Borgfeldt Christer, Bendahl Pär-Ola, Fernö Mårten, Casslén Bertil
Department of Obstetrics and Gynecology, University Hospital Lund, Sweden.
Gynecol Oncol. 2003 Oct;91(1):112-7. doi: 10.1016/s0090-8258(03)00493-1.
The objective was to evaluate the preoperative blood concentration of tissue plasminogen activator (tPA) as a discriminator between malignant and benign ovarian tumors, and as a potential marker of postoperative prognosis in patients with ovarian cancer.
The concentration of tPA was assayed with ELISA (Imulyse Biopool) in preoperative plasma samples obtained from 111 patients with adnexal lesions. Tumors were classified as benign (n = 25), borderline malignant (n = 11), well-differentiated (G1, n = 22), moderately differentiated (G2, n = 11), and poorly differentiated malignant (G3, n = 42). The median follow-up time of patients with malignant tumors was 5.6 years (range 2.1-13.2 years) and 37 patients died during the follow-up period.
Patients with moderately and poorly differentiated tumors had higher levels of plasma tPA compared to those with well-differentiated tumors (P = 0.004 and P = 0.005). No significant differences in the plasma tPA levels were observed between patients with benign, borderline, and well-differentiated tumors. The tPA levels were not different between stages nor within stage Ia-c. In a multivariate Cox proportional hazards model including stage, grade, age, and plasma tPA dichotomized at the median (> or =9 vs <9 ng/mL), high levels of tPA were significantly associated with shorter survival: HR = 4.4 (95% CI 2.0-9.8, P = 0.0003). In the univariate analyze high levels of tPA showed HR = 4.5 (95% CI 2.1-9.6, P = 0.0003).
High concentration of plasma tPA was an independent marker for poor prognosis in patients with ovarian cancer in our study. Plasma tPA did, however, not discriminate between benign and malignant adnexal lesions.
评估术前组织纤溶酶原激活物(tPA)的血液浓度,以区分恶性和良性卵巢肿瘤,并作为卵巢癌患者术后预后的潜在标志物。
采用酶联免疫吸附测定法(Imulyse Biopool)检测111例附件病变患者术前血浆样本中tPA的浓度。肿瘤分为良性(n = 25)、交界性恶性(n = 11)、高分化(G1,n = 22)、中分化(G2,n = 11)和低分化恶性(G3,n = 42)。恶性肿瘤患者的中位随访时间为5.6年(范围2.1 - 13.2年),37例患者在随访期间死亡。
中分化和低分化肿瘤患者的血浆tPA水平高于高分化肿瘤患者(P = 0.004和P = 0.005)。在良性、交界性和高分化肿瘤患者之间,血浆tPA水平未观察到显著差异。tPA水平在各分期之间以及Ia - c期内均无差异。在一个多变量Cox比例风险模型中,包括分期、分级、年龄和血浆tPA(以中位数9 ng/mL为界分为≥9 ng/mL与<9 ng/mL),tPA水平高与较短生存期显著相关:风险比(HR)= 4.4(95%置信区间2.0 - 9.8,P = 0.0003)。在单变量分析中,tPA水平高显示HR = 4.5(95%置信区间2.1 - 9.6,P = 0.0003)。
在我们的研究中,血浆tPA浓度高是卵巢癌患者预后不良的独立标志物。然而,血浆tPA并不能区分良性和恶性附件病变。