Barr Chloe E, Njoku Kelechi, Owens Gemma L, Crosbie Emma J
Manchester Academic Health Science Centre, Department of Obstetrics and Gynaecology, St Mary's Hospital, Manchester University NHS Foundation Trust, Manchester M13 9WL, UK.
Division of Cancer Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester M13 9WL, UK.
Cancers (Basel). 2023 Feb 16;15(4):1256. doi: 10.3390/cancers15041256.
The symptoms of ovarian cancer are vague, and current risk assessment tools such as serum CA125 and transvaginal ultrasound scan fail to reliably detect the disease early. This study aimed to evaluate urine CA125 and HE4 as diagnostic biomarkers for ovarian cancer in symptomatic women. Paired urine and serum samples were collected from women undergoing treatment for ovarian cancer (cases) or investigations for gynaecological symptoms (controls). Biomarkers were measured using an automated chemiluminescent enzyme immunoassay analyser. Standard diagnostic accuracy metrics were calculated. In total, 114 women were included, of whom 17 (15%) were diagnosed with an epithelial ovarian malignancy. Levels of urine CA125 and HE4 were significantly elevated in women with ovarian cancer compared to controls [CA125: 8.5 U/mL (IQR: 2.4-19.5) vs. 2.3 U/mL (IQR: 1.0-6.4), = 0.01. HE4: 12.0 nmol/L (IQR: 10.3-23.1) vs. 6.7 nmol/L (IQR: 3.4-13.6), = 0.006]. Urine CA125 and HE4 detected ovarian cancer with an AUC of 0.69 (95% CI: 0.55-0.82) and 0.71 (95% CI: 0.69-0.82), respectively ( = 0.73). A combination of urine CA125 and HE4 at optimal thresholds had a sensitivity of 82.4% (95% CI: 56.6-96.2) and was comparable to the sensitivity of serum CA125 [88.2% (95% CI: 63.6-98.5)]. Larger studies are required to confirm our findings, standardise urine collection, and evaluate optimal biomarker thresholds. Urine CA125 and HE4 may be useful non-invasive diagnostic tools to triage women for formal ovarian cancer investigations.
卵巢癌的症状不明确,目前诸如血清CA125和经阴道超声扫描等风险评估工具无法可靠地早期检测出该疾病。本研究旨在评估尿CA125和人附睾蛋白4(HE4)作为有症状女性卵巢癌诊断生物标志物的价值。从接受卵巢癌治疗的女性(病例组)或因妇科症状接受检查的女性(对照组)中收集配对的尿液和血清样本。使用自动化学发光酶免疫分析分析仪测量生物标志物。计算标准诊断准确性指标。总共纳入了114名女性,其中17名(15%)被诊断为上皮性卵巢恶性肿瘤。与对照组相比,卵巢癌女性的尿CA125和HE4水平显著升高[CA125:8.5 U/mL(四分位间距:2.4 - 19.5)对2.3 U/mL(四分位间距:1.0 - 6.4),P = 0.01。HE4:12.0 nmol/L(四分位间距:10.3 - 23.1)对6.7 nmol/L(四分位间距:3.4 - 13.6),P = 0.006]。尿CA125和HE4检测卵巢癌的曲线下面积(AUC)分别为0.69(95%可信区间:0.55 - 0.82)和0.71(95%可信区间:0.69 - 0.82)(P = 0.73)。尿CA125和HE4在最佳阈值下联合使用的灵敏度为82.4%(95%可信区间:56.6 - 96.2),与血清CA125的灵敏度[88.2%(95%可信区间:63.6 - 98.5)]相当。需要更大规模的研究来证实我们的发现、规范尿液收集并评估最佳生物标志物阈值。尿CA125和HE4可能是用于对女性进行正式卵巢癌检查分流的有用非侵入性诊断工具。