University of Gothenburg, Institute of Clinical Sciences, Department of Obstetrics and Gynecology, S-41345 Gothenburg, Sweden.
Gynecol Oncol. 2013 Oct;131(1):52-8. doi: 10.1016/j.ygyno.2013.07.094. Epub 2013 Jul 25.
To evaluate the diagnostic performance of HE4 and CA125 in patients presenting with suspicious malignant ovarian cysts. We especially wanted to investigate the levels of HE4 and CA125 with regard to the gene and histology-unifying model of type I and type II epithelial ovarian cancer (EOC).
Plasma from 373 women presenting with a suspicious malignant ovarian cyst was collected prior to surgery. Histology, grade, and stage were determined according to FIGO-classification. HE4 and CA125 were analyzed using ELISA, and the markers were evaluated for significance separately and in combination. Receiver operating curves, the area under the curve, sensitivity and specificity were estimated.
The combination of HE4 and CA125 resulted in the best diagnostic power in comparing benign tumors to EOC (ROC AUC 0.93, sensitivity 94.4% at 75% specificity) for type II. Diagnostic power in type I (ROC AUC 0.79, sensitivity 61.9% at 75% specificity) was less impressive. In particular, mucinous benign vs. malignant tumors could not significantly be separated by the dual marker combination. Impressively high ROC AUC 0.99 was found for the late stage type II EOC with 100% sensitivity at 75% specificity.
HE4 and CA125 have a good ability to diagnose the more aggressive type II tumors but a poor diagnostic ability when patients are presenting with slow-growing type I in the early stage. Our results support the hypothesis that EOC should be looked upon as several different diseases, and that we lack biomarkers for sub-groups of EOC.
评估 HE4 和 CA125 在疑似恶性卵巢囊肿患者中的诊断性能。我们特别希望研究 HE4 和 CA125 的水平,针对 I 型和 II 型上皮性卵巢癌(EOC)的基因和组织学统一模型。
在手术前收集了 373 名患有疑似恶性卵巢囊肿的女性的血浆。根据 FIGO 分类确定组织学、分级和分期。使用 ELISA 分析 HE4 和 CA125,并分别评估单独和联合使用标记物的意义。估计接收者操作曲线、曲线下面积、敏感性和特异性。
HE4 和 CA125 的组合在将良性肿瘤与 EOC 进行比较时具有最佳的诊断能力(ROC AUC 0.93,特异性为 75%时敏感性为 94.4%),对于 II 型。I 型(ROC AUC 0.79,特异性为 75%时敏感性为 61.9%)的诊断能力较差。特别是,粘液性良性与恶性肿瘤之间不能通过双标记物组合明显分离。令人印象深刻的是,晚期 II 型 EOC 的 ROC AUC 为 0.99,特异性为 75%时敏感性为 100%。
HE4 和 CA125 具有良好的诊断 II 型侵袭性更强的肿瘤的能力,但在早期缓慢生长的 I 型患者中诊断能力较差。我们的结果支持这样一种假设,即 EOC 应该被视为几种不同的疾病,并且我们缺乏 EOC 亚组的生物标志物。