Thymidylate synthase protein expression in primary colorectal cancer: Lack of correlation with outcome and response to fluorouracil in metastatic disease sites

被引:71
作者
Johnston, PG
Benson, AB
Catalano, P
Rao, MS
O'Dwyer, PJ
Allegra, CJ
机构
[1] Queens Univ Belfast, Belfast City Hosp, Dept Oncol, Canc Res Ctr, Belfast BT9 7AB, Antrim, North Ireland
[2] Northwestern Univ, Robert H Lurie Comprehens Canc Ctr, Clin Invest Program, Chicago, IL 60611 USA
[3] Dana Farber Canc Inst, Dept Biostat Sci, Eastern Cooperat Oncol Grp, Ctr Stat, Boston, MA 02115 USA
[4] Northwestern Mem Hosp, Chicago, IL USA
[5] Univ Penn, Philadelphia, PA 19104 USA
[6] NCI, Med Branch, Bethesda, MD 20892 USA
关键词
D O I
10.1200/JCO.2003.07.039
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: The aim of this study was to investigate the utility of quantitating thymidylate synthase (TS) in the primary tumor as a surrogate for metastatic disease sites to predict the likelihood of response and outcome to fluorouracil (FU) treatment in patients with metastatic colorectal cancer. Methods: TS protein expression was evaluated using the TS 106 antibody and the avidin biotin labeling immunahistochemical technique in primary tumor samples from 219 patients with metastatic colorectal cancer. The patients were a representative sample of those patients enrolled into the Eastern Cooperative Oncology Group E2290 protocol that evaluated five separate FU-containing regimens in patients with metastatic residual or recurrent colorectal carcinoma. Results: Our retrospective analysis found that the level and extent of TS protein expression in the primary tumor did not correlate with overall survival in patients with metastatic or recurrent colorectal cancer. A trend toward a direct correlation between the level of TS protein expression and response was noted in tumors that expressed high TS levels. This response advantage for patients expressing high TS levels in the primary tumor was apparent regardless of what FU-based treatment the patient received but was most apparent in the subgroup treated with leucovorin, in which the level of TS expression and response to FU and leucovorin reached statistical significance (P = .034). No significant interaction could be detected between the addition of leucovorin to FU and the level of TS expression in the primary tumor. Conclusion: This study demonstrated that measurement of TS protein levels in the primary tumor tissue does not aid in predicting outcome or response to FU in a metastatic disease site. These assays must be performed on biopsy tissue from the metastatic disease site that is used to radiologically assess response and outcome to treatment. (C) 2003 by American Society of Clinical Oncology.
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页码:815 / 819
页数:5
相关论文
共 21 条
[1]   Investigation of the prognostic and predictive value of thymidylate synthase, p53, and Ki-67 in patients with locally advanced colon cancer [J].
Allegra, CJ ;
Parr, AL ;
Wold, LE ;
Mahoney, MR ;
Sargent, DJ ;
Johnston, P ;
Klein, P ;
Behan, K ;
O'Connell, MJ ;
Levitt, R ;
Kugler, JW ;
Tirona, MT ;
Goldberg, RM .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (07) :1735-1743
[2]  
Aschele C, 2000, CLIN CANCER RES, V6, P4797
[3]  
Cascinu S, 1999, CLIN CANCER RES, V5, P1996
[4]   New concepts for the development and use of antifolates [J].
Chu, E ;
Grem, JL ;
Johnston, PG ;
Allegra, CJ .
STEM CELLS, 1996, 14 (01) :41-46
[5]   THYMIDYLATE SYNTHETASE - TARGET ENZYME IN CANCER CHEMOTHERAPY [J].
DANENBERG, PV .
BIOCHIMICA ET BIOPHYSICA ACTA, 1977, 473 (02) :73-92
[6]   Resistance to Tomudex (ZD1694): Multifactorial in human breast and colon carcinoma cell lines [J].
Drake, JC ;
Allegra, CJ ;
Moran, RG ;
Johnston, PG .
BIOCHEMICAL PHARMACOLOGY, 1996, 51 (10) :1349-1355
[7]   Lack of correlation between thymidylate synthase levels in primary colorectal tumours and subsequent response to chemotherapy [J].
Findlay, MPN ;
Cunningham, D ;
Morgan, G ;
Clinton, S ;
Hardcastle, A ;
Aherne, GW .
BRITISH JOURNAL OF CANCER, 1997, 75 (06) :903-909
[8]   Higher levels of thymidylate synthase gene expression are observed in pulmonary as compared with hepatic metastases of colorectal adenocarcinoma [J].
Gorlick, R ;
Metzger, R ;
Danenberg, KD ;
Salonga, D ;
Miles, JS ;
Longo, GSA ;
Fu, J ;
Banerjee, D ;
Klimstra, D ;
Jhanwar, S ;
Danenberg, PV ;
Kemeny, N ;
Bertino, JR .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (04) :1465-1469
[9]  
GREM JL, 1990, CANC CHEMOTHERAPY PR, P180
[10]   MECHANISMS OF ACQUIRED-RESISTANCE TO THE QUINAZOLINE THYMIDYLATE SYNTHASE INHIBITOR ZD1694 (TOMUDEX) IN ONE MOUSE AND 3 HUMAN CELL-LINES [J].
JACKMAN, AL ;
KELLAND, LR ;
KIMBELL, R ;
BROWN, M ;
GIBSON, W ;
AHERNE, GW ;
HARDCASTLE, A ;
BOYLE, FT .
BRITISH JOURNAL OF CANCER, 1995, 71 (05) :914-924