regorafenib治疗的难治性结直肠癌患者中的Stanniocalcin 1: TEXCAN和CORRECT试验的事后生物标志物分析

IF 3.3 Q3 ONCOLOGY
Angélique Vienot, Dewi Vernerey, Adeline Bouard, Elodie Klajer, Stefano Kim, Christophe Tournigand, Christophe Louvet, Thierry André, Benoît Rousseau, Mylène Wespiser, Laurie Spehner, Ying A Wang, Anke Weispfenning, Emmanuelle Dochy, Christophe Borg
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引用次数: 0

摘要

化疗难治性转移性结直肠癌(mCRC)缺乏抗血管生成药物的生物标志物。我们在TEXCAN和CORRECT试验中研究了瑞非尼治疗患者的STC1与预后之间的关系。采用ELISA法检测化疗难治性mCRC患者的基线血浆STC1蛋白水平,TEXCAN组(regorafenib组n=48)和CORRECT组(安慰剂组n=211;regorafenib n = 435)。采用Cox比例风险模型评估STC1水平与总生存期(OS)的关系。化疗难治性mCRC患者的STC1中位值(1211 pg/mL)比先前未治疗的患者(215 pg/mL)增加。使用优化的截止值,STC1是OS的预后(HR 2.12, 95% CI 1.79, 2.50;P
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Stanniocalcin 1 in Patients with Refractory Colorectal Cancer Treated with Regorafenib: A Post Hoc Biomarker Analysis of the TEXCAN and CORRECT Trials.

Abstract: Biomarkers for antiangiogenic drugs in chemorefractory metastatic colorectal cancer (mCRC) are lacking. We investigated the relationship between stanniocalcin 1 (STC1) and outcomes in patients treated with regorafenib in the TEXCAN and CORRECT trials. Baseline plasma STC1 protein levels were measured by ELISA from patients with chemorefractory mCRC enrolled in TEXCAN (regorafenib n = 48) and CORRECT (placebo n = 211; regorafenib n = 435). The relationship between STC1 levels and overall survival (OS) was assessed using a Cox proportional hazards model. The median STC1 value was increased in patients with chemorefractory mCRC (1,211 pg/mL) compared with previously untreated patients (215 pg/mL). Using an optimized cut-off, STC1 was prognostic for OS [HR = 2.12, 95% confidence interval (CI), 1.79–2.50; P < 0.001], with a median OS of 7.63 months in the STC1-low group (<1,436.87 pg/mL; n = 400) and 3.81 months in the STC1-high group (≥1,436.87 pg/mL; n = 246). The interaction P value of lactate dehydrogenase and treatment revealed no predictive effect of lactate dehydrogenase levels on OS in terms of regorafenib (P = 0.598). A predictive analysis suggested a significant association between STC1 and regorafenib for OS (interaction P = 0.049). The median OS with regorafenib versus placebo was 8.32 versus 6.54 months in the STC1-low group (HR = 0.83, 95% CI, 0.66–1.03; P = 0.087) and 4.41 versus 3.09 months in the STC1-high group (HR = 0.64, 95% CI, 0.49–0.84; P = 0.001). Altogether, high STC1 protein levels have a predictive potential to characterize a population of patients with chemorefractory mCRC and poor prognosis in whom regorafenib has an increased level of efficacy.

Significance: STC1 is a protein secreted by intratumor endothelial cells in which plasma concentrations increase in patients with chemorefractory mCRC. Based on analyses of patients with refractory mCRC in the TEXCAN and CORRECT trials, we found that STC1 plasma levels had a prognostic role for OS, with high levels associated with poor outcome. A predictive role for baseline STC1 levels was pointed out for regorafenib efficacy.

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