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[人附睾蛋白4,一种上皮性卵巢癌的新型标志物:分析性能评估]

[HE4, a novel marker for epithelial ovarian cancer: evaluation of analytical performances].

作者信息

Lamy Pierre-Jean, Roques Sylvie, Viglianti Cathy, Fabbro Michel, Montels Frédéric

机构信息

Laboratoire de Biologie Spécialisée, Service d'Oncologie Gynécologique, CRLC Val d'Aurelle-Paul Lamarque, Montpellier.

出版信息

Ann Biol Clin (Paris). 2010 May-Jun;68(3):325-9. doi: 10.1684/abc.2010.0435.

Abstract

Human epididymis protein 4 (HE4) is a novel marker for ovarian cancer. HE4 exhibits a high sensitivity to detect ovarian cancer and can be used with CA125 as a predictor of malignancy. Additional uses of HE4 are as an aid of monitoring response to therapy for patients with invasive ovarian cancer and as a marker to detect recurrences in the follow-up after treatment of the primary tumor. The HE4 EIA, an enzyme immunoassay for the quantitative determination of HE4 in human serum developed by Fujirebio Diagnostic Inc. (Tokyo, Japan), is now available with a CE-IVD label in Europe (Diasource, Nivelles, Belgium). The aim of the study was to evaluate according to the COFRAC LAB GTA 04 guide, the analytical performance of the test, using 4 standardized samples (target values: 49.8, 140.4, 167.6 and 415.2 pmol/L) and serum samples from patients with ovarian cancer treated in our institution. Intra- and inter-assay precisions showed coefficients of variation less than 10%. The low limit of detection (4 pmol/L) and the limit of quantitation (8 pmol/L) are suitable for clinical samples assessment. The assay mean dilution linearity is 100 +/- 10% (90 to 107% of recovery). Globally, the uncertainty varied from 13.1% (low values) to 28.1% (elevated values). We conclude that the HE4 EIA from Fujirebio Diagnostic Inc. displayed convenient analytical performances that allows its use it clinical practice.

摘要

人附睾蛋白4(HE4)是一种新型的卵巢癌标志物。HE4在检测卵巢癌方面具有很高的敏感性,可与CA125一起作为恶性肿瘤的预测指标。HE4的其他用途包括辅助监测侵袭性卵巢癌患者的治疗反应,以及作为检测原发性肿瘤治疗后随访中复发情况的标志物。富士瑞必欧诊断公司(日本东京)开发的用于定量测定人血清中HE4的酶免疫测定法(HE4 EIA),目前在欧洲已获得CE-IVD标签(比利时尼韦勒的Diasource公司)。本研究的目的是根据COFRAC LAB GTA 04指南,使用4个标准化样品(目标值:49.8、140.4、167.6和415.2 pmol/L)以及在我们机构接受治疗的卵巢癌患者的血清样品,评估该检测方法的分析性能。批内和批间精密度显示变异系数小于10%。检测下限(4 pmol/L)和定量限(8 pmol/L)适用于临床样品评估。该检测方法的平均稀释线性为100±10%(回收率为90%至107%)。总体而言,不确定度从13.1%(低值)到28.1%(高值)不等。我们得出结论,富士瑞必欧诊断公司的HE4 EIA表现出便捷的分析性能,使其能够在临床实践中使用。

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