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组织型纤溶酶原激活剂作为乳腺癌复发的可能指标:一项初步前瞻性研究。

Tissue Plasminogen Activator as a Possible Indicator of Breast Cancer Relapse: A Preliminary, Prospective Study.

作者信息

Wrzeszcz Katarzyna, Słomka Artur, Zarychta Elżbieta, Rhone Piotr, Ruszkowska-Ciastek Barbara

机构信息

Department of Pathophysiology, Faculty of Pharmacy, Nicolaus Copernicus University, Collegium Medicum, 85-094 Bydgoszcz, Poland.

Clinical Ward of Breast Cancer and Reconstructive Surgery, Oncology Centre Prof. F. Łukaszczyk Memorial Hospital, 85-796 Bydgoszcz, Poland.

出版信息

J Clin Med. 2022 Apr 25;11(9):2398. doi: 10.3390/jcm11092398.

Abstract

(1) Background: The fundamental causes of breast cancer mortality are the cancer spread and hypercoagulability state. The study aimed to evaluate the prognostic efficacy of the fibrinolytic profile concerning 5-year follow-up. (2) Methods: We investigated the predictive potential of the plasma activity of urokinase plasminogen activator (u-PA) and plasminogen activator inhibitor type 1 (PAI-1) as well as antigen of tissue plasminogen activator (t-PA), u-PA, PAI-1, and PAI-1/t-PA and PAI-1/u-PA complexes in 41 breast cancer patients. The median follow-up was 66 months, with full evidence of the first event. (3) Results: A significantly lower level of PAI-1 antigen was noted in IBrC patients with lymph node involvement (N1) than in patients with free lymph node metastases (N0). According to ROC curve analysis, a t-PA antigen was the strongest predictor of disease relapse (the area under the curve, AUC = 0.799; p < 0.0006). Patients with PAI-1 activity < 3.04 U/mL had significantly better disease-free survival (DFS) compared to those with PAI-1 activity > 3.04 U/mL. Patients with both t-PA antigen lower than 1.41 ng/mL (cut-off according to median value) and lower than 1.37 ng/mL (cut-off according to ROC curve) had significantly shorter DFS (p = 0.0086; p = 0.0029). (4) Conclusions: The results suggest that a higher plasma t-PA antigen level or lower PAI-1 activity are linked to better outcomes in breast cancer patients.

摘要

(1) 背景:乳腺癌死亡的根本原因是癌症扩散和高凝状态。本研究旨在评估纤维蛋白溶解谱在5年随访中的预后效果。(2) 方法:我们调查了41例乳腺癌患者中尿激酶型纤溶酶原激活剂(u-PA)和纤溶酶原激活物抑制剂1型(PAI-1)的血浆活性以及组织纤溶酶原激活剂(t-PA)、u-PA、PAI-1、PAI-1/t-PA和PAI-1/u-PA复合物的抗原的预测潜力。中位随访时间为66个月,首次事件有充分证据。(3) 结果:有淋巴结受累(N1)的原位乳腺癌(IBrC)患者的PAI-1抗原水平明显低于无淋巴结转移(N0)的患者。根据ROC曲线分析,t-PA抗原是疾病复发的最强预测因子(曲线下面积,AUC = 0.799;p < 0.0006)。与PAI-1活性> 3.04 U/mL的患者相比,PAI-1活性< 3.04 U/mL的患者无病生存期(DFS)明显更好。t-PA抗原低于1.41 ng/mL(根据中位数确定的临界值)且低于1.37 ng/mL(根据ROC曲线确定的临界值)的患者DFS明显更短(p = 0.0086;p = 0.0029)。(4) 结论:结果表明,较高的血浆t-PA抗原水平或较低的PAI-1活性与乳腺癌患者更好的预后相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6ea/9104124/5c2c57fb1e07/jcm-11-02398-g001.jpg

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