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[超敏前列腺特异抗原检测试剂盒在前列腺癌低水平前列腺特异抗原测定中的应用价值]

[Usefulness of hyper sensitive PSA assay kits for determination on low range of prostate specific antigen in prostate cancer].

作者信息

Akimoto S, Akakura K, Ohki T, Shimazaki J, Kuriyama M, Kawada Y

机构信息

Department of Urology, School of Medicine, Chiba University.

出版信息

Nihon Hinyokika Gakkai Zasshi. 1995 Feb;86(2):256-62. doi: 10.5980/jpnjurol1989.86.256.

Abstract

Prostate specific antigen (PSA) levels after total prostatectomy or radiation therapy to localized prostate cancer and also during endocrine therapy are within normal range. Therefore, it is necessary to use hyper sensitive PSA assay kits for early detection of relapse. The present study was undertaken to evaluate two hyper sensitive assay kits (Delfia kit, lower limit 0.1 ng/ml, Kabi Pharmacia Diagnostics Co. and Markit M kit, 0.5 ng/ml, Dainippon Pharmaceutical Co.) and to compare them with conventional PSA kit (Eiken Chemical Co., 1.0 ng/ml). Total of 291 sera were examined: patients consisted of 10 total prostatectomy+endocrine therapy, 9 radiation therapy+endocrine therapy, 5 radiation therapy alone and 44 endocrine therapy alone. Values of endocrine therapy alone were divided into two groups according to duration after start of treatment; more or less than 5 years. The following results were obtained. 1. In non-relapse patients after total prostatectomy+endocrine therapy and radiation+endocrine therapy, PSA showed under lower limit with hyper sensitive kit. On the contrary, conventional kit indicated more than 1.0 ng/ml. 2. Radiation therapy alone kept PSA in detectable range with hyper sensitive kit in spite of no sign of relapse. 3. In non-relapsed patients under endocrine therapy alone, long duration (more than 5 years after start of treatment) decreased PSA in non detectable values with hyper sensitive kits. In this case, conventional kit still showed PSA as more than 1 ng/ml. 4. Doubling time at relapse was estimated similar with Delfia kit and Markit M kit, and much longer with conventional kit. It is concluded that hyper sensitive kit is more useful to manage patients after therapy than conventional kit.

摘要

前列腺癌根治术或局部前列腺癌放射治疗后以及内分泌治疗期间,前列腺特异性抗原(PSA)水平均在正常范围内。因此,有必要使用超敏PSA检测试剂盒来早期检测复发情况。本研究旨在评估两种超敏检测试剂盒(Delfia试剂盒,下限为0.1 ng/ml,卡比药业诊断公司生产;Markit M试剂盒,0.5 ng/ml,日本大日本制药公司生产),并将它们与传统PSA试剂盒(荣化学公司生产,1.0 ng/ml)进行比较。共检测了291份血清样本:患者包括10例接受前列腺癌根治术+内分泌治疗、9例接受放射治疗+内分泌治疗、5例仅接受放射治疗以及44例仅接受内分泌治疗。仅接受内分泌治疗的患者根据治疗开始后的持续时间分为两组:5年及以上和5年以下。结果如下:1. 在接受前列腺癌根治术+内分泌治疗和放射治疗+内分泌治疗后未复发的患者中,超敏试剂盒检测显示PSA低于下限。相反,传统试剂盒显示PSA超过1.0 ng/ml。2. 仅接受放射治疗的患者,尽管没有复发迹象,但超敏试剂盒仍能检测到PSA处于可检测范围内。3. 在仅接受内分泌治疗且未复发的患者中,治疗开始后较长时间(超过5年),超敏试剂盒检测显示PSA降至不可检测值。在这种情况下,传统试剂盒仍显示PSA超过1 ng/ml。4. 复发时的倍增时间,Delfia试剂盒和Markit M试剂盒估计相似,而传统试剂盒则长得多。结论是,与传统试剂盒相比,超敏试剂盒在治疗后患者管理中更有用。

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