酶的放射免疫测定。参照组非酸化血清中的平均浓度为1.3±0.4(M±SD)ng/ml,良性增生组为1.6±0.8 ng/ml。前列腺癌诊断的鉴别值上限确定为3 ng/ml。以此值计算,前列腺癌阳性结果的总体百分比为61%(65/106)。A期大于3 ng/ml的病例数为3/18(17%),B期为8/27(30%),C期为7/13(54%),D期为47/48(98%)。其他来源癌症中有8%(2/25)呈阳性结果。将放射免疫技术的测定结果与34例未经治疗的前列腺癌(各期混合)中以对硝基苯磷酸为底物测量酶活性所获得的结果进行了比较。当两种技术在相同理想条件下,在采血后尽快使用新鲜血清进行测量时,放射免疫法12例中有10例(83%)结果异常,酶活性测量法12例中有8例(67%)结果异常。相比之下,在常规条件下,放射免疫技术的阳性百分比为77%(17/22),而酶活性测量仅为36%(8/22)。因此,放射免疫测量似乎比酶活性测量更可靠。