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

被引:34
作者
Grimminger, P. P. [2 ,3 ]
Shi, M. [4 ]
Barrett, C. [4 ]
Lebwohl, D. [4 ]
Danenberg, K. D. [5 ]
Brabender, J. [3 ]
Vigen, C. L. P. [6 ]
Danenberg, P. V. [2 ]
Winder, T. [1 ]
Lenz, H-J [1 ]
机构
[1] Univ So Calif, Keck Sch Med, Div Med Oncol, Norris Comprehens Canc Ctr, Los Angeles, CA 90033 USA
[2] Univ So Calif, Keck Sch Med, Dept Mol Biol & Biochem, Norris Comprehens Canc Ctr, Los Angeles, CA 90033 USA
[3] Univ Cologne, Dept General Visceral & Tumor Surg, D-50931 Cologne, Germany
[4] Novartis Pharmaceut, E Hanover, NJ USA
[5] Response Genet Inc, Los Angeles, CA USA
[6] Univ So Calif, Keck Sch Med, Div Biostat, Los Angeles, CA 90033 USA
关键词
colorectal cancer; CONFIRM; prognostic; FOLFOX4; PTK/ZK; survival; THYMIDYLATE SYNTHASE EXPRESSION; NUCLEOTIDE EXCISION-REPAIR; COLORECTAL-CANCER; GENE-EXPRESSION; DIHYDROPYRIMIDINE DEHYDROGENASE; PREOPERATIVE CHEMORADIOTHERAPY; PROTRACTED-INFUSION; PROGNOSTIC VALUE; FLUOROURACIL; SURVIVAL;
D O I
10.1038/tpj.2011.29
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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. The Pharmacogenomics Journal (2012) 12, 404-411; doi:10.1038/tpj.2011.29; published online 26 July 2011
引用
收藏
页码:404 / 411
页数:8
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