Dorn Julia, Schmitt Manfred, Kates Ronald, Schmalfeldt Barbara, Kiechle Marion, Scorilas Andreas, Diamandis Eleftherios P, Harbeck Nadia
Department of Obstetrics and Gynecology, Klinikum Rechts der Isar, Technical University of Munich, Munich, Germany.
Clin Cancer Res. 2007 Mar 15;13(6):1742-8. doi: 10.1158/1078-0432.CCR-06-2482.
Proteolytic factors of the human tissue kallikrein (hK) family and the plasminogen activation system play a key role in tumor progression in various malignancies. We determined antigen levels of urokinase-type plasminogen activator (uPA), its inhibitor PAI-1, and hK5-8, hK10, hK11, and hK13 by ELISA in primary tumor tissue extracts of 142 International Federation of Gynecology and Obstetrics (FIGO) I to IV ovarian cancer patients (median follow-up 41 months).
After radical surgery, absence of macroscopically visible residual tumor (RT) was achieved in 72 patients; all patients received postoperative platinum-containing chemotherapy. Significant univariate predictors of poor progression-free survival (PFS) were RT (>0), FIGO stages (III/IV versus I/II/III), ascites volume >500 mL, nodal status, and the difference between PAI-1 and uPA (fractionally ranked). In multivariate analysis, significant independent factors for poor PFS were RT [hazard ratio (HR), 4.53] and low hK11 fractional rank (HR, 0.30). Univariate predictors of poor overall survival were RT, FIGO stages, nodal status, ascites volume, nuclear grade, and low hK10 and hK13. In multivariate analysis, significant independent factors for poor overall survival were RT (HR, 7.49), ascites (HR, 1.97), and low hK10 (HR, 0.196). We constructed a multivariate scoring model estimating RT probability, based on ascites [odds ratio (OR), 13.1], nuclear grade (OR, 2.92), hK6 (OR, 8.54), and hK13 (OR, 0.14), with good in-sample predictive performance (area under receiver operating characteristic, 0.833).
In view of risks and benefits of radical surgery, such a score could support preoperative risk stratification and identify candidates for alternative therapeutic strategies. These results highlight the distinct roles of the hKs for different disease end points in ovarian cancer and their potential to support individualized therapy decisions.
人组织激肽释放酶(hK)家族的蛋白水解因子和纤溶酶原激活系统在多种恶性肿瘤的肿瘤进展中起关键作用。我们通过酶联免疫吸附测定法(ELISA)测定了142例国际妇产科联盟(FIGO)I至IV期卵巢癌患者(中位随访41个月)原发肿瘤组织提取物中尿激酶型纤溶酶原激活剂(uPA)、其抑制剂PAI-1以及hK5 - 8、hK10、hK11和hK13的抗原水平。
根治性手术后,72例患者实现了肉眼可见无残留肿瘤(RT);所有患者均接受了含铂术后化疗。无进展生存期(PFS)差的单因素显著预测因素为RT(>0)、FIGO分期(III/IV期与I/II/III期)、腹水体积>500 mL、淋巴结状态以及PAI-1与uPA的差异(分级排序)。多因素分析中,PFS差的显著独立因素为RT [风险比(HR),4.53]和hK11分级排序低(HR,0.30)。总生存期差的单因素预测因素为RT、FIGO分期、淋巴结状态、腹水体积、核分级以及hK10和hK13低。多因素分析中,总生存期差的显著独立因素为RT(HR,7.49)、腹水(HR,1.97)和hK10低(HR,0.196)。我们构建了一个基于腹水[比值比(OR),13.1]、核分级(OR,2.92)、hK6(OR,8.54)和hK13(OR,0.14)估计RT概率的多因素评分模型,其样本内预测性能良好(受试者操作特征曲线下面积,0.833)。
鉴于根治性手术的风险和益处,这样一个评分可以支持术前风险分层并识别替代治疗策略的候选者。这些结果突出了hKs在卵巢癌不同疾病终点中的不同作用及其支持个体化治疗决策的潜力。