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CONFIRM-1 和 -2 临床试验中转移性结直肠癌患者的 TS 和 ERCC-1 mRNA 表达与临床结局。

TS and ERCC-1 mRNA expressions and clinical outcome in patients with metastatic colon cancer in CONFIRM-1 and -2 clinical trials.

机构信息

Department of Molecular Biology and Biochemistry, University of Southern California/Norris Comprehensive Cancer Center, Keck School of Medicine, Los Angeles, CA, USA.

出版信息

Pharmacogenomics J. 2012 Oct;12(5):404-11. doi: 10.1038/tpj.2011.29. Epub 2011 Jul 26.

Abstract

To validate established cutoff levels of thymidylate synthase (TS) and excision repair cross-complementing (ERCC-1) intratumoral mRNA expressions in tumor samples from metastatic colorectal cancer (mCRC) patients treated with PTK787/ZK222584 (PTK/ZK). From 122 samples of patients with mCRC enrolled in CONFIRM-1 (Colorectal Oral Novel Therapy for the Inhibition of Angiogenesis and Retarding of Metastases) or CONFIRM-2, mRNA was isolated of microdissected formalin-fixed paraffin-embedded samples and quantitated using TaqMan-based technology. Existing TS and ERCC-1 cutoff levels were tested for their prognostic value in first-line and second-line therapy. TS expression was associated with overall survival (OS) in first-line, but not second-line therapy. ERCC-1 was associated with OS in patients treated with first-line and second-line FOLFOX4. In first-line FOLFOX4, combination of high TS and/or high ERCC-1 was associated with shorter OS. A correlation was observed between ERCC-1 expression and benefit from PTK/ZK+FOLFOX4 treatment. TS and ERCC-1 expression is associated with clinical outcome in mCRC. Baseline TS and ERCC-1 levels may allow the selection of patients who benefit from FOLFOX4 chemotherapy.

摘要

为了验证在转移性结直肠癌(mCRC)患者的肿瘤样本中,胸腺嘧啶核苷合成酶(TS)和切除修复交叉互补基因 1(ERCC-1)的肿瘤内 mRNA 表达的既定截止水平,这些患者接受了 PTK787/ZK222584(PTK/ZK)的治疗。从参加 CONFIRM-1(结直肠口服新型抗血管生成和转移抑制疗法)或 CONFIRM-2 的 122 名 mCRC 患者的样本中,分离了微切割福尔马林固定石蜡包埋样本中的 mRNA,并使用 TaqMan 技术进行定量。对现有 TS 和 ERCC-1 的截止水平进行了测试,以评估其在一线和二线治疗中的预后价值。在一线治疗中,TS 表达与总生存期(OS)相关,但在二线治疗中不相关。ERCC-1 与一线和二线 FOLFOX4 治疗的患者的 OS 相关。在一线 FOLFOX4 治疗中,高 TS 和/或高 ERCC-1 联合与较短的 OS 相关。观察到 ERCC-1 表达与 PTK/ZK+FOLFOX4 治疗获益之间存在相关性。TS 和 ERCC-1 的表达与 mCRC 的临床结果相关。基线 TS 和 ERCC-1 水平可能允许选择从 FOLFOX4 化疗中获益的患者。

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