Department of Surgical Gastroenterology, Hvidovre University Hospital, Hvidovre, Denmark.
Ann Oncol. 2011 Feb;22(2):369-75. doi: 10.1093/annonc/mdq354. Epub 2010 Jul 19.
The aim was to evaluate the association between plasma tissue inhibitor of metalloproteinase-1 (TIMP-1) and serum carcinoembryonic antigen (CEA) levels and outcome in patients with metastatic colorectal cancer (mCRC) receiving XELOX (combination chemotherapy with capecitabine and oxaliplatin) as first-line treatment.
One hundred and twenty patients were included. Blood samples were collected before treatment and 3 weeks later before the next treatment cycle. Plasma TIMP-1 and serum CEA levels were correlated to treatment outcome.
No significant associations between baseline TIMP-1 or CEA levels and best response to treatment or progression-free survival (PFS) could be demonstrated. In contrast, high baseline plasma TIMP-1 levels were associated with poor overall survival (OS), P = 0.008, hazard ratio (HR) = 1.80 [95% confidence interval (CI): 1.17-2.78]. Furthermore, increase in TIMP-1 levels from baseline to immediately before the second cycle of chemotherapy had a significant negative effect on survival (P = 0.03, HR = 1.30, 95% CI: 1.02-1.65) while a decrease in TIMP-1 was significantly associated with a higher objective response rate (P = 0.03).
Both high baseline and subsequent increase in TIMP-1 levels were associated with shorter OS in patients with mCRC receiving XELOX as first-line treatment, whereas baseline TIMP-1 levels were not associated with response or PFS following XELOX treatment.
本研究旨在评估转移性结直肠癌(mCRC)患者接受 XELOX(卡培他滨联合奥沙利铂的联合化疗)一线治疗时,血浆组织金属蛋白酶抑制剂-1(TIMP-1)和血清癌胚抗原(CEA)水平与预后的关系。
共纳入 120 例患者。在治疗前和下一治疗周期前 3 周采集血样。将血浆 TIMP-1 和血清 CEA 水平与治疗结果相关联。
基线 TIMP-1 或 CEA 水平与最佳治疗反应或无进展生存期(PFS)之间无显著相关性。相比之下,高基线血浆 TIMP-1 水平与总生存期(OS)较差相关,P=0.008,风险比(HR)=1.80[95%置信区间(CI):1.17-2.78]。此外,从基线到化疗第二周期前 TIMP-1 水平的升高对生存有显著的负面影响(P=0.03,HR=1.30,95%CI:1.02-1.65),而 TIMP-1 的降低与更高的客观缓解率显著相关(P=0.03)。
在接受 XELOX 一线治疗的 mCRC 患者中,基线时及随后 TIMP-1 水平升高均与 OS 较短相关,而基线 TIMP-1 水平与 XELOX 治疗后的反应或 PFS 无关。