Department of Obstetrics & Gynaecology, National University of Singapore, Singapore, Singapore.
Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Vic., Australia.
BJOG. 2018 Mar;125(4):421-431. doi: 10.1111/1471-0528.14835. Epub 2017 Sep 4.
To investigate haptoglobin within ovarian cyst fluid (OCF) as a diagnostic biomarker for epithelial ovarian cancer (EOC) and develop an in vitro diagnostic point-of-care device test (IVDPCT) for use in the operating theatre.
Retrospective and prospective cohort study.
South-East Asia.
Women with suspicious ovarian cysts.
Proteomic, immunohistochemical and ELISA methods measured haptoglobin in OCF to differentiate benign and EOCs. Diagnostic performance of haptoglobin was compared with CA125, risk malignancy indices (RMI) and frozen section. Blinded validation of the IVDPCT was performed.
Prediction of malignancy.
Haptoglobin concentration measured by ELISA was 0.70 ± 0.09 mg/ml in patients with benign cysts (n = 87), 6.22 ± 0.53 mg/ml in early stage-EOC (n = 17), and 6.57 ± 0.65 mg/ml in late stage-EOC (n = 20). Haptoglobin in EOCs was significantly higher than in benign cysts (P < 0.0001). Haptoglobin using rapid colorimetric assay (RCA) on a training set had a sensitivity of 97.3% and a specificity 92.0%, comparable to ELISA and frozen sections. The haptoglobin AUROC curve was 0.999 (95% CI 0.997-1.000) compared with 0.895 (95% CI 0.814-0.977, P < 0.05) for CA125. Haptoglobin performed significantly better than all the RMIs (P < 0.01). Blinded validation studies showed a minor drop in average diagnostic performance (sensitivity 85.2% and specificity 90.5%) compared with the training set. However, when compared with frozen section, haptoglobin was no worse in diagnostic accuracy for malignancy.
Haptoglobin was identified as a biomarker for the detection of EOC with potential as a point-of-care diagnostic tool.
Haptoglobin within ovarian cyst fluid: a biomarker for epithelial ovarian cancer and point-of-care diagnostics.
研究卵巢囊液中的触珠蛋白作为上皮性卵巢癌(EOC)的诊断生物标志物,并开发一种用于手术室的体外诊断即时检测设备测试(IVDPCT)。
回顾性和前瞻性队列研究。
东南亚。
疑似卵巢囊肿的女性。
蛋白质组学、免疫组织化学和 ELISA 方法测量卵巢囊液中的触珠蛋白以区分良性和 EOC。触珠蛋白的诊断性能与 CA125、风险恶性指数(RMI)和冷冻切片进行比较。对 IVDPCT 进行了盲法验证。
预测恶性肿瘤。
通过 ELISA 测量的触珠蛋白浓度在良性囊肿患者(n=87)中为 0.70±0.09mg/ml,早期 EOC 患者(n=17)中为 6.22±0.53mg/ml,晚期 EOC 患者(n=20)中为 6.57±0.65mg/ml。EOC 中的触珠蛋白明显高于良性囊肿(P<0.0001)。在训练集上使用快速比色法(RCA)的触珠蛋白具有 97.3%的敏感性和 92.0%的特异性,与 ELISA 和冷冻切片相当。触珠蛋白的 AUROC 曲线为 0.999(95%CI 0.997-1.000),而 CA125 的 AUROC 曲线为 0.895(95%CI 0.814-0.977,P<0.05)。触珠蛋白的性能明显优于所有 RMIs(P<0.01)。盲法验证研究显示,与训练集相比,平均诊断性能略有下降(敏感性 85.2%,特异性 90.5%)。然而,与冷冻切片相比,触珠蛋白在恶性肿瘤的诊断准确性方面并没有更差。
触珠蛋白被鉴定为检测上皮性卵巢癌的生物标志物,具有成为即时护理诊断工具的潜力。
卵巢囊液中的触珠蛋白:上皮性卵巢癌的生物标志物和即时护理诊断。