Knauf S, Taillon-Miller P, Helmkamp B F, Bonfiglio T A, Beecham J B
Gynecol Oncol. 1984 Mar;17(3):349-55. doi: 10.1016/0090-8258(84)90220-8.
An improved NB/70K assay which can be used to reproducibly and accurately measure the NB/70K content of unextracted serum samples has been developed. Analysis of pretreatment serum samples has indicated that the NB/70K assay shows selectivity for ovarian cancer with respect to nonmalignant ovarian cysts and tumors as well as controls; if one considers 10 units of NB/70K as a significant level of antigen, then there are no false positives in the benign and control groups, while 10 of 21 in the ovarian cancer group have significant NB/70K levels. When NB/70K levels of ovarian cancer patients are compared to those of patients with non-ovarian malignant disease, only 4 of 23 patients with non-ovarian cancers had significantly elevated NB/70K levels. However, none of these 4 false positives had levels greater than 20 units.
已开发出一种改进的NB/70K检测方法,可用于重复性地、准确地测量未提取血清样本中的NB/70K含量。对预处理血清样本的分析表明,NB/70K检测方法相对于非恶性卵巢囊肿、肿瘤以及对照而言,对卵巢癌具有选择性;如果将10个单位的NB/70K视为抗原的显著水平,那么良性组和对照组中没有假阳性,而卵巢癌组21例中有10例NB/70K水平显著。当将卵巢癌患者的NB/70K水平与非卵巢恶性疾病患者的水平进行比较时,23例非卵巢癌患者中只有4例NB/70K水平显著升高。然而,这4例假阳性患者的水平均未超过20个单位。