Blomberg Kristian, Hansen Torben F, Brasen Claus L, Madsen Jeppe B, Jensen Lars H, Thomsen Caroline B
Department of Health Science, University of Southern Denmark, 5000 Odense, Denmark.
Danish Colorectal Cancer Center South, Department of Oncology, University Hospital of Southern Denmark, 7100 Vejle, Denmark.
Cancers (Basel). 2021 Oct 12;13(20):5100. doi: 10.3390/cancers13205100.
The soluble urokinase-type plasminogen activator receptor (suPAR) is prognostic for overall survival (OS) in colorectal cancer (CRC). Our study explored the association between baseline suPAR and OS and progression-free survival (PFS) in metastatic CRC (mCRC). It is also the first study to explore the association between the initial change in suPAR level and OS, PFS and the first CT response evaluation. The study included 132 patients with mCRC treated with chemotherapy (FOLFIRI) with or without an EGFR-inhibitor. Blood samples were drawn before the first treatment cycle and in between the first and second treatment cycle. suPAR levels were determined using an ELISA assay. Using the Kaplan-Meyer method, we demonstrated a significantly shorter OS for patients with suPAR levels above the median (HR = 1.79, 95%CI = 1.10-2.92, = 0.01). We also showed association between plasma suPAR level, gender and performance status (PS). However, we could not show any association with PFS, and analysis on the change in suPAR level provided no significant results. The results showing association between baseline suPAR and OS are in line with previous findings.
可溶性尿激酶型纤溶酶原激活物受体(suPAR)可预测结直肠癌(CRC)患者的总生存期(OS)。我们的研究探讨了转移性结直肠癌(mCRC)患者基线suPAR水平与OS及无进展生存期(PFS)之间的关联。这也是第一项探索suPAR水平的初始变化与OS、PFS及首次CT反应评估之间关联的研究。该研究纳入了132例接受化疗(FOLFIRI)联合或不联合表皮生长因子受体(EGFR)抑制剂治疗的mCRC患者。在第一个治疗周期前以及第一个和第二个治疗周期之间采集血样。采用酶联免疫吸附测定(ELISA)法测定suPAR水平。使用Kaplan - Meyer方法,我们发现suPAR水平高于中位数的患者OS显著缩短(风险比[HR]=1.79,95%置信区间[CI]=1.10 - 2.92,P = 0.01)。我们还发现血浆suPAR水平与性别及体能状态(PS)之间存在关联。然而,我们未发现其与PFS存在任何关联,并且对suPAR水平变化的分析未得出显著结果。基线suPAR与OS之间存在关联的结果与先前的研究结果一致。