Riisbro R, Stephens R W, Brünner N, Christensen I J, Nielsen H J, Heilmann L, von Tempelhoff G F
Finsen Laboratory, Rigshospitalet, DK-2100 Copenhagen, Denmark.
Gynecol Oncol. 2001 Sep;82(3):523-31. doi: 10.1006/gyno.2001.6324.
The present study was planned to measure preoperative levels of soluble urokinase plasminogen activator receptor (suPAR) in plasma from patients with gynecological diseases, and to test for a relationship to clinical and biochemical patient characteristics.
Using a specific and sensitive kinetic ELISA, suPAR levels were determined in preoperative citrate plasma samples from 53 ovarian, 34 endometrial, and 30 cervical cancer patients, 17 patients with benign ovarian tumors, and 28 patients with benign endometrial diseases. In addition, suPAR was measured in citrate samples from 31 female blood donors.
suPAR was measurable in all samples. No significant difference was found between plasma suPAR in the blood donors and the patients with benign diseases (P = 0.58). The groups of cancer patients had suPAR levels that were significantly higher than those found in the blood donors (P < 0.0001, P < 0.0001, and P = 0.001 for patients with ovarian, endometrial, and cervical cancer, respectively). In all groups of cancer patients a trend toward increasing suPAR levels with increasing FIGO stage was noted (P = 0.0003, P = 0.02, and P = 0.01 for patients with ovarian, endometrial, and cervical cancer, respectively). Using the median suPAR level to dichotomize the ovarian cancer patients, FIGO stages I-III, a significantly increased risk of progression/relapse was found for patients with high suPAR levels (Hazard ratio (HR) = 3.1, 95% CI: 1.1-8.8, P = 0.03). A multivariate analysis was performed, including suPAR, FIGO stage, and CA-125. Only FIGO stage III compared with FIGO stage I was significant (HR = 15, 95% CI: 1.8-129, P = 0.01). Survival analyses were not performed in the endometrial or cervical cancer patients due to few progressions/relapses during the follow-up period.
This study concludes that patients with gynecological cancers have elevated plasma suPAR levels as compared with healthy female blood donors and patients with benign gynecological diseases. In addition, high preoperative plasma levels of suPAR are significantly associated with poor outcome of ovarian cancer patients. However, additional studies are needed to further validate the clinical usefulness of plasma suPAR measurements in the management of ovarian cancer patients.
本研究旨在测定妇科疾病患者术前血浆中可溶性尿激酶型纤溶酶原激活物受体(suPAR)的水平,并检测其与患者临床及生化特征之间的关系。
采用特异性和敏感性均较高的动力学酶联免疫吸附测定法(ELISA),测定53例卵巢癌、34例子宫内膜癌、30例宫颈癌患者,17例卵巢良性肿瘤患者及28例子宫内膜良性疾病患者术前枸橼酸盐血浆样本中的suPAR水平。此外,还测定了31名女性献血者枸橼酸盐样本中的suPAR水平。
所有样本中均可检测到suPAR。献血者与良性疾病患者血浆中的suPAR水平无显著差异(P = 0.58)。癌症患者组的suPAR水平显著高于献血者(卵巢癌、子宫内膜癌和宫颈癌患者的P值分别为P < 0.0001、P < 0.0001和P = 0.001)。在所有癌症患者组中,均发现随着国际妇产科联盟(FIGO)分期增加,suPAR水平有升高趋势(卵巢癌、子宫内膜癌和宫颈癌患者的P值分别为P = 0.0003、P = 0.02和P = 0.01)。以suPAR水平中位数对卵巢癌患者(FIGO分期I - III期)进行二分法分析,发现suPAR水平高的患者进展/复发风险显著增加(风险比(HR)= 3.1,95%置信区间:1.1 - 8.8,P = 0.03)。进行了多因素分析,纳入suPAR、FIGO分期和CA - 125。仅FIGO III期与FIGO I期相比差异有统计学意义(HR = 15,95%置信区间:1.8 - 129,P = 0.01)。由于子宫内膜癌和宫颈癌患者在随访期间进展/复发较少,未对其进行生存分析。
本研究得出结论,与健康女性献血者及妇科良性疾病患者相比,妇科癌症患者血浆suPAR水平升高。此外,术前血浆suPAR水平高与卵巢癌患者预后不良显著相关。然而,需要进一步研究以进一步验证血浆suPAR检测在卵巢癌患者管理中的临床实用性。