Uemura M, Winant R C, Brandt A E
New Material R/D Laboratory, Konishiroku Photo Industries Co., Ltd., Tokyo, Japan.
Cancer Res. 1988 Sep 15;48(18):5335-41.
Serum galactosyltransferase isoenzyme II (GT-II) was assayed in 409 coded serum samples obtained from the National Cancer Institute Tumor Serum Bank using a monoclonal antibody-based immunoassay. The serum panel consisted of samples from patients with confirmed, metastatic ovarian, breast, stomach, esophageal, pancreatic, lung, colorectal, bladder, prostate, and cervical cancer, as well as benign disease controls corresponding to each cancer type, and confirmed healthy normal controls. The serum panel was matched for age and sex; 176 of 179 cancer patients had metastatic disease, and many had undergone previous therapy. GT-II was significantly elevated (P less than 0.01) in all pairwise tests (Wilcoxon) comparing cancer cases with normals and cancer cases with benign disease cases of the same site. A cutpoint of 200 milliunits of GT-II activity/ml of serum was selected, and only one of 50 normal control sera was elevated above this value, yielding a specificity of 98%. The overall sensitivity of the GT-II assay was 55.3%, with higher sensitivity shown by pancreatic (77%), prostate (65%), esophageal (64%), cervical (59%), and bladder cancer (58%).
使用基于单克隆抗体的免疫测定法,对从美国国立癌症研究所肿瘤血清库获取的409份编码血清样本中的血清半乳糖基转移酶同工酶II(GT-II)进行了检测。血清样本组包括确诊为转移性卵巢癌、乳腺癌、胃癌、食管癌、胰腺癌、肺癌、结直肠癌、膀胱癌、前列腺癌和宫颈癌的患者的样本,以及每种癌症类型对应的良性疾病对照样本和确诊的健康正常对照样本。血清样本组在年龄和性别上进行了匹配;179名癌症患者中有176名患有转移性疾病,许多人此前接受过治疗。在所有将癌症病例与正常对照以及癌症病例与同一部位良性疾病病例进行比较的成对检验(Wilcoxon检验)中,GT-II显著升高(P小于0.01)。选择血清GT-II活性200毫单位/毫升作为临界值,50份正常对照血清中只有1份高于此值,特异性为98%。GT-II检测的总体敏感性为55.3%,胰腺癌(77%)、前列腺癌(65%)、食管癌(64%)、宫颈癌(59%)和膀胱癌(58%)的敏感性更高。