ERCC1 and thymidylate synthase mRNA levels predict survival for colorectal cancer patients receiving combination oxaliplatin and fluorouracil chemotherapy

被引:545
作者
Shirota, Y
Stoehlmacher, J
Brabender, J
Xiang, YP
Uetake, H
Danenberg, KD
Groshen, S
Tsao-Wei, DD
Danenberg, PV
Lenz, HJ
机构
[1] Univ So Calif, Kenneth Norris Jr Comprehens Canc Ctr, Gastrointestinal Oncol Program, Los Angeles, CA 90033 USA
[2] Response Genet Inc, Los Angeles, CA USA
关键词
D O I
10.1200/JCO.2001.19.23.4298
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To test the hypotheses of whether the relative mRNA expression of the thymidylate synthase (TS) gene and the excision cross-complementing (ERCC1) gene are associated with response to and survival of fluorouracil (5-FU)/oxaliplatin chemotherapy in metastatic colorectal cancer. Patients and Methods: Patients had progressive stage IV disease after unsuccessful 5-FU and irinotecan chemotherapy. All patients were evaluated for eligibility for a compassionate 5-FU/oxaliplatin protocol. cDNA was derived from paraffin-embedded tumor specimens to determine TS and ERCC1 mRNA expression relative to the internal reference gene beta-actin using fluorescence-based, real-time reverse transcriptase polymerase chain reaction. Results: The median TS gene expression level from 50 metastasized tumors was 3.4 x 10(-3) (minimum expression, 0.18 x 10(-3); maximum expression, 11.5 x 10(-3)), and the median ERCC1 gene expression level was 2.53 x 10(-3) (minimum, 0.0; maximum, 14.61 x 10(-3)). The gene expression cutoff values for chemotherapy nonresponse were 7.5 x 10(-3) for TS and 4.9 x 10(-3) for ERCC1. The median survival time for patients with TS less than or equal to 7.5 x 10(-3) (43 of 50 patients) was 10.2 months, compared with 1.5 months for patients with TS greater than 7.5 x 10(-3) (p <.001). Patients with ERCC1 expression <less than or equal to> 4.9 x 10(-3) (40 of 50 patients) had a median survival time of 10.2 months, compared with 1.9 months for patients with ERCC1 expression greater than 4.9 x 10(-3) (P <.001). A TS of 7.5 x 10(-3) segregated significantly into response, stable disease, and progression (P =.02), whereas the association between ERCC1 and response did not reach statistical significance (P =.29). Conclusion: These data suggest that intratumoral ERCC1 mRNA and TS mRNA expression levels are independent predictive markers of survival for 5-FU and oxaliplatin combination chemotherapy in 5-FU-resistant metastatic colorectal cancer. Precise definition of the best TS cut point will require further analysis in a large, prospective study. J Clin Oncol 19:4298-4304. (C) 2001 by American Society of Clinical Oncology.
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页码:4298 / 4304
页数:7
相关论文
共 35 条
[1]   Factors predicting for efficacy of oxaliplatin in combination with 5-fluorouracil (5-FU)±folinic acid (FA) in a compassionate-use cohort of 370 5-FU-resistant advanced colorectal cancer (CRC) patients [J].
Bensmaïne, MA ;
de Gramont, A ;
Brienza, S ;
Marty, M ;
Lévi, F ;
Ducreux, M ;
François, E ;
Gamelin, E ;
Bleiberg, H ;
Bleuzen, P ;
Simon, J ;
Cvitkovic, E .
EUROPEAN JOURNAL OF CANCER, 2000, 36 (18) :2335-2343
[2]  
Bleiberg H, 1996, SEMIN ONCOL, V23, P42
[3]   Reduced expression levels of nucleotide excision repair genes in lung cancer: a case-control analysis [J].
Cheng, L ;
Spitz, MR ;
Hong, WK ;
Wei, QY .
CARCINOGENESIS, 2000, 21 (08) :1527-1530
[4]   Oxaliplatin - A review of its pharmacological properties and clinical efficacy in metastatic colorectal cancer and its potential in other malignancies [J].
Culy, CR ;
Clemett, D ;
Wiseman, LR .
DRUGS, 2000, 60 (04) :895-924
[5]  
DABOLKAR M, 1992, J NATL CANCER I, V84, P1512
[6]   Oxaliplatin with high-dose leucovorin and 5-fluorouracil 48 hour continuous infusion in pretreated metastatic colorectal cancer [J].
deGramont, A ;
Vignoud, J ;
Tournigand, C ;
Louvet, C ;
Andre, T ;
Varette, C ;
Raymond, E ;
Moreau, S ;
LeBail, N ;
Krulik, M .
EUROPEAN JOURNAL OF CANCER, 1997, 33 (02) :214-219
[7]   Cisplatin and adriamycin resistance are associated with MutL alpha and mismatch repair deficiency in an ovarian tumor cell line [J].
Drummond, JT ;
Anthoney, A ;
Brown, R ;
Modrich, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (33) :19645-19648
[8]   Comparative cytotoxicity of oxaliplatin and cisplatin in non-seminomatous germ cell cancer cell lines [J].
Dunn, TA ;
Schmoll, HJ ;
Grunwald, V ;
Bokemeyer, C ;
Casper, J .
INVESTIGATIONAL NEW DRUGS, 1997, 15 (02) :109-114
[9]  
Fink D, 1996, CANCER RES, V56, P4881
[10]  
Fink D, 1997, CANCER RES, V57, P1841