Ishii M
Saitama Cancer Center.
Gan To Kagaku Ryoho. 1995 Aug;22(9):1139-45.
The clinical features and limitations of the usefulness of 10 kinds of main tumor markers such as AFP, CEA, CA 19-9 etc. are described in detail in this paper. This review is concerned with the limitation of the clinical usefulness of tumor marker. Evaluation of tumor marker is directed toward usefulness for diagnosis and the monitoring of cancer. The main weak points in the diagnosis of cancer by tumor marker have been insufficient sensitivity for detection of cancer and specificity to cancer. The sensitivity for detection of early cancer by tumor marker is especially low, and many tumor markers have ordinarily high false positive incidence for benign liver disease. On the other hand, limitation of specificity to organ is found in most tumor markers. Most tumor markers generally considered to be organ-specific are in fact, non-organ-specific, such as CA 19-9, which is thought to be specific to pancreatic cancer. On the other hand, there are few strictly organ-specific tumor markers such as prostate-specific antigen (PSA) and PIVKA-II. The usefulness of tumor marker for monitoring cancer is considered far better than that for diagnosis of cancer. However, a tumor marker in cases with less than the cut-off value is not available for monitoring of cancer.
本文详细描述了甲胎蛋白(AFP)、癌胚抗原(CEA)、糖类抗原19-9(CA 19-9)等10种主要肿瘤标志物的临床特征及其应用局限性。本综述关注肿瘤标志物临床应用的局限性。肿瘤标志物的评估旨在用于癌症诊断和监测。肿瘤标志物在癌症诊断中的主要弱点在于检测癌症的敏感性不足以及对癌症的特异性不强。肿瘤标志物检测早期癌症的敏感性尤其低,而且许多肿瘤标志物对良性肝病通常具有较高的假阳性发生率。另一方面,大多数肿瘤标志物存在对器官特异性的局限性。大多数通常被认为是器官特异性的肿瘤标志物实际上并非器官特异性,例如被认为是胰腺癌特异性标志物的CA 19-9。另一方面,严格意义上器官特异性的肿瘤标志物很少,如前列腺特异性抗原(PSA)和异常凝血酶原-II(PIVKA-II)。肿瘤标志物用于癌症监测的效用被认为远优于其用于癌症诊断的效用。然而,低于临界值情况下的肿瘤标志物无法用于癌症监测。