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Serum placental-like alkaline phosphatase (PLAP): a novel combined enzyme linked immunoassay for monitoring ovarian cancer.

机译:血清胎盘样碱性磷酸酶(PLAP):一种用于监测卵巢癌的新型联合酶联免疫法。

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摘要

A new combined enzyme linked immunoassay (ELISA) was developed to measure both serum placental-like alkaline phosphatase (PLAP) activity (PLAPA) and concentration (PLAPC) in the same microtitre plate using an Imperial Cancer Research Fund monoclonal antibody, designated H17E2. PLAP A and PLAP C were determined together with an existing marker, CA125 in 397 serial samples from 87 patients with epithelial ovarian cancer. Retrospective assessment showed the sensitivity to increase from 73% with CA125 alone, to 88% using CA125 and PLAP A, and to 93% with all three markers in 261 samples from the patients with known active disease at the time of sampling. When the results for all 397 samples were included in the analysis, however, the specificity, sensitivity, accuracy and predictive powers of this monoclonal antibody were not sufficiently high to assist in the prospective follow up of patients with ovarian cancer. This was due to a significant number of false positive and false negative results. Our data indicate that PLAP A or PLAP C estimation with H17E2 may, therefore, only be of value in the management of those patients with known active disease who are already known to be "marker positive" for this antigen.
机译:开发了一种新的联合酶联免疫测定(ELISA)方法,使用帝国癌症研究基金(Imperial Cancer Research Fund)单克隆抗体(H17E2)在同一微量滴定板中测量血清胎盘样碱性磷酸酶(PLAP)活性(PLAPA)和浓度(PLAPC)。在87例上皮性卵巢癌患者的397份连续样本中确定了PLAP A和PLAP C以及现有标记CA125。回顾性评估显示,在抽样时,已知活动性疾病患者的261个样本中,敏感性从单独使用CA125的73%提高到使用CA125和PLAP A的88%,使用所有三个标记物提高到93%。但是,当将所有397个样品的结果都包括在分析中时,该单克隆抗体的特异性,敏感性,准确性和预测能力不够高,无法辅助卵巢癌患者的前瞻性随访。这是由于大量的假阳性和假阴性结果。我们的数据表明,因此,用H17E2进行PLAP A或PLAP C评估可能仅对那些已知已对该抗原“标志物阳性”的已知活动性疾病患者有效。

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