Henic Emir, Borgfeldt Christer, Christensen Ib Jarle, Casslén Bertil, Høyer-Hansen Gunilla
Department of Obstetrics and Gynecology, University Hospital Lund, Lund, Sweden.
Clin Cancer Res. 2008 Sep 15;14(18):5785-93. doi: 10.1158/1078-0432.CCR-08-0096.
To evaluate the plasma level of different forms of soluble urokinase plasminogen activator receptor (suPAR) as discriminators between malignant, borderline, and benign ovarian tumors and as prognostic markers in patients with ovarian cancer.
The different suPAR forms were measured in preoperative plasma samples obtained from 335 patients with adnexal lesions using three different time-resolved fluoresence assays (TR-FIA): TR-FIA 1 measuring intact suPAR, suPAR(I-III), TR-FIA 2 measuring the total amount of suPAR(I-III) and the cleaved form, suPAR(II-III), and TR-FIA 3 measuring the liberated uPAR(I). Tumors were classified as benign (n = 211), borderline (possibly malignant; n = 30), and well (n = 19), moderately (n = 15), and poorly (n = 60) differentiated malignant.
All uPAR forms as well as CA125 were statistically significant in univariate analysis discriminating between benign, borderline, and invasive tumors. Restricting the analysis of invasive tumors to early stage (I and II) showed similar results. A combination of CA125 and suPAR(I-III) + suPAR(II-III) discriminated between malignant (all stages) and benign tumors [AUC, 0.94; 95% confidence interval (95% CI), 0.90-0.98] as well as borderline and benign tumors (AUC, 0.78; 95% CI, 0.67-0.89). All suPAR forms were markers for poor prognosis in univariate analyses, and high preoperative plasma level of uPAR(I) is an independent predictor of poor prognosis (hazard ratio, 1.84; 95% CI, 1.15-2.95; P = 0.011) in multivariate analyses including age and CA125.
High concentration of plasma uPAR(I) is an independent preoperative marker of poor prognosis in patients with ovarian cancer. The combination of plasma suPAR(I-III) + suPAR(II-III) and CA125 discriminates between malignant and benign tumors with an AUC of 0.94.
评估不同形式的可溶性尿激酶型纤溶酶原激活物受体(suPAR)的血浆水平,以鉴别恶性、交界性和良性卵巢肿瘤,并作为卵巢癌患者的预后标志物。
使用三种不同的时间分辨荧光分析法(TR-FIA),对335例附件病变患者术前采集的血浆样本中的不同suPAR形式进行检测:TR-FIA 1检测完整的suPAR,即suPAR(I-III);TR-FIA 2检测suPAR(I-III)的总量和裂解形式suPAR(II-III);TR-FIA 3检测游离的uPAR(I)。肿瘤分为良性(n = 211)、交界性(可能为恶性;n = 30)以及高分化(n = 19)、中分化(n = 15)和低分化(n = 60)的恶性肿瘤。
在鉴别良性、交界性和浸润性肿瘤的单因素分析中,所有uPAR形式以及CA125均具有统计学意义。将浸润性肿瘤的分析局限于早期(I期和II期)显示出相似的结果。CA125与suPAR(I-III)+ suPAR(II-III)的组合可鉴别恶性(所有分期)和良性肿瘤【曲线下面积(AUC),0.94;95%置信区间(95%CI),0.90 - 0.98】以及交界性和良性肿瘤(AUC,0.78;95%CI,0.67 - 0.89)。在单因素分析中,所有suPAR形式均为预后不良的标志物,在包括年龄和CA125的多因素分析中,术前血浆uPAR(I)水平高是预后不良的独立预测因素(风险比,1.84;95%CI),1.15 - 2.95;P = 0.011)。
血浆uPAR(I)浓度高是卵巢癌患者术前预后不良的独立标志物。血浆suPAR(I-III)+ suPAR(II-III)与CA125的组合鉴别恶性和良性肿瘤的AUC为0.94。